-
1
-
-
0026715570
-
Molecular basis for differences in susceptibility to toxicants, introduction
-
Boobis, A.R., Molecular basis for differences in susceptibility to toxicants, introduction. Toxicol. Lett. 64/65, 109, 1992.
-
(1992)
Toxicol. Lett.
, vol.64-65
, pp. 109
-
-
Boobis, A.R.1
-
2
-
-
0028237729
-
Inter-individual variations in human liver cytochrome P-450 enzymes involved in the oxidation of drugs, carcinogens and toxic chemicals, Studies with liver microsomes of 30 Japanese and 30 Caucasians
-
Shimada, T., Yamazaki, H., Mimura, M., Inui, Y., and Guengerich, F.P., Inter-individual variations in human liver cytochrome P-450 enzymes involved in the oxidation of drugs, carcinogens and toxic chemicals, Studies with liver microsomes of 30 Japanese and 30 Caucasians. J. Pharmacol. Exp. Ther. 270, 414, 1994.
-
(1994)
J. Pharmacol. Exp. Ther.
, vol.270
, pp. 414
-
-
Shimada, T.1
Yamazaki, H.2
Mimura, M.3
Inui, Y.4
Guengerich, F.P.5
-
3
-
-
0028960012
-
Polymorphism in drug conjugation in man, is it a factor of concern in drug toxicity or efficacy?
-
Mulder, G.J., Polymorphism in drug conjugation in man, is it a factor of concern in drug toxicity or efficacy? Eur. J. Pharm. Sci. 3, 57, 1995.
-
(1995)
Eur. J. Pharm. Sci.
, vol.3
, pp. 57
-
-
Mulder, G.J.1
-
4
-
-
0029095756
-
Glutathione conjugation with 1-chloro-2, 4-dinitrobenzene (CDNB), inter-individual variability in human liver, lung, kidney and intestine
-
Temellini, A., Castiglioni, M., Giuliani, L., Mussi, A., Giulianotti, P.C., Pietrabissa, A., Angeletti, C.A., Mosca, F., and Pacifici, G.M., Glutathione conjugation with 1-chloro-2, 4-dinitrobenzene (CDNB), inter-individual variability in human liver, lung, kidney and intestine. Int. J. Clin. Pharmacol. Ther. 33, 498, 1995.
-
(1995)
Int. J. Clin. Pharmacol. Ther.
, vol.33
, pp. 498
-
-
Temellini, A.1
Castiglioni, M.2
Giuliani, L.3
Mussi, A.4
Giulianotti, P.C.5
Pietrabissa, A.6
Angeletti, C.A.7
Mosca, F.8
Pacifici, G.M.9
-
5
-
-
0029760232
-
Inter-individual variability in catalytic activity and immunoreactivity of three major human liver cytochrome P450 isozymes
-
Transon, C., Lecoeur, S., Leemann, T., Beaune, P., and Dayer, P., Inter-individual variability in catalytic activity and immunoreactivity of three major human liver cytochrome P450 isozymes. Eur. J. Clin. Pharmacol. 51, 79, 1996.
-
(1996)
Eur. J. Clin. Pharmacol.
, vol.51
, pp. 79
-
-
Transon, C.1
Lecoeur, S.2
Leemann, T.3
Beaune, P.4
Dayer, P.5
-
6
-
-
0030588284
-
Inter-individual variability in metabolic activation in humans in vivo
-
Boobis, A.R., Inter-individual variability in metabolic activation in humans in vivo. Environ. Toxicol. and Pharmacol. 2, 161, 1996.
-
(1996)
Environ. Toxicol. and Pharmacol.
, vol.2
, pp. 161
-
-
Boobis, A.R.1
-
7
-
-
0028950447
-
A note on individual differences in the urinary excretion of optical enantiomers of styrene metabolites and of styrene-derived mercapturic acids in humans
-
Hallier, E., Goergens, H.W., Karels, H., and Golka, K., A note on individual differences in the urinary excretion of optical enantiomers of styrene metabolites and of styrene-derived mercapturic acids in humans. Arch. Toxicol. 69, 300, 1995.
-
(1995)
Arch. Toxicol.
, vol.69
, pp. 300
-
-
Hallier, E.1
Goergens, H.W.2
Karels, H.3
Golka, K.4
-
8
-
-
0028343118
-
Genotoxic risk for humans due to work place exposure to ethylene oxide, remarkable individual differences in susceptibility
-
Fuchs, J., Wullenweber, U., Hengstler, J.G., Bienfait, H.G., Hiltl, G., and Oesch, F., Genotoxic risk for humans due to work place exposure to ethylene oxide, remarkable individual differences in susceptibility. Arch, Toxicol. 68, 343, 1994.
-
(1994)
Arch, Toxicol.
, vol.68
, pp. 343
-
-
Fuchs, J.1
Wullenweber, U.2
Hengstler, J.G.3
Bienfait, H.G.4
Hiltl, G.5
Oesch, F.6
-
9
-
-
0028997489
-
Inter-individual differences in the concentration of 1-hydroxypyrene-glucuronide in urine and polycyclic aromatic hydrocarbon-DNA adducts in peripheral white blood cells after charbroiled beef consumption
-
Kang, D.H., Rothman, N., Poirier, M.C., Greenberg, A., Hsu, C.H., Schwartz, B.S., Baser, M.E., Groopman, J.D., Weston, A., and Strickland, P.T., Inter-individual differences in the concentration of 1-hydroxypyrene-glucuronide in urine and polycyclic aromatic hydrocarbon-DNA adducts in peripheral white blood cells after charbroiled beef consumption. Carcinogenesis, 16, 1079, 1995.
-
(1995)
Carcinogenesis
, vol.16
, pp. 1079
-
-
Kang, D.H.1
Rothman, N.2
Poirier, M.C.3
Greenberg, A.4
Hsu, C.H.5
Schwartz, B.S.6
Baser, M.E.7
Groopman, J.D.8
Weston, A.9
Strickland, P.T.10
-
10
-
-
0013552024
-
Overview of pharmacogenetics
-
Kalow, W., Pergamon Press Inc., New York
-
Du, B.N. La, Overview of pharmacogenetics. In: Pharmacogenetics of drug metabolism, Kalow, W., Pergamon Press Inc., New York, 1992, 1-12.
-
(1992)
Pharmacogenetics of Drug Metabolism
, pp. 1-12
-
-
La Du, B.N.1
-
11
-
-
0013490724
-
Molecular genetics and the future of pharmacogenetics
-
Kalow, W., Pergamon Press Inc., New York
-
11. Meyer, U.A., Molecular genetics and the future of pharmacogenetics. In: Pharmacogenetics of Drug Metabolism, Kalow, W., Pergamon Press Inc., New York, 1992, 879-888.
-
(1992)
Pharmacogenetics of Drug Metabolism
, pp. 879-888
-
-
Meyer, U.A.1
-
12
-
-
0023215491
-
Genetic factors in toxicology. Implications for toxicological screening
-
Festing, M.F.W., Genetic factors in toxicology. Implications for toxicological screening. CRC Crit. Rev. Toxicol. 18, 1, 1987.
-
(1987)
CRC Crit. Rev. Toxicol.
, vol.18
, pp. 1
-
-
Festing, M.F.W.1
-
13
-
-
0026716854
-
Genetically determined differences in drug metabolism as a risk factor in drug toxicity
-
Eichelbaum, M., Kroemer, H.K., and Mikus, G., Genetically determined differences in drug metabolism as a risk factor in drug toxicity. Toxicol. Lett. 64/ 65, 115, 1992.
-
(1992)
Toxicol. Lett.
, vol.64-65
, pp. 115
-
-
Eichelbaum, M.1
Kroemer, H.K.2
Mikus, G.3
-
14
-
-
0028225674
-
Genetic and individual differences in the process of biotransformation and their relevance for occupational medicine
-
Bolt, H.M., Genetic and individual differences in the process of biotransformation and their relevance for occupational medicine. Med. Lav. 85, 37, 1994.
-
(1994)
Med. Lav.
, vol.85
, pp. 37
-
-
Bolt, H.M.1
-
15
-
-
0027186219
-
Genetically determined adverse durg reactions involving metabolism
-
Lennard, M.S., Genetically determined adverse durg reactions involving metabolism. Drug Safety, 9, 60, 1993.
-
(1993)
Drug Safety
, vol.9
, pp. 60
-
-
Lennard, M.S.1
-
16
-
-
0025729217
-
Clinical consequences of polymorphic drug oxidation
-
Alvan, G., Clinical consequences of polymorphic drug oxidation. Fundam. Clin. Pharmacol. 5, 209, 1991.
-
(1991)
Fundam. Clin. Pharmacol.
, vol.5
, pp. 209
-
-
Alvan, G.1
-
17
-
-
0025797108
-
Genetic and environmental factors causing variation in drug response
-
Vesell, E.S., Genetic and environmental factors causing variation in drug response. Mutat. Res. 247, 241, 1991.
-
(1991)
Mutat. Res.
, vol.247
, pp. 241
-
-
Vesell, E.S.1
-
18
-
-
0028289040
-
Clinical implications of genetic polymorphism in drug metabolism
-
Tucker, G.T., Clinical implications of genetic polymorphism in drug metabolism. J. Pharm. Pharmacol. 46, 417, 1994.
-
(1994)
J. Pharm. Pharmacol.
, vol.46
, pp. 417
-
-
Tucker, G.T.1
-
19
-
-
0013524402
-
Genetic and inter-ethnic variability in drug metabolism, What are the clinical consequences?
-
Besancon, May 1995, Alvan, G., Balant, L.P., Bechtel, P.R., Boobis, A.R., Gram, L.F., Paintaud, G., and Pithan, K., Luxembourg, EU
-
Gram, L.F., Brosen, K., Sindrup, S., and Skjelbo, E., Genetic and inter-ethnic variability in drug metabolism, What are the clinical consequences? In: Proceedings of the COST B1 European Conference on Specificity and Variability in Drug Metabolism, Besancon, May 1995, Alvan, G., Balant, L.P., Bechtel, P.R., Boobis, A.R., Gram, L.F., Paintaud, G., and Pithan, K., Luxembourg, EU, 1995, 235-245.
-
(1995)
Proceedings of the COST B1 European Conference on Specificity and Variability in Drug Metabolism
, pp. 235-245
-
-
Gram, L.F.1
Brosen, K.2
Sindrup, S.3
Skjelbo, E.4
-
20
-
-
0029808456
-
Influence of pharmacogenetics on drug disposition and response
-
Eichelbaum, M. and Evert, B., Influence of pharmacogenetics on drug disposition and response. Clin. Exp. Pharmacol. Physiol. 23, 983, 1996.
-
(1996)
Clin. Exp. Pharmacol. Physiol.
, vol.23
, pp. 983
-
-
Eichelbaum, M.1
Evert, B.2
-
21
-
-
0031023815
-
Pharmacogenetics, a laboratory tool for optimizing therapeutic efficiency
-
Linder, M.W., Prough, R.A., and Valdes, R., Jr., Pharmacogenetics, a laboratory tool for optimizing therapeutic efficiency. Clin. Chem. 43, 254, 1997.
-
(1997)
Clin. Chem.
, vol.43
, pp. 254
-
-
Linder, M.W.1
Prough, R.A.2
Valdes R., Jr.3
-
22
-
-
0025540484
-
Metabolic factors in cancer susceptibility
-
Wolf, C.R., Metabolic factors in cancer susceptibility. Cancer Surveys, 9, 437, 1990.
-
(1990)
Cancer Surveys
, vol.9
, pp. 437
-
-
Wolf, C.R.1
-
23
-
-
0025569330
-
The contribution of inherited predisposition to cancer incidence
-
Easton, D. and Peto, J., The contribution of inherited predisposition to cancer incidence. Cancer Surv. 9, 395, 1990.
-
(1990)
Cancer Surv.
, vol.9
, pp. 395
-
-
Easton, D.1
Peto, J.2
-
24
-
-
0025817167
-
Is environmental carcinogenesis modulated by host polymorphism?
-
Idle, J.R., Is environmental carcinogenesis modulated by host polymorphism? Mutat. Res. 247, 259, 1991.
-
(1991)
Mutat. Res.
, vol.247
, pp. 259
-
-
Idle, J.R.1
-
25
-
-
0026240006
-
Relevance of metabolic polymorphisms to human carcinogenesis, evaluation of epidemiologic evidence
-
Caporaso, N., Landi, M.T., and Vineis, P., Relevance of metabolic polymorphisms to human carcinogenesis, evaluation of epidemiologic evidence. Pharmacogenetics 1, 4, 1991.
-
(1991)
Pharmacogenetics
, vol.1
, pp. 4
-
-
Caporaso, N.1
Landi, M.T.2
Vineis, P.3
-
26
-
-
0025859220
-
Role of genetics and drug metabolism in human cancer risk
-
Nebert, D.W., Role of genetics and drug metabolism in human cancer risk. Mutat. Res. 247, 267, 1991.
-
(1991)
Mutat. Res.
, vol.247
, pp. 267
-
-
Nebert, D.W.1
-
27
-
-
0026922775
-
Host factors in lung cancer risk, a review of interdisciplinary studies
-
Amos, C.I., Caporaso, N.E., and Weston, A., Host factors in lung cancer risk, a review of interdisciplinary studies. Cancer Epidemiol. Biomark. Prevent. 1, 505, 1992.
-
(1992)
Cancer Epidemiol. Biomark. Prevent.
, vol.1
, pp. 505
-
-
Amos, C.I.1
Caporaso, N.E.2
Weston, A.3
-
28
-
-
0028365397
-
Mechanisms of carcinogenesis and individual susceptibility to cancer
-
Venitt, S., Mechanisms of carcinogenesis and individual susceptibility to cancer. Clin. Chem. 40, 1421, 1994.
-
(1994)
Clin. Chem.
, vol.40
, pp. 1421
-
-
Venitt, S.1
-
29
-
-
0029000305
-
Cancer genes, single and susceptibility, exposing the difference
-
Caporaso, N. and Goldstein, A., Cancer genes, single and susceptibility, exposing the difference. Pharmacogenetics 5, 59, 1995.
-
(1995)
Pharmacogenetics
, vol.5
, pp. 59
-
-
Caporaso, N.1
Goldstein, A.2
-
30
-
-
0027026424
-
The pharmacogenetics of chemical carcinogenesis
-
Idle, J.R., Armstrong, M., Boddy, A.V., Boustead, C., Cholerton, S., Cooper, J., Daly, A.K., Ellis, J., Gregory, W., Hadidi, H., Hofer, C., Holt, J., Leathart, J., McCracken, N., Monkman, S.C., Painter, J.E., Taber, H., Walker, D., and Yule, M., The pharmacogenetics of chemical carcinogenesis. Pharmacogenetics 2, 246, 1992.
-
(1992)
Pharmacogenetics
, vol.2
, pp. 246
-
-
Idle, J.R.1
Armstrong, M.2
Boddy, A.V.3
Boustead, C.4
Cholerton, S.5
Cooper, J.6
Daly, A.K.7
Ellis, J.8
Gregory, W.9
Hadidi, H.10
Hofer, C.11
Holt, J.12
Leathart, J.13
McCracken, N.14
Monkman, S.C.15
Painter, J.E.16
Taber, H.17
Walker, D.18
Yule, M.19
-
31
-
-
0027032111
-
Metabolic cytochrome P450 genotypes and assessment of individual susceptibility to lung cancer
-
Hirvonen, A., Husgafvel-Pursiainen, K., Anttila, S., Karjalainen, A., Sorsa, M., and Vainio, H., Metabolic cytochrome P450 genotypes and assessment of individual susceptibility to lung cancer. Pharmacogenetics 2, 259, 1992.
-
(1992)
Pharmacogenetics
, vol.2
, pp. 259
-
-
Hirvonen, A.1
Husgafvel-Pursiainen, K.2
Anttila, S.3
Karjalainen, A.4
Sorsa, M.5
Vainio, H.6
-
32
-
-
0027033317
-
Genetic polymorphism of cytochromes P450, inter-ethnic differences and relationship to incidence of lung cancer
-
Ingelman -Sundberg, M., Johansson, I., Persson, I., Yue, Q.-Y., Dahl, M.-L., Bertilsson, L., and Sjoqvist, F., Genetic polymorphism of cytochromes P450, inter-ethnic differences and relationship to incidence of lung cancer. Pharmacogenetics 2, 264, 1992.
-
(1992)
Pharmacogenetics
, vol.2
, pp. 264
-
-
Ingelman-Sundberg, M.1
Johansson, I.2
Persson, I.3
Yue, Q.-Y.4
Dahl, M.-L.5
Bertilsson, L.6
Sjoqvist, F.7
-
33
-
-
0002006730
-
Polymorphic enzymes and cancer risk, Concepts, methodology and data review
-
Kalow, W., Pergamon Press Inc., New York
-
Roots, I., Drakoulis, N., and Brockmoller, J., Polymorphic enzymes and cancer risk, Concepts, methodology and data review. In: Pharmacogenetics of Drug Metabolism, Kalow, W., Pergamon Press Inc., New York, 1992, 815-841.
-
(1992)
Pharmacogenetics of Drug Metabolism
, pp. 815-841
-
-
Roots, I.1
Drakoulis, N.2
Brockmoller, J.3
-
34
-
-
0027463280
-
Cancer risk related to genetic polymorphisms in carcinogen metabolism and DNA repair
-
Poulsen, H.E., Loft, S., and Wassermann, K., Cancer risk related to genetic polymorphisms in carcinogen metabolism and DNA repair. Pharmacol. Toxicol. (Suppl. 71), s93, 1993.
-
(1993)
Pharmacol. Toxicol.
, Issue.SUPPL. 71
-
-
Poulsen, H.E.1
Loft, S.2
Wassermann, K.3
-
35
-
-
0027984719
-
Metabolic polymorphisms in carcinogen metabolising enzymes and cancer susceptibility
-
Wolf, C.R., Smith, C.A.D., and Forman, D., Metabolic polymorphisms in carcinogen metabolising enzymes and cancer susceptibility. Br. Med. Bull. 50, 718, 1994.
-
(1994)
Br. Med. Bull.
, vol.50
, pp. 718
-
-
Wolf, C.R.1
Smith, C.A.D.2
Forman, D.3
-
36
-
-
0028568658
-
Genotyping for polymorphisms in xenobiotic metabolism as a predictor of disease susceptibility
-
Daly, A.K., Cholerton, S., Armstrong, M., and Idle, J.R., Genotyping for polymorphisms in xenobiotic metabolism as a predictor of disease susceptibility. Environ. Health Perspect. 102 (Suppl. 9), 55, 1994.
-
(1994)
Environ. Health Perspect.
, vol.102
, Issue.SUPPL. 9
, pp. 55
-
-
Daly, A.K.1
Cholerton, S.2
Armstrong, M.3
Idle, J.R.4
-
37
-
-
0029021815
-
Diagnosis of polymorphisms in carcinogen-activating and inactivating enzymes and cancer susceptibility - A review
-
Raunio, H., Husgafvel-Pursiainen, K., Anttila, S., Hietanen, E., Hirvonen, A., and Pelkonen, O., Diagnosis of polymorphisms in carcinogen-activating and inactivating enzymes and cancer susceptibility - a review. Gene, 159, 113, 1995.
-
(1995)
Gene
, vol.159
, pp. 113
-
-
Raunio, H.1
Husgafvel-Pursiainen, K.2
Anttila, S.3
Hietanen, E.4
Hirvonen, A.5
Pelkonen, O.6
-
38
-
-
0029558569
-
Metabolic polymorphisms and cancer susceptibility
-
Smith, G., Stanley, L.A., Sim, E., Strange, R.C., and Wolf, C.R., Metabolic polymorphisms and cancer susceptibility. Cancer Surv. 25, 27, 1995.
-
(1995)
Cancer Surv.
, vol.25
, pp. 27
-
-
Smith, G.1
Stanley, L.A.2
Sim, E.3
Strange, R.C.4
Wolf, C.R.5
-
39
-
-
0001360416
-
Genetic matabolic polymorphisms and the risk of cancer, a review of the literature
-
d'Errico, A., Taioli, E., Chen, X., and Vineis, P., Genetic matabolic polymorphisms and the risk of cancer, a review of the literature. Biomarkers 1, 149, 1996.
-
(1996)
Biomarkers
, vol.1
, pp. 149
-
-
D'Errico, A.1
Taioli, E.2
Chen, X.3
Vineis, P.4
-
40
-
-
0031105286
-
The role of carcinogen-metabolizing enzyme polymorphisms in cancer susceptibility
-
Gonzalez, F.J., The role of carcinogen-metabolizing enzyme polymorphisms in cancer susceptibility. Reprod. Toxicol. 11, 397, 1997.
-
(1997)
Reprod. Toxicol.
, vol.11
, pp. 397
-
-
Gonzalez, F.J.1
-
41
-
-
0027304210
-
Polymorphisms of the CYP1A1 and glutathione S-transferase genes associated with susceptibility to lung cancer in relation to ciggarette dose in a Japanese population
-
Nakachi, K., Imai, K., Hayashi, S-i., and Kawajiri, K., Polymorphisms of the CYP1A1 and glutathione S-transferase genes associated with susceptibility to lung cancer in relation to ciggarette dose in a Japanese population. Cancer Res. 53, 2994, 1993.
-
(1993)
Cancer Res.
, vol.53
, pp. 2994
-
-
Nakachi, K.1
Imai, K.2
Hayashi, S.-I.3
Kawajiri, K.4
-
42
-
-
0028228772
-
Restriction fragment length polymorphism of the human CYP2E1 (cytochrome P450IIE1) gene and susceptibility to lung cancer, possible relevance to low smoking exposure
-
Uematsu, F., Ikawa, S., Kikuchi, H., Sagami, I., Kanamaru, R., Abe, T., Satoh, K., Motomiya, M., and Watanabe, M., Restriction fragment length polymorphism of the human CYP2E1 (cytochrome P450IIE1) gene and susceptibility to lung cancer, possible relevance to low smoking exposure. Pharmacogenetics 4, 58, 1994.
-
(1994)
Pharmacogenetics
, vol.4
, pp. 58
-
-
Uematsu, F.1
Ikawa, S.2
Kikuchi, H.3
Sagami, I.4
Kanamaru, R.5
Abe, T.6
Satoh, K.7
Motomiya, M.8
Watanabe, M.9
-
43
-
-
0028283887
-
Combined effect of CYP1A1 inducibility and GSTM1 polymorphism on histological type of lung cancer
-
Anttila, S., Hirvonen, A., Husgafvel-Pursiainen, K., Karjalainen, A., Nurminen, T., and Vainio, H., Combined effect of CYP1A1 inducibility and GSTM1 polymorphism on histological type of lung cancer. Carcinogenesis 15, 1133, 1994.
-
(1994)
Carcinogenesis
, vol.15
, pp. 1133
-
-
Anttila, S.1
Hirvonen, A.2
Husgafvel-Pursiainen, K.3
Karjalainen, A.4
Nurminen, T.5
Vainio, H.6
-
44
-
-
0019990268
-
Ethnic differences in drug metabolism
-
Kalow, W., Ethnic differences in drug metabolism. Clin. Pharmacokin. 7, 373, 1982.
-
(1982)
Clin. Pharmacokin.
, vol.7
, pp. 373
-
-
Kalow, W.1
-
45
-
-
0026486899
-
Cytochrome P-450IIE1 genetic polymorphisms, racial variation, and lung cancer risk
-
Kato, S., Shields, P.G., Caporaso, N.E., Hoover, R.N., Trump, B.F., Sugimura, H., Weston, A., and Harris, C.C., Cytochrome P-450IIE1 genetic polymorphisms, racial variation, and lung cancer risk. Cancer Res. 52, 6712, 1992.
-
(1992)
Cancer Res.
, vol.52
, pp. 6712
-
-
Kato, S.1
Shields, P.G.2
Caporaso, N.E.3
Hoover, R.N.4
Trump, B.F.5
Sugimura, H.6
Weston, A.7
Harris, C.C.8
-
46
-
-
0028334418
-
Genetic basis for differences in debrisoquin polymorphism between a Spanish and other white populations
-
Agundez, J.A.G., Martinez, C., Ledesma, M.C., Ladona, M.G., Ladero, J.M., and Benitez, J., Genetic basis for differences in debrisoquin polymorphism between a Spanish and other white populations. Clin. Pharmacol. Ther. 55, 412, 1994.
-
(1994)
Clin. Pharmacol. Ther.
, vol.55
, pp. 412
-
-
Agundez, J.A.G.1
Martinez, C.2
Ledesma, M.C.3
Ladona, M.G.4
Ladero, J.M.5
Benitez, J.6
-
47
-
-
0028024393
-
Ethnic variation in the CYP2E1 gene, polymorphism analysis of 695 African-Americans, European Americans and Taiwanese
-
Stephens, E.A., Taylor, J.A., Kaplan, N., Yang, C.-H., Hsieh, L.L., Lucier, G.W., and Bell, D.A., Ethnic variation in the CYP2E1 gene, polymorphism analysis of 695 African-Americans, European Americans and Taiwanese. Pharmacogenetics 4, 185, 1994.
-
(1994)
Pharmacogenetics
, vol.4
, pp. 185
-
-
Stephens, E.A.1
Taylor, J.A.2
Kaplan, N.3
Yang, C.-H.4
Hsieh, L.L.5
Lucier, G.W.6
Bell, D.A.7
-
48
-
-
0001451028
-
Genetic contribution to inter-ethnic variations in drug oxidation
-
Besancon, May, Alvan, G., Balant, L.P., Bechtel, P.R., Boobis, A.R., Gram, L.F., Paintaud, G., and Pithan, K., Eds. Luxembourg, EU, 1995
-
Dahl, M.-L., Bertilsson, L., Chang, M., Rob, H.-K., Abdi, Y.A., Yue, Q.-Y., Sawe, J., Masimerembwa, C., Johansson, I., Ingelman-Sundberg, M., and Sjoqvist, F., Genetic contribution to inter-ethnic variations in drug oxidation. In Proceedings of the COST B1 European Conference on Specificity and Variability in Drug Metabolism, Besancon, May 1995, Alvan, G., Balant, L.P., Bechtel, P.R., Boobis, A.R., Gram, L.F., Paintaud, G., and Pithan, K., Eds. Luxembourg, EU, 1995, 111-124
-
(1995)
Proceedings of the COST B1 European Conference on Specificity and Variability in Drug Metabolism
, pp. 111-124
-
-
Dahl, M.-L.1
Bertilsson, L.2
Chang, M.3
Rob, H.-K.4
Abdi, Y.A.5
Yue, Q.-Y.6
Sawe, J.7
Masimerembwa, C.8
Johansson, I.9
Ingelman-Sundberg, M.10
Sjoqvist, F.11
-
49
-
-
0026785516
-
High susceptibility to lung cancer analyzed in terms of combined genoytypes of P450IA1 and Mu-class glutathione S-transferase genes
-
Hayashi, S.-i., Watanabe, J., and Kawajiri, K., High susceptibility to lung cancer analyzed in terms of combined genoytypes of P450IA1 and Mu-class glutathione S-transferase genes. Jpn. J. Cancer Res. 83, 866, 1992.
-
(1992)
Jpn. J. Cancer Res.
, vol.83
, pp. 866
-
-
Hayashi, S.-I.1
Watanabe, J.2
Kawajiri, K.3
-
50
-
-
0030588194
-
Influence of environmental and genetic factors on variation in human response to DNA damaging agents
-
Green, M.H.L., Influence of environmental and genetic factors on variation in human response to DNA damaging agents. Environ. Toxicol. and Pharmacol. 2, 151, 1996.
-
(1996)
Environ. Toxicol. and Pharmacol.
, vol.2
, pp. 151
-
-
Green, M.H.L.1
-
51
-
-
0024348327
-
Analysis of mercapturic acids as a tool in biotransformation, biomonitoring and toxicological studies
-
Vermeulen, N.P.E., Analysis of mercapturic acids as a tool in biotransformation, biomonitoring and toxicological studies. Trends Pharmacol. Sci. 10, 177, 1989.
-
(1989)
Trends Pharmacol. Sci.
, vol.10
, pp. 177
-
-
Vermeulen, N.P.E.1
-
52
-
-
0027050667
-
Mercapturic acids, protein adducts, and DNA adducts as biomarkers of electrophilic chemicals
-
van Welie, R.T.H., van Dijck, R.G.J.M., and Vermeulen, N.P.E., Mercapturic acids, protein adducts, and DNA adducts as biomarkers of electrophilic chemicals. Crit. Rev. Toxicol. 22, 271, 1992.
-
(1992)
Crit. Rev. Toxicol.
, vol.22
, pp. 271
-
-
Van Welie, R.T.H.1
Van Dijck, R.G.J.M.2
Vermeulen, N.P.E.3
-
53
-
-
0022273488
-
Future directions in the use of DNA adducts as internal dosimeters for monitoring human exposure to environmental mutagens and carcinogens
-
Harris, C.C., Future directions in the use of DNA adducts as internal dosimeters for monitoring human exposure to environmental mutagens and carcinogens. Environ. Health Perspect. 62, 185, 1985.
-
(1985)
Environ. Health Perspect.
, vol.62
, pp. 185
-
-
Harris, C.C.1
-
54
-
-
0023631254
-
Biochemical and molecular epidemiology of human cancer, Indicators of carcinogen exposure, DNA damage, and genetic predisposition
-
Harris, C.C., Weston, A., Willey, J.C., Trivers, G.E., and Mann, D.L., Biochemical and molecular epidemiology of human cancer, Indicators of carcinogen exposure, DNA damage, and genetic predisposition. Environ. Health Perspect. 75, 109, 1987.
-
(1987)
Environ. Health Perspect.
, vol.75
, pp. 109
-
-
Harris, C.C.1
Weston, A.2
Willey, J.C.3
Trivers, G.E.4
Mann, D.L.5
-
55
-
-
0024381995
-
Markers of exposure to carcinogens
-
Wogan, G.N., Markers of exposure to carcinogens. Environ. Health Perspect. 81, 9, 1989.
-
(1989)
Environ. Health Perspect.
, vol.81
, pp. 9
-
-
Wogan, G.N.1
-
56
-
-
0026092659
-
Distribution of ethylene oxide in human blood and its implications for biomonitoring
-
Fost, U., Hallier, E., Ottenwalder, H., Bolt, H.M., and Peter, H., Distribution of ethylene oxide in human blood and its implications for biomonitoring. Hum. Exp. Toxicol. 10, 25, 1991.
-
(1991)
Hum. Exp. Toxicol.
, vol.10
, pp. 25
-
-
Fost, U.1
Hallier, E.2
Ottenwalder, H.3
Bolt, H.M.4
Peter, H.5
-
57
-
-
0028918693
-
Effects of variation in detoxification rate on dose monitoring adducts
-
Fost, U., Tornqvist, M., Leutbecher, M., Granath, F., Hallier, E., and Ehrenberg, L., Effects of variation in detoxification rate on dose monitoring adducts. Hum. Exp. Toxicol. 14, 201, 1995.
-
(1995)
Hum. Exp. Toxicol.
, vol.14
, pp. 201
-
-
Fost, U.1
Tornqvist, M.2
Leutbecher, M.3
Granath, F.4
Hallier, E.5
Ehrenberg, L.6
-
58
-
-
0028283889
-
Comparison of 7-medG formation in white blood cells, liver and target organs in rats treated with methylating carcinogens
-
Bianchini, F. and Wild, C.P., Comparison of 7-medG formation in white blood cells, liver and target organs in rats treated with methylating carcinogens. Carcinogenesis 15, 1137-1141, 1994.
-
(1994)
Carcinogenesis
, vol.15
, pp. 1137-1141
-
-
Bianchini, F.1
Wild, C.P.2
-
59
-
-
0028567130
-
Effect of route of administration of environmental methylating agents on 7-methylguanine formation in white blood cells and internal organs, implications for molecular epidemiology
-
Bianchini, F. and Wild, C.P., Effect of route of administration of environmental methylating agents on 7-methylguanine formation in white blood cells and internal organs, implications for molecular epidemiology. Cancer Lett. 87, 131, 1994.
-
(1994)
Cancer Lett.
, vol.87
, pp. 131
-
-
Bianchini, F.1
Wild, C.P.2
-
60
-
-
0027315493
-
Carcinogen-DNA adducts in exfoliated urothelial cells: Techniques for noninvasive human monitoring
-
Talaska, G., Schamer, M., Skipper, P., Tannenbaum, S., Caporaso, N., Kadlubar, F., Bartsch, H., and Vineis, P., Carcinogen-DNA adducts in exfoliated urothelial cells: techniques for noninvasive human monitoring. Env. Health Perspect. 99, 289, 1993.
-
(1993)
Env. Health Perspect.
, vol.99
, pp. 289
-
-
Talaska, G.1
Schamer, M.2
Skipper, P.3
Tannenbaum, S.4
Caporaso, N.5
Kadlubar, F.6
Bartsch, H.7
Vineis, P.8
-
61
-
-
0026673948
-
Relevance of urinary DNA adducts as markers of carcinogen exposure
-
Shuker, D.E.G. and Farmer, P.B., Relevance of urinary DNA adducts as markers of carcinogen exposure. Chem. Res. Toxicol. 5, 450, 1992.
-
(1992)
Chem. Res. Toxicol.
, vol.5
, pp. 450
-
-
Shuker, D.E.G.1
Farmer, P.B.2
-
62
-
-
0030250252
-
Chromosome abberations, micronuclei, aneuploidy, sister chromatid exchanges, and cancer risk assessment
-
Tucker, J.D. and Preston, R.J., Chromosome abberations, micronuclei, aneuploidy, sister chromatid exchanges, and cancer risk assessment. Mutat. Res. 365, 147, 1996.
-
(1996)
Mutat. Res.
, vol.365
, pp. 147
-
-
Tucker, J.D.1
Preston, R.J.2
-
63
-
-
0028641692
-
Pharmacogenetics, detecting sensitive populations
-
Shields, P.G., Pharmacogenetics, detecting sensitive populations. Environ. Health Perspect. 102 (Suppl. 11), 81, 1994.
-
(1994)
Environ. Health Perspect.
, vol.102
, Issue.SUPPL. 11
, pp. 81
-
-
Shields, P.G.1
-
64
-
-
0029016980
-
Assessment of cancer susceptibility in humans by use of genetic polymorphisms in carcinogen metabolism
-
Ikawa, S., Uematsu, F., Watanabe, K.-i., Kimpara, T., Osada, M., Hossain, A., Sagami, I., Kikuchi, H., and Watanabe, M., Assessment of cancer susceptibility in humans by use of genetic polymorphisms in carcinogen metabolism. Pharmacogenetics, 5, S154, 1995.
-
(1995)
Pharmacogenetics
, vol.5
-
-
Ikawa, S.1
Uematsu, F.2
Watanabe, K.-I.3
Kimpara, T.4
Osada, M.5
Hossain, A.6
Sagami, I.7
Kikuchi, H.8
Watanabe, M.9
-
65
-
-
0028856846
-
Molecular basis of polymorphic drug metabolism
-
Daly, A.K., Molecular basis of polymorphic drug metabolism. J. Mol. Med. 73, 539, 1995.
-
(1995)
J. Mol. Med.
, vol.73
, pp. 539
-
-
Daly, A.K.1
-
66
-
-
0029963622
-
Human drug-metabolizing enzyme polymorphisms: Effects on risk of toxicity and cancer
-
Nebert, D.W., Human drug-metabolizing enzyme polymorphisms: effects on risk of toxicity and cancer. DNA and Cell Biol. 15, 273, 1996.
-
(1996)
DNA and Cell Biol.
, vol.15
, pp. 273
-
-
Nebert, D.W.1
-
67
-
-
0030995879
-
Molecular mechanisms of genetic polymorphisms of drug metabolism
-
Meyer, U.A. and Zanger, U.M., Molecular mechanisms of genetic polymorphisms of drug metabolism. Ann. Rev. Pharmacol. Toxicol. 37, 269, 1997.
-
(1997)
Ann. Rev. Pharmacol. Toxicol.
, vol.37
, pp. 269
-
-
Meyer, U.A.1
Zanger, U.M.2
-
68
-
-
0023558113
-
Guidelines for human gene nomenclature
-
Shows, T.B., McAlpine, P.J., Boucheir, C., Collins, F.S., Conneally, P.M., Prezal, J., Gershowitz, H., Goodfellow, P.N., Hall, J.G., Issitt, P., Jones, C.A., Knowles, B.B., Lewis, M., McKusic, V.A., Meisler, M., Morton, N.E., Rubinstein, P., Schanfield, M.S., Schmickel, R.D., Skolnick, M.H., Spence, M.A., Sutherland, G.R., Traver, M., Van Cong, N., and Willard, H.F., Guidelines for human gene nomenclature. Cytogen. Cell Genet. 46, 11, 1987.
-
(1987)
Cytogen. Cell Genet.
, vol.46
, pp. 11
-
-
Shows, T.B.1
McAlpine, P.J.2
Boucheir, C.3
Collins, F.S.4
Conneally, P.M.5
Prezal, J.6
Gershowitz, H.7
Goodfellow, P.N.8
Hall, J.G.9
Issitt, P.10
Jones, C.A.11
Knowles, B.B.12
Lewis, M.13
McKusic, V.A.14
Meisler, M.15
Morton, N.E.16
Rubinstein, P.17
Schanfield, M.S.18
Schmickel, R.D.19
Skolnick, M.H.20
Spence, M.A.21
Sutherland, G.R.22
Traver, M.23
Van Cong, N.24
Willard, H.F.25
more..
-
69
-
-
0028831941
-
Nomenclature for N-acetyltransferases
-
Vatsis, K.P., Weber, W.W., Bell, D.A., Dupret, J.-M., Price Evans, D.A., Grant, D.M., Hein, D.W., Lin, H.J., Meyer, U.A., Relling, M.V., Sim, E., Suzuki, T., and Yamazoe, Y., Nomenclature for N-acetyltransferases. Pharmacogenetics, 5, 1, 1995.
-
(1995)
Pharmacogenetics
, vol.5
, pp. 1
-
-
Vatsis, K.P.1
Weber, W.W.2
Bell, D.A.3
Dupret, J.-M.4
Price Evans, D.A.5
Grant, D.M.6
Hein, D.W.7
Lin, H.J.8
Meyer, U.A.9
Relling, M.V.10
Sim, E.11
Suzuki, T.12
Yamazoe, Y.13
-
70
-
-
0021813284
-
N-Acetylation pharmacogenetics
-
Weber, W.W. and Hein, D.W., N-Acetylation pharmacogenetics. Pharmacol. Rev. 37, 25, 1985.
-
(1985)
Pharmacol. Rev.
, vol.37
, pp. 25
-
-
Weber, W.W.1
Hein, D.W.2
-
71
-
-
0024345871
-
N-Acetyltransferase
-
Price Evans, D.A., N-Acetyltransferase. Pharmac. Ther. 42, 157, 1989.
-
(1989)
Pharmac. Ther.
, vol.42
, pp. 157
-
-
Price Evans, D.A.1
-
72
-
-
26444539817
-
Genetic control of isoniazid metabolism in man
-
Price Evans, D.A. and Manley, K.A., Genetic control of isoniazid metabolism in man. Br. Med. J. 2, 485, 1960.
-
(1960)
Br. Med. J.
, vol.2
, pp. 485
-
-
Price Evans, D.A.1
Manley, K.A.2
-
74
-
-
0025231840
-
Acetylation pharmacogenetics; The slow acetylator phenotype is caused by decreased or absent arylamine N-Acetyltransferase in human liver
-
Grant, D.M., Morike, K., Eichelbaum, M., and Meyer, U.A., Acetylation pharmacogenetics; The slow acetylator phenotype is caused by decreased or absent arylamine N-Acetyltransferase in human liver. J. Clin. Invest. 85, 968, 1990.
-
(1990)
J. Clin. Invest.
, vol.85
, pp. 968
-
-
Grant, D.M.1
Morike, K.2
Eichelbaum, M.3
Meyer, U.A.4
-
75
-
-
0025967717
-
Monomorphic and polymorphic human arylamine N-Acetyltransferases, A comparison of liver isozymes and expressed products of two cloned genes
-
Grant, D.M., Blum, M., Beer, M., and Meyer, U.A., Monomorphic and polymorphic human arylamine N-Acetyltransferases, A comparison of liver isozymes and expressed products of two cloned genes. Mol. Pharmacol. 39, 184, 1991.
-
(1991)
Mol. Pharmacol.
, vol.39
, pp. 184
-
-
Grant, D.M.1
Blum, M.2
Beer, M.3
Meyer, U.A.4
-
76
-
-
0026335694
-
Expression of monomorphic arylamine N-acetyltransferase (NAT1) in human leukocytes
-
Cribb, A.E., Grant, D.M., Miller, M.A., and Spielberg, S.P., Expression of monomorphic arylamine N-acetyltransferase (NAT1) in human leukocytes. J. Pharmacol. Exp. Ther. 259, 1241, 1991.
-
(1991)
J. Pharmacol. Exp. Ther.
, vol.259
, pp. 1241
-
-
Cribb, A.E.1
Grant, D.M.2
Miller, M.A.3
Spielberg, S.P.4
-
77
-
-
0025344002
-
Human arylamine N-acetyl-transferase genes: Isolation, chromosomal localization, and functional expression
-
Blum, M., Grant, D.M., McBride, W., Heim, M., and Meyer, U.A., Human arylamine N-acetyl-transferase genes: isolation, chromosomal localization, and functional expression. DNA Cell. Biol. 9, 193, 1990.
-
(1990)
DNA Cell. Biol.
, vol.9
, pp. 193
-
-
Blum, M.1
Grant, D.M.2
McBride, W.3
Heim, M.4
Meyer, U.A.5
-
78
-
-
0025880699
-
Structure and restriction fragment length polymorphism of genes for human liver arylamine N-acetyltransferases
-
Ebisawa, T. and Deguchi, T., Structure and restriction fragment length polymorphism of genes for human liver arylamine N-acetyltransferases. Biochem. Biophys. Res. Commun. 177, 1252, 1991.
-
(1991)
Biochem. Biophys. Res. Commun.
, vol.177
, pp. 1252
-
-
Ebisawa, T.1
Deguchi, T.2
-
79
-
-
0028298396
-
Biochemical individuality and its implications for drug and carcinogen metabolism: Recent insights from acetyltransferase and cytochrome P4501A2 phenotyping and genotyping in humans
-
Kadlubar, F.F., Biochemical individuality and its implications for drug and carcinogen metabolism: recent insights from acetyltransferase and cytochrome P4501A2 phenotyping and genotyping in humans. Drug Metab. Rev. 26, 37, 1994.
-
(1994)
Drug Metab. Rev.
, vol.26
, pp. 37
-
-
Kadlubar, F.F.1
-
80
-
-
0026768271
-
Polymorphisms of N-acetyltransferase genes
-
Grant, D.M., Blum, M., and Meyer, U.A., Polymorphisms of N-acetyltransferase genes. Xenobiotica, 22, 1073, 1992.
-
(1992)
Xenobiotica
, vol.22
, pp. 1073
-
-
Grant, D.M.1
Blum, M.2
Meyer, U.A.3
-
81
-
-
0028044081
-
Polymorphism of human acetyl-transferases
-
Meyer, U.A., Polymorphism of human acetyl-transferases. Environ. Health. Perspect. 102(Suppl. 6), 213, 1994.
-
(1994)
Environ. Health. Perspect.
, vol.102
, Issue.SUPPL. 6
, pp. 213
-
-
Meyer, U.A.1
-
82
-
-
0000756778
-
Detection of a new polymorphism of human arylamine N-acetyltransferase NAT1 using p-amino-salicylic acid as an in vivo probe
-
Grant, D.M., Vohra, P., Avis, Y., and Ima, A., Detection of a new polymorphism of human arylamine N-acetyltransferase NAT1 using p-amino-salicylic acid as an in vivo probe. J. Basic Clin. Physiol. Pharmacol. 3 (Suppl.), 244, 1992.
-
(1992)
J. Basic Clin. Physiol. Pharmacol.
, vol.3
, Issue.SUPPL.
, pp. 244
-
-
Grant, D.M.1
Vohra, P.2
Avis, Y.3
Ima, A.4
-
83
-
-
0027182143
-
Structural heterogeinity of Caucasian N-acetyltransferase at the NAT1 gene locus
-
Vatsis, K.P. and Weber, W.W., Structural heterogeinity of Caucasian N-acetyltransferase at the NAT1 gene locus. Arch. Biochem. Biophys. 301, 71, 1993.
-
(1993)
Arch. Biochem. Biophys.
, vol.301
, pp. 71
-
-
Vatsis, K.P.1
Weber, W.W.2
-
84
-
-
0013830743
-
Partial purification and properties of the isoniazid trans-acetylase in human liver. Its relationship to the acetylation of p-aminosalicylic acid
-
Jenne, J.W. and Orser, M., Partial purification and properties of the isoniazid trans-acetylase in human liver. Its relationship to the acetylation of p-aminosalicylic acid. J. Clin. Invest. 44, 1992, 1965.
-
(1965)
J. Clin. Invest.
, vol.44
, pp. 1992
-
-
Jenne, J.W.1
Orser, M.2
-
85
-
-
0018092881
-
Genetic variation in N-acetylation of carcinogenic arylamines by human and rabbit liver
-
Glowinski, I.B., Radtke, H.E., and Weber, W.W., Genetic variation in N-acetylation of carcinogenic arylamines by human and rabbit liver. Mol. Pharmacol. 14, 940, 1978.
-
(1978)
Mol. Pharmacol.
, vol.14
, pp. 940
-
-
Glowinski, I.B.1
Radtke, H.E.2
Weber, W.W.3
-
86
-
-
0019297993
-
Characterization of human lymphocyte N-acetyltransferase and its relationship to the isoniazid acetylator polymorphism
-
McQueen, C.A. and Weber, W.W., Characterization of human lymphocyte N-acetyltransferase and its relationship to the isoniazid acetylator polymorphism. Biochem. Genet. 18, 889, 1980.
-
(1980)
Biochem. Genet.
, vol.18
, pp. 889
-
-
McQueen, C.A.1
Weber, W.W.2
-
87
-
-
0026071623
-
Kinetics of acetyl CoA, Arylamine N-acetyltransferase from rapid and slow acetylator human liver
-
Kilbane, A.J., Petroff, T., and Weber, W.W., Kinetics of acetyl CoA, Arylamine N-acetyltransferase from rapid and slow acetylator human liver. Drug Metab. Dispos. 19, 503, 1991.
-
(1991)
Drug Metab. Dispos.
, vol.19
, pp. 503
-
-
Kilbane, A.J.1
Petroff, T.2
Weber, W.W.3
-
88
-
-
0026674776
-
Arylamine N-acetyltransferase in human red blood cells
-
Ward, A., Hickman, D., Gordon, J.W., and Sim, E., Arylamine N-acetyltransferase in human red blood cells. Biochem. Pharmacol. 44, 1099, 1992.
-
(1992)
Biochem. Pharmacol.
, vol.44
, pp. 1099
-
-
Ward, A.1
Hickman, D.2
Gordon, J.W.3
Sim, E.4
-
89
-
-
0027218299
-
Individual variability in p-aminobenzoic acid N-acetylation by human N-acetyltransferase (NAT1) of peripheral blood
-
Weber, W.W. and Vatsis, K.P., Individual variability in p-aminobenzoic acid N-acetylation by human N-acetyltransferase (NAT1) of peripheral blood. Pharmacogenetics 3, 209, 1993.
-
(1993)
Pharmacogenetics
, vol.3
, pp. 209
-
-
Weber, W.W.1
Vatsis, K.P.2
-
90
-
-
0028043708
-
Structure-function studies of human arylamine N-acetyltransferases NAT1 and NAT2: Functional analysis of recombinant NAT1/NAT2 chimeras expressed in Escherichia coli
-
Dupret, J.-M., Goodfellow, G.H., Janezic, S.A., and Grant, D.M., Structure-function studies of human arylamine N-acetyltransferases NAT1 and NAT2: functional analysis of recombinant NAT1/NAT2 chimeras expressed in Escherichia coli. J. Biol. Chem. 269, 26830, 1994.
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 26830
-
-
Dupret, J.-M.1
Goodfellow, G.H.2
Janezic, S.A.3
Grant, D.M.4
-
91
-
-
0028285248
-
Acetylator phenotyping, the urinary metabolite ratio in slow acetylators correlates with a marker of systemic NAT1 activity
-
Cribb, A.E., Isbrucker, R., Levatte, T., Tsui, T., Gillespie, C.T., and Renton, K.W., Acetylator phenotyping, the urinary metabolite ratio in slow acetylators correlates with a marker of systemic NAT1 activity. Pharmacogenetics 4, 166, 1994.
-
(1994)
Pharmacogenetics
, vol.4
, pp. 166
-
-
Cribb, A.E.1
Isbrucker, R.2
Levatte, T.3
Tsui, T.4
Gillespie, C.T.5
Renton, K.W.6
-
92
-
-
0027476961
-
Molecular genetics of the N-acetyl-transferases
-
Grant, D.M., Molecular genetics of the N-acetyl-transferases. Pharmacogenetics 3, 45, 1993.
-
(1993)
Pharmacogenetics
, vol.3
, pp. 45
-
-
Grant, D.M.1
-
93
-
-
0027281895
-
Metabolic activation and deactivation of arylamine carcinogens by recombinant human NAT1 and polymorphic NAT2 acetyltransferases
-
Hein, D.W., Doll, M.A., Rustan, T.D., Gray, K., Feng, Y., Ferguson, R.J., and Grant, D.M., Metabolic activation and deactivation of arylamine carcinogens by recombinant human NAT1 and polymorphic NAT2 acetyltransferases. Carcinogenesis 14, 1633, 1993.
-
(1993)
Carcinogenesis
, vol.14
, pp. 1633
-
-
Hein, D.W.1
Doll, M.A.2
Rustan, T.D.3
Gray, K.4
Feng, Y.5
Ferguson, R.J.6
Grant, D.M.7
-
94
-
-
0028040059
-
Metabolic activation of aromatic and heterocyclic N-hydroxyarylamines by wild-type and mutant recombinant human NAT1 and NAT2 acetyltransferases
-
Hein, D.W., Rustan, T.D., Ferguson, R.J., Doll, M.A., and Gray, K., Metabolic activation of aromatic and heterocyclic N-hydroxyarylamines by wild-type and mutant recombinant human NAT1 and NAT2 acetyltransferases. Arch. Toxicol. 68, 129, 1994.
-
(1994)
Arch. Toxicol.
, vol.68
, pp. 129
-
-
Hein, D.W.1
Rustan, T.D.2
Ferguson, R.J.3
Doll, M.A.4
Gray, K.5
-
95
-
-
0026650976
-
N- and O-acetylation of aromatic and heterocyclic amine carcinogens by human monomorphic and polymorphic acetyltransferases expressed in COS-1 cells
-
Minchin, R.F., Reeves, P.T., Teitel, C.H., McManus, M.E., Mojarrabi, B., Ilett, K.F., and Kadlubar, F.F., N- and O-acetylation of aromatic and heterocyclic amine carcinogens by human monomorphic and polymorphic acetyltransferases expressed in COS-1 cells. Biochem. Biophys. Res. Commun. 185, 839, 1992.
-
(1992)
Biochem. Biophys. Res. Commun.
, vol.185
, pp. 839
-
-
Minchin, R.F.1
Reeves, P.T.2
Teitel, C.H.3
McManus, M.E.4
Mojarrabi, B.5
Ilett, K.F.6
Kadlubar, F.F.7
-
96
-
-
0027076179
-
Polymorphisms for aromatic amine metabolism in humans, Relevance for human carcinogenesis
-
Kadlubar, F.F., Butler, M.A., Kaderlik, K.R., Chou, H.-C., and Lang, N.P., Polymorphisms for aromatic amine metabolism in humans, Relevance for human carcinogenesis. Environ. Health Perspect. 98, 69, 1992.
-
(1992)
Environ. Health Perspect.
, vol.98
, pp. 69
-
-
Kadlubar, F.F.1
Butler, M.A.2
Kaderlik, K.R.3
Chou, H.-C.4
Lang, N.P.5
-
97
-
-
0026701773
-
The role of human acetylation polymorphism in the metabolic activation of the food carcinogen 2-amino-3-methylimidazo [4,5-f]quinoline (IQ)
-
Probst, M.R., Blum, M., Fasshauer, I., D'Orazio, D., Meyer, U.A., and Wild, D., The role of human acetylation polymorphism in the metabolic activation of the food carcinogen 2-amino-3-methylimidazo [4,5-f]quinoline (IQ). Carcinogenesis 13, 1713, 1992.
-
(1992)
Carcinogenesis
, vol.13
, pp. 1713
-
-
Probst, M.R.1
Blum, M.2
Fasshauer, I.3
D'Orazio, D.4
Meyer, U.A.5
Wild, D.6
-
98
-
-
0025237412
-
Cloning and expression of cDNAs for polymorphic and monomorphic arylamine N-acetyltransferases from human liver
-
Ohsako, S. and Deguchi, T., Cloning and expression of cDNAs for polymorphic and monomorphic arylamine N-acetyltransferases from human liver. J. Biol. Chem. 265, 4630, 1990
-
(1990)
J. Biol. Chem.
, vol.265
, pp. 4630
-
-
Ohsako, S.1
Deguchi, T.2
-
99
-
-
0031589171
-
Identification of a novel allele at the human NAT1 acetyltransferase locus
-
Doll, M.A., Jiang, W., Deitz, A.C., Rustan, T.D., and Hein, D.W., Identification of a novel allele at the human NAT1 acetyltransferase locus. Biochem. Biophys. Res. Commun. 233, 584, 1997.
-
(1997)
Biochem. Biophys. Res. Commun.
, vol.233
, pp. 584
-
-
Doll, M.A.1
Jiang, W.2
Deitz, A.C.3
Rustan, T.D.4
Hein, D.W.5
-
100
-
-
0024309783
-
Nucleotide sequence of an intronless gene for a human arylamine N-acetyltransferase related to polymorphic drug acetylation
-
Grant, D.M., Blum, M., Demierre, A., and Meyer, U.A., Nucleotide sequence of an intronless gene for a human arylamine N-acetyltransferase related to polymorphic drug acetylation. Nucl. Acids Res. 17, 3978, 1989.
-
(1989)
Nucl. Acids Res.
, vol.17
, pp. 3978
-
-
Grant, D.M.1
Blum, M.2
Demierre, A.3
Meyer, U.A.4
-
101
-
-
0025948280
-
Molecular mechanisms of slow acetylation of drugs and carcinogens in humans
-
Blum, M., Demierre, A., Grant, D.M., Heim, M., and Meyer, U.A., Molecular mechanisms of slow acetylation of drugs and carcinogens in humans. Proc. Natl. Acad. Sci. U.S.A. 88, 5237, 1991.
-
(1991)
Proc. Natl. Acad. Sci. U.S.A.
, vol.88
, pp. 5237
-
-
Blum, M.1
Demierre, A.2
Grant, D.M.3
Heim, M.4
Meyer, U.A.5
-
102
-
-
0025917067
-
Diverse point mutations in the human gene for polymorphic N-acetyltransferase
-
Vatsis, K.P., Martell, K.J., and Weber, W.W., Diverse point mutations in the human gene for polymorphic N-acetyltransferase. Proc. Natl. Acad. Sci. U.S.A.88, 6333, 1991.
-
(1991)
Proc. Natl. Acad. Sci. U.S.A.
, vol.88
, pp. 6333
-
-
Vatsis, K.P.1
Martell, K.J.2
Weber, W.W.3
-
103
-
-
0027306025
-
The structure and characteristics of a fourth allele of polymorphic N-acetyltransferase gene found in the Japanese population
-
Abe, M., Deguchi, T., and Suzuki, T., The structure and characteristics of a fourth allele of polymorphic N-acetyltransferase gene found in the Japanese population. Biochem. Biophys. Res. Commun. 191, 811, 1993.
-
(1993)
Biochem. Biophys. Res. Commun.
, vol.191
, pp. 811
-
-
Abe, M.1
Deguchi, T.2
Suzuki, T.3
-
104
-
-
0026935909
-
Genotyping human polymorphic arylamine N-acetyltransferase, identification of new slow allotypic variants
-
Hickman, D., Risch, A., Camilleri, J.P., and Sim, E., Genotyping human polymorphic arylamine N-acetyltransferase, identification of new slow allotypic variants. Pharmacogenetics, 2, 217, 1992.
-
(1992)
Pharmacogenetics
, vol.2
, pp. 217
-
-
Hickman, D.1
Risch, A.2
Camilleri, J.P.3
Sim, E.4
-
106
-
-
0028829841
-
Determination of human NAT2 acetylator genotype by restriction fragment length polymorphism and allele-specific amplification
-
Doll, M.A., Fretland, A.J., Deitz, A.C., and Hein, D.W., Determination of human NAT2 acetylator genotype by restriction fragment length polymorphism and allele-specific amplification. Anal. Biochem. 231, 413, 1995.
-
(1995)
Anal. Biochem.
, vol.231
, pp. 413
-
-
Doll, M.A.1
Fretland, A.J.2
Deitz, A.C.3
Hein, D.W.4
-
107
-
-
0026713308
-
Sequences and expression of alleles of polymorphic arylamine N-acetyltransferase of human liver
-
Deguchi, T., Sequences and expression of alleles of polymorphic arylamine N-acetyltransferase of human liver. J. Biol. Chem. 267, 18140, 1992.
-
(1992)
J. Biol. Chem.
, vol.267
, pp. 18140
-
-
Deguchi, T.1
-
108
-
-
0025364134
-
Correlations between acetylator phenotype and genotypes of polymorphic arylamine N-acetyltransferase in human liver
-
Deguchi, T., Mashimo, M., and Suzuki, T., Correlations between acetylator phenotype and genotypes of polymorphic arylamine N-acetyltransferase in human liver. J. Biol. Chem. 265, 12757, 1990.
-
(1990)
J. Biol. Chem.
, vol.265
, pp. 12757
-
-
Deguchi, T.1
Mashimo, M.2
Suzuki, T.3
-
109
-
-
0028270681
-
Ethnic distribution of slow acetylator mutations in the polymorphic N-acetyltransferase (NAT2) gene
-
Lin, H.J., Han, C.-Y., Lin, B.K., and Hardy, S., Ethnic distribution of slow acetylator mutations in the polymorphic N-acetyltransferase (NAT2) gene. Pharmacogenetics 4, 125, 1994.
-
(1994)
Pharmacogenetics
, vol.4
, pp. 125
-
-
Lin, H.J.1
Han, C.-Y.2
Lin, B.K.3
Hardy, S.4
-
110
-
-
0013524405
-
Human N-Acetyltransferase variant r4 at the NAT2 locus
-
Vatsis, K.P., Rodgers, L., and Weber, W.W., Human N-Acetyltransferase variant r4 at the NAT2 locus. The Pharmacologist 35, 204, 1993.
-
(1993)
The Pharmacologist
, vol.35
, pp. 204
-
-
Vatsis, K.P.1
Rodgers, L.2
Weber, W.W.3
-
111
-
-
0029662087
-
NAT2*12A (803A→G) codes for rapid arylamine N-acetylation in humans
-
Cascorbi, I., Brockmoller, J., Bauer, S., Reum, T., and Roots, I., NAT2*12A (803A→G) codes for rapid arylamine N-acetylation in humans. Pharmacogenetics 6, 257, 1996.
-
(1996)
Pharmacogenetics
, vol.6
, pp. 257
-
-
Cascorbi, I.1
Brockmoller, J.2
Bauer, S.3
Reum, T.4
Roots, I.5
-
112
-
-
0027183777
-
Genotype/phenotype discordance for human arylamine N-acetyltransferase (NAT2) reveals a new slow-acetylator allele common in African-Americans
-
Bell, D.A., Taylor, J.A., Butler, M.A., Stephens, E.A., Wiest, J., Brubaker, L.H., Kadlubar, F.F., and Lucier, G.W., Genotype/phenotype discordance for human arylamine N-acetyltransferase (NAT2) reveals a new slow-acetylator allele common in African-Americans. Carcinogenesis 14, 1689, 1993.
-
(1993)
Carcinogenesis
, vol.14
, pp. 1689
-
-
Bell, D.A.1
Taylor, J.A.2
Butler, M.A.3
Stephens, E.A.4
Wiest, J.5
Brubaker, L.H.6
Kadlubar, F.F.7
Lucier, G.W.8
-
113
-
-
0026785642
-
Molecular genotyping of N-acetylation polymorphism to predict phenotype
-
Mashimo, M., Suzuki, T., Abe, M., and Deguchi, T., Molecular genotyping of N-acetylation polymorphism to predict phenotype. Hum. Genet. 90, 139, 1992.
-
(1992)
Hum. Genet.
, vol.90
, pp. 139
-
-
Mashimo, M.1
Suzuki, T.2
Abe, M.3
Deguchi, T.4
-
114
-
-
0027384793
-
Correlation between N-acetyl-transferase activity and NAT2 genotype in Chinese males
-
Rothman, N., Hayes, R.B., Bi, W., Caporaso, N., Broly, F., Woosley, R.L., Yin, S., Feng, P., You, X., and Meyer, U.A., Correlation between N-acetyl-transferase activity and NAT2 genotype in Chinese males. Pharmacogenetics, 3, 250, 1993.
-
(1993)
Pharmacogenetics
, vol.3
, pp. 250
-
-
Rothman, N.1
Hayes, R.B.2
Bi, W.3
Caporaso, N.4
Broly, F.5
Woosley, R.L.6
Yin, S.7
Feng, P.8
You, X.9
Meyer, U.A.10
-
115
-
-
0031063347
-
A new mutation C759T in the polymorphic N-acetyltransferase (NAT2) gene
-
Woolhouse, N.M., Qureshi, M.M., and Rayoumi, R.A.L., A new mutation C759T in the polymorphic N-acetyltransferase (NAT2) gene. Pharmacogenetics, 7, 83, 1997.
-
(1997)
Pharmacogenetics
, vol.7
, pp. 83
-
-
Woolhouse, N.M.1
Qureshi, M.M.2
Rayoumi, R.A.L.3
-
116
-
-
0029163589
-
Arylamine N-acetyltransferase (NAT2) mutations and their allelic linkage in unrelated Caucasian individuals, correlation with phenotypic activity
-
Cascorbi, I., Drakoulis, N., Brockmoller, J., Maurer, A., Sperling, K., and Roots, I., Arylamine N-acetyltransferase (NAT2) mutations and their allelic linkage in unrelated Caucasian individuals, Correlation with phenotypic activity. Am. J. Hum. Genet. 57, 581, 1995.
-
(1995)
Am. J. Hum. Genet.
, vol.57
, pp. 581
-
-
Cascorbi, I.1
Drakoulis, N.2
Brockmoller, J.3
Maurer, A.4
Sperling, K.5
Roots, I.6
-
117
-
-
0025572192
-
Hydroxylation polymorphisms of debrisoquine and mephenytoin in European populations
-
Alvan, G., Bechtel, P., Iselius, L., and Gundert-Remy, U., Hydroxylation polymorphisms of debrisoquine and mephenytoin in European populations. Eur. J. Clin. Pharmacol. 39, 533, 1990.
-
(1990)
Eur. J. Clin. Pharmacol.
, vol.39
, pp. 533
-
-
Alvan, G.1
Bechtel, P.2
Iselius, L.3
Gundert-Remy, U.4
-
118
-
-
0027282007
-
The GSTM1 null genotype as a potential risk modifier for squamous cell carcinoma of the lung
-
Hirvonen, A., Husgafvel-Pursiainen, K., Anttila, S., and Vainio, H., The GSTM1 null genotype as a potential risk modifier for squamous cell carcinoma of the lung. Carcinogenesis. 14, 1479, 1993.
-
(1993)
Carcinogenesis
, vol.14
, pp. 1479
-
-
Hirvonen, A.1
Husgafvel-Pursiainen, K.2
Anttila, S.3
Vainio, H.4
-
119
-
-
0027450886
-
Genotype and phenotype of glutathione-S-transferase class μ isoenzymes μ and ψ in lung cancer patients and controls
-
Brockmoller, J., Kerb, R., Drakoulis, N., Nitz, M., and Roots, I., Genotype and phenotype of glutathione-S-transferase class μ isoenzymes μ and ψ in lung cancer patients and controls. Cancer Res. 53, 1004, 1993.
-
(1993)
Cancer Res.
, vol.53
, pp. 1004
-
-
Brockmoller, J.1
Kerb, R.2
Drakoulis, N.3
Nitz, M.4
Roots, I.5
-
120
-
-
0029130808
-
Genotyping and phenotyping determination of polymorphic glutathione transferase T1 in a Swedish population
-
Warholm, M., Rane, A., Aleandrie, A.-K., Monaghan, G., and Rannug, A., Genotyping and phenotyping determination of polymorphic glutathione transferase T1 in a Swedish population. Pharmacogenetics 5, 252, 1995.
-
(1995)
Pharmacogenetics
, vol.5
, pp. 252
-
-
Warholm, M.1
Rane, A.2
Aleandrie, A.-K.3
Monaghan, G.4
Rannug, A.5
-
121
-
-
0021684926
-
Mephenytoin hydroxylation deficiency in Caucasians: Frequency of a new oxidative drug metabolism polymorphism
-
Wedlund, P.J., Asianian, W.S., McAllister, C.B., Wilkinson, G.R., and Branch, R.A., Mephenytoin hydroxylation deficiency in Caucasians: frequency of a new oxidative drug metabolism polymorphism. Clin. Pharmacol. Ther. 36, 773, 1984.
-
(1984)
Clin. Pharmacol. Ther.
, vol.36
, pp. 773
-
-
Wedlund, P.J.1
Asianian, W.S.2
McAllister, C.B.3
Wilkinson, G.R.4
Branch, R.A.5
-
122
-
-
0027276869
-
Genetic basis for a lower prevalence of deficient CYP2D6 oxidative drug metabolism phenotypes in black Americans
-
Evans, W.E., Relling, M.V., Rahman, A., McLeod, H.L., Scott, E.P., and Lin, J.-S., Genetic basis for a lower prevalence of deficient CYP2D6 oxidative drug metabolism phenotypes in black Americans. J. Clin. Invest. 91, 2150, 1993.
-
(1993)
J. Clin. Invest.
, vol.91
, pp. 2150
-
-
Evans, W.E.1
Relling, M.V.2
Rahman, A.3
McLeod, H.L.4
Scott, E.P.5
Lin, J.-S.6
-
123
-
-
0029086208
-
Polymorphism of glutathione-S-transferase M1 and lung cancer risk among African-Americans and Caucasians in Los Angeles County
-
California
-
London, S.J., Daly, A.K., Cooper, J., Navidi, W.C., Carpenter, C.L., and Idle, J.R., Polymorphism of glutathione-S-transferase M1 and lung cancer risk among African-Americans and Caucasians in Los Angeles County, California. J. Natl. Cancer Inst. 87, 1246, 1995.
-
(1995)
J. Natl. Cancer Inst.
, vol.87
, pp. 1246
-
-
London, S.J.1
Daly, A.K.2
Cooper, J.3
Navidi, W.C.4
Carpenter, C.L.5
Idle, J.R.6
-
124
-
-
0029881659
-
Simultaneous characterization of glutathione-S-transferase M1 and T1 polymorphisms by polymerase chain reaction in American whites and blacks
-
Chen, C.-L., Liu, Q., and Relling, M.V., Simultaneous characterization of glutathione-S-transferase M1 and T1 polymorphisms by polymerase chain reaction in American whites and blacks. Pharmacogenetics 6, 187, 1996.
-
(1996)
Pharmacogenetics
, vol.6
, pp. 187
-
-
Chen, C.-L.1
Liu, Q.2
Relling, M.V.3
-
125
-
-
0029002341
-
Ethnic differences in the prevalence of the homozygous deleted genotype of glutathione-S-transferase theta
-
Nelson, H.H., Wiencke, J.K., Christian, D.C., Cheng, T.J., Zuo, Z.-F., Schwartz, B.S., Lee, B.-K., Spitz, M.R., Wang, M., Xu, X., and Kelsey, K.T., Ethnic differences in the prevalence of the homozygous deleted genotype of glutathione-S-transferase theta. Carcinogenesis. 16, 1243, 1995.
-
(1995)
Carcinogenesis
, vol.16
, pp. 1243
-
-
Nelson, H.H.1
Wiencke, J.K.2
Christian, D.C.3
Cheng, T.J.4
Zuo, Z.-F.5
Schwartz, B.S.6
Lee, B.-K.7
Spitz, M.R.8
Wang, M.9
Xu, X.10
Kelsey, K.T.11
-
126
-
-
0024442372
-
Metoprolol and mephenytoin oxidation polymorphisms in far eastern oriental subjects, Japanese versus mainland Chinese
-
Horai, Y., Nakano, M., Ishizaki, T., Ishikawa, K., Zhou, H.-H., Zhou, B.-J., Liao, C.-L., and Zhang, L.-M., Metoprolol and mephenytoin oxidation polymorphisms in far Eastern Oriental subjects, Japanese versus mainland Chinese. Clin. Pharmacol. Ther. 46, 198, 1989.
-
(1989)
Clin. Pharmacol. Ther.
, vol.46
, pp. 198
-
-
Horai, Y.1
Nakano, M.2
Ishizaki, T.3
Ishikawa, K.4
Zhou, H.-H.5
Zhou, B.-J.6
Liao, C.-L.7
Zhang, L.-M.8
-
127
-
-
0029010611
-
Distribution of GSTM1 null genotype in relation to gender, age and smoking status in Japanese lung cancer patients
-
Kihara, M., Noda, K., and Kihara, M., Distribution of GSTM1 null genotype in relation to gender, age and smoking status in Japanese lung cancer patients. Pharmacogenetics 5, s74, 1995.
-
(1995)
Pharmacogenetics
, vol.5
-
-
Kihara, M.1
Noda, K.2
Kihara, M.3
-
128
-
-
0030012268
-
Genetic polymorphisms of debrisoquine and S-mephenytoin oxidation metabolism in Chinese populations, a meta-analysis
-
Xie, H.-G., Xu, Z.-H., Luo, X., Huang, S.-L., Zeng, F.-D., and Zhou, H.-H., Genetic polymorphisms of debrisoquine and S-mephenytoin oxidation metabolism in Chinese populations, a meta-analysis. Pharmacogenetics 6, 235. 1996.
-
(1996)
Pharmacogenetics
, vol.6
, pp. 235
-
-
Xie, H.-G.1
Xu, Z.-H.2
Luo, X.3
Huang, S.-L.4
Zeng, F.-D.5
Zhou, H.-H.6
-
129
-
-
0028971978
-
Glutathione-S-transferase (GSTT1) genetic polymorphism among Chinese, Malays and Indians in Singapore
-
Lee, E.J.D., Wong, J.Y.Y., Yeoh, P.N., and Gong, N.H., Glutathione-S-transferase (GSTT1) genetic polymorphism among Chinese, Malays and Indians in Singapore. Pharmacogenetics 5, 332, 1995.
-
(1995)
Pharmacogenetics
, vol.5
, pp. 332
-
-
Lee, E.J.D.1
Wong, J.Y.Y.2
Yeoh, P.N.3
Gong, N.H.4
-
130
-
-
0026705708
-
Incidence of S-mephenytoin hydroxylation deficiency in a Korean population and the interphenotypic differences in diazepam pharmacokinetics
-
Sohn, D.-R., Kusaka, M., Ishizaki, T., Shin, S.-G., Jang, I.-J., Shin, J.-G., and Chiba, K., Incidence of S-mephenytoin hydroxylation deficiency in a Korean population and the interphenotypic differences in diazepam pharmacokinetics. Clin. Pharmacol. Ther. 52, 160, 1992.
-
(1992)
Clin. Pharmacol. Ther.
, vol.52
, pp. 160
-
-
Sohn, D.-R.1
Kusaka, M.2
Ishizaki, T.3
Shin, S.-G.4
Jang, I.-J.5
Shin, J.-G.6
Chiba, K.7
-
131
-
-
0025887858
-
N-acetyltransferase polymorphism: Comparison of phenotype and genotype in humans
-
Hickman, D. and Sim, E., N-acetyltransferase polymorphism: comparison of phenotype and genotype in humans. Biochem. Pharmacol. 42, 1007, 1991.
-
(1991)
Biochem. Pharmacol.
, vol.42
, pp. 1007
-
-
Hickman, D.1
Sim, E.2
-
132
-
-
0027771328
-
Polymorphic N-acetyl-transferase (NAT2) in Amerindian populations of Panama and Columbia, high frequencies of point mutation 857A as found in allele S3/M3
-
Arias, T.D., Jorge, L.F., Griese, E.-U., Inaba, T., and Eichelbaum, M., Polymorphic N-acetyl-transferase (NAT2) in Amerindian populations of Panama and Columbia, high frequencies of point mutation 857A as found in allele S3/M3. Pharmacogenetics 3, 328, 1993.
-
(1993)
Pharmacogenetics
, vol.3
, pp. 328
-
-
Arias, T.D.1
Jorge, L.F.2
Griese, E.-U.3
Inaba, T.4
Eichelbaum, M.5
-
133
-
-
0028286844
-
Molecular genetics of human polymorphic N-acetyltransferase, enzymatic analysis of 15 recombinant wild-type, mutant, and chimeric NAT2 allozymes
-
Hein, D.W., Ferguson, R.J., Doll, M.A., Rustan, T.O., and Gray, K., Molecular genetics of human polymorphic N-acetyltransferase, enzymatic analysis of 15 recombinant wild-type, mutant, and chimeric NAT2 allozymes. Hum. Mol. Genet. 3, 729, 1994.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 729
-
-
Hein, D.W.1
Ferguson, R.J.2
Doll, M.A.3
Rustan, T.O.4
Gray, K.5
-
134
-
-
0029117480
-
Metabolic activation of N-hydroxyarylamines and N-hydroxyarylamides by 16 recombinant human NAT2 allozymes: Effects of 7 specific NAT 2 nucleic acid substitutions
-
Hein, D.W., Doll, M.A., Rustan, T.O., and Ferguson, R.J., Metabolic activation of N-hydroxyarylamines and N-hydroxyarylamides by 16 recombinant human NAT2 allozymes: effects of 7 specific NAT 2 nucleic acid substitutions. Cancer Res. 55, 3531, 1995.
-
(1995)
Cancer Res.
, vol.55
, pp. 3531
-
-
Hein, D.W.1
Doll, M.A.2
Rustan, T.O.3
Ferguson, R.J.4
-
135
-
-
0029143503
-
Enzyme kinetic properties of human recombinant arylamine N-acetyltransferase 2 allotypic variants expressed in Escherichia coli
-
Hickman, D., Palamanda, J.R., Unadkat, J.D., and Sim, E., Enzyme kinetic properties of human recombinant arylamine N-acetyltransferase 2 allotypic variants expressed in Escherichia coli. Biochem. Pharmacol. 50, 697, 1995.
-
(1995)
Biochem. Pharmacol.
, vol.50
, pp. 697
-
-
Hickman, D.1
Palamanda, J.R.2
Unadkat, J.D.3
Sim, E.4
-
136
-
-
0026648960
-
Site-directed mutagenesis of recombinant human arylamine N-acetyltransferase expressed in Escherichia coli: Evidence for direct involvement of Cys68 in the catalytic mechanism of polymorphic human NAT 2
-
Dupret, J.-M. and Grant, D.M., Site-directed mutagenesis of recombinant human arylamine N-acetyltransferase expressed in Escherichia coli: evidence for direct involvement of Cys68 in the catalytic mechanism of polymorphic human NAT 2. J. Biol. Chem. 267, 7381, 1992.
-
(1992)
J. Biol. Chem.
, vol.267
, pp. 7381
-
-
Dupret, J.-M.1
Grant, D.M.2
-
137
-
-
0028844578
-
Polymorphism in the N-acetyltransferase 1 (NAT1) polyadenylation signal, association of the NAT1*10 allele with higher N-acetylation activity in bladder and colon tissue
-
Bell, D.A., Badawi, A.F., Lang, N.P., Ilett, K.F., Kadlubar, F.F., and Hirvonen, A., Polymorphism in the N-acetyltransferase 1 (NAT1) polyadenylation signal, association of the NAT1*10 allele with higher N-acetylation activity in bladder and colon tissue. Cancer Res. 55, 5226, 1995.
-
(1995)
Cancer Res.
, vol.55
, pp. 5226
-
-
Bell, D.A.1
Badawi, A.F.2
Lang, N.P.3
Ilett, K.F.4
Kadlubar, F.F.5
Hirvonen, A.6
-
138
-
-
0029835661
-
Human N-acetylation of benzidine: Role of NAT1 and NAT2
-
Zenser, T.V., Lakshmi, V.M., Rustan, T.D., Doll, M.A., Deitz, A.C., Davis, B.B., and Hein, D.W., Human N-acetylation of benzidine: role of NAT1 and NAT2. Cancer Res. 56, 3941, 1996.
-
(1996)
Cancer Res.
, vol.56
, pp. 3941
-
-
Zenser, T.V.1
Lakshmi, V.M.2
Rustan, T.D.3
Doll, M.A.4
Deitz, A.C.5
Davis, B.B.6
Hein, D.W.7
-
139
-
-
0014384060
-
Madras study of supervised once-weekly chemotherapy
-
Menon, N.K., Madras study of supervised once-weekly chemotherapy. Bull. Int. un Tuberc. 41, 316, 1968.
-
(1968)
Bull. Int. un Tuberc.
, vol.41
, pp. 316
-
-
Menon, N.K.1
-
140
-
-
84965909752
-
Clinical applications of antibiotic and chemotherapeutic agents
-
Mitchison, D.A., II. Clinical applications of antibiotic and chemotherapeutic agents. Proc. Roy. Soc. Med. 64, 537, 1971.
-
(1971)
Proc. Roy. Soc. Med.
, vol.64
, pp. 537
-
-
Mitchison D.A. II1
-
141
-
-
0013536878
-
Effect of acetylation phenotype on the antihypertensive response to hydralazine
-
Pasanen, M., Pasanen, A., and Jounela, A., Effect of acetylation phenotype on the antihypertensive response to hydralazine. Scand. J. Clin. Lab. Invest. 31 (Suppl. 130), 12, 1973.
-
(1973)
Scand. J. Clin. Lab. Invest.
, vol.31
, Issue.SUPPL. 130
, pp. 12
-
-
Pasanen, M.1
Pasanen, A.2
Jounela, A.3
-
142
-
-
0016684049
-
Acetylator phenotype and the antihypertensive response to hydralazine
-
Jounela, A.J., Pasanen, M., and Mattila, M.J., Acetylator phenotype and the antihypertensive response to hydralazine. Acta Med. Scand. 197, 303, 1975.
-
(1975)
Acta Med. Scand.
, vol.197
, pp. 303
-
-
Jounela, A.J.1
Pasanen, M.2
Mattila, M.J.3
-
143
-
-
0017365752
-
Acetylator phenotyping of tuberculosis patients using matrix isoniazid or sulfadimidine and its prognostic significance for treatment with several intermittent isoniazid-containing regimens
-
Ellard, G.A. and Gammon, P.T., Acetylator phenotyping of tuberculosis patients using matrix isoniazid or sulfadimidine and its prognostic significance for treatment with several intermittent isoniazid-containing regimens. Br. J. Clin. Pharmacol. 4, 5, 1977.
-
(1977)
Br. J. Clin. Pharmacol.
, vol.4
, pp. 5
-
-
Ellard, G.A.1
Gammon, P.T.2
-
144
-
-
0019407216
-
Prizidilol, an antihypertensive with precapillary vasodilator and β-adrenoceptor blocking actions, in primary hypertension
-
Larsson, R., Karlberg, B.E., Norlander, B., and Wirsen, A., Prizidilol, an antihypertensive with precapillary vasodilator and β-adrenoceptor blocking actions, in primary hypertension. Clin. Pharmacol. Ther. 29, 588, 1981.
-
(1981)
Clin. Pharmacol. Ther.
, vol.29
, pp. 588
-
-
Larsson, R.1
Karlberg, B.E.2
Norlander, B.3
Wirsen, A.4
-
145
-
-
0015336460
-
Relation of hydralazine plasma concentration to dosage and hypotensive action
-
Zacest, R. and Koch-Weser, J., Relation of hydralazine plasma concentration to dosage and hypotensive action. Clin. Pharmacol. Ther. 13, 420, 1972.
-
(1972)
Clin. Pharmacol. Ther.
, vol.13
, pp. 420
-
-
Zacest, R.1
Koch-Weser, J.2
-
146
-
-
0016268028
-
Acetylator phenotype, minimal maintenance dose and haemolytic effect of dapsone in dermatitis herpetiformis
-
Forstrom, L., Mattila, M.J., and Mustakallio, K.K., Acetylator phenotype, minimal maintenance dose and haemolytic effect of dapsone in dermatitis herpetiformis. Ann. Clin. Res. 6, 308, 1974.
-
(1974)
Ann. Clin. Res.
, vol.6
, pp. 308
-
-
Forstrom, L.1
Mattila, M.J.2
Mustakallio, K.K.3
-
147
-
-
0019869340
-
Plasma concentration and acetylator phenotype determine response to oral hydralazine
-
Shepherd, A.M.M., McNay, J.L., Ludden, T.M., Lin, M.-S., and Musgrave, G.E., Plasma concentration and acetylator phenotype determine response to oral hydralazine. Hypertension 3, 580, 1981.
-
(1981)
Hypertension
, vol.3
, pp. 580
-
-
Shepherd, A.M.M.1
McNay, J.L.2
Ludden, T.M.3
Lin, M.-S.4
Musgrave, G.E.5
-
148
-
-
0021367521
-
Should the acetylator phenotype be determined when prescribing hydralazine for hypertension
-
Ramsay, L.E., Silas, J.H., Ollerenshaw, J.D., Tucker, G.T., Phillips, F.C., and Freestone, S., Should the acetylator phenotype be determined when prescribing hydralazine for hypertension? Eur. J. Clin. Pharmacol. 26, 39, 1984.
-
(1984)
Eur. J. Clin. Pharmacol.
, vol.26
, pp. 39
-
-
Ramsay, L.E.1
Silas, J.H.2
Ollerenshaw, J.D.3
Tucker, G.T.4
Phillips, F.C.5
Freestone, S.6
-
149
-
-
0025947335
-
Paradoxical relationship between acetylator phenotype and amonafide toxicity
-
Ratain, M.J., Mick, R., Berezin, F., Janisch, L., Schilsky, R.L., Williams, S.F., and Smiddy, J., Paradoxical relationship between acetylator phenotype and amonafide toxicity. Clin. Pharmacol. Ther. 50, 573, 1991.
-
(1991)
Clin. Pharmacol. Ther.
, vol.50
, pp. 573
-
-
Ratain, M.J.1
Mick, R.2
Berezin, F.3
Janisch, L.4
Schilsky, R.L.5
Williams, S.F.6
Smiddy, J.7
-
150
-
-
0000995035
-
Peripheral neuritis due to isoniazid
-
Devadatta, S., Gangadharam, P.R.J., Andrews, R.H., Fox, W., Ramakrishnan, C.V., Selkon, J.B., and Vein, S., Peripheral neuritis due to isoniazid. Bull Wld. Hlth. Org. 23, 587, 1960.
-
(1960)
Bull Wld. Hlth. Org.
, vol.23
, pp. 587
-
-
Devadatta, S.1
Gangadharam, P.R.J.2
Andrews, R.H.3
Fox, W.4
Ramakrishnan, C.V.5
Selkon, J.B.6
Vein, S.7
-
151
-
-
0014823763
-
Relationship of acetyl transferase activity to antinuclear antibodies and toxic symptoms in hypertensive patients treated with hydralazine
-
Perry, H.M., Tan, E.M., Carmody, S., and Sakamoto, A., Relationship of acetyl transferase activity to antinuclear antibodies and toxic symptoms in hypertensive patients treated with hydralazine. J. Lab. Clin. Med. 76, 114, 1970.
-
(1970)
J. Lab. Clin. Med.
, vol.76
, pp. 114
-
-
Perry, H.M.1
Tan, E.M.2
Carmody, S.3
Sakamoto, A.4
-
152
-
-
0015321166
-
Acetylator phenotype and adverse effects of sulphasalazine in healthy subjects
-
Schroder, H. and Price Evans, D.A., Acetylator phenotype and adverse effects of sulphasalazine in healthy subjects. Gut 13, 278, 1972.
-
(1972)
Gut
, vol.13
, pp. 278
-
-
Schroder, H.1
Price Evans, D.A.2
-
153
-
-
0015916139
-
Adverse reactions during salicylazosulfapyridine therapy and the relation with drag metabolism and acetylator phenotype
-
Das, K.M., Eastwood, M.A., McManus, J.P.A., and Sircus, W., Adverse reactions during salicylazosulfapyridine therapy and the relation with drag metabolism and acetylator phenotype. N. Engl. J. Med. 289, 491, 1973.
-
(1973)
N. Engl. J. Med.
, vol.289
, pp. 491
-
-
Das, K.M.1
Eastwood, M.A.2
McManus, J.P.A.3
Sircus, W.4
-
154
-
-
0016760218
-
Antinuclear antibodies during procainamide treatment and drag acetylation
-
Davies, D.M., Beedie, M.A., and Rawlins, M.D., Antinuclear antibodies during procainamide treatment and drag acetylation. Br. Med. J. 3, 682, 1975.
-
(1975)
Br. Med. J.
, vol.3
, pp. 682
-
-
Davies, D.M.1
Beedie, M.A.2
Rawlins, M.D.3
-
155
-
-
0016699528
-
Effects of long-term treatment with procaine amide
-
Henningsen, N.C., Cederberg, A., Hanson, A., and Johansson, B.W., Effects of long-term treatment with procaine amide. Acta Med. Scand. 198, 475, 1975.
-
(1975)
Acta Med. Scand.
, vol.198
, pp. 475
-
-
Henningsen, N.C.1
Cederberg, A.2
Hanson, A.3
Johansson, B.W.4
-
156
-
-
0017146043
-
Acetylator phenotype in patients with hydralazine-induced lupoid syndrome
-
Strandberg, I., Boman, G., Hassler, L., and Sjoqvist, F., Acetylator phenotype in patients with hydralazine-induced lupoid syndrome. Acta Med. Scand. 200, 367, 1976.
-
(1976)
Acta Med. Scand.
, vol.200
, pp. 367
-
-
Strandberg, I.1
Boman, G.2
Hassler, L.3
Sjoqvist, F.4
-
157
-
-
0018099670
-
Effect of acetylator phenotype on the rate at which procainamide induces antinuclear antibodies and the lupus syndrome
-
Woosley, R.L., Drayer, D.E., Reidenberg, M.M., Nies, A.S., Carr, K., and Oates, J.A., Effect of acetylator phenotype on the rate at which procainamide induces antinuclear antibodies and the lupus syndrome. N. Engl. J. Med. 298, 1157, 1978.
-
(1978)
N. Engl. J. Med.
, vol.298
, pp. 1157
-
-
Woosley, R.L.1
Drayer, D.E.2
Reidenberg, M.M.3
Nies, A.S.4
Carr, K.5
Oates, J.A.6
-
158
-
-
0018868978
-
Hydralazine-induced systemic lupus erythematosus, influence of HLA-DR and sex on susceptibility
-
Batchelor, J.R., Welsh, K.I., Mansilla Tinoco, R., Dollery, C.T., Hughes, G.R.V., Bernstein, R., Ryan, P., Naish, P.F., Aber, G.M., Bing, R.F., and Russell, G.L., Hydralazine-induced systemic lupus erythematosus, Influence of HLA-DR and sex on susceptibility. Lancet, 1107, 1980.
-
(1980)
Lancet
, pp. 1107
-
-
Batchelor, J.R.1
Welsh, K.I.2
Mansilla Tinoco, R.3
Dollery, C.T.4
Hughes, G.R.V.5
Bernstein, R.6
Ryan, P.7
Naish, P.F.8
Aber, G.M.9
Bing, R.F.10
Russell, G.L.11
-
159
-
-
0019867906
-
Acetylator phenotype and serum levels of sulfapyridine in patients with inflammatory bowel disease
-
Sharp, M.E., Wallace, S.M., Hindmarsh, K.W., and Brown, M.A., Acetylator phenotype and serum levels of sulfapyridine in patients with inflammatory bowel disease. Eur. J. Clin. Pharmacol. 21, 243, 1981.
-
(1981)
Eur. J. Clin. Pharmacol.
, vol.21
, pp. 243
-
-
Sharp, M.E.1
Wallace, S.M.2
Hindmarsh, K.W.3
Brown, M.A.4
-
160
-
-
0020662982
-
The effect of the acetylator phenotype on the metabolism of sulfasalazine in man
-
Azad Khan, A.K., Nurazzaman, M., and Truelove, S.C.,The effect of the acetylator phenotype on the metabolism of sulfasalazine in man. J. Med. Genet. 20, 30, 1983.
-
(1983)
J. Med. Genet.
, vol.20
, pp. 30
-
-
Azad Khan, A.K.1
Nurazzaman, M.2
Truelove, S.C.3
-
161
-
-
0022453306
-
Differences in metabolism of sulfonamides predisposing to idiosyncratic toxicity
-
Shear, N.H., Spielberg, S.P., Grant, D.M., Tang, B.K., and Kalow, W., Differences in metabolism of sulfonamides predisposing to idiosyncratic toxicity. Ann. Intern. Med. 105, 179, 1986.
-
(1986)
Ann. Intern. Med.
, vol.105
, pp. 179
-
-
Shear, N.H.1
Spielberg, S.P.2
Grant, D.M.3
Tang, B.K.4
Kalow, W.5
-
162
-
-
0026078504
-
Prominence of slow acetylator phenotype among patients with sulfonamide hypersensitivity reactions
-
Rieder, M.J., Shear, N.H., Kanee, A., Tang, B.K., and Spielberg, S.P., Prominence of slow acetylator phenotype among patients with sulfonamide hypersensitivity reactions. Clin. Pharmacol. Ther. 49, 13, 1991.
-
(1991)
Clin. Pharmacol. Ther.
, vol.49
, pp. 13
-
-
Rieder, M.J.1
Shear, N.H.2
Kanee, A.3
Tang, B.K.4
Spielberg, S.P.5
-
163
-
-
0029130809
-
A slow acetylator genotype is a risk factor for sulphonamide-induced toxic epidermal necrolysis and Stevens-Johnson syndrome
-
Wolkenstein, P., Carriere, V., Charue, D., Bastuji-Garin, S., Revuz, J., Roujeau, J.-C., Beaune, P., and Bagot, M., A slow acetylator genotype is a risk factor for sulphonamide-induced toxic epidermal necrolysis and Stevens-Johnson syndrome. Pharmacogenetics 5, 255, 1995.
-
(1995)
Pharmacogenetics
, vol.5
, pp. 255
-
-
Wolkenstein, P.1
Carriere, V.2
Charue, D.3
Bastuji-Garin, S.4
Revuz, J.5
Roujeau, J.-C.6
Beaune, P.7
Bagot, M.8
-
164
-
-
0000147088
-
Further investigations of the role of acetylation in sulfonamide hypersensitivity reactions
-
Nuss, C.E., Grant, D.M., Spielberg, S.P., and Cribb, A.E., Further investigations of the role of acetylation in sulfonamide hypersensitivity reactions. Biomarkers 1, 267, 1996.
-
(1996)
Biomarkers
, vol.1
, pp. 267
-
-
Nuss, C.E.1
Grant, D.M.2
Spielberg, S.P.3
Cribb, A.E.4
-
165
-
-
0030426571
-
N-Acetyltransferases: Pharmacogenetics and clinical consequences of polymorphic drug metabolism
-
Spielberg, S.P., N-Acetyltransferases: pharmacogenetics and clinical consequences of polymorphic drug metabolism. J. Pharmacokin. Biopharm. 24, 509, 1996.
-
(1996)
J. Pharmacokin. Biopharm.
, vol.24
, pp. 509
-
-
Spielberg, S.P.1
-
166
-
-
0028236383
-
Genetically based N-acetyl-transferase metabolic polymorphism and low-level environmental exposure to carcinogens
-
Vineis, P., Bartsch, H., Caporaso, N., Harrington, A.M., Kadlubar, F.F., Landi, M.T., Malaveille, C., Shields, P.G., Skipper, P., Talaska, G., and Tannenbaum, S.R., Genetically based N-acetyl-transferase metabolic polymorphism and low-level environmental exposure to carcinogens. Nature, 369, 154, 1994.
-
(1994)
Nature
, vol.369
, pp. 154
-
-
Vineis, P.1
Bartsch, H.2
Caporaso, N.3
Harrington, A.M.4
Kadlubar, F.F.5
Landi, M.T.6
Malaveille, C.7
Shields, P.G.8
Skipper, P.9
Talaska, G.10
Tannenbaum, S.R.11
-
167
-
-
9344264042
-
The impact of inter-individual variation in NAT2 activity on benzidine urinary metabolites and urothelial DNA adducts in exposed workers
-
Rothman, N., Bhatnagar, V.K., Hayes, R.B., Zenser, T.V., Kashyap, S.K., Buffer, M.A., Bell, D.A., Lakshmi, V., Jaeger, M., Kashyap, R., Hirvonen, A., Schulte, P.A., Dosemeci, M., Hsu, F., Parikh, D.J., Davis, B.B., and Talaska, G., The impact of inter-individual variation in NAT2 activity on benzidine urinary metabolites and urothelial DNA adducts in exposed workers. Proc. Natl. Acad. Sci. U.S.A. 93, 5084, 1996.
-
(1996)
Proc. Natl. Acad. Sci. U.S.A.
, vol.93
, pp. 5084
-
-
Rothman, N.1
Bhatnagar, V.K.2
Hayes, R.B.3
Zenser, T.V.4
Kashyap, S.K.5
Buffer, M.A.6
Bell, D.A.7
Lakshmi, V.8
Jaeger, M.9
Kashyap, R.10
Hirvonen, A.11
Schulte, P.A.12
Dosemeci, M.13
Hsu, F.14
Parikh, D.J.15
Davis, B.B.16
Talaska, G.17
-
168
-
-
0028879678
-
Role of aromatic amine acetyltransferase, NAT1 and NAT2, in carcinogen-DNA adduct formation in the human urinary bladder
-
Badawi, A.F., Hirvonen, A., Bell, D.A., Lang, N.P., and Kadlubar, F.F., Role of aromatic amine acetyltransferase, NAT1 and NAT2, in carcinogen-DNA adduct formation in the human urinary bladder. Cancer Res. 55, 5230, 1995.
-
(1995)
Cancer Res.
, vol.55
, pp. 5230
-
-
Badawi, A.F.1
Hirvonen, A.2
Bell, D.A.3
Lang, N.P.4
Kadlubar, F.F.5
-
169
-
-
0023096984
-
Acetylation phenotype in colorectal carcinoma
-
Ilett, K.F., David, B.M., Detchon, P., Castleden, W.M., and Kwa, R., Acetylation phenotype in colorectal carcinoma. Cancer Res. 47, 1466, 1987.
-
(1987)
Cancer Res.
, vol.47
, pp. 1466
-
-
Ilett, K.F.1
David, B.M.2
Detchon, P.3
Castleden, W.M.4
Kwa, R.5
-
170
-
-
0025324003
-
Aromatic amine acetyltransferase as a marker for colorectal cancer: Environmental and demographic associations
-
Wohlleb, J.C., Hunter, C.F., Blass, B., Kadlubar, F.F., Chu, D.Z.J., and Lang, N.P., Aromatic amine acetyltransferase as a marker for colorectal cancer:
-
(1990)
Int. J. Cancer
, vol.46
, pp. 22
-
-
Wohlleb, J.C.1
Hunter, C.F.2
Blass, B.3
Kadlubar, F.F.4
Chu, D.Z.J.5
Lang, N.P.6
-
171
-
-
0027999623
-
Rapid metabolic phenotypes for acetyltransferase and cytochrome P4501A2 and putative exposure to food-borne heterocyclic amines increase the risk for colorectal cancer or polyps
-
Lang, N.P., Butler, M.A., Massengill, J., Lawson, M., Stotts, R.C., Hauer-Jensen, M., and Kadlubar, F.F., Rapid metabolic phenotypes for acetyltransferase and cytochrome P4501A2 and putative exposure to food-borne heterocyclic amines increase the risk for colorectal cancer or polyps. Cancer Epidemiol. Biomark. Prevent. 3, 675, 1994.
-
(1994)
Cancer Epidemiol. Biomark. Prevent.
, vol.3
, pp. 675
-
-
Lang, N.P.1
Butler, M.A.2
Massengill, J.3
Lawson, M.4
Stotts, R.C.5
Hauer-Jensen, M.6
Kadlubar, F.F.7
-
172
-
-
0019976311
-
Role of N-acetyltransferase phenotypes in bladder cancer carcinogenesis: A pharmacogenetic epidemiological approach to bladder cancer
-
Cartwright, R.A., Rogers, H.J., Barbara-Hall, D., Glashan, R.W., Ahmad, R.A., Higgins, E., and Kahn, M.A., Role of N-acetyltransferase phenotypes in bladder cancer carcinogenesis: a pharmacogenetic epidemiological approach to bladder cancer. Lancet III, 842, 1982.
-
(1982)
Lancet
, vol.3
, pp. 842
-
-
Cartwright, R.A.1
Rogers, H.J.2
Barbara-Hall, D.3
Glashan, R.W.4
Ahmad, R.A.5
Higgins, E.6
Kahn, M.A.7
-
173
-
-
0021931373
-
N-Acetyltransferase phenotypes in the urinary bladder carcinogenesis of a low-risk population
-
Mommsen, S., Barfod, N.M., and Aagaard, J., N-Acetyltransferase phenotypes in the urinary bladder carcinogenesis of a low-risk population. Carcinogenesis 6, 199, 1985.
-
(1985)
Carcinogenesis
, vol.6
, pp. 199
-
-
Mommsen, S.1
Barfod, N.M.2
Aagaard, J.3
-
174
-
-
0028224431
-
Acetylator phenotype, aminobiphenyl-hemoglobin adduct levels, and bladder cancer risk in white, black, and Asian men in Los Angeles
-
California
-
Yu, M.C., Skipper, P.L., Taghizadeh, K., Tannanbaum, S.R., Chan, K.K., Henderson, B.E., and Ross, R.K., Acetylator phenotype, aminobiphenyl-hemoglobin adduct levels, and bladder cancer risk in white, black, and Asian men in Los Angeles, California. J. Natl. Canc. Inst. 86, 712, 1994.
-
(1994)
J. Natl. Canc. Inst.
, vol.86
, pp. 712
-
-
Yu, M.C.1
Skipper, P.L.2
Taghizadeh, K.3
Tannanbaum, S.R.4
Chan, K.K.5
Henderson, B.E.6
Ross, R.K.7
-
175
-
-
0028909978
-
Slow N-acetylation genotype is a susceptibility factor in occupational and smoking related bladder cancer
-
Risch, A., Wallace, D.M.A., Bathers, S., and Sim, E., Slow N-acetylation genotype is a susceptibility factor in occupational and smoking related bladder cancer. Hum. Mol. Genet. 4, 231, 1995.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 231
-
-
Risch, A.1
Wallace, D.M.A.2
Bathers, S.3
Sim, E.4
-
176
-
-
0029815779
-
Combined analysis of inherited polymorphisms in arylamine N-acetyltransferase 2, glutathione-S-transferases M1 and T1, microsomal epoxide hydrolase, and cytochrome P450 enzymes as modulators of bladder cancer risk
-
Brockmoller, J., Cascorbi, I., Kerb, R., and Roots, I., Combined analysis of inherited polymorphisms in arylamine N-acetyltransferase 2, glutathione-S-transferases M1 and T1, microsomal epoxide hydrolase, and cytochrome P450 enzymes as modulators of bladder cancer risk. Cancer Res. 56, 3915, 1996.
-
(1996)
Cancer Res.
, vol.56
, pp. 3915
-
-
Brockmoller, J.1
Cascorbi, I.2
Kerb, R.3
Roots, I.4
-
177
-
-
0029163025
-
Polyadenylation polymorphism in the acetyltransferase I gene (NAT1) increases risk of colorectal cancer
-
Bell, D.A., Stephens, E.A., Castranio, T., Umbach, D.M., Watson, M., Deakin, M., Elder, J., Hendrickse, C., Duncan, H., and Strange, R.C., Polyadenylation polymorphism in the acetyltransferase I gene (NAT1) increases risk of colorectal cancer. Cancer Res. 55, 3537, 1995.
-
(1995)
Cancer Res.
, vol.55
, pp. 3537
-
-
Bell, D.A.1
Stephens, E.A.2
Castranio, T.3
Umbach, D.M.4
Watson, M.5
Deakin, M.6
Elder, J.7
Hendrickse, C.8
Duncan, H.9
Strange, R.C.10
-
178
-
-
0000319425
-
The role of N-acetylation polymorphisms at NAT1 and NAT2 in smoking-associated bladder cancer
-
Taylor, J.A., Umbach, D.M., Stephens, E., Paulson, D., Robertson, C., Mohler, J.L., and Bell, D.A., The role of N-acetylation polymorphisms at NAT1 and NAT2 in smoking-associated bladder cancer, Proc. Am. Ass. Cancer Res. 36, 282, 1995.
-
(1995)
Proc. Am. Ass. Cancer Res.
, vol.36
, pp. 282
-
-
Taylor, J.A.1
Umbach, D.M.2
Stephens, E.3
Paulson, D.4
Robertson, C.5
Mohler, J.L.6
Bell, D.A.7
-
179
-
-
0026529664
-
Metabolic polymorphisms affecting activation of toxic and mutagenic arylamines
-
Bock, K.W., Metabolic polymorphisms affecting activation of toxic and mutagenic arylamines. Trends Pharmacol. Sci. 13, 223, 1992.
-
(1992)
Trends Pharmacol. Sci.
, vol.13
, pp. 223
-
-
Bock, K.W.1
-
180
-
-
0029559744
-
Genetic susceptibility and carcinogen-DNA adduct formation in human urinary bladder carcinogenesis
-
Kadlubar, F.F. and Badawi, A.F., Genetic susceptibility and carcinogen-DNA adduct formation in human urinary bladder carcinogenesis. Toxicol. Lett. 82/ 83, 627, 1995.
-
(1995)
Toxicol. Lett.
, vol.82-83
, pp. 627
-
-
Kadlubar, F.F.1
Badawi, A.F.2
-
181
-
-
0029906406
-
Interplay between heterocyclic amines in cooked meat and metabolic phenotype in the etiology of colon cancer
-
Vineis, P. and McMichael, A., Interplay between heterocyclic amines in cooked meat and metabolic phenotype in the etiology of colon cancer. Cancer Causes and Control 7, 479, 1996.
-
(1996)
Cancer Causes and Control
, vol.7
, pp. 479
-
-
Vineis, P.1
McMichael, A.2
-
182
-
-
0029062796
-
Acetylation polymorphism and prevalence of colorectal adenomas
-
Probst-Hensch, N.M., Haile, R.W., Ingles, S.A., Longnecker, M.P., Han, C.-Y., Lin, B.K., Lee, D.B., Sakamoto, G.T., Frankl, H.D., Lee, E.R., and Lin, H.J., Acetylation polymorphism and prevalence of colorectal adenomas. Cancer Res. 55, 2017 1995.
-
(1995)
Cancer Res.
, vol.55
, pp. 2017
-
-
Probst-Hensch, N.M.1
Haile, R.W.2
Ingles, S.A.3
Longnecker, M.P.4
Han, C.-Y.5
Lin, B.K.6
Lee, D.B.7
Sakamoto, G.T.8
Frankl, H.D.9
Lee, E.R.10
Lin, H.J.11
-
183
-
-
0027324277
-
Human acetylator genotype: Relationship to colorectal cancer incidence and arylamine N-acetyltransferase expression in colon cytosol
-
Rodriquez, J.W., Kirlin, W.G., Ferguson, R.J., Doll, M.A., Gray, K., Rustan, T.D., Lee, M.E., Kemp, K., Urso, P., and Hein, D.W., Human acetylator genotype: relationship to colorectal cancer incidence and arylamine N-acetyltransferase expression in colon cytosol. Arch. Toxicol. 67, 445, 1993.
-
(1993)
Arch. Toxicol.
, vol.67
, pp. 445
-
-
Rodriquez, J.W.1
Kirlin, W.G.2
Ferguson, R.J.3
Doll, M.A.4
Gray, K.5
Rustan, T.D.6
Lee, M.E.7
Kemp, K.8
Urso, P.9
Hein, D.W.10
-
184
-
-
0029806517
-
Lack of association between the polyadenylation polymorphism in the NAT1 (acetyltransferase 1) gene and colorectal adenomas
-
Probst-Hensch, N.M., Haile, R.W., Li, D.S., Sakamoto, G.T., Louie, A.D., Lin, B.K., Frankl, H.D., Lee, E.R., and Lin, H.J., Lack of association between the polyadenylation polymorphism in the NAT1 (acetyltransferase 1) gene and colorectal adenomas. Carcinogenesis, 17, 2125, 1996.
-
(1996)
Carcinogenesis
, vol.17
, pp. 2125
-
-
Probst-Hensch, N.M.1
Haile, R.W.2
Li, D.S.3
Sakamoto, G.T.4
Louie, A.D.5
Lin, B.K.6
Frankl, H.D.7
Lee, E.R.8
Lin, H.J.9
-
185
-
-
0029096522
-
Lung cancer and mutations at the polymorphic NAT2 gene locus
-
Martinez, C., Agundez, J.A.G., Olivera, M., Martin, R., Ladero, J.M., and Benitez, J., Lung cancer and mutations at the polymorphic NAT2 gene locus. Pharmacogenetics 5, 207, 1995.
-
(1995)
Pharmacogenetics
, vol.5
, pp. 207
-
-
Martinez, C.1
Agundez, J.A.G.2
Olivera, M.3
Martin, R.4
Ladero, J.M.5
Benitez, J.6
-
186
-
-
0029837310
-
Homozygous rapid arylamine N-acetyltransferase (NAT2) genotype as a susceptibility factor for lung cancer
-
Cascorbi, L., Brockmoller, J., Mrozikiewicz, P.M., Bauer, S., Loddenkemper, R., and Roots, I., Homozygous rapid arylamine N-acetyltransferase (NAT2) genotype as a susceptibility factor for lung cancer. Cancer Res. 56, 3961, 1996.
-
(1996)
Cancer Res.
, vol.56
, pp. 3961
-
-
Cascorbi, L.1
Brockmoller, J.2
Mrozikiewicz, P.M.3
Bauer, S.4
Loddenkemper, R.5
Roots, I.6
-
187
-
-
8944256082
-
Nomenclature for human CYP2D6 alleles
-
Daly, A.K., Brockmoller, J., Broly, F., Eichelbaum, M., Evans, W.E., Gonzalez, F.J., Huang, J.-D., Idle, J.R., Ingelman-Sundberg, M., Ishizaki, T., Jacqz-Aigrain, E., Meyer, U.A., Nebert, D.W., Steen, V.M., Wolf, C.R., and Zanger, U.M., Nomenclature for human CYP2D6 alleles. Pharmacogenetics 6, 193, 1996.
-
(1996)
Pharmacogenetics
, vol.6
, pp. 193
-
-
Daly, A.K.1
Brockmoller, J.2
Broly, F.3
Eichelbaum, M.4
Evans, W.E.5
Gonzalez, F.J.6
Huang, J.-D.7
Idle, J.R.8
Ingelman-Sundberg, M.9
Ishizaki, T.10
Jacqz-Aigrain, E.11
Meyer, U.A.12
Nebert, D.W.13
Steen, V.M.14
Wolf, C.R.15
Zanger, U.M.16
-
188
-
-
0029854529
-
A C4887A polymorphism in exon 7 of human CYP1A1. Population frequency, mutation linkages, and impact on lung cancer susceptibility
-
Cascorbi, I., Brockmoller, J., and Roots, I., A C4887A polymorphism in exon 7 of human CYP1A1. Population frequency, mutation linkages, and impact on lung cancer susceptibility. Cancer Res. 56, 4965, 1996.
-
(1996)
Cancer Res.
, vol.56
, pp. 4965
-
-
Cascorbi, I.1
Brockmoller, J.2
Roots, I.3
-
189
-
-
9044254525
-
P450 superfamily, update on new sequences, gene mapping, accession numbers and nomenclature
-
Nelson, D.R., Koymans, L., Kamataki, T., Stegeman, J.J., Feyereisen, R., Waxman, D.J., Waterman, M.R., Gotoh, O., Coon, M.J., Estabrook, R.W., Gunsalus, I.C., and Nebert, D.W., P450 superfamily, update on new sequences, gene mapping, accession numbers and nomenclature. Pharmacogenetics, 6, 1 1996.
-
(1996)
Pharmacogenetics
, vol.6
, pp. 1
-
-
Nelson, D.R.1
Koymans, L.2
Kamataki, T.3
Stegeman, J.J.4
Feyereisen, R.5
Waxman, D.J.6
Waterman, M.R.7
Gotoh, O.8
Coon, M.J.9
Estabrook, R.W.10
Gunsalus, I.C.11
Nebert, D.W.12
-
190
-
-
0026750647
-
The human hepatic cytochromes P450 involved in drug metabolism
-
Wrighton, S.A. and Stevens, J.C., The human hepatic cytochromes P450 involved in drug metabolism. Crit. Rev. Toxicol. 22, 1, 1992.
-
(1992)
Crit. Rev. Toxicol.
, vol.22
, pp. 1
-
-
Wrighton, S.A.1
Stevens, J.C.2
-
191
-
-
0028876897
-
Oxygen and xenobiotic reductase activities of cytochrome P450
-
Goeptar, A.R., Scheerens, H., and Vermeulen, N.P.E., Oxygen and xenobiotic reductase activities of cytochrome P450. Crit. Rev. Toxicol. 25, 25, 1995.
-
(1995)
Crit. Rev. Toxicol.
, vol.25
, pp. 25
-
-
Goeptar, A.R.1
Scheerens, H.2
Vermeulen, N.P.E.3
-
192
-
-
0025992864
-
Oxidation of toxic and carcinogenic chemicals by human cytochrome P-450 enzymes
-
Guengerich, F.P. and Shimada, T., Oxidation of toxic and carcinogenic chemicals by human cytochrome P-450 enzymes. Chem. Res. Toxicol. 4, 391, 1991.
-
(1991)
Chem. Res. Toxicol.
, vol.4
, pp. 391
-
-
Guengerich, F.P.1
Shimada, T.2
-
193
-
-
0026661470
-
Metabolic activation of carcinogens
-
Guengerich, F.P., Metabolic activation of carcinogens. Pharmacol. Ther. 54, 17, 1992.
-
(1992)
Pharmacol. Ther.
, vol.54
, pp. 17
-
-
Guengerich, F.P.1
-
194
-
-
0028272001
-
Role of human cytochromes P450 in the metabolic activation of chemical carcinogens and toxins
-
Gonzalez, F.J. and Gelboin, H.V., Role of human cytochromes P450 in the metabolic activation of chemical carcinogens and toxins. Drug Metab. Rev. 26, 165, 1994.
-
(1994)
Drug Metab. Rev.
, vol.26
, pp. 165
-
-
Gonzalez, F.J.1
Gelboin, H.V.2
-
195
-
-
0023061373
-
P450 genes, structure, evolution, and regulation
-
Nebert, D.W. and Gonzalez, F.J., P450 genes, structure, evolution, and regulation. Ann. Rev. Biochem. 56, 945, 1987.
-
(1987)
Ann. Rev. Biochem.
, vol.56
, pp. 945
-
-
Nebert, D.W.1
Gonzalez, F.J.2
-
196
-
-
0024236331
-
The molecular biology of cytochrome P450s
-
Gonzalez, F.J., The molecular biology of cytochrome P450s. Pharmacol. Rev. 40, 243, 1989.
-
(1989)
Pharmacol. Rev.
, vol.40
, pp. 243
-
-
Gonzalez, F.J.1
-
197
-
-
0025067462
-
Molecular genetics of the P-450 superfamily
-
Gonzalez, F.J., Molecular genetics of the P-450 superfamily. Pharmacol. Ther. 45, 1, 1990.
-
(1990)
Pharmacol. Ther.
, vol.45
, pp. 1
-
-
Gonzalez, F.J.1
-
198
-
-
0029588524
-
The role of cytochrome P450 enzymes in hepatic and extrahepatic drug toxicity
-
Park, B.K., Pirmohamed, M., and Kitteringham, N.R., The role of cytochrome P450 enzymes in hepatic and extrahepatic drug toxicity. Pharmacol. Ther. 68, 385, 1995.
-
(1995)
Pharmacol. Ther.
, vol.68
, pp. 385
-
-
Park, B.K.1
Pirmohamed, M.2
Kitteringham, N.R.3
-
200
-
-
0030831220
-
Modeling the active sites of cytochrome P450s and glutathione-S-transferases, two of the most important biotransformation enzymes
-
de Groot, M.J. and Vermeulen, N.P.E., Modeling the active sites of cytochrome P450s and glutathione-S-transferases, two of the most important biotransformation enzymes. Drug. Metab. Rev. 29, 747, 1997.
-
(1997)
Drug. Metab. Rev.
, vol.29
, pp. 747
-
-
De Groot, M.J.1
Vermeulen, N.P.E.2
-
201
-
-
0022431968
-
Assignment of the human 2,3,7,8-tetrachlorodibenzo-p-dioxin-inducible cytochrome P1-450 gene to chromosome 15
-
Hildebrand, C.E., Gonzalez, F.J., McBride, O.W., and Nebert, D.W., Assignment of the human 2,3,7,8-tetrachlorodibenzo-p-dioxin-inducible cytochrome P1-450 gene to chromosome 15. Nucl. Acids Res. 13, 2009, 1985.
-
(1985)
Nucl. Acids Res.
, vol.13
, pp. 2009
-
-
Hildebrand, C.E.1
Gonzalez, F.J.2
McBride, O.W.3
Nebert, D.W.4
-
202
-
-
0022432242
-
Human P1-450 gene sequence and correlation of mRNA with genetic differences in benzo[a]pyrene metabolism
-
Jaiswal, A.K., Gonzalez, F.J., and Nebert, D.W., Human P1-450 gene sequence and correlation of mRNA with genetic differences in benzo[a]pyrene metabolism. Nucl. Acids Res. 13, 4503, 1985.
-
(1985)
Nucl. Acids Res.
, vol.13
, pp. 4503
-
-
Jaiswal, A.K.1
Gonzalez, F.J.2
Nebert, D.W.3
-
203
-
-
0023663556
-
Msp 1 polymorphism detected with a cDNA probe for the P-450 I family on chromosome 15
-
Spurr, N.K., Gough, A.C., Stevenson, K., and Wolf, C.R., Msp 1 polymorphism detected with a cDNA probe for the P-450 I family on chromosome 15. Nucl. Acids Res. 15, 5901, 1987.
-
(1987)
Nucl. Acids Res.
, vol.15
, pp. 5901
-
-
Spurr, N.K.1
Gough, A.C.2
Stevenson, K.3
Wolf, C.R.4
-
204
-
-
0001238051
-
Subchromosomal localization of the dioxin-inducible P450 locus (CYP1) and description of two RFLPs detected with a 3′ P450 cDNA probe
-
Bale, A.E., Nebert, D.W., and McBride, O.W., Subchromosomal localization of the dioxin-inducible P450 locus (CYP1) and description of two RFLPs detected with a 3′ P450 cDNA probe. Cytogen. Cell Genet. 46, 574, 1987.
-
(1987)
Cytogen. Cell Genet.
, vol.46
, pp. 574
-
-
Bale, A.E.1
Nebert, D.W.2
McBride, O.W.3
-
205
-
-
0025288756
-
Pst I polymorphism at the human P1450 gene on chromosome 15
-
Haugen, A., Willey, J., Borresen, A.L., and Tefre, T., Pst I polymorphism at the human P1450 gene on chromosome 15. Nucl. Acids Res. 18, 3114, 1990.
-
(1990)
Nucl. Acids Res.
, vol.18
, pp. 3114
-
-
Haugen, A.1
Willey, J.2
Borresen, A.L.3
Tefre, T.4
-
206
-
-
0025737529
-
PCR detection of an A/G polymorphism within exon 7 of the CYP1A1 gene
-
Hayashi, S.-i., Watanabe, J., Nakachi, K., and Kawajiri, K., PCR detection of an A/G polymorphism within exon 7 of the CYP1A1 gene. Nucl. Acids Res. 19, 4797, 1991.
-
(1991)
Nucl. Acids Res.
, vol.19
, pp. 4797
-
-
Hayashi, S.-I.1
Watanabe, J.2
Nakachi, K.3
Kawajiri, K.4
-
207
-
-
0025914145
-
Genetic linkage of lung cancer-associated Msp I polymorphisms with amino acid replacement in the heme binding region of the human cytochrome P450IAI gene
-
Hayashi, S.-i., Watanabe, J., Nakachi, K., and Kawajiri, K., Genetic linkage of lung cancer-associated Msp I polymorphisms with amino acid replacement in the heme binding region of the human cytochrome P450IAI gene. J. Biochem. 110, 407, 1991.
-
(1991)
J. Biochem.
, vol.110
, pp. 407
-
-
Hayashi, S.-I.1
Watanabe, J.2
Nakachi, K.3
Kawajiri, K.4
-
208
-
-
0027429541
-
Relationship between genotype and function of the human CYP1A1 gene
-
Cosma, G., Crofts, F., Taioli, E., Toniolo, P., and Garte, S., Relationship between genotype and function of the human CYP1A1 gene. J. Toxicol. Environ. Health 40, 309, 1993a.
-
(1993)
J. Toxicol. Environ. Health
, vol.40
, pp. 309
-
-
Cosma, G.1
Crofts, F.2
Taioli, E.3
Toniolo, P.4
Garte, S.5
-
209
-
-
0028182661
-
I462V mutation in the human CYP1A1 gene, Lack of correlation with either the Msp I 1.9 kb (M2) allele or CYP1A1 inducibility in a three-generation family of East Mediterranean descent
-
Wedlund, P.J., Kimura, S., Gonzalez, F.J., and Nebert, D.W., I462V mutation in the human CYP1A1 gene, Lack of correlation with either the Msp I 1.9 kb (M2) allele or CYP1A1 inducibility in a three-generation family of East Mediterranean descent. Pharmacogenetics 4, 21, 1994.
-
(1994)
Pharmacogenetics
, vol.4
, pp. 21
-
-
Wedlund, P.J.1
Kimura, S.2
Gonzalez, F.J.3
Nebert, D.W.4
-
210
-
-
0028209022
-
Polymorphisms in the human CYP1A1 gene as susceptibility factors for lung cancer, exon-7 mutation (4889 A to G), and a T to C mutation in the 3′-flanking region
-
Drakoulis, N., Cascorbi, I., Brockmoller, J., Gross, C.R., and Roots, I., Polymorphisms in the human CYP1A1 gene as susceptibility factors for lung cancer, exon-7 mutation (4889 A to G), and a T to C mutation in the 3′-flanking region. Clin. Investig. 72, 240, 1994.
-
(1994)
Clin. Investig.
, vol.72
, pp. 240
-
-
Drakoulis, N.1
Cascorbi, I.2
Brockmoller, J.3
Gross, C.R.4
Roots, I.5
-
211
-
-
0027364894
-
A novel CYP1A1 gene polymorphism in African-Americans
-
Crofts, F., Cosma, G.N., Currie, D., Taioli, E., Toniolo, P., and Garte, S.J., A novel CYP1A1 gene polymorphism in African-Americans. Carcinogenesis 14, 1729, 1993.
-
(1993)
Carcinogenesis
, vol.14
, pp. 1729
-
-
Crofts, F.1
Cosma, G.N.2
Currie, D.3
Taioli, E.4
Toniolo, P.5
Garte, S.J.6
-
212
-
-
0030005971
-
Distribution of composite CYP1A1 genotypes in Africans, African-Americans and Caucasians
-
Garte, S.J., Trachman, J., Crofts, F., Toniolo, P., Buxbaum, J., Bayo, S., and Taioli, E., Distribution of composite CYP1A1 genotypes in Africans, African-Americans and Caucasians. Hum. Hered. 46, 121, 1996.
-
(1996)
Hum. Hered.
, vol.46
, pp. 121
-
-
Garte, S.J.1
Trachman, J.2
Crofts, F.3
Toniolo, P.4
Buxbaum, J.5
Bayo, S.6
Taioli, E.7
-
213
-
-
0027246408
-
Susceptibility markers in normal subjects: A pilot study for the investigation of 2,3,7,8-tetrachlorodibenzo-p-dioxin-related diseases
-
Landi, M.T., Bertazzi, P.A., Clark, G., Lucier, G.W., Garte, S.J., Cosma, G., Shields, P.G., and Caporaso, N.E., Susceptibility markers in normal subjects: a pilot study for the investigation of 2,3,7,8-tetrachlorodibenzo-p-dioxin-related diseases. Chemosphere 27, 375, 1993.
-
(1993)
Chemosphere
, vol.27
, pp. 375
-
-
Landi, M.T.1
Bertazzi, P.A.2
Clark, G.3
Lucier, G.W.4
Garte, S.J.5
Cosma, G.6
Shields, P.G.7
Caporaso, N.E.8
-
214
-
-
0028020326
-
Association between CYP1A1 genotype, mRNA expression and enzymatic activity in humans
-
Landi, M.T., Bertazzi, P.A., Shields, P.G., Clark, G., Lucier, G.W., Garte, S.J., Cosma, G., and Caporaso, N.E., Association between CYP1A1 genotype, mRNA expression and enzymatic activity in humans. Pharmacogenetics 4, 242, 1994.
-
(1994)
Pharmacogenetics
, vol.4
, pp. 242
-
-
Landi, M.T.1
Bertazzi, P.A.2
Shields, P.G.3
Clark, G.4
Lucier, G.W.5
Garte, S.J.6
Cosma, G.7
Caporaso, N.E.8
-
215
-
-
0028557312
-
Functional significance of different human CYP1A1 genotypes
-
Crofts, F., Taioli, E., Trachman, J., Cosma, G.N., Currie, D., Toniolo, P., and Garte, S.J., Functional significance of different human CYP1A1 genotypes. Carcinogenesis 15, 2961, 1994.
-
(1994)
Carcinogenesis
, vol.15
, pp. 2961
-
-
Crofts, F.1
Taioli, E.2
Trachman, J.3
Cosma, G.N.4
Currie, D.5
Toniolo, P.6
Garte, S.J.7
-
216
-
-
0025845934
-
Human CYP1A1 gene: Cosegregation of the enzyme inducibility phenotype and an RFLP
-
Petersen, D.D., McKinney, C.E., Ikeya, K., Smith, H.H., Bale, A.E., McBride, O.W., and Nebert, D.W., Human CYP1A1 gene: cosegregation of the enzyme inducibility phenotype and an RFLP. Am. J. Hum. Genet. 48, 720, 1991.
-
(1991)
Am. J. Hum. Genet.
, vol.48
, pp. 720
-
-
Petersen, D.D.1
McKinney, C.E.2
Ikeya, K.3
Smith, H.H.4
Bale, A.E.5
McBride, O.W.6
Nebert, D.W.7
-
217
-
-
0030028660
-
The relationship between aryl hydrocarbon hydroxylase and polymorphisms of the CYP1A1 gene
-
Kiyohara, C., Hirohata, T., and Inutsuka, S., The relationship between aryl hydrocarbon hydroxylase and polymorphisms of the CYP1A1 gene. Jpn. J. Cancer Res. 87, 18, 1996.
-
(1996)
Jpn. J. Cancer Res.
, vol.87
, pp. 18
-
-
Kiyohara, C.1
Hirohata, T.2
Inutsuka, S.3
-
218
-
-
0027458138
-
The Ah-receptor, genetics, structure and function
-
Swanson, H.I. and Bradfield, C.A., The Ah-receptor, genetics, structure and function. Pharmacogenetics 3, 213, 1993.
-
(1993)
Pharmacogenetics
, vol.3
, pp. 213
-
-
Swanson, H.I.1
Bradfield, C.A.2
-
219
-
-
0029020636
-
Polymorphic forms of the Ah receptor and induction of the CYP1A1 gene
-
Fujii-Kuriyama, Y., Ema, M., Mimura, J., Matsushita, N., and Sogawa, K., Polymorphic forms of the Ah receptor and induction of the CYP1A1 gene. Pharmacogenetics 5, S149, 1995.
-
(1995)
Pharmacogenetics
, vol.5
-
-
Fujii-Kuriyama, Y.1
Ema, M.2
Mimura, J.3
Matsushita, N.4
Sogawa, K.5
-
220
-
-
0029078019
-
Genetic polymorphisms of drug-metabolizing enzymes and lung cancer susceptibility
-
Kawajiri, K., Watanabe, J., Eguchi, H., and Hayashi, S.-i., Genetic polymorphisms of drug-metabolizing enzymes and lung cancer susceptibility. Pharmacogenetics 5, S70, 1995.
-
(1995)
Pharmacogenetics
, vol.5
-
-
Kawajiri, K.1
Watanabe, J.2
Eguchi, H.3
Hayashi, S.-I.4
-
221
-
-
0029069369
-
Polymorphisms of human Ah receptor gene are not involved in lung cancer
-
Kawajiri, K., Watanabe, J., Eguchi, H., Nakachi, K., Kiyohara, C., and Hayashi, S.-i., Polymorphisms of human Ah receptor gene are not involved in lung cancer. Pharmacogenetics 5, 151, 1995.
-
(1995)
Pharmacogenetics
, vol.5
, pp. 151
-
-
Kawajiri, K.1
Watanabe, J.2
Eguchi, H.3
Nakachi, K.4
Kiyohara, C.5
Hayashi, S.-I.6
-
222
-
-
0029841793
-
Characterization of purified human recombinant cytochrome P4501A1-Ile462 and -Val462: Assessment of a role for the rare allele in carcinogenesis
-
Zhang, Z.-Y., Fasco, M.J., Huang, L., Guengerich, F.P., and Kaminsky, L.S., Characterization of purified human recombinant cytochrome P4501A1-Ile462 and -Val462: assessment of a role for the rare allele in carcinogenesis. Cancer Res. 56, 3926, 1996.
-
(1996)
Cancer Res.
, vol.56
, pp. 3926
-
-
Zhang, Z.-Y.1
Fasco, M.J.2
Huang, L.3
Guengerich, F.P.4
Kaminsky, L.S.5
-
223
-
-
0031550543
-
In vitro kinetics of two human CYP1A1 variant enzymes suggested to be associated with inter-individual differences in cancer susceptibility
-
Persson, I., Johansson, I., and Ingelman-Sundberg, M., In vitro kinetics of two human CYP1A1 variant enzymes suggested to be associated with inter-individual differences in cancer susceptibility. Biochem. Biophys. Res. Commun. 231, 227, 1997.
-
(1997)
Biochem. Biophys. Res. Commun.
, vol.231
, pp. 227
-
-
Persson, I.1
Johansson, I.2
Ingelman-Sundberg, M.3
-
224
-
-
0027056293
-
Polycyclic aromatic hydrocarbon-DNA adducts and the CYP1A1 restriction fragment length polymorphism
-
Shields, P.G., Sugimura, H., Caporaso, N.E., Petruzzelli, S.F., Bowman, E.D., Trump, B.F., Weston, A., and Harris, C.C., Polycyclic aromatic hydrocarbon-DNA adducts and the CYP1A1 restriction fragment length polymorphism. Environ. Health Perspect. 98, 191, 1992.
-
(1992)
Environ. Health Perspect.
, vol.98
, pp. 191
-
-
Shields, P.G.1
Sugimura, H.2
Caporaso, N.E.3
Petruzzelli, S.F.4
Bowman, E.D.5
Trump, B.F.6
Weston, A.7
Harris, C.C.8
-
225
-
-
0027220611
-
Polycyclic aromatic hydrocarbon-DNA adducts in human lung and cancer susceptibility genes
-
Shields, P.G., Bowman, E.D., Harrington, A.M., Doan, V.T., and Weston, A., Polycyclic aromatic hydrocarbon-DNA adducts in human lung and cancer susceptibility genes. Cancer Res. 53, 3486, 1993.
-
(1993)
Cancer Res.
, vol.53
, pp. 3486
-
-
Shields, P.G.1
Bowman, E.D.2
Harrington, A.M.3
Doan, V.T.4
Weston, A.5
-
226
-
-
0028364382
-
Aromatic DNA adducts, micronuclei and genetic polymorphism for CYP1A1 and GSTT1 in chimney sweeps
-
Ichiba, M., Hagmar, L., Rannug, A., Högstedt, B., Alexandrie, A.-K., Carstensen, U., and Hemminki, K., Aromatic DNA adducts, micronuclei and genetic polymorphism for CYP1A1 and GSTT1 in chimney sweeps. Carcinogenesis 15, 1347, 1994.
-
(1994)
Carcinogenesis
, vol.15
, pp. 1347
-
-
Ichiba, M.1
Hagmar, L.2
Rannug, A.3
Högstedt, B.4
Alexandrie, A.-K.5
Carstensen, U.6
Hemminki, K.7
-
227
-
-
0030045915
-
Association of CYP1A1 germ line polymorphisms with mutations of the p53 gene in lung cancer
-
Kawajiri, K., Eguchi, H., Nakachi, K., Sekiya, T., and Yamamoto, M., Association of CYP1A1 germ line polymorphisms with mutations of the p53 gene in lung cancer. Cancer Res. 56, 72, 1996.
-
(1996)
Cancer Res.
, vol.56
, pp. 72
-
-
Kawajiri, K.1
Eguchi, H.2
Nakachi, K.3
Sekiya, T.4
Yamamoto, M.5
-
228
-
-
0013491081
-
A new CYP polymorphism to complicate drug development: Deficient C-oxidation of nicotine, a comment
-
Maenpaa, J. and Wrighton, S.A., A new CYP polymorphism to complicate drug development: deficient C-oxidation of nicotine, a comment. Hum. Exp. Toxicol. 15, 82, 1996.
-
(1996)
Hum. Exp. Toxicol.
, vol.15
, pp. 82
-
-
Maenpaa, J.1
Wrighton, S.A.2
-
229
-
-
8044258385
-
Role of human cytochrome P4502A6 in C-oxidation of nicotine
-
Nakajima, M., Yamamoto, T., Nunoya, K.-i., Yokoi, T., Nagashima, K., Inoue, K., Funae, Y., Shimada, N., Kamataki, T., and Kuroiwa, Y., Role of human cytochrome P4502A6 in C-oxidation of nicotine. Drug Metab. Dispos. 24, 1212, 1996.
-
(1996)
Drug Metab. Dispos.
, vol.24
, pp. 1212
-
-
Nakajima, M.1
Yamamoto, T.2
Nunoya, K.-I.3
Yokoi, T.4
Nagashima, K.5
Inoue, K.6
Funae, Y.7
Shimada, N.8
Kamataki, T.9
Kuroiwa, Y.10
-
230
-
-
0029591606
-
Organization and evolution of the cytochrome P450 CYP2A-2B-2F subfamily gene cluster on human chromosome 19
-
Hoffman, S.M.G., Fernandez-Salguero, P., Gonzalez, F.J., and Mohrenweiser, H.W., Organization and evolution of the cytochrome P450 CYP2A-2B-2F subfamily gene cluster on human chromosome 19. J. Mol. Evol. 41, 894, 1995.
-
(1995)
J. Mol. Evol.
, vol.41
, pp. 894
-
-
Hoffman, S.M.G.1
Fernandez-Salguero, P.2
Gonzalez, F.J.3
Mohrenweiser, H.W.4
-
231
-
-
0029099107
-
A genetic polymorphism in coumarin 7-hydroxylation, Sequence of the human CYP2A genes and identification of variant CYP2A6 alleles
-
Fernandez-Salguero, P., Hoffman, S.M.G., Cholerton, S., Mohrenweiser, H., Raunio, H., Rautio, A., Pelkonen, O., Huang, J.-d., Evans, W.E., Idle, J.R., and Gonzalez, F.J., A genetic polymorphism in coumarin 7-hydroxylation, Sequence of the human CYP2A genes and identification of variant CYP2A6 alleles. Am. J. Hum. Genet. 57, 651, 1995.
-
(1995)
Am. J. Hum. Genet.
, vol.57
, pp. 651
-
-
Fernandez-Salguero, P.1
Hoffman, S.M.G.2
Cholerton, S.3
Mohrenweiser, H.4
Raunio, H.5
Rautio, A.6
Pelkonen, O.7
Huang, J.-D.8
Evans, W.E.9
Idle, J.R.10
Gonzalez, F.J.11
-
232
-
-
0028798734
-
Expression and alternative splicing of the cytochrome P450 CYP2A7
-
Ding, S., Lake, B.G., Friedberg, T., and Wolf, C.R., Expression and alternative splicing of the cytochrome P450 CYP2A7. Biochem. J. 306, 161, 1995.
-
(1995)
Biochem. J.
, vol.306
, pp. 161
-
-
Ding, S.1
Lake, B.G.2
Friedberg, T.3
Wolf, C.R.4
-
233
-
-
0028590127
-
Biochemistry and molecular biology of the human CYP2C subfamily
-
Goldstein, J.A. and de Morals, S.M.F., Biochemistry and molecular biology of the human CYP2C subfamily. Pharmacogenetics 4, 285, 1994.
-
(1994)
Pharmacogenetics
, vol.4
, pp. 285
-
-
Goldstein, J.A.1
De Morals, S.M.F.2
-
234
-
-
0029128881
-
The substrate binding site of human liver cytochrome P450 2C9, an approach using designed tienilic acid derivatives and molecular modeling
-
Mancy, A., Broto, P., Dijols, S., Dansette, P.M., and Mansuy, D., The substrate binding site of human liver cytochrome P450 2C9, an approach using designed tienilic acid derivatives and molecular modeling. Biochemistry 34, 10365, 1995.
-
(1995)
Biochemistry
, vol.34
, pp. 10365
-
-
Mancy, A.1
Broto, P.2
Dijols, S.3
Dansette, P.M.4
Mansuy, D.5
-
235
-
-
0023879378
-
Human cytochrome P-450 PB-1: A multigene family involved in mephenytoin and steroid oxidations that maps to chromosome 10
-
Meehan, R.R., Gosden, J.R., Rout, D., Hastie, N.D., Friedberg, T., Adesnik, M., Buckland, R., van Heyningen, V., Fletcher, J., Spurr, N.K., Sweeney, J., and Wolf, C.R., Human cytochrome P-450 PB-1: a multigene family involved in mephenytoin and steroid oxidations that maps to chromosome 10. Am J. Hum. Genet. 42, 26, 1988.
-
(1988)
Am J. Hum. Genet.
, vol.42
, pp. 26
-
-
Meehan, R.R.1
Gosden, J.R.2
Rout, D.3
Hastie, N.D.4
Friedberg, T.5
Adesnik, M.6
Buckland, R.7
Van Heyningen, V.8
Fletcher, J.9
Spurr, N.K.10
Sweeney, J.11
Wolf, C.R.12
-
236
-
-
0029122980
-
A 2.4-megabase physical map spanning the CYP2C gene cluster on chromosome 10q24
-
Gray, I.C., Nobile, C., Muresu, R., Ford, and Spurr, N.K., A 2.4-megabase physical map spanning the CYP2C gene cluster on chromosome 10q24. Genomics 28, 328, 1995.
-
(1995)
Genomics
, vol.28
, pp. 328
-
-
Gray, I.C.1
Nobile, C.2
Muresu, R.3
Ford4
Spurr, N.K.5
-
237
-
-
0023121619
-
Cloning and sequence determination of a complementary DNA related to human liver microsomal cytochrome P-450 S-mephenytoin 4-hydroxylase
-
Umbenhauer, D.R., Martin, M.V., Lloyd, R.S., and Guengerich, F.P., Cloning and sequence determination of a complementary DNA related to human liver microsomal cytochrome P-450 S-mephenytoin 4-hydroxylase. Biochemistry, 26, 1094, 1987.
-
(1987)
Biochemistry
, vol.26
, pp. 1094
-
-
Umbenhauer, D.R.1
Martin, M.V.2
Lloyd, R.S.3
Guengerich, F.P.4
-
238
-
-
0023650353
-
cDNA and amino acid sequences of two members of the human P450IIC gene subfamily
-
Kimura, S., Pastewka, J., Gelboin, H.V., and Gonzalez, F.J., cDNA and amino acid sequences of two members of the human P450IIC gene subfamily. Nucl. Acids Res. 15, 10053, 1987.
-
(1987)
Nucl. Acids Res.
, vol.15
, pp. 10053
-
-
Kimura, S.1
Pastewka, J.2
Gelboin, H.V.3
Gonzalez, F.J.4
-
239
-
-
0023443243
-
Nucleotide sequence of a human liver cytochrome P-450 related to the rat male specific form
-
Yasumori, T., Kawano, S., Nagata, K., Shimada, M., Yamazoe, Y., and Kato, R., Nucleotide sequence of a human liver cytochrome P-450 related to the rat male specific form. J. Biochem. 102, 1075, 1987.
-
(1987)
J. Biochem.
, vol.102
, pp. 1075
-
-
Yasumori, T.1
Kawano, S.2
Nagata, K.3
Shimada, M.4
Yamazoe, Y.5
Kato, R.6
-
240
-
-
0023718998
-
Characterization of cDNAs, mRNAs, and proteins related to human liver microsomal cytochrome P-450 S)-mephenytoin 4′-hydroxylase
-
Ged, C., Umbenhauer, D.R., Bellew, T.M., Bork, R.W., Srivastava, P.K., Shinriki, N., Lloyd, R.S., and Guengerich, F.P., Characterization of cDNAs, mRNAs, and proteins related to human liver microsomal cytochrome P-450 S)-mephenytoin 4′-hydroxylase. Biochemistry, 27, 6929, 1988.
-
(1988)
Biochemistry
, vol.27
, pp. 6929
-
-
Ged, C.1
Umbenhauer, D.R.2
Bellew, T.M.3
Bork, R.W.4
Srivastava, P.K.5
Shinriki, N.6
Lloyd, R.S.7
Guengerich, F.P.8
-
241
-
-
85038195291
-
Polymorphism in the human cytochrome P450 2C9 gene
-
Seattle
-
Bhasker, C.R., Birkett, D.J., Veronese, M.E., and Miners, J.O., Polymorphism in the human cytochrome P450 2C9 gene. In: Proceedings of the ISSX Meeting, Seattle, 1995, 105.
-
(1995)
Proceedings of the ISSX Meeting
, pp. 105
-
-
Bhasker, C.R.1
Birkett, D.J.2
Veronese, M.E.3
Miners, J.O.4
-
242
-
-
0028861660
-
Detection of CYP2C9 polymorphism based on the polymerase chain reaction in Chinese
-
Wang, S.-L., Huang, J.-d., Lai, M.-D., and Tsai, J.-J., Detection of CYP2C9 polymorphism based on the polymerase chain reaction in Chinese. Pharmacogenetics 5, 37-42, 1995.
-
(1995)
Pharmacogenetics
, vol.5
, pp. 37-42
-
-
Wang, S.-L.1
Huang, J.-D.2
Lai, M.-D.3
Tsai, J.-J.4
-
243
-
-
0029658591
-
The role of the CYP2C9; Leu359 allelic variant in the tolbutamide polymorphism
-
Sullivan-Klose, T.H., Ghanayem, B.I., Bell, D.A., Zhang, Z.-Y., Kaminsky, L.S., Shenfield, G.M., Miners, J.O., Birkett, D.J., and Goldstein, J.A., The role of the CYP2C9; Leu359 allelic variant in the tolbutamide polymorphism. Pharmacogenetics 6, 341, 1996.
-
(1996)
Pharmacogenetics
, vol.6
, pp. 341
-
-
Sullivan-Klose, T.H.1
Ghanayem, B.I.2
Bell, D.A.3
Zhang, Z.-Y.4
Kaminsky, L.S.5
Shenfield, G.M.6
Miners, J.O.7
Birkett, D.J.8
Goldstein, J.A.9
-
244
-
-
0029798351
-
Genetic analysis of the cytochrome P450 2C9 locus
-
Stubbins, M.J., Harries, L.W., Smith, G., Tarbit, M.H., and Wolf, C.R., Genetic analysis of the cytochrome P450 2C9 locus. Pharmacogenetics 6, 429, 1996.
-
(1996)
Pharmacogenetics
, vol.6
, pp. 429
-
-
Stubbins, M.J.1
Harries, L.W.2
Smith, G.3
Tarbit, M.H.4
Wolf, C.R.5
-
245
-
-
0029564238
-
Genetic polymorphism of CYP2C9 and its effect on warfarin maintanance dose requirement in patients undergoing anticoagulation therapy
-
Furuya, H., Fernandez-Salguero, P., Gregory, W., Taber, H., Steward, A., Gonzalez, F.J., and Idle, J.R., Genetic polymorphism of CYP2C9 and its effect on warfarin maintanance dose requirement in patients undergoing anticoagulation therapy. Pharmacogenetics 5, 289, 1995.
-
(1995)
Pharmacogenetics
, vol.5
, pp. 289
-
-
Furuya, H.1
Fernandez-Salguero, P.2
Gregory, W.3
Taber, H.4
Steward, A.5
Gonzalez, F.J.6
Idle, J.R.7
-
246
-
-
0018395301
-
Pharmacogenetics of tolbutamide metabolism in humans
-
Scott, J. and Poffenbarger, P.L., Pharmacogenetics of tolbutamide metabolism in humans. Diabetes 28, 41, 1979.
-
(1979)
Diabetes
, vol.28
, pp. 41
-
-
Scott, J.1
Poffenbarger, P.L.2
-
247
-
-
0025884407
-
A screening test for slow metabolisers of tolbutamide
-
Page, M.A., Boutagy, J.S., and Shenfield, G.M., A screening test for slow metabolisers of tolbutamide. Br. J. Clin. Pharmacol. 31, 649, 1991.
-
(1991)
Br. J. Clin. Pharmacol.
, vol.31
, pp. 649
-
-
Page, M.A.1
Boutagy, J.S.2
Shenfield, G.M.3
-
248
-
-
0013520394
-
Genetic factors influencing the metabolism of tolbutamide
-
Kalow, W., Ed, Pergamon Press Inc., New York
-
Back, D.J. and Orme, M. L'E., Genetic factors influencing the metabolism of tolbutamide. In: Pharmacogenetics of Drug Metabolism, Kalow, W., Ed, Pergamon Press Inc., New York, 1992, 737-746.
-
(1992)
Pharmacogenetics of Drug Metabolism
, pp. 737-746
-
-
Back, D.J.1
Orme, M.L'E.2
-
249
-
-
0027529381
-
Tolbutamide hydroxylation in humans, lack of bimodality in 106 healthy subjects
-
Veronese, M.E., Miners, J.O., Rees, D.L.P., and Birkett, D.J., Tolbutamide hydroxylation in humans, lack of bimodality in 106 healthy subjects. Pharmacogenetics 3, 86, 1993
-
(1993)
Pharmacogenetics
, vol.3
, pp. 86
-
-
Veronese, M.E.1
Miners, J.O.2
Rees, D.L.P.3
Birkett, D.J.4
-
250
-
-
0000966446
-
Insufficient parahydroxylation as a cause of diphenylhydantoin toxocity
-
Kutt, H. and Wolk, M., Insufficient parahydroxylation as a cause of diphenylhydantoin toxocity. Neurology 14, 542, 1964.
-
(1964)
Neurology
, vol.14
, pp. 542
-
-
Kutt, H.1
Wolk, M.2
-
251
-
-
0018853387
-
Inheritance of phenytoin hypometabolism: A kinetic study of one family
-
Vasko, M.R., Bell, R.D., Daly, D.D., and Pippenger, C.E., Inheritance of phenytoin hypometabolism: a kinetic study of one family. Clin Pharmacol. Ther. 27, 96, 1980.
-
(1980)
Clin Pharmacol. Ther.
, vol.27
, pp. 96
-
-
Vasko, M.R.1
Bell, R.D.2
Daly, D.D.3
Pippenger, C.E.4
-
252
-
-
0024262689
-
Inheritance of poor phenytoin parahydroxylation capacity in a Dutch family
-
Vermeij, P., Ferrari, M.D., Buruma, O.J.S., Veenema, H., and de Wolff, F.A., Inheritance of poor phenytoin parahydroxylation capacity in a Dutch family. Clin. Pharmacol. Ther. 44, 588, 1988.
-
(1988)
Clin. Pharmacol. Ther.
, vol.44
, pp. 588
-
-
Vermeij, P.1
Ferrari, M.D.2
Buruma, O.J.S.3
Veenema, H.4
De Wolff, F.A.5
-
253
-
-
0025266722
-
Phenytoin, pharmacogenetic polymorphism of 4′-hydroxylation
-
Inaba, T., Phenytoin, pharmacogenetic polymorphism of 4′-hydroxylation. Pharmac. Ther. 46, 341, 1990.
-
(1990)
Pharmac. Ther.
, vol.46
, pp. 341
-
-
Inaba, T.1
-
254
-
-
0029134950
-
Phenytoin disposition and toxicity, role of pharmacogenetic and inter-ethnic factors
-
Edeki, T.L. and Brase, D.A., Phenytoin disposition and toxicity, role of pharmacogenetic and inter-ethnic factors. Drug Metab. Rev. 27, 449, 1995.
-
(1995)
Drug Metab. Rev.
, vol.27
, pp. 449
-
-
Edeki, T.L.1
Brase, D.A.2
-
255
-
-
0030034642
-
Relationship between mephenytoin, phenytoin and tolbutamide hydroxylations in healthy African subjects
-
Horsmans, Y., Kanyinda, J.M., and Desager, J.P., Relationship between mephenytoin, phenytoin and tolbutamide hydroxylations in healthy African subjects. Pharmacol. Toxicol. 78, 86, 1996.
-
(1996)
Pharmacol. Toxicol.
, vol.78
, pp. 86
-
-
Horsmans, Y.1
Kanyinda, J.M.2
Desager, J.P.3
-
256
-
-
0027397054
-
Site-directed mutation studies of human liver cytochrome P-450 isoenzymes in the CYP2C subfamily
-
Veronese, M.E., Doecke, C.J., MacKenzie, P.I., McManus, M.E., Miners, J.O., Rees, D.L.P., Gasser, R., Meyer, U.A., and Birkett, D.J., Site-directed mutation studies of human liver cytochrome P-450 isoenzymes in the CYP2C subfamily. Biochem. J. 289, 533, 1993.
-
(1993)
Biochem. J.
, vol.289
, pp. 533
-
-
Veronese, M.E.1
Doecke, C.J.2
Mackenzie, P.I.3
McManus, M.E.4
Miners, J.O.5
Rees, D.L.P.6
Gasser, R.7
Meyer, U.A.8
Birkett, D.J.9
-
257
-
-
0028210729
-
Impaired (S)-warfarin metabolism catalysed by the R144C allelic variant of CYP2C9
-
Rettie, A.E., Wienckers, L.C., Gonzalez, F.J., Trager, W.F., and Korzekwa, K.R., Impaired (S)-warfarin metabolism catalysed by the R144C allelic variant of CYP2C9. Pharmacogenetics, 4, 39, 1994.
-
(1994)
Pharmacogenetics
, vol.4
, pp. 39
-
-
Rettie, A.E.1
Wienckers, L.C.2
Gonzalez, F.J.3
Trager, W.F.4
Korzekwa, K.R.5
-
258
-
-
0027452620
-
Correlation of human cytochrome P4502C substrate specificities with primary structure. Warfarin as a probe
-
Kaminsky, L.S., de Morais, S.M.F., Faletto, M.B., Dunbar, D.A., and Goldstein, J.A., Correlation of human cytochrome P4502C substrate specificities with primary structure. Warfarin as a probe. Mol. Pharmacol. 43, 234, 1993.
-
(1993)
Mol. Pharmacol.
, vol.43
, pp. 234
-
-
Kaminsky, L.S.1
De Morais, S.M.F.2
Faletto, M.B.3
Dunbar, D.A.4
Goldstein, J.A.5
-
259
-
-
0030587544
-
Allelic variants of human cytochrome P4502C9, Baculovirus-mediated expression, purification, structural characterization, substrate stereoselectivity, and prochiral selectivity of the wild-type and 1359L mutant forms
-
Haining, R.L., Hunter, A.P., Veronese, M.E., Trager, W.F., and Rettie, A.E., Allelic variants of human cytochrome P4502C9, Baculovirus-mediated expression, purification, structural characterization, substrate stereoselectivity, and prochiral selectivity of the wild-type and 1359L mutant forms. Arch. Biochem. Biophys. 333, 447, 1996.
-
(1996)
Arch. Biochem. Biophys.
, vol.333
, pp. 447
-
-
Haining, R.L.1
Hunter, A.P.2
Veronese, M.E.3
Trager, W.F.4
Rettie, A.E.5
-
260
-
-
0029744762
-
Effect of CYP2C polymorphisms on the pharmacokinetics of phenytoin in Japanese patients with epilepsy
-
Hashimoto, Y., Otsuki, Y., Odani, A., Takano, M., Hattori, H., Furusho, K., and Inui, K.-i., Effect of CYP2C polymorphisms on the pharmacokinetics of phenytoin in Japanese patients with epilepsy. Biol. Pharm. Bull. 19, 1103, 1996.
-
(1996)
Biol. Pharm. Bull.
, vol.19
, pp. 1103
-
-
Hashimoto, Y.1
Otsuki, Y.2
Odani, A.3
Takano, M.4
Hattori, H.5
Furusho, K.6
Inui, K.-I.7
-
261
-
-
0029865596
-
Genetic analysis of the cytochrome P-450IIC18 (CYP2C18) gene and a novel member of the CYP2C subfamily
-
Tsuneoka, Y., Matsuo, Y., Okuyama, E., Watanabe, Y., and Ichikawa, Y., Genetic analysis of the cytochrome P-450IIC18 (CYP2C18) gene and a novel member of the CYP2C subfamily. FEBS Lett. 384, 281, 1996.
-
(1996)
FEBS Lett.
, vol.384
, pp. 281
-
-
Tsuneoka, Y.1
Matsuo, Y.2
Okuyama, E.3
Watanabe, Y.4
Ichikawa, Y.5
-
262
-
-
0030580125
-
Genotype analysis of the CYP2C19 gene in the Japanese population
-
Tsuneoka, Y., Fukushima, K., Matsuo, Y., Ichikawa, Y., and Watanabe, Y., Genotype analysis of the CYP2C19 gene in the Japanese population. Life Sci. 59, 1711, 1996.
-
(1996)
Life Sci.
, vol.59
, pp. 1711
-
-
Tsuneoka, Y.1
Fukushima, K.2
Matsuo, Y.3
Ichikawa, Y.4
Watanabe, Y.5
-
263
-
-
0030606689
-
Novel 2-point linked mutations in the 5′-flanking region of human CYP2C18
-
Iwahashi, K., Okuyama, E., Furukawa, A., Nakamura, K., Miyatake, R., Matsuo, Y., and Ichikawa, Y., Novel 2-point linked mutations in the 5′-flanking region of human CYP2C18. Clin. Chim. Acta, 252, 197, 1996.
-
(1996)
Clin. Chim. Acta
, vol.252
, pp. 197
-
-
Iwahashi, K.1
Okuyama, E.2
Furukawa, A.3
Nakamura, K.4
Miyatake, R.5
Matsuo, Y.6
Ichikawa, Y.7
-
264
-
-
0029868939
-
Identification of a new non-functional CYP2C18 allele in Japanese, substitution of T204 to A in exon 2 generates a premature stop codon
-
Komai, K., Sumida, K., Kaneko, H., and Nakatsuka, I., Identification of a new non-functional CYP2C18 allele in Japanese, substitution of T204 to A in exon 2 generates a premature stop codon. Pharmacogenetics 6, 117, 1996.
-
(1996)
Pharmacogenetics
, vol.6
, pp. 117
-
-
Komai, K.1
Sumida, K.2
Kaneko, H.3
Nakatsuka, I.4
-
265
-
-
0024360705
-
Genetic polymorphism of S-mephenytoin hydroxylation
-
Wilkinson, G.R., Guengerich, F.P., and Branch, R.A., Genetic polymorphism of S-mephenytoin hydroxylation. Pharmac. Ther. 43, 53, 1989.
-
(1989)
Pharmac. Ther.
, vol.43
, pp. 53
-
-
Wilkinson, G.R.1
Guengerich, F.P.2
Branch, R.A.3
-
266
-
-
0028626297
-
S-mephenytoin pharmacogenetics and its clinical implications in Asian ethnic populations
-
Sohn, D.R., Shin, S.G., and Ishizaki, T., S-mephenytoin pharmacogenetics and its clinical implications in Asian ethnic populations. Asia Pacific J. Pharmacol. 9, 287, 1994.
-
(1994)
Asia Pacific J. Pharmacol.
, vol.9
, pp. 287
-
-
Sohn, D.R.1
Shin, S.G.2
Ishizaki, T.3
-
267
-
-
0029783939
-
Genetic polymorphism of S-mephenytoin 4′-hydroxylation
-
Daniel, H.I. and Edeki, T.I., Genetic polymorphism of S-mephenytoin 4′-hydroxylation. Psychopharmacol. Bull. 32, 219, 1996.
-
(1996)
Psychopharmacol. Bull.
, vol.32
, pp. 219
-
-
Daniel, H.I.1
Edeki, T.I.2
-
268
-
-
0021237993
-
Pharmacogenetics of mephenytoin, A new drug hydroxylation polymorphism in man
-
Kupfer, A. and Preisig, R., Pharmacogenetics of mephenytoin, A new drug hydroxylation polymorphism in man. Eur. J. Clin. Pharmacol. 26, 753, 1984.
-
(1984)
Eur. J. Clin. Pharmacol.
, vol.26
, pp. 753
-
-
Kupfer, A.1
Preisig, R.2
-
269
-
-
0021333271
-
Stereoselectivity of the arene epoxide pathway of mephenytoin hydroxylation in man
-
Kupfer, A., Lawson, J., and Branch, R.A., Stereoselectivity of the arene epoxide pathway of mephenytoin hydroxylation in man. Epilepsia 25, 1, 1984.
-
(1984)
Epilepsia
, vol.25
, pp. 1
-
-
Kupfer, A.1
Lawson, J.2
Branch, R.A.3
-
270
-
-
0022503196
-
Family studies of mephenytoin hydroxylation deficiency
-
Inaba, T., Jurima, M., and Kalow, W., Family studies of mephenytoin hydroxylation deficiency. Am. J. Hum. Genet. 68, 768, 1986.
-
(1986)
Am. J. Hum. Genet.
, vol.68
, pp. 768
-
-
Inaba, T.1
Jurima, M.2
Kalow, W.3
-
271
-
-
0023189074
-
S-mephenytoin 4-hydroxylase is inherited as an autosomal-recessive trait in Japanese families
-
Ward, S.A., Goto, F., Nakamura, K., Jacqz, E., Wilkinson, G.R., and Branch, R.A., S-mephenytoin 4-hydroxylase is inherited as an autosomal-recessive trait in Japanese families. Clin. Pharmcol. Ther. 42, 96, 1987.
-
(1987)
Clin. Pharmcol. Ther.
, vol.42
, pp. 96
-
-
Ward, S.A.1
Goto, F.2
Nakamura, K.3
Jacqz, E.4
Wilkinson, G.R.5
Branch, R.A.6
-
272
-
-
0022916809
-
Mephenytoin-type polymorphism of drug oxidation, purification and characterization of a human liver cytochrome P-450 isozyme catalyzing microsomal mephenytoin hydroxylation
-
Gut, J., Meier, U.T., Catin, T., and Meyer, U.A., Mephenytoin-type polymorphism of drug oxidation, purification and characterization of a human liver cytochrome P-450 isozyme catalyzing microsomal mephenytoin hydroxylation. Biochem. Biophys. Acta 884, 435, 1986.
-
(1986)
Biochem. Biophys. Acta
, vol.884
, pp. 435
-
-
Gut, J.1
Meier, U.T.2
Catin, T.3
Meyer, U.A.4
-
273
-
-
0022344457
-
Mephenytoin hydroxylation polymorphism: Characterization of the enzymatic deficiency in liver microsomes of poor metabolizers phenotyped in vivo
-
Meier, U.T., Dayer, P., Male, P.-J., Kronbach, T., and Meyer, U.A., Mephenytoin hydroxylation polymorphism: characterization of the enzymatic deficiency in liver microsomes of poor metabolizers phenotyped in vivo. Clin. Pharmacol. Ther. 38, 488, 1985.
-
(1985)
Clin. Pharmacol. Ther.
, vol.38
, pp. 488
-
-
Meier, U.T.1
Dayer, P.2
Male, P.-J.3
Kronbach, T.4
Meyer, U.A.5
-
274
-
-
0027445449
-
Isolation and characterization of human liver cytochrome P450 2C19: Correlation between 2C19 and S-mephenytoin 4′-hydroxylation
-
Wrighton, S.A., Stevens, J.C., Becker, G.W., and Vandenbranden, M., Isolation and characterization of human liver cytochrome P450 2C19: correlation between 2C19 and S-mephenytoin 4′-hydroxylation. Arch. Biochem. Biophys. 306, 240, 1993.
-
(1993)
Arch. Biochem. Biophys.
, vol.306
, pp. 240
-
-
Wrighton, S.A.1
Stevens, J.C.2
Becker, G.W.3
Vandenbranden, M.4
-
275
-
-
0028279041
-
Evidence that CYP2C 19 is the major (S)-mephenytoin 4′-hydroxylase in humans
-
Goldstein, J.A., Faletto, M.B., Romkes-Sparks, M., Sullivan, T., Kitareewan, S., Raucy, J.L., Lasker, J.M., and Ghanayem, B.I., Evidence that CYP2C 19 is the major (S)-mephenytoin 4′-hydroxylase in humans. Biochemistry 33, 1743, 1994.
-
(1994)
Biochemistry
, vol.33
, pp. 1743
-
-
Goldstein, J.A.1
Faletto, M.B.2
Romkes-Sparks, M.3
Sullivan, T.4
Kitareewan, S.5
Raucy, J.L.6
Lasker, J.M.7
Ghanayem, B.I.8
-
276
-
-
0028842707
-
The effects of selective serotonin reuptake inhibitors on S-mephenytoin 4′-hydroxylase activity in human liver microsomes
-
4152
-
Kobayashi, K., Yamamoto, T., Chiba, K., Tani, M., Ishizaki, T., and Kuroiwa, Y., The effects of selective serotonin reuptake inhibitors on S-mephenytoin 4′-hydroxylase activity in human liver microsomes. Br. J. Clin. Pharmacol. 40, 481 1995, 4152.
-
(1995)
Br. J. Clin. Pharmacol.
, vol.40
, pp. 481
-
-
Kobayashi, K.1
Yamamoto, T.2
Chiba, K.3
Tani, M.4
Ishizaki, T.5
Kuroiwa, Y.6
-
277
-
-
0025763625
-
Cloning and expression of complementary DNAs for multiple members of the human cytochrome P450IIC subfamily
-
Romkes, M., Faletto, M.B., Blaisdell, J.A., Raucy, J.L., and Goldstein, J.A., Cloning and expression of complementary DNAs for multiple members of the human cytochrome P450IIC subfamily. Biochemistry 30, 3247, 1991.
-
(1991)
Biochemistry
, vol.30
, pp. 3247
-
-
Romkes, M.1
Faletto, M.B.2
Blaisdell, J.A.3
Raucy, J.L.4
Goldstein, J.A.5
-
278
-
-
0028260641
-
The major genetic defect responsible for the polymorphism of S-mephenytoin metabolism in humans
-
de Morals, S.M.F., Wilkinson, G.R., Blaisdell, J., Nakamura, K., Meyer, U.A., and Goldstein, J.A., The major genetic defect responsible for the polymorphism of S-mephenytoin metabolism in humans. J. Biol. Chem. 269, 15419, 1994.
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 15419
-
-
De Morals, S.M.F.1
Wilkinson, G.R.2
Blaisdell, J.3
Nakamura, K.4
Meyer, U.A.5
Goldstein, J.A.6
-
279
-
-
0028044085
-
Identification of a new genetic defect responsible for the polymorphism of (S)-mephenytoin metabolism in Japanese
-
de Morais, S.M.F., Wilkinson, G.R., Blaisdell, J., Meyer, U.A., Nakamura, K., and Goldstein, J.A., Identification of a new genetic defect responsible for the polymorphism of (S)-mephenytoin metabolism in Japanese. Mol. Pharmacol. 46, 594, 1994.
-
(1994)
Mol. Pharmacol.
, vol.46
, pp. 594
-
-
De Morais, S.M.F.1
Wilkinson, G.R.2
Blaisdell, J.3
Meyer, U.A.4
Nakamura, K.5
Goldstein, J.A.6
-
280
-
-
0029994586
-
Evidence that poor metabolizers of (S)-mephenytoin could be identified by haplotypes of CYP2C19 in Japanese
-
Takakubo, F., Kuwano, A., and Kondo, I., Evidence that poor metabolizers of (S)-mephenytoin could be identified by haplotypes of CYP2C19 in Japanese. Pharmacogenetics 6, 265, 1996.
-
(1996)
Pharmacogenetics
, vol.6
, pp. 265
-
-
Takakubo, F.1
Kuwano, A.2
Kondo, I.3
-
281
-
-
0030444707
-
Genotyping of S-mephenytoin 4′-hydroxylation in an extended Japanese population
-
Kubota, T., Chiba, K., and Ishizaki, T., Genotyping of S-mephenytoin 4′-hydroxylation in an extended Japanese population. Clin. Pharmacol. Ther. 60, 661, 1996.
-
(1996)
Clin. Pharmacol. Ther.
, vol.60
, pp. 661
-
-
Kubota, T.1
Chiba, K.2
Ishizaki, T.3
-
282
-
-
0028860954
-
Genetic analysis of the S-mephenytoin polymorphism in a Chinese population
-
de Morals, S.M.F., Goldstein, J.A., Xie, H.-G., Huang, S.-L., Lu, Y.-Q., Xia, H., Xiao, Z.-S., Ile, N., and Zhou, H.-H., Genetic analysis of the S-mephenytoin polymorphism in a Chinese population. Clin. Pharmcol. Ther. 58, 404, 1995.
-
(1995)
Clin. Pharmcol. Ther.
, vol.58
, pp. 404
-
-
De Morals, S.M.F.1
Goldstein, J.A.2
Xie, H.-G.3
Huang, S.-L.4
Lu, Y.-Q.5
Xia, H.6
Xiao, Z.-S.7
Ile, N.8
Zhou, H.-H.9
-
283
-
-
0030904031
-
Frequencies of the defective CYP2C19 alleles responsible for the mephenytoin poor metabolizer phenotype in various Oriental, Caucasian, Saudi Arabian and American black populations
-
Goldstein, J.A., Ishizaki, T., Chiba, K., de Morais, S.M.F., Bell, D., Krahn, P.M., and Price Evans, D.A., Frequencies of the defective CYP2C19 alleles responsible for the mephenytoin poor metabolizer phenotype in various Oriental, Caucasian, Saudi Arabian and American black populations. Pharmacogenetics 7, 59, 1997.
-
(1997)
Pharmacogenetics
, vol.7
, pp. 59
-
-
Goldstein, J.A.1
Ishizaki, T.2
Chiba, K.3
De Morais, S.M.F.4
Bell, D.5
Krahn, P.M.6
Price Evans, D.A.7
-
284
-
-
0030473384
-
CYP2C19 genotype and phenotype determined by omeprazole in a Korean population
-
Roh, H.-K., Dahl, M.-L., Tybring, G., Yamada, H., Cha, Y.-N., and Bertilsson, L., CYP2C19 genotype and phenotype determined by omeprazole in a Korean population. Pharmacogenetics 6, 547, 1996.
-
(1996)
Pharmacogenetics
, vol.6
, pp. 547
-
-
Roh, H.-K.1
Dahl, M.-L.2
Tybring, G.3
Yamada, H.4
Cha, Y.-N.5
Bertilsson, L.6
-
285
-
-
0030462277
-
S-mephenytoin hydroxylation phenotype and CYP2C19 genotype among Ethiopians
-
Persson, I., Aklillu, E., Rodrigues, F., Bertilsson, L., and Ingelman-Sundberg, M., S-mephenytoin hydroxylation phenotype and CYP2C19 genotype among Ethiopians. Pharmacogenetics 6, 521, 1996.
-
(1996)
Pharmacogenetics
, vol.6
, pp. 521
-
-
Persson, I.1
Aklillu, E.2
Rodrigues, F.3
Bertilsson, L.4
Ingelman-Sundberg, M.5
-
286
-
-
0030975288
-
High frequencies of CYP2C19 mutations and poor metabolism of proguanil in Vanuatu
-
Kaneko, A., Kaneko, O., Taleo, G., Björkman, A., and Kobayakawa, T., High frequencies of CYP2C19 mutations and poor metabolism of proguanil in Vanuatu. Lancet 349, 921, 1997.
-
(1997)
Lancet
, vol.349
, pp. 921
-
-
Kaneko, A.1
Kaneko, O.2
Taleo, G.3
Björkman, A.4
Kobayakawa, T.5
-
287
-
-
0026469799
-
Enantioselective amitriptyline metabolism in patients phenotyped for two cytochrome P450 isozymes
-
Breyer-Pfaff, U., Pfandl, B., Nill, K., Nusser, E., Monney, C., Jonzier-Perey, M., Baettig, D., and Baumann, P., Enantioselective amitriptyline metabolism in patients phenotyped for two cytochrome P450 isozymes. Clin. Pharmacol. Ther. 52, 350, 1992.
-
(1992)
Clin. Pharmacol. Ther.
, vol.52
, pp. 350
-
-
Breyer-Pfaff, U.1
Pfandl, B.2
Nill, K.3
Nusser, E.4
Monney, C.5
Jonzier-Perey, M.6
Baettig, D.7
Baumann, P.8
-
288
-
-
0024580554
-
Importance of genetic factors in the regulation of diazepam metabolism: Relationship to S-mephenytoin, but not debrisoquine, hydroxylation phenotype
-
Bertilsson, L., Henthorn, T.K., Sanz, E., Tybring, G., Sawe, J., and Villen, T., Importance of genetic factors in the regulation of diazepam metabolism: relationship to S-mephenytoin, but not debrisoquine, hydroxylation phenotype. Clin. Pharmacol. Ther. 45, 348, 1989.
-
(1989)
Clin. Pharmacol. Ther.
, vol.45
, pp. 348
-
-
Bertilsson, L.1
Henthorn, T.K.2
Sanz, E.3
Tybring, G.4
Sawe, J.5
Villen, T.6
-
289
-
-
0025129339
-
Factors influencing the metabolism of diazepam
-
Bertilsson, L., Baillie, T.A., and Reviriego, J., Factors influencing the metabolism of diazepam. Pharmacol. Ther. 45, 85, 1990.
-
(1990)
Pharmacol. Ther.
, vol.45
, pp. 85
-
-
Bertilsson, L.1
Baillie, T.A.2
Reviriego, J.3
-
290
-
-
0029842851
-
The elimination of diazepam in Chinese subjects is dependent on the mephenytoin oxidation phenotype
-
Wan, J., Xia, H., He, N., Lu, Y.-Q., and Zhou, H.-H., The elimination of diazepam in Chinese subjects is dependent on the mephenytoin oxidation phenotype. Br. J. Clin. Pharmacol. 42, 471, 1996.
-
(1996)
Br. J. Clin. Pharmacol.
, vol.42
, pp. 471
-
-
Wan, J.1
Xia, H.2
He, N.3
Lu, Y.-Q.4
Zhou, H.-H.5
-
291
-
-
0025253095
-
Polymorphism in hydroxylation of mephenytoin and hexobarbital stereoisomers in relation to hepatic P-450 human-2
-
Yasumori, T., Murayama, N., Yamazoe, Y., and Kato, R., Polymorphism in hydroxylation of mephenytoin and hexobarbital stereoisomers in relation to hepatic P-450 human-2. Clin. Pharmacol. Ther. 47, 313, 1990.
-
(1990)
Clin. Pharmacol. Ther.
, vol.47
, pp. 313
-
-
Yasumori, T.1
Murayama, N.2
Yamazoe, Y.3
Kato, R.4
-
292
-
-
0023928098
-
Oxidative metabolism of hexobarbital in human liver: Relationship to polymorphic S-mephenytoin 4-hydroxylation
-
Knodell, R.G., Dubey, R.K., Wilkinson, G.R., and Guengerich, F.P., Oxidative metabolism of hexobarbital in human liver: relationship to polymorphic S-mephenytoin 4-hydroxylation. J. Pharmacol. Exp. Ther. 245, 845, 1988.
-
(1988)
J. Pharmacol. Exp. Ther.
, vol.245
, pp. 845
-
-
Knodell, R.G.1
Dubey, R.K.2
Wilkinson, G.R.3
Guengerich, F.P.4
-
293
-
-
0025964524
-
The mephenytoin oxidation polymorphism is partially responsible for the N-demethylation of imipramine
-
Skjelbo, E., Brosen, K., Hallas, J., and Gram, L.F., The mephenytoin oxidation polymorphism is partially responsible for the N-demethylation of imipramine. Clin. Pharmacol. Ther. 49, 18, 1991.
-
(1991)
Clin. Pharmacol. Ther.
, vol.49
, pp. 18
-
-
Skjelbo, E.1
Brosen, K.2
Hallas, J.3
Gram, L.F.4
-
294
-
-
0030055999
-
Steady-state plasma concentrations of imipramine and desipramine in relation to S-mephenytoin 4′-hydroxylation status in Japanese depressive patients
-
Koyama, E., Tanaka, T., Chiba, K., Kawakatsu, S., Morinobu, S., Totsuka, S., and Ishizaki, T., Steady-state plasma concentrations of imipramine and desipramine in relation to S-mephenytoin 4′-hydroxylation status in Japanese depressive patients. J. Clin. Psychopharmacol. 16, 286, 1996.
-
(1996)
J. Clin. Psychopharmacol.
, vol.16
, pp. 286
-
-
Koyama, E.1
Tanaka, T.2
Chiba, K.3
Kawakatsu, S.4
Morinobu, S.5
Totsuka, S.6
Ishizaki, T.7
-
295
-
-
0022212549
-
Stereoselective mephobarbital hydroxylation coseggregates with mephenytoin hydroxylation
-
Kupfer, A. and Branch, R.A., Stereoselective mephobarbital hydroxylation coseggregates with mephenytoin hydroxylation. Clin. Pharmacol. Ther. 38, 414, 1985.
-
(1985)
Clin. Pharmacol. Ther.
, vol.38
, pp. 414
-
-
Kupfer, A.1
Branch, R.A.2
-
296
-
-
0022623877
-
Polymorphic metabolism of mephenytoin in man, Pharmacokinetic interaction with a co-regulated substrate, mephobarbital
-
Jacqz, E., Hall, S.D., Branch, R.A., and Wilkinson, G.R., Polymorphic metabolism of mephenytoin in man, Pharmacokinetic interaction with a co-regulated substrate, mephobarbital. Clin. Pharmacol. Ther. 39, 646, 1986.
-
(1986)
Clin. Pharmacol. Ther.
, vol.39
, pp. 646
-
-
Jacqz, E.1
Hall, S.D.2
Branch, R.A.3
Wilkinson, G.R.4
-
297
-
-
0025299490
-
Slow omeprazole metabolizers are also poor S-mephenytoin hydroxyl-ators
-
Andersson, T., Regardh, C.-G., Dahl-Puustinen, M.-L., and Bertilsson, L., Slow omeprazole metabolizers are also poor S-mephenytoin hydroxyl-ators. Ther. Drug Monitor. 12, 415, 1990.
-
(1990)
Ther. Drug Monitor.
, vol.12
, pp. 415
-
-
Andersson, T.1
Regardh, C.-G.2
Dahl-Puustinen, M.-L.3
Bertilsson, L.4
-
298
-
-
0029955476
-
Ethnic and genetic determinants of omeprazole disposition and effect
-
Caraco, Y., Lagerstrom, P.-O., and Wood, A.J.J., Ethnic and genetic determinants of omeprazole disposition and effect. Clin. Pharmacol. Ther. 60, 157, 1996.
-
(1996)
Clin. Pharmacol. Ther.
, vol.60
, pp. 157
-
-
Caraco, Y.1
Lagerstrom, P.-O.2
Wood, A.J.J.3
-
299
-
-
0030937510
-
Differential stereoselective pharmacokinetics of pantoprazole, a proton pump inhibitor in extensive and poor metabolizers of pantoprazole-A preliminary study
-
Tanaka, M., Yamazaki, H., Hakusui, H., Nakamichi, N., and Sekino, H., Differential stereoselective pharmacokinetics of pantoprazole, a proton pump inhibitor in extensive and poor metabolizers of pantoprazole-A preliminary study. Chirality 9, 17, 1997.
-
(1997)
Chirality
, vol.9
, pp. 17
-
-
Tanaka, M.1
Yamazaki, H.2
Hakusui, H.3
Nakamichi, N.4
Sekino, H.5
-
300
-
-
0025735576
-
The activation of the biguanide antimalarial proguanil co-segregates with the mephenytoin oxidation polymorphism-a panel study
-
Ward, S.A., Helsby, N.A., Skjelbo, E., Brosen, K., Gram, L.F., and Breckenridge, A.M., The activation of the biguanide antimalarial proguanil co-segregates with the mephenytoin oxidation polymorphism-a panel study. Br. J. Clin. Pharmacol. 31, 689, 1991.
-
(1991)
Br. J. Clin. Pharmacol.
, vol.31
, pp. 689
-
-
Ward, S.A.1
Helsby, N.A.2
Skjelbo, E.3
Brosen, K.4
Gram, L.F.5
Breckenridge, A.M.6
-
301
-
-
0029960882
-
Chloroguanide metabolism in relation to the efficacy in malaria prophylaxis and the S-mephenytoin oxidation in Tanzanians
-
Skjelbo, E., Mutabingwa, T.K., Bygbjerg, I., Nielsen, K.K., Gram, L.F., and Brosen, K., Chloroguanide metabolism in relation to the efficacy in malaria prophylaxis and the S-mephenytoin oxidation in Tanzanians. Clin. Pharmacol. Ther. 59, 304, 1996.
-
(1996)
Clin. Pharmacol. Ther.
, vol.59
, pp. 304
-
-
Skjelbo, E.1
Mutabingwa, T.K.2
Bygbjerg, I.3
Nielsen, K.K.4
Gram, L.F.5
Brosen, K.6
-
302
-
-
0024534047
-
Propranolol's metabolism is determined by both mephenytoin and debrisoquin hydroxylase activities
-
Ward, S.A., Walle, T., Walle, K., Wilkinson, G.R., and Branch, R.A., Propranolol's metabolism is determined by both mephenytoin and debrisoquin hydroxylase activities. Clin. Pharmacol. Then. 45, 72, 1989.
-
(1989)
Clin. Pharmacol. Then.
, vol.45
, pp. 72
-
-
Ward, S.A.1
Walle, T.2
Walle, K.3
Wilkinson, G.R.4
Branch, R.A.5
-
303
-
-
0029018767
-
The hydroxylation of omeprazole correlates with S-mephenytoin metabolism: A population study
-
Balian, J.D., Sukhova, N., Harris, J.W., Hewett, J., Pickle, L., Goldstein, J.A., Woosley, R.L., and Flockhart, D.A., The hydroxylation of omeprazole correlates with S-mephenytoin metabolism: a population study. Clin. Pharmacol. Ther. 57, 662, 1995.
-
(1995)
Clin. Pharmacol. Ther.
, vol.57
, pp. 662
-
-
Balian, J.D.1
Sukhova, N.2
Harris, J.W.3
Hewett, J.4
Pickle, L.5
Goldstein, J.A.6
Woosley, R.L.7
Flockhart, D.A.8
-
304
-
-
0029587180
-
Use of omeprazole as a probe drug for CYP2C19 phenotype in Swedish Caucasians, comparison with S-mephenytoin hydroxylation phenotype and CYP2C19 genotype
-
Chang, M., Dahl, M.-L., Tybring, G., Gotharson, E., and Bertilsson, L., Use of omeprazole as a probe drug for CYP2C19 phenotype in Swedish Caucasians, comparison with S-mephenytoin hydroxylation phenotype and CYP2C19 genotype. Pharmacogenetics 5, 358-363, 1995.
-
(1995)
Pharmacogenetics
, vol.5
, pp. 358-363
-
-
Chang, M.1
Dahl, M.-L.2
Tybring, G.3
Gotharson, E.4
Bertilsson, L.5
-
305
-
-
0029877643
-
Pharmacokinetic evaluation of proguanil, a probe phenotyping drug for the mephenytoin hydroxylase polymorphism
-
Somogyi, A.A., Reinhard, H.A., and Bochner, F., Pharmacokinetic evaluation of proguanil, a probe phenotyping drug for the mephenytoin hydroxylase polymorphism. Br. J. Clin. Pharmacol. 41, 175, 1996.
-
(1996)
Br. J. Clin. Pharmacol.
, vol.41
, pp. 175
-
-
Somogyi, A.A.1
Reinhard, H.A.2
Bochner, F.3
-
306
-
-
0029055448
-
Phenotyping and genotyping of S-mephenytoin hydroxylase (cytochrome P450 2C19) in a shona population of Zimbabwe
-
Masimirembwa, C., Bertilsson, L., Johansson, I., Hasler, J.A., and Ingelman-Sundberg, M., Phenotyping and genotyping of S-mephenytoin hydroxylase (cytochrome P450 2C19) in a shona population of Zimbabwe. Clin. Pharmacol. Ther. 57, 656, 1995.
-
(1995)
Clin. Pharmacol. Ther.
, vol.57
, pp. 656
-
-
Masimirembwa, C.1
Bertilsson, L.2
Johansson, I.3
Hasler, J.A.4
Ingelman-Sundberg, M.5
-
307
-
-
0028865992
-
A multifamily study on the relationship between CYP2C19 genotype and S-mephenytoin oxidation phenotype
-
Brosen, K., de Morals, S.M.F., Meyer, U.A., and Goldstein, J.A., A multifamily study on the relationship between CYP2C19 genotype and S-mephenytoin oxidation phenotype. Pharmacogenetics 5, 312, 1995.
-
(1995)
Pharmacogenetics
, vol.5
, pp. 312
-
-
Brosen, K.1
De Morals, S.M.F.2
Meyer, U.A.3
Goldstein, J.A.4
-
308
-
-
0028998678
-
Phenotyping of CYP2C19 with enantiospecific HPLC-quantification of R- and S- mephenytoin and comparison with the intron4/exon5 G→A-splice site mutation
-
Brockmoller, J., Rost, K.L., Gross, D., Schenkel, A., and Roots, L., Phenotyping of CYP2C19 with enantiospecific HPLC-quantification of R- and S- mephenytoin and comparison with the intron4/exon5 G→A-splice site mutation. Pharmacogenetics 5, 80, 1995.
-
(1995)
Pharmacogenetics
, vol.5
, pp. 80
-
-
Brockmoller, J.1
Rost, K.L.2
Gross, D.3
Schenkel, A.4
Roots, L.5
-
309
-
-
0028214359
-
The role of S-mephenytoin 4′-hydroxylase in imipramine metabolism by human liver microsomes, a two-enzyme kinetic analysis of N-demethylation and 2-hydroxylation
-
Chiba, K., Saitoh, A., Koyama, E., Tani, M., Hayashi, M., and Ishizaki, T., The role of S-mephenytoin 4′-hydroxylase in imipramine metabolism by human liver microsomes, a two-enzyme kinetic analysis of N-demethylation and 2-hydroxylation. Br. J. Clin. Pharmacol. 37, 237, 1994.
-
(1994)
Br. J. Clin. Pharmacol.
, vol.37
, pp. 237
-
-
Chiba, K.1
Saitoh, A.2
Koyama, E.3
Tani, M.4
Hayashi, M.5
Ishizaki, T.6
-
310
-
-
0027471030
-
Genetically determined drug-metabolizing activity and desipramine-associated cardiotoxicity: A case report
-
Bluhm, R.E., Wilkinson, G.R., Shelton, R., and Branch, R.A., Genetically determined drug-metabolizing activity and desipramine-associated cardiotoxicity: a case report. Clin. Pharmacol. Ther. 53, 89, 1993.
-
(1993)
Clin. Pharmacol. Ther.
, vol.53
, pp. 89
-
-
Bluhm, R.E.1
Wilkinson, G.R.2
Shelton, R.3
Branch, R.A.4
-
311
-
-
0025223056
-
Diazepam metabolism in native Chinese poor and extensive hydroxylators of S-mephenytoin: Inter-ethnic differences in comparison with white subjects
-
Zhang, Y., Reviriego, J., Lou, Y.-q., Sjoqvist, F., and Bertilsson, L., Diazepam metabolism in native Chinese poor and extensive hydroxylators of S-mephenytoin: inter-ethnic differences in comparison with white subjects. Clin. Pharmacol. Ther. 48, 496, 1990.
-
(1990)
Clin. Pharmacol. Ther.
, vol.48
, pp. 496
-
-
Zhang, Y.1
Reviriego, J.2
Lou, Y.-Q.3
Sjoqvist, F.4
Bertilsson, L.5
-
312
-
-
0027208084
-
Why are diazepam metabolism and polymorphic S-mephenytoin hydroxylation associated with each other in white and Korean populations but not in Chinese populations
-
Bertilsson, L. and Kalow, W.,Why are diazepam metabolism and polymorphic S-mephenytoin hydroxylation associated with each other in white and Korean populations but not in Chinese populations. Clin. Pharmacol. Ther. 53, 608, 1993.
-
(1993)
Clin. Pharmacol. Ther.
, vol.53
, pp. 608
-
-
Bertilsson, L.1
Kalow, W.2
-
313
-
-
0027272518
-
Proguanil metabolism is determined by the mephenytoin oxidation polymorphism in Vietnamese living in Denmark
-
Brosen, K., Skjelbo, E., and Flachs, H., Proguanil metabolism is determined by the mephenytoin oxidation polymorphism in Vietnamese living in Denmark. Br. J. Clin. Pharmacol. 36, 105, 1993.
-
(1993)
Br. J. Clin. Pharmacol.
, vol.36
, pp. 105
-
-
Brosen, K.1
Skjelbo, E.2
Flachs, H.3
-
314
-
-
0029815579
-
Proguanil polymorphism does not affect antimalarial activity of proguanil combined with atovaquone in vitro
-
Edstein, M.D., Yeo, A.E.T., Kyle, D.E., Looareesuwan, S., Wilairatana, P., and Rieckmann, K.H., Proguanil polymorphism does not affect antimalarial activity of proguanil combined with atovaquone in vitro, Transact. R. Soc. Trop. Med. Hyg. 90, 418, 1996.
-
(1996)
Transact. R. Soc. Trop. Med. Hyg.
, vol.90
, pp. 418
-
-
Edstein, M.D.1
Yeo, A.E.T.2
Kyle, D.E.3
Looareesuwan, S.4
Wilairatana, P.5
Rieckmann, K.H.6
-
315
-
-
0026816971
-
Polymorphic hydroxylation of S-mephenytoin and omeprazole metabolism in Caucasian and Chinese subjects
-
Andersson, T., Regardh, C.-G., Lou, Y.-C., Zhang, Y., Dahl, M.-L., and Bertilsson, L., Polymorphic hydroxylation of S-mephenytoin and omeprazole metabolism in Caucasian and Chinese subjects. Pharmacogenetics 2, 25, 1992.
-
(1992)
Pharmacogenetics
, vol.2
, pp. 25
-
-
Andersson, T.1
Regardh, C.-G.2
Lou, Y.-C.3
Zhang, Y.4
Dahl, M.-L.5
Bertilsson, L.6
-
316
-
-
0029858783
-
Human CYP2C19 is a major omeprazole 5-hydroxylase, as demonstrated with recombinant cytochrome P450 enzymes
-
Karam, W.G, Goldstein, J.A., Lasker, J.M., and Ghanayem, B.I., Human CYP2C19 is a major omeprazole 5-hydroxylase, as demonstrated with recombinant cytochrome P450 enzymes. Drug Metab. Dispos. 24, 1081, 1996.
-
(1996)
Drug Metab. Dispos.
, vol.24
, pp. 1081
-
-
Karam, W.G.1
Goldstein, J.A.2
Lasker, J.M.3
Ghanayem, B.I.4
-
317
-
-
0017695082
-
Polymorphic hydroxylation of debrisoquine in man
-
Mahgoub, A., Dring, L.G., Idle, J.R., Lancaster, R., and Smith, R.L., Polymorphic hydroxylation of debrisoquine in man. Lancet, 584, 1977.
-
(1977)
Lancet
, pp. 584
-
-
Mahgoub, A.1
Dring, L.G.2
Idle, J.R.3
Lancaster, R.4
Smith, R.L.5
-
318
-
-
0018900001
-
A family and population study of the genetic polymorphism of debrisoquine oxidation in a white British population
-
Price Evans, D.A., Mahgoub, A., Sloan, T.P., Idle, J.R., and Smith, R.L., A family and population study of the genetic polymorphism of debrisoquine oxidation in a white British population. J. Med. Genet. 17, 102, 1980.
-
(1980)
J. Med. Genet.
, vol.17
, pp. 102
-
-
Price Evans, D.A.1
Mahgoub, A.2
Sloan, T.P.3
Idle, J.R.4
Smith, R.L.5
-
319
-
-
0020582521
-
Genetically determined oxidation capacity and the disposition of debrisoquine
-
Sloan, T.P., Lancaster, R., Shah, R.R., Idle, J.R., and Smith, R.L., Genetically determined oxidation capacity and the disposition of debrisoquine. Br. J. Clin. Pharmacol. 15, 443, 1983.
-
(1983)
Br. J. Clin. Pharmacol.
, vol.15
, pp. 443
-
-
Sloan, T.P.1
Lancaster, R.2
Shah, R.R.3
Idle, J.R.4
Smith, R.L.5
-
320
-
-
0018615011
-
Defective N-oxidation of sparteine in man: A new pharmacogenetic defect
-
Eichelbaum, M., Spannbrucker, N., Steincke, B., and Dengler, H.J., Defective N-oxidation of sparteine in man: a new pharmacogenetic defect. Eur. J. Clin. Pharmacol. 16, 183, 1979.
-
(1979)
Eur. J. Clin. Pharmacol.
, vol.16
, pp. 183
-
-
Eichelbaum, M.1
Spannbrucker, N.2
Steincke, B.3
Dengler, H.J.4
-
321
-
-
0018714764
-
Influence of the defective metabolism of sparteine on its pharmacokinetics
-
Eichelbaum, M., Spannbrucker, N., and Dengler, H.J., Influence of the defective metabolism of sparteine on its pharmacokinetics. Eur. J. Clin. Pharmacol. 16, 189, 1979.
-
(1979)
Eur. J. Clin. Pharmacol.
, vol.16
, pp. 189
-
-
Eichelbaum, M.1
Spannbrucker, N.2
Dengler, H.J.3
-
322
-
-
0020068049
-
Polymorphic oxidation of sparteine and debrisoquine, related pharmacogenetic entities
-
Eichelbaum, M., Bertilsson, L., Sawe, J., and Zekorn, C., Polymorphic oxidation of sparteine and debrisoquine, related pharmacogenetic entities. Clin. Pharmacol. Ther. 31, 184, 1982.
-
(1982)
Clin. Pharmacol. Ther.
, vol.31
, pp. 184
-
-
Eichelbaum, M.1
Bertilsson, L.2
Sawe, J.3
Zekorn, C.4
-
323
-
-
0022179340
-
A family study of genetic and environmental factors determining polymorphic hydroxylation of debrisoquine
-
Steiner, E., Iselius, L., Alvan, G., Lindsten, J., and Sjoqvist, F., A family study of genetic and environmental factors determining polymorphic hydroxylation of debrisoquine. Clin. Pharmacol. Ther. 38, 394, 1985.
-
(1985)
Clin. Pharmacol. Ther.
, vol.38
, pp. 394
-
-
Steiner, E.1
Iselius, L.2
Alvan, G.3
Lindsten, J.4
Sjoqvist, F.5
-
324
-
-
0023684586
-
Absence of hepatic cytochrome P450bufI causes genetically deficient debrisoquine oxidation in man
-
Zanger, U.M., Vilbois, F., Hardwick, J.P., and Meyer, U.A., Absence of hepatic cytochrome P450bufI causes genetically deficient debrisoquine oxidation in man. Biochemistry 27, 5447, 1988.
-
(1988)
Biochemistry
, vol.27
, pp. 5447
-
-
Zanger, U.M.1
Vilbois, F.2
Hardwick, J.P.3
Meyer, U.A.4
-
325
-
-
0023854270
-
Characterization of the common genetic defects in humans deficient in debrisoquine metabolism
-
Gonzalez, F.J., Skoda, R.C, Kimura, S., Umeno, M., Zanger, U.M., Nebert, D.W., Gelboin, H.V., Hardwick, J.P., and Meyer, U.A., Characterization of the common genetic defects in humans deficient in debrisoquine metabolism. Nature 331, 442, 1988.
-
(1988)
Nature
, vol.331
, pp. 442
-
-
Gonzalez, F.J.1
Skoda, R.C.2
Kimura, S.3
Umeno, M.4
Zanger, U.M.5
Nebert, D.W.6
Gelboin, H.V.7
Hardwick, J.P.8
Meyer, U.A.9
-
326
-
-
0028997955
-
"It's the genes, stupid": Molecular bases and clinical consequences of genetic cytochrome P450 2D6 polymorphism
-
Kroemer, H.K. and Eichelbaum, M., "It's the genes, stupid": molecular bases and clinical consequences of genetic cytochrome P450 2D6 polymorphism. Life Sci. 56, 2285, 1995.
-
(1995)
Life Sci.
, vol.56
, pp. 2285
-
-
Kroemer, H.K.1
Eichelbaum, M.2
-
327
-
-
0029028932
-
Geographical/Interracial differences in polymorphic drug oxidation; current state of knowledge of cytochromes P450 (CYP) 2D6 and 2C19
-
Bertilsson, L., Geographical/Interracial differences in polymorphic drug oxidation; current state of knowledge of cytochromes P450 (CYP) 2D6 and 2C19. Clin. Pharmacokinet. 29, 192, 1995.
-
(1995)
Clin. Pharmacokinet.
, vol.29
, pp. 192
-
-
Bertilsson, L.1
-
328
-
-
0027477948
-
Polymorphism of debrisoquine and mephenytoin hydroxylation among Estonians
-
Kiivet, R.A., Svensson, J.-O., Bertilsson, L., and Sjoqvist, F., Polymorphism of debrisoquine and mephenytoin hydroxylation among Estonians. Pharmacol. Toxicol. 72, 113, 1993.
-
(1993)
Pharmacol. Toxicol.
, vol.72
, pp. 113
-
-
Kiivet, R.A.1
Svensson, J.-O.2
Bertilsson, L.3
Sjoqvist, F.4
-
329
-
-
84920227522
-
Low frequency of slow debrisoquine hydroxylation in a native Chinese population
-
Lou, Y.-C., Ying, L., Bertilsson, L., and Sjoqvist, F., Low frequency of slow debrisoquine hydroxylation in a native Chinese population. Lancet 852, 1987.
-
(1987)
Lancet
, pp. 852
-
-
Lou, Y.-C.1
Ying, L.2
Bertilsson, L.3
Sjoqvist, F.4
-
330
-
-
0026506140
-
Pronounced differences between native Chinese and Swedish populations in the polymorphic hydroxylations of debrisoquine and S-mephenytoin
-
Bertilsson, L., Lou, Y.-Q., Du, Y.-L., Liu, Y., Kuang, T.-Y., Liao, X.-M., Wang, K.-Y., Reviriego, J., Iselius, L., and Sjoqvist, F., Pronounced differences between native Chinese and Swedish populations in the polymorphic hydroxylations of debrisoquine and S-mephenytoin. Clin. Pharmacol. Ther. 51, 388, 1992.
-
(1992)
Clin. Pharmacol. Ther.
, vol.51
, pp. 388
-
-
Bertilsson, L.1
Lou, Y.-Q.2
Du, Y.-L.3
Liu, Y.4
Kuang, T.-Y.5
Liao, X.-M.6
Wang, K.-Y.7
Reviriego, J.8
Iselius, L.9
Sjoqvist, F.10
-
331
-
-
0024359574
-
Clinical significance of the sparteine/debrisoquine oxidation polymorphism
-
Brosen, K. and Gram, L.F., Clinical significance of the sparteine/debrisoquine oxidation polymorphism. Eur. J. Clin. Pharmacol. 36, 537, 1989.
-
(1989)
Eur. J. Clin. Pharmacol.
, vol.36
, pp. 537
-
-
Brosen, K.1
Gram, L.F.2
-
332
-
-
0001668414
-
The genetic polymorphism of debrisoquine/sparteine metabolism: Clinical aspects
-
Kalow, W., Ed., Pergamon Press Inc., New York
-
Eichelbaum, M. and Gross, A.S., The genetic polymorphism of debrisoquine/sparteine metabolism: clinical aspects. In: Pharmacogenetics of Drug Metabolism. Kalow, W., Ed., Pergamon Press Inc., New York, 1992, 625-648
-
(1992)
Pharmacogenetics of Drug Metabolism
, pp. 625-648
-
-
Eichelbaum, M.1
Gross, A.S.2
-
333
-
-
0027483214
-
Genetically variable metabolism of antidepressants and neuroleptics in man
-
Dahl, M.-L. and Bertilsson, L., Genetically variable metabolism of antidepressants and neuroleptics in man. Pharmacogenetics 3, 61, 1993.
-
(1993)
Pharmacogenetics
, vol.3
, pp. 61
-
-
Dahl, M.-L.1
Bertilsson, L.2
-
334
-
-
0020059423
-
High plasma concentrations of β-receptor blocking drugs and deficient debrisoquine hydroxylation
-
Alvan, G., von Bahr, C., Seideman, P., and Sjoqvist, F., High plasma concentrations of β-receptor blocking drugs and deficient debrisoquine hydroxylation. The Lancet, 333, 1982.
-
(1982)
The Lancet
, pp. 333
-
-
Alvan, G.1
Von Bahr, C.2
Seideman, P.3
Sjoqvist, F.4
-
335
-
-
0021717945
-
Relationship of N-demethylation of amiflamine and its metabolite to debrisoquine hydroxylation polymorphism
-
Alvan, G., Grind, M., Graffner, C., and Sjoqvist, F., Relationship of N-demethylation of amiflamine and its metabolite to debrisoquine hydroxylation polymorphism. Clin. Pharmacol. Ther. 36, 515, 1984.
-
(1984)
Clin. Pharmacol. Ther.
, vol.36
, pp. 515
-
-
Alvan, G.1
Grind, M.2
Graffner, C.3
Sjoqvist, F.4
-
336
-
-
0020592679
-
Amitriptyline metabolism: Relationship to polymorphic debrisoquine hydroxylation
-
Mellstrom, B., Bertilsson, L., Lou, Y.-C., Sawe, J., and Sjoqvist, F., Amitriptyline metabolism: relationship to polymorphic debrisoquine hydroxylation. Clin. Pharmacol. Ther. 34, 516, 1983.
-
(1983)
Clin. Pharmacol. Ther.
, vol.34
, pp. 516
-
-
Mellstrom, B.1
Bertilsson, L.2
Lou, Y.-C.3
Sawe, J.4
Sjoqvist, F.5
-
337
-
-
0022481136
-
Amitriptyline metabolism: Association with debrisoquine hydroxylation in nonsmokers
-
Mellstrom, B., Sawe, J., Bertilsson, L., and Sjoqvist, F., Amitriptyline metabolism: association with debrisoquine hydroxylation in nonsmokers. Clin. Pharmacol. Ther. 39, 369, 1986.
-
(1986)
Clin. Pharmacol. Ther.
, vol.39
, pp. 369
-
-
Mellstrom, B.1
Sawe, J.2
Bertilsson, L.3
Sjoqvist, F.4
-
338
-
-
0022692071
-
Amitriptyline pharmacokinetics and clinical response, II. Metabolic polymorphism assessed by hydroxylation of debrisoquine and mephenytoin
-
Baumann, P., Jonzier-Perey, M., Koeb, L., Kupfer, A., Tinguely, D., and Schopf, J., Amitriptyline pharmacokinetics and clinical response, II. Metabolic polymorphism assessed by hydroxylation of debrisoquine and mephenytoin. Int. Clin. Psychopharmacol. 1, 102, 1986.
-
(1986)
Int. Clin. Psychopharmacol.
, vol.1
, pp. 102
-
-
Baumann, P.1
Jonzier-Perey, M.2
Koeb, L.3
Kupfer, A.4
Tinguely, D.5
Schopf, J.6
-
339
-
-
0027410086
-
The metabolism of aprindine in relation to the sparteine/debrisoquine polymorphism
-
Ebner, T. and Eichelbaum, M., The metabolism of aprindine in relation to the sparteine/debrisoquine polymorphism. Br. J. Clin. Pharmacol. 35, 426, 1993.
-
(1993)
Br. J. Clin. Pharmacol.
, vol.35
, pp. 426
-
-
Ebner, T.1
Eichelbaum, M.2
-
340
-
-
0021848782
-
Effect of oxidative polymorphism (debrisoquine/sparteine type) on hepatic first-pass metabolism of bufuralol
-
Dayer, P., Balant, L., Kupfer, A., Striberni, R., and Leemann, T., Effect of oxidative polymorphism (debrisoquine/sparteine type) on hepatic first-pass metabolism of bufuralol. Eur. J. Clin. Pharmacol. 28, 317, 1985.
-
(1985)
Eur. J. Clin. Pharmacol.
, vol.28
, pp. 317
-
-
Dayer, P.1
Balant, L.2
Kupfer, A.3
Striberni, R.4
Leemann, T.5
-
341
-
-
0022869718
-
Stereo-and regioselectivity of hepatic oxidation in man-Effect of the debrisoquine/sparteine phenotype on bufuralol hydroxylation
-
Dayer, P., Leemann, T., Kupfer, A., Kronbach, T., and Meyer, U.A., Stereo-and regioselectivity of hepatic oxidation in man-Effect of the debrisoquine/ sparteine phenotype on bufuralol hydroxylation. Eur. J. Clin. Pharmacol. 31, 313, 1986.
-
(1986)
Eur. J. Clin. Pharmacol.
, vol.31
, pp. 313
-
-
Dayer, P.1
Leemann, T.2
Kupfer, A.3
Kronbach, T.4
Meyer, U.A.5
-
342
-
-
0021947109
-
Discovery of altered pharmacokinetics of CGP 15 210 G in poor hydroxylators of debrisoquine during early drug development
-
Gleiter, C.H., Aichele, G., Nilsson, E., Henhen, N., Antonin, K.H., and Bieck, P.R., Discovery of altered pharmacokinetics of CGP 15 210 G in poor hydroxylators of debrisoquine during early drug development. Br. J. Clin. Pharmacol. 20, 81, 1985.
-
(1985)
Br. J. Clin. Pharmacol.
, vol.20
, pp. 81
-
-
Gleiter, C.H.1
Aichele, G.2
Nilsson, E.3
Henhen, N.4
Antonin, K.H.5
Bieck, P.R.6
-
343
-
-
0027472058
-
Pharmacokinetics of citalopram in relation to the sparteine and the mephenytoin oxidation polymorphisms
-
Sindrup, S.H., Brosen, K., Hansen, M.G.J., Aaes-Jorgensen, T., Overo, K.F., and Gram, L.F., Pharmacokinetics of citalopram in relation to the sparteine and the mephenytoin oxidation polymorphisms. Ther. Drug. Monitor. 15, 11, 1993.
-
(1993)
Ther. Drug. Monitor.
, vol.15
, pp. 11
-
-
Sindrup, S.H.1
Brosen, K.2
Hansen, M.G.J.3
Aaes-Jorgensen, T.4
Overo, K.F.5
Gram, L.F.6
-
344
-
-
0022898438
-
Importance of oxidative polymorphism and levomepromazine treatment on the steady-state blood concentrations of clomipramine and its major metabolites
-
Balant-Gorgia, A.E., Balant, L.P., Genet, Ch., Dayer, P., Aeschlimann, J.M., and Garrone, G., Importance of oxidative polymorphism and levomepromazine treatment on the steady-state blood concentrations of clomipramine and its major metabolites. Eur. J. Clin. Pharmacol. 31. 449, 1986.
-
(1986)
Eur. J. Clin. Pharmacol.
, vol.31
, pp. 449
-
-
Balant-Gorgia, A.E.1
Balant, L.P.2
Genet, Ch.3
Dayer, P.4
Aeschlimann, J.M.5
Garrone, G.6
-
345
-
-
0026739661
-
Steady-state plasma levels of clomipramine and its metabolites, impact of the sparteine/debrisoquine oxidation polymorphism
-
Kramer Nielsen, K., Brosen, K., Gram, L.F., and the Danish University Antidepressant Group, Steady-state plasma levels of clomipramine and its metabolites, impact of the sparteine/debrisoquine oxidation polymorphism. Eur. J. Clin. Pharmacol. 43, 405, 1992.
-
(1992)
Eur. J. Clin. Pharmacol.
, vol.43
, pp. 405
-
-
Kramer Nielsen, K.1
Brosen, K.2
Gram, L.F.3
-
346
-
-
0020662811
-
The debrisoquine hydroxylation test predicts steady-state plasma levels of desipramine
-
Bertilsson, L. and Aberg-Wistedt, A., The debrisoquine hydroxylation test predicts steady-state plasma levels of desipramine. Br. J. Clin. Pharmac. 15, 388, 1983.
-
(1983)
Br. J. Clin. Pharmac.
, vol.15
, pp. 388
-
-
Bertilsson, L.1
Aberg-Wistedt, A.2
-
347
-
-
0029868823
-
The influence of the sparteine/ debrisoquine genetic polymorphism on the disposition of dexfenfluramine
-
Gross, A.S., Phillips, A.C., Roeutord, A., and Shenfield, G.M., The influence of the sparteine/ debrisoquine genetic polymorphism on the disposition of dexfenfluramine. Br. J. Clin. Pharmacol. 41, 311, 1996
-
(1996)
Br. J. Clin. Pharmacol.
, vol.41
, pp. 311
-
-
Gross, A.S.1
Phillips, A.C.2
Roeutord, A.3
Shenfield, G.M.4
-
348
-
-
0021179863
-
Dextromethorphan as a safe probe for debrisoquine hydroxylation polymorphism
-
Kupfer, A., Schmid, B., Preisig, R., and Pfaff, G., Dextromethorphan as a safe probe for debrisoquine hydroxylation polymorphism. Lancet 517, 1984.
-
(1984)
Lancet
, pp. 517
-
-
Kupfer, A.1
Schmid, B.2
Preisig, R.3
Pfaff, G.4
-
349
-
-
0022338958
-
Polymorphic dextromethorphan metabolism: Co-segregation of oxidative O-demethylation with debrisoquine hydroxylation
-
Schmid, B., Bircher, J., Preisig, R., and Kupfer, A., Polymorphic dextromethorphan metabolism: co-segregation of oxidative O-demethylation with debrisoquine hydroxylation. Clin. Pharmacol. Ther. 38, 618, 1985.
-
(1985)
Clin. Pharmacol. Ther.
, vol.38
, pp. 618
-
-
Schmid, B.1
Bircher, J.2
Preisig, R.3
Kupfer, A.4
-
350
-
-
0029853347
-
The influence of CYP2D6 polymorphism and quinidine on the disposition and antitussive effect of dextromethorphan in humans
-
Capon, D.A., Bochner, F., Kerry, N., Mikus, G., Danz, C., and Somogyi, A.A., The influence of CYP2D6 polymorphism and quinidine on the disposition and antitussive effect of dextromethorphan in humans. Clin. Pharmacol. Ther. 60, 295, 1996.
-
(1996)
Clin. Pharmacol. Ther.
, vol.60
, pp. 295
-
-
Capon, D.A.1
Bochner, F.2
Kerry, N.3
Mikus, G.4
Danz, C.5
Somogyi, A.A.6
-
351
-
-
0023724194
-
Is there a genetic factor in flecainide toxicity
-
Beckmann, J., Hertrampf, R., Gundert-Remy, U., Mikus, G., Gross, A.S., and Eichelbaum, M., Is there a genetic factor in flecainide toxicity? Br. Med. J. 297, 1316, 1988.
-
(1988)
Br. Med. J.
, vol.297
, pp. 1316
-
-
Beckmann, J.1
Hertrampf, R.2
Gundert-Remy, U.3
Mikus, G.4
Gross, A.S.5
Eichelbaum, M.6
-
352
-
-
0029827303
-
The disposition of fluoxetine but not sertraline is altered in poor metabolizers of debrisoquine
-
Hamelin, B.A., Turgeon, J., Vallee, F., Belanger, P.-M., Paquet, F., and LeBel, M., The disposition of fluoxetine but not sertraline is altered in poor metabolizers of debrisoquine. Clin. Pharmacol. Ther. 60, 512, 1996.
-
(1996)
Clin. Pharmacol. Ther.
, vol.60
, pp. 512
-
-
Hamelin, B.A.1
Turgeon, J.2
Vallee, F.3
Belanger, P.-M.4
Paquet, F.5
Lebel, M.6
-
353
-
-
0029860967
-
Disposition of fluvoxamine in humans is determined by the polymorphic CYP2D6 and also by the CYP1A2 activity
-
Carrillo, J.A., Dahl, M.-L., Svensson, J.-O., Alm, C., Rodriguez, I., and Bertilsson, L., Disposition of fluvoxamine in humans is determined by the polymorphic CYP2D6 and also by the CYP1A2 activity. Clin. Pharmacol. Ther. 60, 183, 1996.
-
(1996)
Clin. Pharmacol. Ther.
, vol.60
, pp. 183
-
-
Carrillo, J.A.1
Dahl, M.-L.2
Svensson, J.-O.3
Alm, C.4
Rodriguez, I.5
Bertilsson, L.6
-
354
-
-
0018082438
-
Polymorphism of carbon oxidation of drugs and clinical implications
-
Sloan, T.P., Mahgoub, A., Lancaster, R., Idle, J.R., and Smith, R.L., Polymorphism of carbon oxidation of drugs and clinical implications. Br. Med. J. 2, 655, 1978.
-
(1978)
Br. Med. J.
, vol.2
, pp. 655
-
-
Sloan, T.P.1
Mahgoub, A.2
Lancaster, R.3
Idle, J.R.4
Smith, R.L.5
-
355
-
-
0026692983
-
Haloperidol disposition is dependent on debrisoquine hydroxylation phenotype
-
Llerena, A., Alm, C., Dahl, M.-L., Ekqvist, B., and Bertilsson, L., Haloperidol disposition is dependent on debrisoquine hydroxylation phenotype. Ther. Drug Monitor. 14, 92, 1992.
-
(1992)
Ther. Drug Monitor.
, vol.14
, pp. 92
-
-
Llerena, A.1
Alm, C.2
Dahl, M.-L.3
Ekqvist, B.4
Bertilsson, L.5
-
356
-
-
0023905440
-
First-pass metabolism of imipramine and desipramine: Impact of the sparteine oxidation phenotype
-
Brosen, K. and Gram, L.F., First-pass metabolism of imipramine and desipramine: impact of the sparteine oxidation phenotype. Clin. Pharmacol. Ther. 43, 400, 1988.
-
(1988)
Clin. Pharmacol. Ther.
, vol.43
, pp. 400
-
-
Brosen, K.1
Gram, L.F.2
-
357
-
-
0022510805
-
Steady-state concentrations of imipramine and its metabolites in relation to the sparteine/debrisoquine polymorphism
-
Brosen, K., Klysner, R., Gram, L.F., Otton, S.V., Bech, P., and Bertilsson, L., Steady-state concentrations of imipramine and its metabolites in relation to the sparteine/debrisoquine polymorphism. Eur. J. Clin. Pharmacol. 30, 679, 1986.
-
(1986)
Eur. J. Clin. Pharmacol.
, vol.30
, pp. 679
-
-
Brosen, K.1
Klysner, R.2
Gram, L.F.3
Otton, S.V.4
Bech, P.5
Bertilsson, L.6
-
358
-
-
0023032092
-
Imipramine demethylation and hydroxylation, impact of the sparteine oxidation phenotype
-
Brosen, K., Otton, S.V., and Gram, L.F., Imipramine demethylation and hydroxylation, Impact of the sparteine oxidation phenotype. Clin. Pharmacol. Ther. 40, 543, 1986.
-
(1986)
Clin. Pharmacol. Ther.
, vol.40
, pp. 543
-
-
Brosen, K.1
Otton, S.V.2
Gram, L.F.3
-
359
-
-
0024216319
-
Importance of oxidative polymorphism on clinical efficacy and side-effects of imipramine-a retrospective study
-
Meyer, J.W., Woggon, B., and Kupfer, A., Importance of oxidative polymorphism on clinical efficacy and side-effects of imipramine-a retrospective study. Pharmacopsychiatry 21, 365, 1988.
-
(1988)
Pharmacopsychiatry
, vol.21
, pp. 365
-
-
Meyer, J.W.1
Woggon, B.2
Kupfer, A.3
-
360
-
-
0023217521
-
The pharmacokinetics of indoramin and 6-hydroxy-indoramin in poor and extensive hydroxylators of debrisoquine
-
Pierce, D.M., Smith, S.E., and Franklin, R.A., The pharmacokinetics of indoramin and 6-hydroxy-indoramin in poor and extensive hydroxylators of debrisoquine. Eur. J. Clin. Pharmacol. 33, 59, 1987.
-
(1987)
Eur. J. Clin. Pharmacol.
, vol.33
, pp. 59
-
-
Pierce, D.M.1
Smith, S.E.2
Franklin, R.A.3
-
361
-
-
0018674294
-
Inter-individual and interspecies variation in the metabolism of the hallucinogen 4-methoxyamphetamine
-
Kitchen, I., Tremblay, J., Andre, J., Dring, L.G., Idle, J.R., Smith, R.L., and Williams, R.T., Inter-individual and interspecies variation in the metabolism of the hallucinogen 4-methoxyamphetamine. Xenobiotica 9, 397, 1979.
-
(1979)
Xenobiotica
, vol.9
, pp. 397
-
-
Kitchen, I.1
Tremblay, J.2
Andre, J.3
Dring, L.G.4
Idle, J.R.5
Smith, R.L.6
Williams, R.T.7
-
362
-
-
0022356746
-
Metabolism of methoxy-phenamine in extensive and poor metabolizers of debrisoquine
-
Roy, S.D., Hawes, E.M., McKay, G., Korchinski, E.D., and Midha, K.K., Metabolism of methoxy-phenamine in extensive and poor metabolizers of debrisoquine. Clin. Pharmacol. Ther. 38, 128, 1985.
-
(1985)
Clin. Pharmacol. Ther.
, vol.38
, pp. 128
-
-
Roy, S.D.1
Hawes, E.M.2
McKay, G.3
Korchinski, E.D.4
Midha, K.K.5
-
363
-
-
0021082394
-
Differential stereoselectivemetabolism of metoprolol in extensive and poor debrisoquine metabolizers
-
Lennard, M.S., Tucker, G.T., Silas, J.H., Freestone, S., Ramsay, L.E., and Woods, H.F., Differential stereoselectivemetabolism of metoprolol in extensive and poor debrisoquine metabolizers. Clin. Pharmacol. Ther. 34, 732, 1983.
-
(1983)
Clin. Pharmacol. Ther.
, vol.34
, pp. 732
-
-
Lennard, M.S.1
Tucker, G.T.2
Silas, J.H.3
Freestone, S.4
Ramsay, L.E.5
Woods, H.F.6
-
364
-
-
0027390996
-
Stereoselective hydroxylation of mexiletine in human liver microsomes, implication of P450IID6 - A preliminary report
-
Vandamme, N., Broly, F., Libersa, C., Courseau, C., and Lhermitte, M., Stereoselective hydroxylation of mexiletine in human liver microsomes, Implication of P450IID6 - a preliminary report. J. Cardiovasc. Pharmacol. 21, 77, 1993.
-
(1993)
J. Cardiovasc. Pharmacol.
, vol.21
, pp. 77
-
-
Vandamme, N.1
Broly, F.2
Libersa, C.3
Courseau, C.4
Lhermitte, M.5
-
365
-
-
0026776937
-
Debrisoquine hydroxylation phenotypes of patients with high versus low to normal serum antidepressant concentrations
-
Tacke, U., Leinonen, E., Lillsunde, P., Seppala, T., Arvela, P., Pelkonen, O., and Ylitalo, P., Debrisoquine hydroxylation phenotypes of patients with high versus low to normal serum antidepressant concentrations. J. Clin. Psychopharmacol. 12, 262, 1992.
-
(1992)
J. Clin. Psychopharmacol.
, vol.12
, pp. 262
-
-
Tacke, U.1
Leinonen, E.2
Lillsunde, P.3
Seppala, T.4
Arvela, P.5
Pelkonen, O.6
Ylitalo, P.7
-
366
-
-
0028118655
-
Poor metabolisers of nicotine and CYP2D6 polymorphism
-
Cholerton, S., Arpanahi, A., McCracken, N., Boustead, C., Taber, H., Johnstone, E., Leathart, J., Daly, A.K., and Idle, J.R., Poor metabolisers of nicotine and CYP2D6 polymorphism. Lancet 343, 62, 1994.
-
(1994)
Lancet
, vol.343
, pp. 62
-
-
Cholerton, S.1
Arpanahi, A.2
McCracken, N.3
Boustead, C.4
Taber, H.5
Johnstone, E.6
Leathart, J.7
Daly, A.K.8
Idle, J.R.9
-
367
-
-
0019199097
-
Nortriptyline and antipyrine clearance in relation to debrisoquine hydroxylation in man
-
Bertilsson, L., Eichelbaum, M., Mellstrom, B., Sawe, J., Schulz, H.-U., and Sjoqvist, F., Nortriptyline and antipyrine clearance in relation to debrisoquine hydroxylation in man. Life Sci. 27, 1673, 1980.
-
(1980)
Life Sci.
, vol.27
, pp. 1673
-
-
Bertilsson, L.1
Eichelbaum, M.2
Mellstrom, B.3
Sawe, J.4
Schulz, H.-U.5
Sjoqvist, F.6
-
368
-
-
0021933958
-
Plasma concentrations of nortriptyline and its 10-hydroxy metabolite in depressed patients - Relationship to the debrisoquine hydroxylation metabolic ratio
-
Nordin, C., Siwers, B., Benitez, J., and Bertilsson, L., Plasma concentrations of nortriptyline and its 10-hydroxy metabolite in depressed patients - relationship to the debrisoquine hydroxylation metabolic ratio. Br. J. Clin. Pharmacol. 19, 832, 1985.
-
(1985)
Br. J. Clin. Pharmacol.
, vol.19
, pp. 832
-
-
Nordin, C.1
Siwers, B.2
Benitez, J.3
Bertilsson, L.4
-
369
-
-
0029926315
-
Steady-state plasma levels of nortryptiline and its 10-hydroxy metabolite, relationship to the CYP2D6 genotype
-
Dahl, M.-L., Bertilsson, L., and Nordin, C., Steady-state plasma levels of nortryptiline and its 10-hydroxy metabolite, relationship to the CYP2D6 genotype. Psychopharmacology 123, 315, 1996.
-
(1996)
Psychopharmacology
, vol.123
, pp. 315
-
-
Dahl, M.-L.1
Bertilsson, L.2
Nordin, C.3
-
370
-
-
0026606822
-
The relationship between paroxetine and the sparteine oxidation polymorphism
-
Sindrup, S.H., Brosen, K., Gram, L.F., Hallas, J., Skjelbo, E., Allen, A., Allen, G.D., Cooper, S.M., Mellows, G., Tasker, T.C.G., and Zussman, B.D.,. The relationship between paroxetine and the sparteine oxidation polymorphism. Clin. Pharmacol. Ther. 51, 278, 1992,
-
(1992)
Clin. Pharmacol. Ther.
, vol.51
, pp. 278
-
-
Sindrup, S.H.1
Brosen, K.2
Gram, L.F.3
Hallas, J.4
Skjelbo, E.5
Allen, A.6
Allen, G.D.7
Cooper, S.M.8
Mellows, G.9
Tasker, T.C.G.10
Zussman, B.D.11
-
371
-
-
0026568846
-
The role of cytochrome P4502D6 in the metabolism of paroxetine by human liver microsomes
-
Bloomer, J.C, Woods, F.R., Haddock, R.E., Lennard, M.S., and Tucker, G.T., The role of cytochrome P4502D6 in the metabolism of paroxetine by human liver microsomes. Br. J. Clin. Pharmacol. 33, 521, 1992
-
(1992)
Br. J. Clin. Pharmacol.
, vol.33
, pp. 521
-
-
Bloomer, J.C.1
Woods, F.R.2
Haddock, R.E.3
Lennard, M.S.4
Tucker, G.T.5
-
372
-
-
0021351640
-
Polymorphic hydroxylation of perhexiline maleate in man
-
Cooper, R.G., Evans, D.A.P., and Whibley, E.J., Polymorphic hydroxylation of perhexiline maleate in man. J. Med. Genet. 21, 27, 1984.
-
(1984)
J. Med. Genet.
, vol.21
, pp. 27
-
-
Cooper, R.G.1
Evans, D.A.P.2
Whibley, E.J.3
-
373
-
-
0023200314
-
Studies on the metabolism of perhexiline in man
-
Cooper, R.G., Evans, D.A.P., and Price, A.H., Studies on the metabolism of perhexiline in man. Eur. J. Clin. Pharmacol. 32, 569, 1987.
-
(1987)
Eur. J. Clin. Pharmacol.
, vol.32
, pp. 569
-
-
Cooper, R.G.1
Evans, D.A.P.2
Price, A.H.3
-
374
-
-
0020075333
-
Impaired oxidation of debrisoquine in patients with perhexiline neuropathy
-
Shah, R.R., Oates, N.S., Idle, J.R., Smith, R.L., and Lockhart, J.D.F., Impaired oxidation of debrisoquine in patients with perhexiline neuropathy. Br. Med. J. 284, 295, 1982.
-
(1982)
Br. Med. J.
, vol.284
, pp. 295
-
-
Shah, R.R.1
Oates, N.S.2
Idle, J.R.3
Smith, R.L.4
Lockhart, J.D.F.5
-
375
-
-
0021146282
-
Impaired oxidation of debrisoquine in patients with perhexiline liver injury
-
Morgan, M.Y., Reshef, R., Shah, R.R., Oates, N.S., Smith, R.L., and Sherlock, S., Impaired oxidation of debrisoquine in patients with perhexiline liver injury. Gut 25, 1057, 1984.
-
(1984)
Gut
, vol.25
, pp. 1057
-
-
Morgan, M.Y.1
Reshef, R.2
Shah, R.R.3
Oates, N.S.4
Smith, R.L.5
Sherlock, S.6
-
376
-
-
0024333471
-
Disposition of perphenazine is related to polymorphic debrisoquine hydroxylation in human beings
-
Dahl-Puustinen, M.-L., Liden, A., Alm, C., Nordin, C., and Bertilsson, L., Disposition of perphenazine is related to polymorphic debrisoquine hydroxylation in human beings. Clin. Pharmacol. Ther. 46, 78, 1989.
-
(1989)
Clin. Pharmacol. Ther.
, vol.46
, pp. 78
-
-
Dahl-Puustinen, M.-L.1
Liden, A.2
Alm, C.3
Nordin, C.4
Bertilsson, L.5
-
377
-
-
0029930015
-
The CYP2D6 genotype predicts the oral clearance of the neuroleptic agents perphenazine and zuclopenthixol
-
Jerling, M., Dahl, M.-L., Aberg-Wistedt, A., Liljenberg, B., Landell, N.-E., Bertilsson, L., and Sjoqvist, F., The CYP2D6 genotype predicts the oral clearance of the neuroleptic agents perphenazine and zuclopenthixol. Clin. Pharmacol. Ther. 59, 423, 1996.
-
(1996)
Clin. Pharmacol. Ther.
, vol.59
, pp. 423
-
-
Jerling, M.1
Dahl, M.-L.2
Aberg-Wistedt, A.3
Liljenberg, B.4
Landell, N.-E.5
Bertilsson, L.6
Sjoqvist, F.7
-
378
-
-
0029738332
-
Steady-state serum concentrations of the neuroleptic perphenazine in relation to CYP2D6 genetic polymorphism
-
Linnet, K. and Wiborg, O., Steady-state serum concentrations of the neuroleptic perphenazine in relation to CYP2D6 genetic polymorphism. Clin. Pharmacol. Ther. 60, 41, 1996.
-
(1996)
Clin. Pharmacol. Ther.
, vol.60
, pp. 41
-
-
Linnet, K.1
Wiborg, O.2
-
379
-
-
0020283172
-
Genetic polymorphism of phenformin 4-hydroxylation
-
Oates, N.S., Shah, R.R., Idle, J.R., and Smith, R.L., Genetic polymorphism of phenformin 4-hydroxylation. Clin. Pharmacol. Ther. 32, 81, 1982.
-
(1982)
Clin. Pharmacol. Ther.
, vol.32
, pp. 81
-
-
Oates, N.S.1
Shah, R.R.2
Idle, J.R.3
Smith, R.L.4
-
380
-
-
0021053140
-
Influence of oxidation polymorphism on phenformin kinetics and dynamics
-
Oates, N.S., Shah, R.R., Idle, J.R., and Smith, R.L., Influence of oxidation polymorphism on phenformin kinetics and dynamics. Clin. Pharmacol. Ther. 34, 827, 1983.
-
(1983)
Clin. Pharmacol. Ther.
, vol.34
, pp. 827
-
-
Oates, N.S.1
Shah, R.R.2
Idle, J.R.3
Smith, R.L.4
-
381
-
-
0023122069
-
Polymorphism of propafenone metabolism and disposition in man, clinical and pharmacokinetic consequences
-
Siddoway, L.A., Thompson, K.A., McAllister, C.B., Wang, T., Wilkinson, G.R., Roden, D.M., and Woosley, R.L., Polymorphism of propafenone metabolism and disposition in man, clinical and pharmacokinetic consequences. Circulation 75, 785, 1987.
-
(1987)
Circulation
, vol.75
, pp. 785
-
-
Siddoway, L.A.1
Thompson, K.A.2
McAllister, C.B.3
Wang, T.4
Wilkinson, G.R.5
Roden, D.M.6
Woosley, R.L.7
-
382
-
-
0025312448
-
The role of genetically determined polymorphic drug metabolism in the betablockade produced by propafenone
-
Lee, J.T., Kroemer, H.K., Silberstein, D.J., Funck-Brentano, C., Lineberry, M.D., Wood, A.J., Roden, D.M., and Woosley, R.L., The role of genetically determined polymorphic drug metabolism in the betablockade produced by propafenone. N. Engl. J. Med. 322, 1764, 1990.
-
(1990)
N. Engl. J. Med.
, vol.322
, pp. 1764
-
-
Lee, J.T.1
Kroemer, H.K.2
Silberstein, D.J.3
Funck-Brentano, C.4
Lineberry, M.D.5
Wood, A.J.6
Roden, D.M.7
Woosley, R.L.8
-
383
-
-
0022342044
-
Pharmacokinetics of N-propylajmaline in relation to polymorphic sparteine oxidation
-
Zekorn, C., Achtert, G., Hausleiter, H.J., Moon, C.H., and Eichelbaum, M., Pharmacokinetics of N-propylajmaline in relation to polymorphic sparteine oxidation. Klin. Wochenschr. 63, 1180, 1985.
-
(1985)
Klin. Wochenschr.
, vol.63
, pp. 1180
-
-
Zekorn, C.1
Achtert, G.2
Hausleiter, H.J.3
Moon, C.H.4
Eichelbaum, M.5
-
384
-
-
0021253107
-
Polymorphic ability to metabolize propranolol alters 4-hydroxypropranolol levels but not beta blockade
-
Raghuram, T.C., Koshakji, R.P., Wilkinson, G.R., and Wood, A.J.J., Polymorphic ability to metabolize propranolol alters 4-hydroxypropranolol levels but not beta blockade. Clin. Pharmacol. Ther. 36, 51, 1984.
-
(1984)
Clin. Pharmacol. Ther.
, vol.36
, pp. 51
-
-
Raghuram, T.C.1
Koshakji, R.P.2
Wilkinson, G.R.3
Wood, A.J.J.4
-
385
-
-
0029897864
-
Plasma levels of the enantiomers of thioridazine, thioridazine 2-sulfoxide, thioridazine 2-sulfone, and thioridazine 5-sulfoxide in poor and extensive metabolizers of dextromethorphan and mephenytoin
-
Eap, C.B., Guentert, T.W., Schaublin-Loidl, M., Stabl, M., Koeb, L., Powell, K., and Baumann, P., Plasma levels of the enantiomers of thioridazine, thioridazine 2-sulfoxide, thioridazine 2-sulfone, and thioridazine 5-sulfoxide in poor and extensive metabolizers of dextromethorphan and mephenytoin. Clin. Pharmacol. Ther. 59, 322, 1996.
-
(1996)
Clin. Pharmacol. Ther.
, vol.59
, pp. 322
-
-
Eap, C.B.1
Guentert, T.W.2
Schaublin-Loidl, M.3
Stabl, M.4
Koeb, L.5
Powell, K.6
Baumann, P.7
-
386
-
-
0025602984
-
Clinical implications of slow sulphoxidation of thioridazine in a poor metabolizer of the debrisoquine type
-
Meyer, J.W., Woggon, B., Baumann, P., and Meyer, U.A., Clinical implications of slow sulphoxidation of thioridazine in a poor metabolizer of the debrisoquine type. Eur. J. Clin. Pharmacol. 39, 613, 1990.
-
(1990)
Eur. J. Clin. Pharmacol.
, vol.39
, pp. 613
-
-
Meyer, J.W.1
Woggon, B.2
Baumann, P.3
Meyer, U.A.4
-
387
-
-
0026086815
-
Plasma levels of thioridazine and metabolites are influenced by the debrisoquine hydroxylation phenotype
-
von Bahr, C., Movin, G., Nordin, C., Liden, A., Hammarlund-Udenaes, M., Hedberg, A., Ring, H., and Sjoqvist, F., Plasma levels of thioridazine and metabolites are influenced by the debrisoquine hydroxylation phenotype. Clin. Pharmacol. Ther. 49, 234, 1991.
-
(1991)
Clin. Pharmacol. Ther.
, vol.49
, pp. 234
-
-
Von Bahr, C.1
Movin, G.2
Nordin, C.3
Liden, A.4
Hammarlund-Udenaes, M.5
Hedberg, A.6
Ring, H.7
Sjoqvist, F.8
-
388
-
-
0022251340
-
Pharmacokinetics and beta-blocking effects of timolol in poor and extensive metabolizers of debrisoquine
-
McGourty, J.C., Silas, J.H., Fleming, J.J., McBurney, A., and Ward, J.W., Pharmacokinetics and beta-blocking effects of timolol in poor and extensive metabolizers of debrisoquine. Clin. Pharmacol. Ther. 38, 409, 1985.
-
(1985)
Clin. Pharmacol. Ther.
, vol.38
, pp. 409
-
-
McGourty, J.C.1
Silas, J.H.2
Fleming, J.J.3
McBurney, A.4
Ward, J.W.5
-
389
-
-
0022182790
-
Timolol and atenolol, relationships between oxidation phenotype, pharmacokinetics and pharmacodynamics
-
Lewis, R.V., Lennard, M.S., Jackson, P.R., Tucker, G.T., Ramsay, L.E., and Woods, H.F., Timolol and atenolol, relationships between oxidation phenotype, pharmacokinetics and pharmacodynamics. Br. J. Clin. Pharmacol. 19, 329, 1985.
-
(1985)
Br. J. Clin. Pharmacol.
, vol.19
, pp. 329
-
-
Lewis, R.V.1
Lennard, M.S.2
Jackson, P.R.3
Tucker, G.T.4
Ramsay, L.E.5
Woods, H.F.6
-
390
-
-
0001343428
-
Single dose pharmacokinetics of tomoxetine in poor and extensive metabolizers of debrisoquine
-
Feher, M.D., Lucas, R.A., Farid, N.A., Idle, J.R., Bergstrom, R.F., Lemberger, L., and Sever, P.S., Single dose pharmacokinetics of tomoxetine in poor and extensive metabolizers of debrisoquine. Br. J. Clin. Pharmacol. 26, 231p, 1988.
-
(1988)
Br. J. Clin. Pharmacol.
, vol.26
-
-
Feher, M.D.1
Lucas, R.A.2
Farid, N.A.3
Idle, J.R.4
Bergstrom, R.F.5
Lemberger, L.6
Sever, P.S.7
-
391
-
-
0030045095
-
Venlafaxine oxidation in vitro is catalyzed by CYP2D6
-
Otton, S.V., Ball, S.E., Cheung, S.W., Inaba, T., Rudolph, R.L., and Sellers, E.M., Venlafaxine oxidation in vitro is catalyzed by CYP2D6. Br. J. Clin. Pharmacol. 41, 149, 1996.
-
(1996)
Br. J. Clin. Pharmacol.
, vol.41
, pp. 149
-
-
Otton, S.V.1
Ball, S.E.2
Cheung, S.W.3
Inaba, T.4
Rudolph, R.L.5
Sellers, E.M.6
-
392
-
-
0025824216
-
Disposition of the neuroleptic zuclopenthixol cosegregates with the polymorphic hydroxylation of debrisoquine in humans
-
Dahl, M.-L., Ekqvist, B., Widen, J., and Bertilsson, L., Disposition of the neuroleptic zuclopenthixol cosegregates with the polymorphic hydroxylation of debrisoquine in humans. Acta Psychiatr. Scand. 84, 99, 1991.
-
(1991)
Acta Psychiatr. Scand.
, vol.84
, pp. 99
-
-
Dahl, M.-L.1
Ekqvist, B.2
Widen, J.3
Bertilsson, L.4
-
393
-
-
0023884310
-
Bioactivation of the narcotic drug codeine in human liver is mediated by the polymorphic monooxygenase catalyzing debrisoquine 4-hydroxylation (cytochrome P-450 db 1/bufI)
-
Dayer, P., Desmeules, J., Leemann, T., and Striberni, R., Bioactivation of the narcotic drug codeine in human liver is mediated by the polymorphic monooxygenase catalyzing debrisoquine 4-hydroxylation (cytochrome P-450 db 1/bufI). Biochem. Biophys. Res. Commun. 152, 411, 1988.
-
(1988)
Biochem. Biophys. Res. Commun.
, vol.152
, pp. 411
-
-
Dayer, P.1
Desmeules, J.2
Leemann, T.3
Striberni, R.4
-
394
-
-
0029963641
-
Formation of morphine from codeine in Chinese subjects of different CYP2D6 genotypes
-
Tseng, C.-Y., Wang, S.-L., Lai, M.-D., Lai, M.-L., and Huang, J.-d., Formation of morphine from codeine in Chinese subjects of different CYP2D6 genotypes. Clin. Pharmacol. Ther. 60, 177, 1996.
-
(1996)
Clin. Pharmacol. Ther.
, vol.60
, pp. 177
-
-
Tseng, C.-Y.1
Wang, S.-L.2
Lai, M.-D.3
Lai, M.-L.4
Huang, J.-D.5
-
395
-
-
0030432381
-
Pharmacogenetic determination of the effects of codeine and prediction of drug interactions
-
Caraco, Y., Sheller, J., and Wood, A.J.J., Pharmacogenetic determination of the effects of codeine and prediction of drug interactions. J. Pharmacol. Exp. Ther. 278, 1165, 1996b.
-
(1996)
J. Pharmacol. Exp. Ther.
, vol.278
, pp. 1165
-
-
Caraco, Y.1
Sheller, J.2
Wood, A.J.J.3
-
396
-
-
0021347053
-
Influence of genetic polymorphism on the metabolism and disposition of encainide in man
-
Wang, T., Roden, D.M., Wolfenden, H.T., Woosley, R.L., Wood, A.J.J., and Wilkinson, G.R., Influence of genetic polymorphism on the metabolism and disposition of encainide in man. J. Pharmacol. Exp. Ther. 228, 605, 1984.
-
(1984)
J. Pharmacol. Exp. Ther.
, vol.228
, pp. 605
-
-
Wang, T.1
Roden, D.M.2
Wolfenden, H.T.3
Woosley, R.L.4
Wood, A.J.J.5
Wilkinson, G.R.6
-
397
-
-
0030471120
-
The hypoalgesic effect of tramadol in relation to CYP2D6
-
Poulsen, L., Arendt-Nielsen, L., Brosen, K., and Sindrup, S.H., The hypoalgesic effect of tramadol in relation to CYP2D6. Clin. Pharmacol. Ther. 60, 636, 1996b.
-
(1996)
Clin. Pharmacol. Ther.
, vol.60
, pp. 636
-
-
Poulsen, L.1
Arendt-Nielsen, L.2
Brosen, K.3
Sindrup, S.H.4
-
398
-
-
0023954396
-
Human debrisoquine 4-hydroxylase (P450IID1), cDNA and deduced amino acid sequence and assignment of the CYP2D locus to chromosome 22
-
Gonzalez, F.J., Vilbois, F., Hardwick, J.P., McBride, O.W., Nebert, D.W., Gelboin, H.V., and Meyer, U.A., Human debrisoquine 4-hydroxylase (P450IID1), cDNA and deduced amino acid sequence and assignment of the CYP2D locus to chromosome 22. Genomics 2, 174, 1988b.
-
(1988)
Genomics
, vol.2
, pp. 174
-
-
Gonzalez, F.J.1
Vilbois, F.2
Hardwick, J.P.3
McBride, O.W.4
Nebert, D.W.5
Gelboin, H.V.6
Meyer, U.A.7
-
399
-
-
0024796958
-
The human debrisoquine 4-hydroxylase (CYP2D) locus: Sequence and identification of the polymorphic CYP2D6 gene, a related gene and a pseudogene
-
Kimura, S., Umeno, M., Skoda, R.C., Meyer, U.A., and Gonzalez, F.J., The human debrisoquine 4-hydroxylase (CYP2D) locus: sequence and identification of the polymorphic CYP2D6 gene, a related gene and a pseudogene. Am. J. Hum. Genet. 45, 889, 1989.
-
(1989)
Am. J. Hum. Genet.
, vol.45
, pp. 889
-
-
Kimura, S.1
Umeno, M.2
Skoda, R.C.3
Meyer, U.A.4
Gonzalez, F.J.5
-
400
-
-
0023196288
-
Chromosomal assignment of human cytochrome P-450 (debrisoquine/sparteine type) to chromosome 22
-
Eichelbaum, M., Baur, M.P., Dengler, H.J., Osikowska-Evers, B.O., Tieves, G., Zekorn, C., and Rittner, C., Chromosomal assignment of human cytochrome P-450 (debrisoquine/sparteine type) to chromosome 22. Br. J. Clin. Pharmacol. 23, 455, 1987.
-
(1987)
Br. J. Clin. Pharmacol.
, vol.23
, pp. 455
-
-
Eichelbaum, M.1
Baur, M.P.2
Dengler, H.J.3
Osikowska-Evers, B.O.4
Tieves, G.5
Zekorn, C.6
Rittner, C.7
-
401
-
-
0027480849
-
Localization of the CYP2D gene locus to human chromosome 22q13.1 by polymerase chain reaction, in situ hybridization, and linkage analysis
-
Gough, A.C., Dale Smith, C.A, Howell, S.M., Wolf, C.R., Bryant, S.P., and Spurt, N.K., Localization of the CYP2D gene locus to human chromosome 22q13.1 by polymerase chain reaction, in situ hybridization, and linkage analysis. Genomics 15, 430, 1993.
-
(1993)
Genomics
, vol.15
, pp. 430
-
-
Gough, A.C.1
Dale Smith, C.A.2
Howell, S.M.3
Wolf, C.R.4
Bryant, S.P.5
Spurt, N.K.6
-
402
-
-
0013524434
-
Progress on CYP2D6 nomenclature
-
Besancon, May 1995, Alvan, G., Balant, L.P., Bechtel, P.R., Boobis, A.R., Gram, L.F., Paintaud, G., and Pithan, K., Eds., Luxembourg. EU
-
Daly, A.K., Eichelbaum, M., Idle, J.R., Ingelman-Sundberg, M., Meyer, U.A., Wolf, C.R., and Zanger, U.M., Progress on CYP2D6 nomenclature. In: Proceedings of the COST BI European Conference on Specificity and Variability in Drug Metabolism, Besancon, May 1995, Alvan, G., Balant, L.P., Bechtel, P.R., Boobis, A.R., Gram, L.F., Paintaud, G., and Pithan, K., Eds., Luxembourg. EU, 1995a, 137-144.
-
(1995)
Proceedings of the COST BI European Conference on Specificity and Variability in Drug Metabolism
, pp. 137-144
-
-
Daly, A.K.1
Eichelbaum, M.2
Idle, J.R.3
Ingelman-Sundberg, M.4
Meyer, U.A.5
Wolf, C.R.6
Zanger, U.M.7
-
403
-
-
0013532951
-
CYP2D6 polymorphism in familial and sporadic Parkinson's disease
-
in press
-
Sabbagh, N., Brice, A., Marez, D., Durr, A., Legrand, M., Lo Guidice, J.-M., Destee, A., Agid, Y., and Broly, F., CYP2D6 polymorphism in familial and sporadic Parkinson's disease. Pharmacogenetics in press, 1997.
-
(1997)
Pharmacogenetics
-
-
Sabbagh, N.1
Brice, A.2
Marez, D.3
Durr, A.4
Legrand, M.5
Lo Guidice, J.-M.6
Destee, A.7
Agid, Y.8
Broly, F.9
-
404
-
-
0027136288
-
Inherited amplification of an active gene in the cytochrome P450 CYP2D locus as a cause of ultrarapid metabolism of debrisoquine
-
Johansson, I., Lundqvist, E., Bertilsson, L., Dahl, M.-L., Sjoqvist, F., and Ingelman-Sundberg, M., Inherited amplification of an active gene in the cytochrome P450 CYP2D locus as a cause of ultrarapid metabolism of debrisoquine. Proc. Natl. Acad. Sci. U.S.A. 90, 11825, 1993.
-
(1993)
Proc. Natl. Acad. Sci. U.S.A.
, vol.90
, pp. 11825
-
-
Johansson, I.1
Lundqvist, E.2
Bertilsson, L.3
Dahl, M.-L.4
Sjoqvist, F.5
Ingelman-Sundberg, M.6
-
405
-
-
0027968799
-
DNA haplotype-dependent differences in the amino acid sequence of debrisoquine 4-hydroxylase (CYP2D6), evidence for two major allozymes in extensive metabolisers
-
Panserat, S., Mura, C., Gerard, N., Vincent-Viry, M., Galteau, M.M., Jacqz-Aigrain, E., and Krishnamoorthy, R., DNA haplotype-dependent differences in the amino acid sequence of debrisoquine 4-hydroxylase (CYP2D6), evidence for two major allozymes in extensive metabolisers. Hum. Genet. 94, 401, 1994.
-
(1994)
Hum. Genet.
, vol.94
, pp. 401
-
-
Panserat, S.1
Mura, C.2
Gerard, N.3
Vincent-Viry, M.4
Galteau, M.M.5
Jacqz-Aigrain, E.6
Krishnamoorthy, R.7
-
406
-
-
0002362985
-
Genetic polymorphism of human drug metabolizing enzymes, recent aspects on polymorphic forms of cytochromes P450
-
Besancon, May 1995, Alvan, G., Balant, L.P., Bechtel, P.R., Boobis, A.R., Gram, L.F., Paintaud, G., and Pithan, K., Eds., Luxembourg, EU
-
Ingelman-Sundberg, M., Oscarson, M., Persson, I., Masimirembwa, C., Dahl, M.-L., Bertilsson, L., Sjoqvist, F., and Johansson, I., Genetic polymorphism of human drug metabolizing enzymes, recent aspects on polymorphic forms of cytochromes P450. In: Proceedings of the COST B1 European Conference on Specificity and Variability in Drug Metabolism, Besancon, May 1995, Alvan, G., Balant, L.P., Bechtel, P.R., Boobis, A.R., Gram, L.F., Paintaud, G., and Pithan, K., Eds., Luxembourg, EU, 1995, 93-110.
-
(1995)
Proceedings of the COST B1 European Conference on Specificity and Variability in Drug Metabolism
, pp. 93-110
-
-
Ingelman-Sundberg, M.1
Oscarson, M.2
Persson, I.3
Masimirembwa, C.4
Dahl, M.-L.5
Bertilsson, L.6
Sjoqvist, F.7
Johansson, I.8
-
407
-
-
0029064096
-
Ultrarapid hydroxylation of debrisoquine in a Swedish population: Analysis of the molecular genetic basis
-
Dahl, M.-L., Johansson, I., Bertilsson, L., Ingelman-Sundberg, M., and Sjoqvist, F., Ultrarapid hydroxylation of debrisoquine in a Swedish population: analysis of the molecular genetic basis. J. Pharmacol. Exp. Ther. 274, 516, 1995.
-
(1995)
J. Pharmacol. Exp. Ther.
, vol.274
, pp. 516
-
-
Dahl, M.-L.1
Johansson, I.2
Bertilsson, L.3
Ingelman-Sundberg, M.4
Sjoqvist, F.5
-
408
-
-
0030432585
-
Frequent distribution of ultrarapid metabolizers of debrisoquine in an Ethiopean population carrying duplicated and multiduplicated functional CYP2D6 alleles
-
Aklillu, E., Persson, I., Bertilsson, L., Johansson, I., Rodriques, F., and Ingelman-Sundberg, M., Frequent distribution of ultrarapid metabolizers of debrisoquine in an Ethiopean population carrying duplicated and multiduplicated functional CYP2D6 alleles. J. Pharmacol. Exp. Ther. 278, 441, 1996.
-
(1996)
J. Pharmacol. Exp. Ther.
, vol.278
, pp. 441
-
-
Aklillu, E.1
Persson, I.2
Bertilsson, L.3
Johansson, I.4
Rodriques, F.5
Ingelman-Sundberg, M.6
-
409
-
-
0025036544
-
Multiple mutations of the human cytochrome P450IID6 gene (CYP2D6) in poor metabolizers of debrisoquine
-
Kagimoto, M., Heim, M., Kagimoto, K., Zeugin, T., and Meyer, U.A., Multiple mutations of the human cytochrome P450IID6 gene (CYP2D6) in poor metabolizers of debrisoquine. J. Biol. Chem. 265, 17209, 1990.
-
(1990)
J. Biol. Chem.
, vol.265
, pp. 17209
-
-
Kagimoto, M.1
Heim, M.2
Kagimoto, K.3
Zeugin, T.4
Meyer, U.A.5
-
410
-
-
0025114258
-
Identification of the primary gene defect at the cytochrome P450 CYP2D locus
-
Gough, A.C., Miles, J.S., Spurr, N.K., Moss, J.E., Gaedigk, A., Eichelbaum, M., and Wolf, C.R., Identification of the primary gene defect at the cytochrome P450 CYP2D locus. Nature 347, 773, 1990.
-
(1990)
Nature
, vol.347
, pp. 773
-
-
Gough, A.C.1
Miles, J.S.2
Spurr, N.K.3
Moss, J.E.4
Gaedigk, A.5
Eichelbaum, M.6
Wolf, C.R.7
-
411
-
-
0025243460
-
The human CYP2D locus associated with a common genetic defect in drug oxidation, A G1934→A base change in intron 3 of a mutant CYP2D6 allele results in an abberrant 3′ splice recognition site
-
Hanioka, N., Kimura, S., Meyer, U.A., and Gonzalez, F.J., The human CYP2D locus associated with a common genetic defect in drug oxidation, A G1934→A base change in intron 3 of a mutant CYP2D6 allele results in an abberrant 3′ splice recognition site. Am. J. Hum. Genet. 47, 994, 1990.
-
(1990)
Am. J. Hum. Genet.
, vol.47
, pp. 994
-
-
Hanioka, N.1
Kimura, S.2
Meyer, U.A.3
Gonzalez, F.J.4
-
412
-
-
0027527966
-
Evidence for a new variant CYP2D6 allele CYP2D6J in a Japanese population associated with lower in vivo rates of sparteine metabolism
-
Yokota, H., Tamura, S., Furuya, H., Kimura, S., Watanabe, M., Kanazawa, I., Kondo, I., and Gonzalez, F.J., Evidence for a new variant CYP2D6 allele CYP2D6J in a Japanese population associated with lower in vivo rates of sparteine metabolism. Pharmacogenetics 3, 256, 1993.
-
(1993)
Pharmacogenetics
, vol.3
, pp. 256
-
-
Yokota, H.1
Tamura, S.2
Furuya, H.3
Kimura, S.4
Watanabe, M.5
Kanazawa, I.6
Kondo, I.7
Gonzalez, F.J.8
-
413
-
-
0025805934
-
Deletion of the entire cytochrome P450 CYP2D6 gene as a cause of impaired drug metabolism in poor metabolizers of the debrisoquine/sparteine polymorphism
-
Gaedigk, A., Blum, M., Gaedigk, R., Eichelbaum, M., and Meyer, U.A., Deletion of the entire cytochrome P450 CYP2D6 gene as a cause of impaired drug metabolism in poor metabolizers of the debrisoquine/sparteine polymorphism. Am. J. Hum. Genet. 48, 943, 1991.
-
(1991)
Am. J. Hum. Genet.
, vol.48
, pp. 943
-
-
Gaedigk, A.1
Blum, M.2
Gaedigk, R.3
Eichelbaum, M.4
Meyer, U.A.5
-
414
-
-
0028844757
-
Homologous unequal cross-over involving a 2.8 Kb direct repeat as a mechanism for the generation of allelic variants of the human cytochrome P450 CYP2D6 gene
-
Steen, V.M., Molven, A., Aarskog, K., and Gulbrandsen, A.-K., Homologous unequal cross-over involving a 2.8 Kb direct repeat as a mechanism for the generation of allelic variants of the human cytochrome P450 CYP2D6 gene. Hum. Mol. Genet. 4, 2251, 1995.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 2251
-
-
Steen, V.M.1
Molven, A.2
Aarskog, K.3
Gulbrandsen, A.-K.4
-
415
-
-
0028305240
-
Identification of a new variant CYP2D6 allele with a single base deletion in exon 3 and its association with the poor metabolizer phenotype
-
Saxena, R., Shaw, G.L., Relling, M.V., Frame, J.N., Moir, D.T., Evans, W.E., Caporaso, N., and Weiffenbach, B., Identification of a new variant CYP2D6 allele with a single base deletion in exon 3 and its association with the poor metabolizer phenotype. Hum. Mol. Genet. 3, 923, 1994.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 923
-
-
Saxena, R.1
Shaw, G.L.2
Relling, M.V.3
Frame, J.N.4
Moir, D.T.5
Evans, W.E.6
Caporaso, N.7
Weiffenbach, B.8
-
416
-
-
0028046321
-
Cloning and sequencing of a new non-functional CYP2D6 allele: Deletion of T1795 in exon 3 generates a premature stop codon
-
Evert, B., Griese, E.-U., and Eichelbaum, M., Cloning and sequencing of a new non-functional CYP2D6 allele: deletion of T1795 in exon 3 generates a premature stop codon. Pharmacogenetics 4, 271, 1994.
-
(1994)
Pharmacogenetics
, vol.4
, pp. 271
-
-
Evert, B.1
Griese, E.-U.2
Eichelbaum, M.3
-
417
-
-
0028929652
-
An inactive cytochrome P450 CYP2D6 allele containing a deletion and a base substitution
-
Daly, A.K., Leathert, J.B.S., London, S.J., and Idle, J.R., An inactive cytochrome P450 CYP2D6 allele containing a deletion and a base substitution. Hum. Genet. 95, 337, 1995.
-
(1995)
Hum. Genet.
, vol.95
, pp. 337
-
-
Daly, A.K.1
Leathert, J.B.S.2
London, S.J.3
Idle, J.R.4
-
418
-
-
0028109283
-
A missense mutation in exon 6 of the CYP2D6 gene leading to a histidine 324 to proline exchange is associated with the poor metabolizer phenotype of sparteine
-
Evert, B., Griese, E.-U., and Eichelbaum, M., A missense mutation in exon 6 of the CYP2D6 gene leading to a histidine 324 to proline exchange is associated with the poor metabolizer phenotype of sparteine. Naunyn-Schmiedeberg's Arch. Pharmacol. 350, 434, 1994b.
-
(1994)
Naunyn-Schmiedeberg's Arch. Pharmacol.
, vol.350
, pp. 434
-
-
Evert, B.1
Griese, E.-U.2
Eichelbaum, M.3
-
419
-
-
0028806579
-
A nonsense mutation in the cytochrome P450 CYP2D6 gene identified in a Caucasian with an enzyme deficiency
-
Broly, F., Marez, D., Lo Guidice, J.-M., Sabbagh, N., Legrand, M., Boone, P., and Meyer, U.A., A nonsense mutation in the cytochrome P450 CYP2D6 gene identified in a Caucasian with an enzyme deficiency. Hum. Genet. 96, 601, 1995.
-
(1995)
Hum. Genet.
, vol.96
, pp. 601
-
-
Broly, F.1
Marez, D.2
Lo Guidice, J.-M.3
Sabbagh, N.4
Legrand, M.5
Boone, P.6
Meyer, U.A.7
-
420
-
-
0029622336
-
An efficient strategy for detection of known and new mutations of the CYP2D6 gene using single strand conformation polymorphism analysis
-
Broly, F., Marez, D., Sabbagh, N., Legrand, M., Millecamps, S., Lo Guidice, J.-M., Boone, P., and Meyer, U.A., An efficient strategy for detection of known and new mutations of the CYP2D6 gene using single strand conformation polymorphism analysis. Pharmacogenetics 5, 373, 1995.
-
(1995)
Pharmacogenetics
, vol.5
, pp. 373
-
-
Broly, F.1
Marez, D.2
Sabbagh, N.3
Legrand, M.4
Millecamps, S.5
Lo Guidice, J.-M.6
Boone, P.7
Meyer, U.A.8
-
421
-
-
0026240145
-
Identification of a new variant CYP2D6 allele lacking the codon encoding Lys-281, possible association with the poor metaboliser phenotype
-
Tyndale, R., Aoyama, T., Broly, F., Matsunaga, T., Inaba, T., Kalow, W., Gelboin, H.V., Meyer, U.A., and Gonzalez, F.J., Identification of a new variant CYP2D6 allele lacking the codon encoding Lys-281, possible association with the poor metaboliser phenotype. Pharmacogenetics 1, 26, 1991.
-
(1991)
Pharmacogenetics
, vol.1
, pp. 26
-
-
Tyndale, R.1
Aoyama, T.2
Broly, F.3
Matsunaga, T.4
Inaba, T.5
Kalow, W.6
Gelboin, H.V.7
Meyer, U.A.8
Gonzalez, F.J.9
-
422
-
-
0027273757
-
Debrisoquine oxidation polymorphism, phenotypic consequences of a 3-base-pair deletion in exon 5 of the CYP2D6 gene
-
Broly, F., and Meyer, U.A., Debrisoquine oxidation polymorphism, phenotypic consequences of a 3-base-pair deletion in exon 5 of the CYP2D6 gene. Pharmacogenetics 3, 123, 1993.
-
(1993)
Pharmacogenetics
, vol.3
, pp. 123
-
-
Broly, F.1
Meyer, U.A.2
-
423
-
-
0027965620
-
Genetic analysis of the Chinese cytochrome P4502D locus: Characterization of variant CYP2D6 genes present in subjects with diminished capacity for debrisoquine hydroxylation
-
Johansson, I., Oscarson, M., Yue, Q.-Y., Bertilsson, L., Sjoqvist, F., and Ingelman-Sundberg, M., Genetic analysis of the Chinese cytochrome P4502D locus: characterization of variant CYP2D6 genes present in subjects with diminished capacity for debrisoquine hydroxylation. Mol. Pharmacol. 46. 452, 1994.
-
(1994)
Mol. Pharmacol.
, vol.46
, pp. 452
-
-
Johansson, I.1
Oscarson, M.2
Yue, Q.-Y.3
Bertilsson, L.4
Sjoqvist, F.5
Ingelman-Sundberg, M.6
-
425
-
-
0028826569
-
A novel CYP2D6 allele with an abolished splice recognition site associated with the poor metabolizer phenotype
-
Marez, D., Sabbagh, N., Legrand, M., Lo-Guidice, J.M., Boone, P., and Broly, F., A novel CYP2D6 allele with an abolished splice recognition site associated with the poor metabolizer phenotype. Pharmacogenetics 5, 305, 1995.
-
(1995)
Pharmacogenetics
, vol.5
, pp. 305
-
-
Marez, D.1
Sabbagh, N.2
Legrand, M.3
Lo-Guidice, J.M.4
Boone, P.5
Broly, F.6
-
426
-
-
0029937877
-
An additional allelic variant of the CYP2D6 gene causing impaired metabolism of sparteine
-
Marez, D., Legrand, M., Sabbagh, N., Lo-Guidice, J.M., Boone, P., and Broly, F., An additional allelic variant of the CYP2D6 gene causing impaired metabolism of sparteine. Hum. Genet. 97, 668, 1996.
-
(1996)
Hum. Genet.
, vol.97
, pp. 668
-
-
Marez, D.1
Legrand, M.2
Sabbagh, N.3
Lo-Guidice, J.M.4
Boone, P.5
Broly, F.6
-
427
-
-
0028846090
-
An unequal cross-over event within the CYP2D gene cluster generates a chimeric CYP2D7/CYP2D6 gene which is associated with the poor metabolizer phenotype
-
Panserat, S., Mura, C., Gerard, N., Vincent-Viry, M., Galteau, M.M., Jacqz-Aigrain, E., and Krishnamoorthy, R., An unequal cross-over event within the CYP2D gene cluster generates a chimeric CYP2D7/CYP2D6 gene which is associated with the poor metabolizer phenotype. Br. J. Clin. Pharmacol. 40, 361, 1995.
-
(1995)
Br. J. Clin. Pharmacol.
, vol.40
, pp. 361
-
-
Panserat, S.1
Mura, C.2
Gerard, N.3
Vincent-Viry, M.4
Galteau, M.M.5
Jacqz-Aigrain, E.6
Krishnamoorthy, R.7
-
428
-
-
0029661560
-
A rare insertion of T226 in exon 1 of CYP2D6 causes a frameshift and is associated with the poor metabolizer phenotype, CYP2D6*15
-
Sachse, C., Brockmoller, J., Bauer, S., Reum, T., and Roots, I., A rare insertion of T226 in exon 1 of CYP2D6 causes a frameshift and is associated with the poor metabolizer phenotype, CYP2D6*15. Pharmacogenetics 6, 269, 1996.
-
(1996)
Pharmacogenetics
, vol.6
, pp. 269
-
-
Sachse, C.1
Brockmoller, J.2
Bauer, S.3
Reum, T.4
Roots, I.5
-
429
-
-
0029736710
-
Characterization and PCR-based detection of two different hybrid CYP2D7P/CYP2D6 alleles associated with the poor metabolizer phenotype
-
Daly, A.K., Fairbrother, K.S., Andreassen, O.A., London, S.J., Idle, J.R., and Steen, V.M., Characterization and PCR-based detection of two different hybrid CYP2D7P/CYP2D6 alleles associated with the poor metabolizer phenotype. Pharmacogenetics 6, 319, 1996.
-
(1996)
Pharmacogenetics
, vol.6
, pp. 319
-
-
Daly, A.K.1
Fairbrother, K.S.2
Andreassen, O.A.3
London, S.J.4
Idle, J.R.5
Steen, V.M.6
-
430
-
-
0029853664
-
A novel mutant variant of the CYP2D6 gene (CYP2D6*17) common in a black African population: Association with diminished debrisoquine hydroxylase activity
-
Masimirembwa, C., Persson, I., Bertilsson, L., Hasler, J., and Ingelman-Sundberg, M., A novel mutant variant of the CYP2D6 gene (CYP2D6*17) common in a black African population: association with diminished debrisoquine hydroxylase activity. Br. J. Clin. Pharmacol. 42, 713, 1996.
-
(1996)
Br. J. Clin. Pharmacol.
, vol.42
, pp. 713
-
-
Masimirembwa, C.1
Persson, I.2
Bertilsson, L.3
Hasler, J.4
Ingelman-Sundberg, M.5
-
431
-
-
0027200680
-
A novel cytochrome P-450IID6 mutant gene associated with Parkinson's disease
-
Tsuneoka, Y., Matsuo, Y., Iwahashi, K., Takeuchi, H., and Ichikawa, Y., A novel cytochrome P-450IID6 mutant gene associated with Parkinson's disease. J Biochem. 114, 263, 1993.
-
(1993)
J Biochem.
, vol.114
, pp. 263
-
-
Tsuneoka, Y.1
Matsuo, Y.2
Iwahashi, K.3
Takeuchi, H.4
Ichikawa, Y.5
-
432
-
-
0027172453
-
A polymorphic Cfo I site in exon 6 of the human cytochrome P450 CYP2D6 gene detected by the polymerase chain reaction
-
Armstrong, M., Idle, J.R., and Daly, A.K., A polymorphic Cfo I site in exon 6 of the human cytochrome P450 CYP2D6 gene detected by the polymerase chain reaction. Hum. Genet. 91, 616, 1993.
-
(1993)
Hum. Genet.
, vol.91
, pp. 616
-
-
Armstrong, M.1
Idle, J.R.2
Daly, A.K.3
-
433
-
-
0027534276
-
Molecular basis for rational megaprescribing in ultrarapid hydroxy lators of debrisoquine
-
Bertilsson, L., Dahl, M.-L., Sjoqvist, F., Aberg-Wistedt, A., Humble, M., Johansson, I., Lundqvist, E., and Ingelman-Sundberg, M., Molecular basis for rational megaprescribing in ultrarapid hydroxy lators of debrisoquine. The Lancet 341, 63, 1993.
-
(1993)
The Lancet
, vol.341
, pp. 63
-
-
Bertilsson, L.1
Dahl, M.-L.2
Sjoqvist, F.3
Aberg-Wistedt, A.4
Humble, M.5
Johansson, I.6
Lundqvist, E.7
Ingelman-Sundberg, M.8
-
434
-
-
0007293059
-
Ultrarapid metabolizers of debrisoquine: Characterization and PCR-based detection of alleles with duplication of the CYP2D6 gene
-
Lovlie, R., Daly, A.K., Molven, A., Idle, J.R., and Steen, V.M., Ultrarapid metabolizers of debrisoquine: characterization and PCR-based detection of alleles with duplication of the CYP2D6 gene. FEBS Letters 392, 30, 1996.
-
(1996)
FEBS Letters
, vol.392
, pp. 30
-
-
Lovlie, R.1
Daly, A.K.2
Molven, A.3
Idle, J.R.4
Steen, V.M.5
-
435
-
-
0028182215
-
Frequency of human CYP2D6 mutant alleles in a normal Chinese population
-
Lee, E.J.D. and Jeyaseelan, K., Frequency of human CYP2D6 mutant alleles in a normal Chinese population. Br. J. Clin. Pharmacol. 37, 605, 1994.
-
(1994)
Br. J. Clin. Pharmacol.
, vol.37
, pp. 605
-
-
Lee, E.J.D.1
Jeyaseelan, K.2
-
436
-
-
0029053644
-
Genetic analysis of the CYP2D locus in relation to debrisoquine hydroxylation capacity in Korean, Japanese and Chinese subjects
-
Dahl, M.-L., Yue, Q.-Y., Roh, H.-K., Johansson, I., Sawe, J., Sjoqvist, F., and Bertilsson, L., Genetic analysis of the CYP2D locus in relation to debrisoquine hydroxylation capacity in Korean, Japanese and Chinese subjects. Pharmacogenetics 5, 159-164, 1995.
-
(1995)
Pharmacogenetics
, vol.5
, pp. 159-164
-
-
Dahl, M.-L.1
Yue, Q.-Y.2
Roh, H.-K.3
Johansson, I.4
Sawe, J.5
Sjoqvist, F.6
Bertilsson, L.7
-
437
-
-
0025950370
-
Debrisoquine/sparteine hydroxylation genotype and phenotype, analysis of common mutations and alleles of CYP2D6 in a European population
-
Broly, F., Gaedigk, A., Heim, M., Eichelbaum, M., Morike, K., and Meyer, U.A., Debrisoquine/sparteine hydroxylation genotype and phenotype, analysis of common mutations and alleles of CYP2D6 in a European population. DNA Cell. Biol. 10, 545, 1991.
-
(1991)
DNA Cell. Biol.
, vol.10
, pp. 545
-
-
Broly, F.1
Gaedigk, A.2
Heim, M.3
Eichelbaum, M.4
Morike, K.5
Meyer, U.A.6
-
438
-
-
0030933378
-
Functional properties of CYP2D6 1 (wild-type) and CYP2D6 7 (His 324 Pro) expressed by recombinant baculovirus in insect cells
-
Evert, B., Eichelbaum, M., Haubruck, H., and Zanger, U.M., Functional properties of CYP2D6 1 (wild-type) and CYP2D6 7 (His 324 Pro) expressed by recombinant baculovirus in insect cells. Naunyn-Schmiedeberg's Arch. Pharmacol. 355, 309, 1997.
-
(1997)
Naunyn-Schmiedeberg's Arch. Pharmacol.
, vol.355
, pp. 309
-
-
Evert, B.1
Eichelbaum, M.2
Haubruck, H.3
Zanger, U.M.4
-
439
-
-
0028882347
-
Propranolol disposition in Chinese subjects of different CYP2D6 genotypes
-
Lai, M.-L., Wang, S.-L., Lai, M.-D., Lin, E.T., Tse, M., and Huang, J.-d., Propranolol disposition in Chinese subjects of different CYP2D6 genotypes. Clin. Pharmacol. Ther. 58, 264, 1995.
-
(1995)
Clin. Pharmacol. Ther.
, vol.58
, pp. 264
-
-
Lai, M.-L.1
Wang, S.-L.2
Lai, M.-D.3
Lin, E.T.4
Tse, M.5
Huang, J.-D.6
-
440
-
-
0028824253
-
Propafenone in a usual dose produces severe side-effects, the impact of genetically determined metabolic status on drug therapy
-
Morike, K., Magadum, S., Mettang, T., Griese, E.U., Machleidt, C., and Kuhlmann, U., Propafenone in a usual dose produces severe side-effects, the impact of genetically determined metabolic status on drug therapy. J. Int. Med. 238, 469, 1995.
-
(1995)
J. Int. Med.
, vol.238
, pp. 469
-
-
Morike, K.1
Magadum, S.2
Mettang, T.3
Griese, E.U.4
Machleidt, C.5
Kuhlmann, U.6
-
441
-
-
0022337949
-
Extremely rapid hydroxylation of debrisoquine: A case report with implication for treatment with nortriptyline and other tricyclic antidepressants
-
Bertilsson, L., Aberg-Wistedt, A., Gustafsson, L.L., and Nordin, C., Extremely rapid hydroxylation of debrisoquine: a case report with implication for treatment with nortriptyline and other tricyclic antidepressants. Ther. Drug Monitor. 7, 478, 1985.
-
(1985)
Ther. Drug Monitor.
, vol.7
, pp. 478
-
-
Bertilsson, L.1
Aberg-Wistedt, A.2
Gustafsson, L.L.3
Nordin, C.4
-
442
-
-
0026501881
-
Polymorphic debrisoquine oxidation and acute neuroleptic-induced adverse effects
-
Spina, E., Ancione, M., Di Rosa, A.E., Meduri, M., and Caputi, A.P., Polymorphic debrisoquine oxidation and acute neuroleptic-induced adverse effects. Eur. J. Clin. Pharmacol. 42, 347, 1992.
-
(1992)
Eur. J. Clin. Pharmacol.
, vol.42
, pp. 347
-
-
Spina, E.1
Ancione, M.2
Di Rosa, A.E.3
Meduri, M.4
Caputi, A.P.5
-
443
-
-
0021119533
-
Clinical pharmacology of antidepressant drugs, Pharmacogenetics
-
Usdin, E., et al., Eds., Raven Press, New York
-
Sjoqvist, F. and Bertilsson, L., Clinical pharmacology of antidepressant drugs, Pharmacogenetics. In: Frontiers in Biochemical and Pharmacological Research in Depression, Usdin, E., et al., Eds., Raven Press, New York, 1984, 359-372
-
(1984)
Frontiers in Biochemical and Pharmacological Research in Depression
, pp. 359-372
-
-
Sjoqvist, F.1
Bertilsson, L.2
-
444
-
-
0026817161
-
Clinical implications of variable antiarrhythmic drug metabolism
-
Buchert, E. and Woosley, R.L., Clinical implications of variable antiarrhythmic drug metabolism. Pharmacogenetics 2, 2, 1992.
-
(1992)
Pharmacogenetics
, vol.2
, pp. 2
-
-
Buchert, E.1
Woosley, R.L.2
-
445
-
-
0029979414
-
Polymorphic drug oxidation: Relevance to the treatment of psychiatric disorders
-
Bertilsson., L. and Dahl., M.-L., Polymorphic drug oxidation: relevance to the treatment of psychiatric disorders. CNS Drugs, 5, 200, 1996.
-
(1996)
CNS Drugs
, vol.5
, pp. 200
-
-
Bertilsson, L.1
Dahl, M.-L.2
-
446
-
-
0031028101
-
Relationship between plasma desipramine levels, CYP2D6 phenotype and clinical response to desipramine, a prospective study
-
Spina, E., Gitto, C., Avenoso, A., Campo, G.M., Caputi, A.P., and Perucca, E., Relationship between plasma desipramine levels, CYP2D6 phenotype and clinical response to desipramine, a prospective study. Eur. J. Clin. Pharmacol. 51, 395, 1997.
-
(1997)
Eur. J. Clin. Pharmacol.
, vol.51
, pp. 395
-
-
Spina, E.1
Gitto, C.2
Avenoso, A.3
Campo, G.M.4
Caputi, A.P.5
Perucca, E.6
-
447
-
-
0027383271
-
The pharmacogenetics of the selective serotonin reuptake inhibitors
-
Brosen, K., The pharmacogenetics of the selective serotonin reuptake inhibitors. Clin. Invest. 71, 1002-1009, 1993.
-
(1993)
Clin. Invest.
, vol.71
, pp. 1002-1009
-
-
Brosen, K.1
-
448
-
-
0029119170
-
The SSRIs, advantages, disadvantages and differences
-
Lane, R., Baldwin, D., and Preskorn, S., The SSRIs, advantages, disadvantages and differences. J. Psychopharmacol. 9 (Suppl.), 163, 1995.
-
(1995)
J. Psychopharmacol.
, vol.9
, Issue.SUPPL.
, pp. 163
-
-
Lane, R.1
Baldwin, D.2
Preskorn, S.3
-
449
-
-
0029738965
-
Dose-dependent inhibition of CYP1A2, CYP2C19 and CYP2D6 by citalopram, fluoxetine, fluvoxamine and paroxetine
-
Jeppesen, U., Gram, L.F., Vistisen, K., Loft, S., Poulsen, H.E., and Brosen, K., Dose-dependent inhibition of CYP1A2, CYP2C19 and CYP2D6 by citalopram, fluoxetine, fluvoxamine and paroxetine. Eur. J. Clin. Pharmacol. 51, 73, 1996.
-
(1996)
Eur. J. Clin. Pharmacol.
, vol.51
, pp. 73
-
-
Jeppesen, U.1
Gram, L.F.2
Vistisen, K.3
Loft, S.4
Poulsen, H.E.5
Brosen, K.6
-
450
-
-
0029622428
-
The pharmacogenetics of codeine hypoalgesia
-
Sindrup, S.H. and Brosen, K., The pharmacogenetics of codeine hypoalgesia. Pharmacogenetics, 5, 335, 1995.
-
(1995)
Pharmacogenetics
, vol.5
, pp. 335
-
-
Sindrup, S.H.1
Brosen, K.2
-
451
-
-
0028923152
-
Patient-controlled analgesia (PCA) with codeine for postoperative pain relief in ten extensive metabolizers and one poor metabolizer of dextro-methorphan
-
Persson, K., Sjostrom, S., Sigurdardottir, I., Molnar, V., Hammarlund-Udenaes, M., and Rane, A., Patient-controlled analgesia (PCA) with codeine for postoperative pain relief in ten extensive metabolizers and one poor metabolizer of dextro-methorphan. Br. J. Clin. Pharmacol. 39, 182, 1995.
-
(1995)
Br. J. Clin. Pharmacol.
, vol.39
, pp. 182
-
-
Persson, K.1
Sjostrom, S.2
Sigurdardottir, I.3
Molnar, V.4
Hammarlund-Udenaes, M.5
Rane, A.6
-
452
-
-
0030472254
-
Codeine and morphine in extensive and poor metabolizers of sparteine, pharmacokinetics, analgesic effect and side effects
-
Poulsen, L., Brosen, K., Arendt-Nielsen, L., Gram, L.F., Elbaek, K., and Sindrup, S.H., Codeine and morphine in extensive and poor metabolizers of sparteine, pharmacokinetics, analgesic effect and side effects. Eur. J. Clin. Pharmacol. 51, 289, 1996.
-
(1996)
Eur. J. Clin. Pharmacol.
, vol.51
, pp. 289
-
-
Poulsen, L.1
Brosen, K.2
Arendt-Nielsen, L.3
Gram, L.F.4
Elbaek, K.5
Sindrup, S.H.6
-
453
-
-
0030948340
-
Effect of codeine on gastrointestinal motility in relation to CYP2D6 phenotype
-
Mikus, G., Trausch, B., Rodewald, C., Hofmann, U., Richter, K., Gramatte, T., and Eichelbaum, M., Effect of codeine on gastrointestinal motility in relation to CYP2D6 phenotype. Clin. Pharmacol. Ther. 61, 459, 1997.
-
(1997)
Clin. Pharmacol. Ther.
, vol.61
, pp. 459
-
-
Mikus, G.1
Trausch, B.2
Rodewald, C.3
Hofmann, U.4
Richter, K.5
Gramatte, T.6
Eichelbaum, M.7
-
454
-
-
0030935567
-
Cytochrome P-4502E1, Its physiological and pathological role
-
Lieber, C.S., Cytochrome P-4502E1, Its physiological and pathological role. Physiol. Rev. 77, 517, 1997.
-
(1997)
Physiol. Rev.
, vol.77
, pp. 517
-
-
Lieber, C.S.1
-
455
-
-
18344405507
-
A Taq I polymorphism in the human P450IIE1 gene on chromosome 10 (CYP2E)
-
McBride, O.W., Umeno, M., Gelboin, H.V., and Gonzalez, F.J., A Taq I polymorphism in the human P450IIE1 gene on chromosome 10 (CYP2E). Nucl. Acids Res. 15, 10071, 1987.
-
(1987)
Nucl. Acids Res.
, vol.15
, pp. 10071
-
-
McBride, O.W.1
Umeno, M.2
Gelboin, H.V.3
Gonzalez, F.J.4
-
456
-
-
0022869269
-
Complementary DNA and protein sequences of ethanol-inducible rat and human cytochrome P-450s
-
Song, B.-J., Gelboin, H.V., Park, S.-S., Yang, C.S., and Gonzalez, F.J., Complementary DNA and protein sequences of ethanol-inducible rat and human cytochrome P-450s. J. Biol. Chem. 261, 16689, 1986
-
(1986)
J. Biol. Chem.
, vol.261
, pp. 16689
-
-
Song, B.-J.1
Gelboin, H.V.2
Park, S.-S.3
Yang, C.S.4
Gonzalez, F.J.5
-
457
-
-
0024244103
-
Human ethanol-inducible P450IIE1: Complete gene sequence, promoter characterization, chromosome mapping, and cDNA directed expression
-
Umeno, M., McBride, O.W., Yang, C.S., Gelboin, H.V., and Gonzalez, F.J., Human ethanol-inducible P450IIE1: complete gene sequence, promoter characterization, chromosome mapping, and cDNA directed expression. Biochemistry, 27, 9006, 1988
-
(1988)
Biochemistry
, vol.27
, pp. 9006
-
-
Umeno, M.1
McBride, O.W.2
Yang, C.S.3
Gelboin, H.V.4
Gonzalez, F.J.5
-
458
-
-
0025907246
-
Two common RFLPs of the human CYP2E gene
-
Uematsu, F., Kikuchi, H., Ohmachi, T., Sagami, I., Motomiya, M., Kamataki, T., Komori, M., and Watanabe, M., Two common RFLPs of the human CYP2E gene. Nucl. Acids Res. 19, 2803, 1991a.
-
(1991)
Nucl. Acids Res.
, vol.19
, pp. 2803
-
-
Uematsu, F.1
Kikuchi, H.2
Ohmachi, T.3
Sagami, I.4
Motomiya, M.5
Kamataki, T.6
Komori, M.7
Watanabe, M.8
-
459
-
-
0026091138
-
Msp 1 polymorphism of the human CYP2E1 gene
-
Uematsu, F., Kikuchi, H., Abe, T., Motomiya, M., Ohmachi, T., Sagami, I., and Watanabe, M., Msp 1 polymorphism of the human CYP2E1 gene. Nucl. Acids Res. 19, 5797, 1991.
-
(1991)
Nucl. Acids Res.
, vol.19
, pp. 5797
-
-
Uematsu, F.1
Kikuchi, H.2
Abe, T.3
Motomiya, M.4
Ohmachi, T.5
Sagami, I.6
Watanabe, M.7
-
460
-
-
0025685483
-
Pst I and Rsa I RFLPs in complete linkage disequilibrium at the CYP2E gene
-
Watanabe, J., Hayashi, S.-i., Nakachi, K., Imai, K., Suda, Y., Sekine, T., and Kawajiri, K., Pst I and Rsa I RFLPs in complete linkage disequilibrium at the CYP2E gene. Nucl. Acids Res. 18, 7194, 1990.
-
(1990)
Nucl. Acids Res.
, vol.18
, pp. 7194
-
-
Watanabe, J.1
Hayashi, S.-I.2
Nakachi, K.3
Imai, K.4
Suda, Y.5
Sekine, T.6
Kawajiri, K.7
-
461
-
-
0028937318
-
Polymorphism at the P450IIE1 locus is not associated with alcoholic liver disease in Caucasian men, alcoholism
-
Carr, L.G., Hartleroad, J.Y., Liang, Y., Mendenhall, C., Moritz, T., and Thomason, H., Polymorphism at the P450IIE1 locus is not associated with alcoholic liver disease in Caucasian men, alcoholism. Clin. Exp. Res. 19, 182, 1995.
-
(1995)
Clin. Exp. Res.
, vol.19
, pp. 182
-
-
Carr, L.G.1
Hartleroad, J.Y.2
Liang, Y.3
Mendenhall, C.4
Moritz, T.5
Thomason, H.6
-
462
-
-
0030889322
-
Genetic polymorphism of human CYP2E1, Characterization of two variant alleles
-
Hu, Y., Oscarson, M., Johansson, I., Yue, Q.-Y., Dahl, M.-L., Tabone, M., Arinco, S., Albano, E., and Ingelman-Sundberg, M., Genetic polymorphism of human CYP2E1, Characterization of two variant alleles. Mol. Pharmacol. 51, 370, 1997.
-
(1997)
Mol. Pharmacol.
, vol.51
, pp. 370
-
-
Hu, Y.1
Oscarson, M.2
Johansson, I.3
Yue, Q.-Y.4
Dahl, M.-L.5
Tabone, M.6
Arinco, S.7
Albano, E.8
Ingelman-Sundberg, M.9
-
463
-
-
0028847431
-
An investigation of whether polymorphisms of cytochrome P4502E1 are genetic markers of susceptibility to alcoholic end-stage organ damage in Chinese populations
-
Chao Y.-C., Young T.-H., Chang W.-K., Tang H.-S. and Hsu C.-T., An investigation of whether polymorphisms of cytochrome P4502E1 are genetic markers of susceptibility to alcoholic end-stage organ damage in Chinese populations, Hepatology 22, 1409, 1995.
-
(1995)
Hepatology
, vol.22
, pp. 1409
-
-
Chao, Y.-C.1
Young, T.-H.2
Chang, W.-K.3
Tang, H.-S.4
Hsu, C.-T.5
-
464
-
-
0027401426
-
Genetic polymorphism of cytochrome P450IIE1 in a Swedish population: Relationship to incidence of lung cancer
-
Persson, I., Johansson, I., Bergling, H., Dahl, M.L., Seidegard, J., Rylander, R., Rannug, A., Hoberg, J., and Ingelman-Sundberg, M., Genetic polymorphism of cytochrome P450IIE1 in a Swedish population: relationship to incidence of lung cancer. FEBS Lett. 319, 207, 1993.
-
(1993)
FEBS Lett.
, vol.319
, pp. 207
-
-
Persson, I.1
Johansson, I.2
Bergling, H.3
Dahl, M.L.4
Seidegard, J.5
Rylander, R.6
Rannug, A.7
Hoberg, J.8
Ingelman-Sundberg, M.9
-
465
-
-
0029145138
-
Cytochrome P4502E1 genetic polymorphisms and risk of nasopharyngeal carcinoma, results from a case-control study conducted in Taiwan
-
Hildesheim, A., Chen, C.-J., Caporaso, N.E., Cheng, Y.-J., Hoover, R.N., Hsu, M.-M., Levine, P.H., Chen, I.-H., Chen, J.-Y., Yang, C.-S., Daly, A.K., and Idle, J.R., Cytochrome P4502E1 genetic polymorphisms and risk of nasopharyngeal carcinoma, Results from a case-control study conducted in Taiwan. Cancer Epidemiol. Biomark. Prevent. 4, 607, 1995.
-
(1995)
Cancer Epidemiol. Biomark. Prevent.
, vol.4
, pp. 607
-
-
Hildesheim, A.1
Chen, C.-J.2
Caporaso, N.E.3
Cheng, Y.-J.4
Hoover, R.N.5
Hsu, M.-M.6
Levine, P.H.7
Chen, I.-H.8
Chen, J.-Y.9
Yang, C.-S.10
Daly, A.K.11
Idle, J.R.12
-
466
-
-
0026062622
-
Genetic polymorphisms in the 5′-flanking region change transcriptional regulation of the human cytochrome P450IIE1 gene
-
Hayashi, S.-i., Watanabe, J., and Kawajiri, K., Genetic polymorphisms in the 5′-flanking region change transcriptional regulation of the human cytochrome P450IIE1 gene. J. Biochem. 110, 559, 1991.
-
(1991)
J. Biochem.
, vol.110
, pp. 559
-
-
Hayashi, S.-I.1
Watanabe, J.2
Kawajiri, K.3
-
467
-
-
0028145234
-
Different regulation and expression of the human CYP2E1 gene due to the Rsa I polymorphism in the 5′-flanking region
-
Watanabe, J., Hayashi, S.-i., and Kawajiri, K., Different regulation and expression of the human CYP2E1 gene due to the Rsa I polymorphism in the 5′-flanking region. J. Biochem. 116, 321, 1994.
-
(1994)
J. Biochem.
, vol.116
, pp. 321
-
-
Watanabe, J.1
Hayashi, S.-I.2
Kawajiri, K.3
-
468
-
-
0028256189
-
Hepatic messenger RNA contents of cytochrome P4502E1 in patients with different P4502E1 genotypes
-
Tsutsumi, M., Wang, J.-S., and Takada, A., Hepatic messenger RNA contents of cytochrome P4502E1 in patients with different P4502E1 genotypes. Int. Hepatol. Commun. 2, 135, 1994.
-
(1994)
Int. Hepatol. Commun.
, vol.2
, pp. 135
-
-
Tsutsumi, M.1
Wang, J.-S.2
Takada, A.3
-
469
-
-
0028673497
-
Hepatic messenger RNA contents of cytochrome P4502E1 in patients with different P4502E1 genotypes
-
Tsutsumi, M., Wang, J.-S., Takase, S., and Takada, A., Hepatic messenger RNA contents of cytochrome P4502E1 in patients with different P4502E1 genotypes. Alcohol & Alcoholism, 29 (S1), 29, 1994.
-
(1994)
Alcohol & Alcoholism
, vol.29
, Issue.S1
, pp. 29
-
-
Tsutsumi, M.1
Wang, J.-S.2
Takase, S.3
Takada, A.4
-
470
-
-
0029878329
-
Human cytochrome P450 2E1 (CYP2E1), from genotype to phenotype
-
Carriere, V., Berthou, F., Baird, S., Belloc, C., Beaune, P., and de Waziers, I., Human cytochrome P450 2E1 (CYP2E1), from genotype to phenotype. Pharmacogenetics 6, 203, 1996.
-
(1996)
Pharmacogenetics
, vol.6
, pp. 203
-
-
Carriere, V.1
Berthou, F.2
Baird, S.3
Belloc, C.4
Beaune, P.5
De Waziers, I.6
-
471
-
-
0013496628
-
7-alkyl-deoxyguauosine (7-alkyldGp) adduct formation in human lung and cytochrome P450 2E1 (CYP2E1) genetic polymorphisms
-
Kato, S., Bowman, D.E., Blomeke, B., Weston, A., and Shields, P.G., 7-Alkyl-deoxyguauosine (7-alkyldGp) adduct formation in human lung and cytochrome P450 2E1 (CYP2E1) genetic polymorphisms. Proc. Am. Assoc. Cancer Res. 34, 144. 1993.
-
(1993)
Proc. Am. Assoc. Cancer Res.
, vol.34
, pp. 144
-
-
Kato, S.1
Bowman, D.E.2
Blomeke, B.3
Weston, A.4
Shields, P.G.5
-
472
-
-
0028355767
-
Relationship in healthy subjects between CYD2E1 genetic polymorphisms and the 6-hydroxylation of chlorzoxazone, a putative measure of CYP2E1 activity
-
Kim, R.B., O'Shea, D., and Wilkinson, G.R., Relationship in healthy subjects between CYD2E1 genetic polymorphisms and the 6-hydroxylation of chlorzoxazone, a putative measure of CYP2E1 activity. Pharmacogenetics 4, 162, 1994.
-
(1994)
Pharmacogenetics
, vol.4
, pp. 162
-
-
Kim, R.B.1
O'Shea, D.2
Wilkinson, G.R.3
-
473
-
-
0013552795
-
Cytochrome P4502E1-dependent metabolism as a biomarker for genetic susceptibility to chemically induced cancers, a pilot study
-
Lechner, M.C., Ed., John Libbey Eurotext, Paris
-
Campleman, S.L., Tamaki, S.J., Hoener, B.-A., and Smith, M.T., Cytochrome P4502E1-dependent metabolism as a biomarker for genetic susceptibility to chemically induced cancers, a pilot study. In: Proceedings of the Cytochrome P450 8th international conference, Lechner, M.C., Ed., John Libbey Eurotext, Paris, 1994, 213-216.
-
(1994)
Proceedings of the Cytochrome P450 8th International Conference
, pp. 213-216
-
-
Campleman, S.L.1
Tamaki, S.J.2
Hoener, B.-A.3
Smith, M.T.4
-
474
-
-
0029035739
-
Interindividual variability of chlorzoxazone 6-hydroxylation in men and women and its relationship to CYP2E1 genetic polymorphisms
-
Kim, R.B., O'Shea, D., and Wilkinson, G.R., Interindividual variability of chlorzoxazone 6-hydroxylation in men and women and its relationship to CYP2E1 genetic polymorphisms. Clin. Pharmacol. Ther. 57, 645, 1995.
-
(1995)
Clin. Pharmacol. Ther.
, vol.57
, pp. 645
-
-
Kim, R.B.1
O'Shea, D.2
Wilkinson, G.R.3
-
475
-
-
0029878392
-
Acetaminophen metabolism in patients with different cytochrome P-4502E1 genotypes
-
Ueshima, Y., Tsutsumi, M., Takase, S., Matsuda, Y., and Kawahara, H., Acetaminophen metabolism in patients with different cytochrome P-4502E1 genotypes. Alcoholism, Clin. Exp. Res. 20, 25a, 1996.
-
(1996)
Alcoholism, Clin. Exp. Res.
, vol.20
-
-
Ueshima, Y.1
Tsutsumi, M.2
Takase, S.3
Matsuda, Y.4
Kawahara, H.5
-
476
-
-
0029881087
-
Effect of the cytochrome P-450IIE1 genotype on ethanol elimination rate in alcoholics and control subjects
-
Ueno, Y., Adachi, J., Imamichi, H., Nishimura, A., and Tatsuno, Y., Effect of the cytochrome P-450IIE1 genotype on ethanol elimination rate in alcoholics and control subjects. Alcoholism, Clin. Exp. Res. 20, 17a, 1996.
-
(1996)
Alcoholism, Clin. Exp. Res.
, vol.20
-
-
Ueno, Y.1
Adachi, J.2
Imamichi, H.3
Nishimura, A.4
Tatsuno, Y.5
-
477
-
-
0029009951
-
Human lung carcinogen-DNA adduct levels mediated by genetic polymorphisms in vivo
-
Kato, S., Bowman, E.D., Harrington, A.M., Blomeke, B., and Shields, P.G., Human lung carcinogen-DNA adduct levels mediated by genetic polymorphisms in vivo. J. Natl. Cancer Inst. 87, 902, 1995.
-
(1995)
J. Natl. Cancer Inst.
, vol.87
, pp. 902
-
-
Kato, S.1
Bowman, E.D.2
Harrington, A.M.3
Blomeke, B.4
Shields, P.G.5
-
478
-
-
0026532612
-
Nomenclature for human glutathione transferases
-
Mannervik, B., Awasthi, Y.C., Board, P.G., Hayes, J.D., Di Ilio, C., Ketterer, B., Listowsky, I., Morgenstern, R., Muramatsu, M., Pearson, W.R., Pickett, C.B., Sato, K., Widersten, M., and Wolf, C.R., Nomenclature for human glutathione transferases. Biochem. J. 282, 305, 1992.
-
(1992)
Biochem. J.
, vol.282
, pp. 305
-
-
Mannervik, B.1
Awasthi, Y.C.2
Board, P.G.3
Hayes, J.D.4
Di Ilio, C.5
Ketterer, B.6
Listowsky, I.7
Morgenstern, R.8
Muramatsu, M.9
Pearson, W.R.10
Pickett, C.B.11
Sato, K.12
Widersten, M.13
Wolf, C.R.14
-
479
-
-
0003215942
-
The structure, genetics and regulation of soluble glutatione-S-transferases
-
Academic Press, San Diego
-
Pickett, C.B. and Lu, A.Y.H., The structure, genetics and regulation of soluble glutatione-S-transferases. In: Glutathione Conjugation, Academic Press, San Diego, 1988, 137-156
-
(1988)
Glutathione Conjugation
, pp. 137-156
-
-
Pickett, C.B.1
Lu, A.Y.H.2
-
480
-
-
0003215939
-
Soluble glutathione transferase isoenzymes
-
Ketterer, B., and Sies, H., Eds., Academic Press. London
-
Ketterer, B., Meyer, D.J., and Clark, A.G., Soluble glutathione transferase isoenzymes, In: Glutathione Conjugation: Its Mechanism and Biological Significance, Ketterer, B., and Sies, H., Eds., Academic Press. London, 1988, 73-135
-
(1988)
Glutathione Conjugation: Its Mechanism and Biological Significance
, pp. 73-135
-
-
Ketterer, B.1
Meyer, D.J.2
Clark, A.G.3
-
481
-
-
0027300033
-
Glutathione-S-transferases, structure, regulation, and therapeutic implications
-
Rushmore, T.H. and Pickett, C.B., Glutathione-S-transferases, structure, regulation, and therapeutic implications. J. Biol. Chem. 268, 11475, 1993.
-
(1993)
J. Biol. Chem.
, vol.268
, pp. 11475
-
-
Rushmore, T.H.1
Pickett, C.B.2
-
482
-
-
0029561598
-
The glutathione-S-transferase supergene family: Regulation of GST and the contribution of the isoenzymes to cancer chemoprevention and drug resistance
-
Hayes, J.D. and Pulford, D.J., The glutathione-S-transferase supergene family: regulation of GST and the contribution of the isoenzymes to cancer chemoprevention and drug resistance. Crit. Rev. Biochem. Mol. Biol. 30, 445, 1995.
-
(1995)
Crit. Rev. Biochem. Mol. Biol.
, vol.30
, pp. 445
-
-
Hayes, J.D.1
Pulford, D.J.2
-
483
-
-
0031021397
-
Structure, catalytic mechanism, and evolution of the glutathione transferases
-
Armstrong, R.N., Structure, catalytic mechanism, and evolution of the glutathione transferases. Chem. Res. Toxicol. 10, 2, 1997.
-
(1997)
Chem. Res. Toxicol.
, vol.10
, pp. 2
-
-
Armstrong, R.N.1
-
484
-
-
0024377341
-
Glutathione-S-transferases, gene structure, regulation, and biological function
-
Pickett, C.B. and Lu, A.Y.H., Glutathione-S-transferases, gene structure, regulation, and biological function. Ann. Rev. Biochem. 58, 743, 1989.
-
(1989)
Ann. Rev. Biochem.
, vol.58
, pp. 743
-
-
Pickett, C.B.1
Lu, A.Y.H.2
-
485
-
-
0025670311
-
Genetic heterogeinity of the human glutathione-S-transferases, a complex of gene families
-
Board, P., Coggan, M., Johnston, P., Ross, V., Suzuki, T., and Webb, G., Genetic heterogeinity of the human glutathione-S-transferases, a complex of gene families. Pharmacol. Ther. 48, 357, 1990.
-
(1990)
Pharmacol. Ther.
, vol.48
, pp. 357
-
-
Board, P.1
Coggan, M.2
Johnston, P.3
Ross, V.4
Suzuki, T.5
Webb, G.6
-
486
-
-
0029854518
-
Glutathione-S-transferase class kappa: Characterization by the cloning of rat mitochondrial GST and identification of a human orthologue
-
Pemble, S.E., Wardle, A.F., and Taylor, J.B., Glutathione-S-transferase class kappa: characterization by the cloning of rat mitochondrial GST and identification of a human orthologue. Biochem. J. 319, 749, 1996.
-
(1996)
Biochem. J.
, vol.319
, pp. 749
-
-
Pemble, S.E.1
Wardle, A.F.2
Taylor, J.B.3
-
487
-
-
0024265036
-
Intracellular binding and transport of hormones and xenobiotics by glutathione-S-transferases
-
Listowsky, I., Abramovitz, M., Homma, H., and Niitsu, Y., Intracellular binding and transport of hormones and xenobiotics by glutathione-S-transferases. Drug Metab. Rev. 19, 305, 1988.
-
(1988)
Drug Metab. Rev.
, vol.19
, pp. 305
-
-
Listowsky, I.1
Abramovitz, M.2
Homma, H.3
Niitsu, Y.4
-
488
-
-
0023756891
-
Protective role of glutathione and glutathione transferases in mutagenesis and carcinogenesis
-
Ketterer, B., Protective role of glutathione and glutathione transferases in mutagenesis and carcinogenesis. Mutat. Res. 202, 343, 1988.
-
(1988)
Mutat. Res.
, vol.202
, pp. 343
-
-
Ketterer, B.1
-
489
-
-
0025228968
-
The role of glutathione and glutathione transferases in chemical carcinogenesis
-
Coles, B. and Ketterer, B., The role of glutathione and glutathione transferases in chemical carcinogenesis. Crit. Rev. Biochem. Mol. Biol. 25, 47, 1990.
-
(1990)
Crit. Rev. Biochem. Mol. Biol.
, vol.25
, pp. 47
-
-
Coles, B.1
Ketterer, B.2
-
490
-
-
0029008428
-
Enzymes and transport systems involved in the formation and disposition of glutathione-S-conjugates
-
Commandeur, J.N.M., Stijntjes, G.J., and Vermeulen, N.P.E., Enzymes and transport systems involved in the formation and disposition of glutathione-S-conjugates. Pharmacol. Rev. 47, 271, 1995.
-
(1995)
Pharmacol. Rev.
, vol.47
, pp. 271
-
-
Commandeur, J.N.M.1
Stijntjes, G.J.2
Vermeulen, N.P.E.3
-
491
-
-
0023758383
-
The human liver glutathione-S-transferase gene superfamily, expression and chromosome mapping of an Hb subunit cDNA
-
DeJong, J.L., Chang, C.-M., Whang-Peng, J., Nutsen, T., and Tu, C.-P.D., The human liver glutathione-S-transferase gene superfamily, expression and chromosome mapping of an Hb subunit cDNA. Nucl. Acids Res. 16, 8541, 1988.
-
(1988)
Nucl. Acids Res.
, vol.16
, pp. 8541
-
-
Dejong, J.L.1
Chang, C.-M.2
Whang-Peng, J.3
Nutsen, T.4
Tu, C.-P.D.5
-
492
-
-
0024413461
-
Chromosomal localisation of human glutathione transferase genes of classes alpha, mu and pi
-
Islam, M.Q., Platz, A., Szpirer, J., Szpirer, C., Levan, G., and Mannervik, B., Chromosomal localisation of human glutathione transferase genes of classes alpha, mu and pi. Hum. Genet. 82, 338, 1989.
-
(1989)
Hum. Genet.
, vol.82
, pp. 338
-
-
Islam, M.Q.1
Platz, A.2
Szpirer, J.3
Szpirer, C.4
Levan, G.5
Mannervik, B.6
-
493
-
-
0025925240
-
The human Hb (mu) class glutathione-S-transferases are encoded by a dispersed gene family
-
DeJong, J.L., Mohandas, T., and Tu, C.-P.D., The human Hb (mu) class glutathione-S-transferases are encoded by a dispersed gene family. Biochem. Biophys. Res. Commun. 180, 15, 1991.
-
(1991)
Biochem. Biophys. Res. Commun.
, vol.180
, pp. 15
-
-
Dejong, J.L.1
Mohandas, T.2
Tu, C.-P.D.3
-
494
-
-
0027050038
-
Chromosomal assignment and linkage analysis of the human glutathione-S-transferase μ gene (GSTM1) using intron specific polymerase chain reaction
-
Zhong, S., Wolf, C.R., and Spurr, N.K., Chromosomal assignment and linkage analysis of the human glutathione-S-transferase μ gene (GSTM1) using intron specific polymerase chain reaction. Hum. Genet. 90, 435, 1992.
-
(1992)
Hum. Genet.
, vol.90
, pp. 435
-
-
Zhong, S.1
Wolf, C.R.2
Spurr, N.K.3
-
495
-
-
0027367823
-
Identification of class-mu glutathione transferase genes GSTM1-GSTM5 on human chromosome 1p13
-
Pearson, W.R., Vorachek, W.R., Xu, S.-j., Berger, R., Hart, I., Vannais, D., and Patterson, D., Identification of class-mu glutathione transferase genes GSTM1-GSTM5 on human chromosome 1p13. Am. J. Hum. Genet. 53, 220, 1993.
-
(1993)
Am. J. Hum. Genet.
, vol.53
, pp. 220
-
-
Pearson, W.R.1
Vorachek, W.R.2
Xu, S.-J.3
Berger, R.4
Hart, I.5
Vannais, D.6
Patterson, D.7
-
496
-
-
0010325553
-
Hereditary differences in the expression of the human glutathione transferase active on trans-stilbene oxide are due to a gene deletion
-
Seidegard, J., Vorachek, W.R., Pero, R.W., and Pearson, W.R., Hereditary differences in the expression of the human glutathione transferase active on trans-stilbene oxide are due to a gene deletion. Proc. Natl. Acad. Sci. U.S.A. 85, 7293, 1988.
-
(1988)
Proc. Natl. Acad. Sci. U.S.A.
, vol.85
, pp. 7293
-
-
Seidegard, J.1
Vorachek, W.R.2
Pero, R.W.3
Pearson, W.R.4
-
497
-
-
0027431942
-
Use of site-directed mutagenesis of allele-specific PCR primers to identify the GSTM1 A, GSTM1 B, GSTM1 A,B and GSTM1 null polymorphisms at the glutathione-S-transferase, GSTM1 locus
-
Fryer, A.A., Zhao, L., Alldersea, J., Pearson, W.R., and Strange, R.C., Use of site-directed mutagenesis of allele-specific PCR primers to identify the GSTM1 A, GSTM1 B, GSTM1 A,B and GSTM1 null polymorphisms at the glutathione-S-transferase, GSTM1 locus. Biochem. J. 295, 313, 1993.
-
(1993)
Biochem. J.
, vol.295
, pp. 313
-
-
Fryer, A.A.1
Zhao, L.2
Alldersea, J.3
Pearson, W.R.4
Strange, R.C.5
-
498
-
-
0025812157
-
Heterologous expression of the allelic variant Mu-class glutathione transferases μ and ψ
-
Widersten, M., Pearson, W.R., Engstrom, A., and Mannervik, B., Heterologous expression of the allelic variant Mu-class glutathione transferases μ and ψ. Biochem. J. 276, 519, 1991.
-
(1991)
Biochem. J.
, vol.276
, pp. 519
-
-
Widersten, M.1
Pearson, W.R.2
Engstrom, A.3
Mannervik, B.4
-
499
-
-
0030906289
-
DNA adducts in human placenta as related to air pollution and to GSTM1 genotype
-
Topinka, J., Binkova, B., Mrackova, G., Stavkova, Z., Benes, I., Dejmek, J., Lenicek, J., and Sram, R.J., DNA adducts in human placenta as related to air pollution and to GSTM1 genotype. Mutat. Res. 390, 59, 1997.
-
(1997)
Mutat. Res.
, vol.390
, pp. 59
-
-
Topinka, J.1
Binkova, B.2
Mrackova, G.3
Stavkova, Z.4
Benes, I.5
Dejmek, J.6
Lenicek, J.7
Sram, R.J.8
-
500
-
-
0028138821
-
Polycyclic aromatic hydrocarbon-DNA adducts in smokers and their relationship to micronutrient levels and the glutathione-S-transferase M1 genotype
-
Grinberg-Funes, R.A., Singh, V.N., Perera, F.P., Bell, D.A., Young, T.L., Dickey, C., Wang, L.W., and Santella, R.M., Polycyclic aromatic hydrocarbon-DNA adducts in smokers and their relationship to micronutrient levels and the glutathione-S-transferase M1 genotype. Carcinogenesis 15, 2449, 1994
-
(1994)
Carcinogenesis
, vol.15
, pp. 2449
-
-
Grinberg-Funes, R.A.1
Singh, V.N.2
Perera, F.P.3
Bell, D.A.4
Young, T.L.5
Dickey, C.6
Wang, L.W.7
Santella, R.M.8
-
501
-
-
0028950709
-
Polycyclic aromatic hydrocarbon-DNA and protein adducts in coat tar treated patients and controls and their relationship to glutathione-S-transferase genotype
-
Santella, R.M., Perera, F.P., Young, T.L., Zhang, Y.-J., Chiamprasert, S., Tang, D., Wang, L.W., Beachman, A., Lin, J.-H., and DeLeo, V.A., Polycyclic aromatic hydrocarbon-DNA and protein adducts in coat tar treated patients and controls and their relationship to glutathione-S-transferase genotype. Mutat. Res. 334, 117, 1995.
-
(1995)
Mutat. Res.
, vol.334
, pp. 117
-
-
Santella, R.M.1
Perera, F.P.2
Young, T.L.3
Zhang, Y.-J.4
Chiamprasert, S.5
Tang, D.6
Wang, L.W.7
Beachman, A.8
Lin, J.-H.9
Deleo, V.A.10
-
502
-
-
0028818149
-
The impact of glutathione-S-transferase M1 and cytochrome P450 1A1 genotypes on white-blood-cell polycyclic aromatic hydrocarbon-DNA adduct levels in humans
-
Rothman, N., Shields, P.G., Poirier, M.C., Harrington, A.M., Ford, D.P., and Strickland, P.T., The impact of glutathione-S-transferase M1 and cytochrome P450 1A1 genotypes on white-blood-cell polycyclic aromatic hydrocarbon-DNA adduct levels in humans. Mol. Carcinogen. 14, 63, 1995.
-
(1995)
Mol. Carcinogen.
, vol.14
, pp. 63
-
-
Rothman, N.1
Shields, P.G.2
Poirier, M.C.3
Harrington, A.M.4
Ford, D.P.5
Strickland, P.T.6
-
503
-
-
0029934267
-
Environmental air pollution and DNA adducts in Copenhagen bus drivers: Effect of GSTM1 and NAT2 genotypes on adduct levels
-
Nielsen, P.S., de Pater, N., Okkels, H., and Autrup, H., Environmental air pollution and DNA adducts in Copenhagen bus drivers: effect of GSTM1 and NAT2 genotypes on adduct levels. Carcinogenesis 17, 1021, 1996.
-
(1996)
Carcinogenesis
, vol.17
, pp. 1021
-
-
Nielsen, P.S.1
De Pater, N.2
Okkels, H.3
Autrup, H.4
-
504
-
-
0001732868
-
Smoking-related DNA adducts and genetic polymorphism for metabolic enzymes in human lymphocytes
-
Ichiba, M., Wang, Y., Oishi, H., Iyadomi, M., Shono, N., and Tomokuni, K., Smoking-related DNA adducts and genetic polymorphism for metabolic enzymes in human lymphocytes. Biomarkers 1, 211, 1996.
-
(1996)
Biomarkers
, vol.1
, pp. 211
-
-
Ichiba, M.1
Wang, Y.2
Oishi, H.3
Iyadomi, M.4
Shono, N.5
Tomokuni, K.6
-
505
-
-
0028857944
-
Glutathione-S-transferase M1 genotype affects aminobiphenyl-hemoglobin adduct levels in white, black, and Asian smokers and nonsmokers
-
Yu, M.C., Ross, R.K., Chan, K.K., Henderson, B.E., Skipper, P.L., Tannenbaum, S.R., and Coetzee, G.A., Glutathione-S-transferase M1 genotype affects aminobiphenyl-hemoglobin adduct levels in white, black, and Asian smokers and nonsmokers. Cancer Epidemiol. Biomark. Prevent. 4, 861, 1995.
-
(1995)
Cancer Epidemiol. Biomark. Prevent.
, vol.4
, pp. 861
-
-
Yu, M.C.1
Ross, R.K.2
Chan, K.K.3
Henderson, B.E.4
Skipper, P.L.5
Tannenbaum, S.R.6
Coetzee, G.A.7
-
506
-
-
0028957898
-
Susceptibility to hepatocellular carcinoma is associated with genetic variation in the enzymatic detoxification of aflatoxin B 1
-
McGlynn, K.A., Rosvold, E.A., Lustbader, E.D., Hu, Y., Clapper, M.L., Zhou, T., Wild, C.P., Xia, X.-L., Baffoe-Bonnie, A., Ofori-Adjei, D., Chen, G.C., London, W.T., Shen, F.-M., and Buetow, K.H., Susceptibility to hepatocellular carcinoma is associated with genetic variation in the enzymatic detoxification of aflatoxin B 1. Proc. Natl. Acad. Sci. U.S.A. 92, 2384, 1995.
-
(1995)
Proc. Natl. Acad. Sci. U.S.A.
, vol.92
, pp. 2384
-
-
McGlynn, K.A.1
Rosvold, E.A.2
Lustbader, E.D.3
Hu, Y.4
Clapper, M.L.5
Zhou, T.6
Wild, C.P.7
Xia, X.-L.8
Baffoe-Bonnie, A.9
Ofori-Adjei, D.10
Chen, G.C.11
London, W.T.12
Shen, F.-M.13
Buetow, K.H.14
-
507
-
-
0026598647
-
Increased cytogenetic damage in smokers deficient in glutathione S-transferase isozyme mu
-
van Poppel, G., de Vogel, N., van Bladeren, P.J., and Kok, F.J., Increased cytogenetic damage in smokers deficient in glutathione S-transferase isozyme mu. Carcinogenesis 13, 303, 1992.
-
(1992)
Carcinogenesis
, vol.13
, pp. 303
-
-
Van Poppel, G.1
De Vogel, N.2
Van Bladeren, P.J.3
Kok, F.J.4
-
508
-
-
0028176307
-
p53 mutations in lung tumors: Relationship to putative susceptibility markers for cancer
-
Ryberg, D., Kure, E., Lystad, S., Skaug, V., Stangeland, L., Mercy, I., Borresen, A.-L., and Haugen, A., p53 Mutations in lung tumors: relationship to putative susceptibility markers for cancer. Cancer Res. 54, 1551, 1994.
-
(1994)
Cancer Res.
, vol.54
, pp. 1551
-
-
Ryberg, D.1
Kure, E.2
Lystad, S.3
Skaug, V.4
Stangeland, L.5
Mercy, I.6
Borresen, A.-L.7
Haugen, A.8
-
509
-
-
0028905381
-
Hprt mutant frequency and GSTM1 genotype in non-smoking healthy individuals
-
Hou, S.-M., Falt, S., and Steen, A.-M., Hprt mutant frequency and GSTM1 genotype in non-smoking healthy individuals. Environ. Mol. Mutagen. 25, 97, 1995.
-
(1995)
Environ. Mol. Mutagen.
, vol.25
, pp. 97
-
-
Hou, S.-M.1
Falt, S.2
Steen, A.-M.3
-
510
-
-
0030581760
-
Induction of sister chromatid exchange by 3,4-epoxybutane-1,2-diol in cultured human lymphocytes of different GSTT1 and GSTM1 genotypes
-
Bernardini, S., Pelin, K., Peltonen, K., Jarventous, H., Hirvonen, A., Neagu, C., Sorsa, M., and Norppa, H., Induction of sister chromatid exchange by 3,4-epoxybutane-1,2-diol in cultured human lymphocytes of different GSTT1 and GSTM1 genotypes. Mutat. Res. 361, 121, 1996.
-
(1996)
Mutat. Res.
, vol.361
, pp. 121
-
-
Bernardini, S.1
Pelin, K.2
Peltonen, K.3
Jarventous, H.4
Hirvonen, A.5
Neagu, C.6
Sorsa, M.7
Norppa, H.8
-
511
-
-
0028926133
-
Influence of GSTMJ genotype on sister chromatid exchange induction by styrene-7,8-oxide and 1,2-epoxy-3-butene in cultured human lymphocytes
-
Uuskula, M., Jarventaus, H., Hirvonen, A., Sorsa, M., and Norppa, H., Influence of GSTMJ genotype on sister chromatid exchange induction by styrene-7,8-oxide and 1,2-epoxy-3-butene in cultured human lymphocytes. Carcinogenesis 16, 947, 1995.
-
(1995)
Carcinogenesis
, vol.16
, pp. 947
-
-
Uuskula, M.1
Jarventaus, H.2
Hirvonen, A.3
Sorsa, M.4
Norppa, H.5
-
512
-
-
0029114981
-
Glutathione-S-transferase M1 (GSTM1) deficiency and lung cancer risk
-
McWilliams, J.E., Sanderson, B.J.S., Harris, E.L., Richert-Boe, K.E., and Henner, W.D., Glutathione-S-transferase M1 (GSTM1) deficiency and lung cancer risk. Cancer Epidemiol. Biomark. Prevent. 4, 589, 1995.
-
(1995)
Cancer Epidemiol. Biomark. Prevent.
, vol.4
, pp. 589
-
-
McWilliams, J.E.1
Sanderson, B.J.S.2
Harris, E.L.3
Richert-Boe, K.E.4
Henner, W.D.5
-
513
-
-
0027485154
-
Human Mu-class glutathione-S-transferases present in liver, skeletal muscle and testicular tissue
-
Hussey, A.J. and Hayes, J.D., Human Mu-class glutathione-S-transferases present in liver, skeletal muscle and testicular tissue. Biochem. Biophys Acta, 1203, 131, 1993.
-
(1993)
Biochem. Biophys Acta
, vol.1203
, pp. 131
-
-
Hussey, A.J.1
Hayes, J.D.2
-
514
-
-
0027527217
-
Immunohistochemical localization of glutathione-S-transferases in human lung
-
Anttila, S., Hirvonen, A., Vainio, H., Husgafvel-Pursiainen, K., Hayes, J.D., and Ketterer, B., Immunohistochemical localization of glutathione-S-transferases in human lung. Cancer Res. 53, 5643, 1993.
-
(1993)
Cancer Res.
, vol.53
, pp. 5643
-
-
Anttila, S.1
Hirvonen, A.2
Vainio, H.3
Husgafvel-Pursiainen, K.4
Hayes, J.D.5
Ketterer, B.6
-
515
-
-
0027056290
-
The human glutathione-S-transferase supergene family: Its polymorphism, and its effects on susceptibility to lung cancer
-
Ketterer, B., Harris, J.M., Talaska, G., Meyer, D.J., Pemble, S.E., Taylor, J.B., Lang, N.P., and Kadlubar, F.F., The human glutathione-S-transferase supergene family: its polymorphism, and its effects on susceptibility to lung cancer. Environ. Health Perspect. 98, 87, 1992.
-
(1992)
Environ. Health Perspect.
, vol.98
, pp. 87
-
-
Ketterer, B.1
Harris, J.M.2
Talaska, G.3
Meyer, D.J.4
Pemble, S.E.5
Taylor, J.B.6
Lang, N.P.7
Kadlubar, F.F.8
-
516
-
-
0029156516
-
Pulmonary expression of glutathione-S-transferase M3 in lung cancer patients: Association with GSTM1 polymorphism, smoking, and asbestos exposure
-
Anttila, S., Luostarinen, L., Hirvonen, A., Elovaara, E., Karjalainen, A., Nurminen, T., Hayes, J.D., Vainio, H., and Ketterer, B., Pulmonary expression of glutathione-S-transferase M3 in lung cancer patients: association with GSTM1 polymorphism, smoking, and asbestos exposure. Cancer Res. 55, 3305, 1995.
-
(1995)
Cancer Res.
, vol.55
, pp. 3305
-
-
Anttila, S.1
Luostarinen, L.2
Hirvonen, A.3
Elovaara, E.4
Karjalainen, A.5
Nurminen, T.6
Hayes, J.D.7
Vainio, H.8
Ketterer, B.9
-
517
-
-
0029560166
-
Identification of polymorphism at the glutathione-S-transferase, GSTM3 locus: Evidence for linkage with GSTM1*A
-
Inskip, A., Elexperu-Camiruaga, J., Buxton, N., Dias, P.S., MacIntosh, J., Campbell, D., Jones, P.W., Yengi, L., Talbot, J.A., Strange, R.C., and Fryer, A.A., Identification of polymorphism at the glutathione-S-transferase, GSTM3 locus: evidence for linkage with GSTM1*A. Biochem. J. 312. 713, 1995.
-
(1995)
Biochem. J.
, vol.312
, pp. 713
-
-
Inskip, A.1
Elexperu-Camiruaga, J.2
Buxton, N.3
Dias, P.S.4
Macintosh, J.5
Campbell, D.6
Jones, P.W.7
Yengi, L.8
Talbot, J.A.9
Strange, R.C.10
Fryer, A.A.11
-
518
-
-
9244246804
-
Polymorphism at the glutathione-S-transferase locus GSTM3: Interactions with cytochrome P450 and glutathione-S-transferase genotypes as risk factors for multiple cutaneous basal cell carcinoma
-
Yengi, L., Inskip, A., Gilford, J., Alldersea, J., Bailey, L., Smith, A., Lear, J.T., Heagerty, A.H., Bowers, B., Hand, P., Hayes, J.D., Jones, P.W., Strange, R.C., and Fryer, A.A., Polymorphism at the glutathione-S-transferase locus GSTM3: interactions with cytochrome P450 and glutathione-S-transferase genotypes as risk factors for multiple cutaneous basal cell carcinoma. Cancer Res. 56, 1974, 1996.
-
(1996)
Cancer Res.
, vol.56
, pp. 1974
-
-
Yengi, L.1
Inskip, A.2
Gilford, J.3
Alldersea, J.4
Bailey, L.5
Smith, A.6
Lear, J.T.7
Heagerty, A.H.8
Bowers, B.9
Hand, P.10
Hayes, J.D.11
Jones, P.W.12
Strange, R.C.13
Fryer, A.A.14
-
519
-
-
0029812343
-
Allelism at the glutathione-S-transferase GSTM3 locus: Interactions with GSTM1 and GSTT1 as risk factors for astrocytoma
-
Hand, P.A., Inskip, A., Gilford, J., Alldersea, J., Elexpuru-Camiruaga, J., Hayes, J.D., Jones, P.W., Strange, R.C., and Freyer, A.A., Allelism at the glutathione-S-transferase GSTM3 locus: interactions with GSTM1 and GSTT1 as risk factors for astrocytoma. Carcinogenesis 17, 1919, 1996.
-
(1996)
Carcinogenesis
, vol.17
, pp. 1919
-
-
Hand, P.A.1
Inskip, A.2
Gilford, J.3
Alldersea, J.4
Elexpuru-Camiruaga, J.5
Hayes, J.D.6
Jones, P.W.7
Strange, R.C.8
Freyer, A.A.9
-
520
-
-
0029922293
-
Chromosomal localization of the gene for the human theta class glutathione transferase (GSTT1)
-
Webb, G., Vaska, V., Coggan, M., and Board, P., Chromosomal localization of the gene for the human theta class glutathione transferase (GSTT1). Genomics 33, 121, 1996.
-
(1996)
Genomics
, vol.33
, pp. 121
-
-
Webb, G.1
Vaska, V.2
Coggan, M.3
Board, P.4
-
521
-
-
0028231093
-
Human glutathione-S-transferase theta (GSTT1): cDNA cloning and the characterization of a genetic polymorphism
-
Pemble, S., Schroder, K.R., Spencer, S.R., Meyer, D.J., Hallier, E., Bolt, H.M., Ketterer, B., and Taylor, J.B., Human glutathione-S-transferase theta (GSTT1): cDNA cloning and the characterization of a genetic polymorphism. Biochem. J. 300, 271, 1994.
-
(1994)
Biochem. J.
, vol.300
, pp. 271
-
-
Pemble, S.1
Schroder, K.R.2
Spencer, S.R.3
Meyer, D.J.4
Hallier, E.5
Bolt, H.M.6
Ketterer, B.7
Taylor, J.B.8
-
522
-
-
0024449745
-
Metabolism of methyl chloride by human erythrocytes
-
Peter, H., Deutschmann, S., Reichel, C., and Hallier, E., Metabolism of methyl chloride by human erythrocytes. Arch. Toxicol. 63, 351, 1989.
-
(1989)
Arch. Toxicol.
, vol.63
, pp. 351
-
-
Peter, H.1
Deutschmann, S.2
Reichel, C.3
Hallier, E.4
-
523
-
-
0027531684
-
Polymorphism of glutathione conjugation of methyl-bromide, ethylene oxide and dichloromethane in human blood, influence on the induction of sister chromatid exchanges (SCE) in lymphocytes
-
Hallier, E., Langhof, T., Dannappel, D., Leutbecher, M., Schroder, K., Goergens, H.W., Muller, A., and Bolt, H.M., Polymorphism of glutathione conjugation of methyl-bromide, ethylene oxide and dichloromethane in human blood, influence on the induction of sister chromatid exchanges (SCE) in lymphocytes. Arch. Toxicol. 67, 173, 1993.
-
(1993)
Arch. Toxicol.
, vol.67
, pp. 173
-
-
Hallier, E.1
Langhof, T.2
Dannappel, D.3
Leutbecher, M.4
Schroder, K.5
Goergens, H.W.6
Muller, A.7
Bolt, H.M.8
-
524
-
-
0028136267
-
Metabolism of dichloromethane (methylene chloride) to formaldehyde in human erythrocytes: Influence of polymorphism of glutathione transferase theta (GSTT1-1)
-
Hallier, E., Schroder, K.R., Asmuth, K., Dommermuth, A., Aust, B., and Goergens, H.W., Metabolism of dichloromethane (methylene chloride) to formaldehyde in human erythrocytes: influence of polymorphism of glutathione transferase theta (GSTT1-1). Arch. Toxicol. 68, 423, 1994.
-
(1994)
Arch. Toxicol.
, vol.68
, pp. 423
-
-
Hallier, E.1
Schroder, K.R.2
Asmuth, K.3
Dommermuth, A.4
Aust, B.5
Goergens, H.W.6
-
525
-
-
0028595674
-
Polymorphic distribution of glutathione transferase activity with methyl chloride in human blood
-
Warholm, M., Alexandrie, A.-K., Hogberg, J., Sigvardsson, K., and Rannug, A., Polymorphic distribution of glutathione transferase activity with methyl chloride in human blood. Pharmacogenetics 4. 307, 1994.
-
(1994)
Pharmacogenetics
, vol.4
, pp. 307
-
-
Warholm, M.1
Alexandrie, A.-K.2
Hogberg, J.3
Sigvardsson, K.4
Rannug, A.5
-
526
-
-
0028917470
-
Polymorphism in the glutathione conjugation activity of human erythrocytes toward ethylene dibromide and 1,2-epoxy-3-(p-nitrophenoxy)-propane
-
Ploemen, J.H.T.M., Wormhoudt, L.W., van Ommen, B., Commandeur, J.N.M., Vermeulen, N.P.E., and van Bladeren, P.J., Polymorphism in the glutathione conjugation activity of human erythrocytes toward ethylene dibromide and 1,2-epoxy-3-(p-nitrophenoxy)-propane. Biochim. Biophys. Acta, 1243, 469, 1995.
-
(1995)
Biochim. Biophys. Acta
, vol.1243
, pp. 469
-
-
Ploemen, J.H.T.M.1
Wormhoudt, L.W.2
Van Ommen, B.3
Commandeur, J.N.M.4
Vermeulen, N.P.E.5
Van Bladeren, P.J.6
-
527
-
-
0029947171
-
Human glutathione-S-transferase T1-1 enhances mutagenicity of 1,2-dibromoethane, dibromomethane and 1,2,3,4-diepoxybutane in Salmonella typhimurium
-
Thier, R., Pemble, S.E., Kramer, H., Taylor, J.B., Guengerich, F.P., and Ketterer, B., Human glutathione-S-transferase T1-1 enhances mutagenicity of 1,2-dibromoethane, dibromomethane and 1,2,3,4-diepoxybutane in Salmonella typhimurium. Carcinogenesis 17, 163, 1996.
-
(1996)
Carcinogenesis
, vol.17
, pp. 163
-
-
Thier, R.1
Pemble, S.E.2
Kramer, H.3
Taylor, J.B.4
Guengerich, F.P.5
Ketterer, B.6
-
528
-
-
0025819022
-
Bimodal distribution of sensitivity to SCE induction by diepoxybutane in human lymphocytes. II. Relationship to baseline SCE frequency
-
Kelsey, K.T., Christiani, D.C., and Wiencke, J.K., Bimodal distribution of sensitivity to SCE induction by diepoxybutane in human lymphocytes. II. Relationship to baseline SCE frequency. Mutat. Res. 248, 27, 1991.
-
(1991)
Mutat. Res.
, vol.248
, pp. 27
-
-
Kelsey, K.T.1
Christiani, D.C.2
Wiencke, J.K.3
-
529
-
-
0029016586
-
Glutathione-S-transferase (GST) theta polymorphism influences background SCE rate
-
Schroder, K.R, Wiebel, F.A., Reich, S., Dannappel, D., Bolt, H.M., and Hallier, E., Glutathione-S-transferase (GST) theta polymorphism influences background SCE rate. Arch. Toxicol. 69, 505, 1995.
-
(1995)
Arch. Toxicol.
, vol.69
, pp. 505
-
-
Schroder, K.R.1
Wiebel, F.A.2
Reich, S.3
Dannappel, D.4
Bolt, H.M.5
Hallier, E.6
-
530
-
-
0025944342
-
Individual susceptibility to induced chromosome damage and its implications for detecting genotoxic exposures in human populations
-
Wiencke, J.K., Wrensch, M.R., Miike, R., and Petrakis, N.L., Individual susceptibility to induced chromosome damage and its implications for detecting genotoxic exposures in human populations. Cancer Res. 51, 5266, 1991.
-
(1991)
Cancer Res.
, vol.51
, pp. 5266
-
-
Wiencke, J.K.1
Wrensch, M.R.2
Miike, R.3
Petrakis, N.L.4
-
531
-
-
0024581717
-
Unsaturated lipids and intestinal bacteria as sources of endogenous production of ethene and ethylene oxide
-
Tornqvist, M., Gustafsson, B., Kautiainen, A., Harms-Ringdahl, M., Granath, F., and Ehrenberg, L., Unsaturated lipids and intestinal bacteria as sources of endogenous production of ethene and ethylene oxide. Carcinogenesis 10, 39, 1989.
-
(1989)
Carcinogenesis
, vol.10
, pp. 39
-
-
Tornqvist, M.1
Gustafsson, B.2
Kautiainen, A.3
Harms-Ringdahl, M.4
Granath, F.5
Ehrenberg, L.6
-
532
-
-
0025872933
-
Bimodal distribution of sensitivity to SCE induction by diepoxybutane in human lymphocytes. I. Correlation with chromosomal abberations
-
Wiencke, J.K., Christiani, D.C., and Kelsey, K.T., Bimodal distribution of sensitivity to SCE induction by diepoxybutane in human lymphocytes. I. Correlation with chromosomal abberations. Mutat. Res. 248, 17, 1991.
-
(1991)
Mutat. Res.
, vol.248
, pp. 17
-
-
Wiencke, J.K.1
Christiani, D.C.2
Kelsey, K.T.3
-
533
-
-
0013524441
-
Mutagenicity of 1,2,3,4-butadiene diepoxide is altered by mammalian θ-class glutathione-S-transferase
-
Thier, R., Persmark, M., Pemble, S.E., Taylor, J.B., Ketterer, B., and Guengerich, F.P, Mutagenicity of 1,2,3,4-butadiene diepoxide is altered by mammalian θ-class glutathione-S-transferase. Naunyn Schmiedeberg's Arch. Pharmacol. 481 (Suppl.), 349, 1992.
-
(1992)
Naunyn Schmiedeberg's Arch. Pharmacol.
, vol.481
, Issue.SUPPL.
, pp. 349
-
-
Thier, R.1
Persmark, M.2
Pemble, S.E.3
Taylor, J.B.4
Ketterer, B.5
Guengerich, F.P.6
-
534
-
-
0028990060
-
Role of GSTT1 and GSTM1 genotypes in determining individual sensitivity to sister chromatid exchange induction by diepoxybutane in cultured human lymphocytes
-
Norppa, H., Hirvonen, A., Jarventaus, H., Uuskula, M., Tasa, G., Ojajarvi, A., and Sorsa, M., Role of GSTT1 and GSTM1 genotypes in determining individual sensitivity to sister chromatid exchange induction by diepoxybutane in cultured human lymphocytes. Carcinogenesis 16, 1261, 1995.
-
(1995)
Carcinogenesis
, vol.16
, pp. 1261
-
-
Norppa, H.1
Hirvonen, A.2
Jarventaus, H.3
Uuskula, M.4
Tasa, G.5
Ojajarvi, A.6
Sorsa, M.7
-
535
-
-
0029928663
-
Influence of erythrocyte glutathione-S-transferase T1 on sister chromatid exchanges induced by diepoxybutane in cultured human lymphocytes
-
Pelin, K., Hirvonen, A., and Norppa, H., Influence of erythrocyte glutathione-S-transferase T1 on sister chromatid exchanges induced by diepoxybutane in cultured human lymphocytes. Mutagenesis 11, 213, 1996.
-
(1996)
Mutagenesis
, vol.11
, pp. 213
-
-
Pelin, K.1
Hirvonen, A.2
Norppa, H.3
-
536
-
-
0029983811
-
Repeated analysis of sister chromatid exchange induction by diepoxybutane in cultured human lymphocytes: Effect of glutathione-S-transferase T1 and M1 genotype
-
Landi, S., Ponzanelli, I., Hirvonen, A., Norppa, H., and Barale, R., Repeated analysis of sister chromatid exchange induction by diepoxybutane in cultured human lymphocytes: effect of glutathione-S-transferase T1 and M1 genotype. Mutat. Res. 351, 79, 1996.
-
(1996)
Mutat. Res.
, vol.351
, pp. 79
-
-
Landi, S.1
Ponzanelli, I.2
Hirvonen, A.3
Norppa, H.4
Barale, R.5
-
537
-
-
0031427094
-
Identification of genetic polymorphisms at the glutathione-S-transferase Pi locus and association with susceptibility to bladder, testicular and prostate cancer
-
Harries, L.W., Stubbins, M.J., Forman, D., Howard, G.C., and Wolf, C.R., Identification of genetic polymorphisms at the glutathione-S-transferase Pi locus and association with susceptibility to bladder, testicular and prostate cancer. Carcinogenesis, 18, 641, 1997.
-
(1997)
Carcinogenesis
, vol.18
, pp. 641
-
-
Harries, L.W.1
Stubbins, M.J.2
Forman, D.3
Howard, G.C.4
Wolf, C.R.5
-
538
-
-
0001638445
-
Epoxide hydrolases
-
Mulder, G.J., Ed.
-
Guenthner, T.M., Epoxide hydrolases. In: Conjugation Reactions in Drug Metabolism, Mulder, G.J., Ed., 1990, 365-404.
-
(1990)
Conjugation Reactions in Drug Metabolism
, pp. 365-404
-
-
Guenthner, T.M.1
-
539
-
-
0023835220
-
Human microsomal xenobiotic epoxide hydrolase. Complementary DNA sequence, complementary DNA-directed expression in COS-1 cells, and chromosomal localization
-
Skoda, R.C., Demierre, A., McBride, O.W., Gonzalez, F.J., and Meyer, U.A., Human microsomal xenobiotic epoxide hydrolase. Complementary DNA sequence, complementary DNA-directed expression in COS-1 cells, and chromosomal localization. J. Biol. Chem. 263, 1549, 1988.
-
(1988)
J. Biol. Chem.
, vol.263
, pp. 1549
-
-
Skoda, R.C.1
Demierre, A.2
McBride, O.W.3
Gonzalez, F.J.4
Meyer, U.A.5
-
540
-
-
0028295652
-
Human microsomal epoxide hydrolase: Genetic polymorphism and functional expression in vitro of amino acid variants
-
Hassett, C., Aicher, L., Sidhu, J.S., and Omiecinski, C.J., Human microsomal epoxide hydrolase: genetic polymorphism and functional expression in vitro of amino acid variants. Hum. Mol. Genet. 3, 421, 1994.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 421
-
-
Hassett, C.1
Aicher, L.2
Sidhu, J.S.3
Omiecinski, C.J.4
-
541
-
-
0031568236
-
Human hepatic microsomal epoxide hydrolase: Comparative analysis of polymorphic expression
-
Hassett, C., Lin, J., Carty, C.L., Laurenzana, E.M., and Omiecinski, C.J., Human hepatic microsomal epoxide hydrolase: comparative analysis of polymorphic expression. Arch. Biochem. Biophys. 337, 275, 1997.
-
(1997)
Arch. Biochem. Biophys.
, vol.337
, pp. 275
-
-
Hassett, C.1
Lin, J.2
Carty, C.L.3
Laurenzana, E.M.4
Omiecinski, C.J.5
-
542
-
-
0028352066
-
Characterization of the microsomal epoxide hydrolase gene in patients with anticonvulsant adverse drug reactions
-
Gaedigk, A., Spielberg, S.P., and Grant, D.M., Characterization of the microsomal epoxide hydrolase gene in patients with anticonvulsant adverse drug reactions. Pharmacogenetics 4, 142, 1994.
-
(1994)
Pharmacogenetics
, vol.4
, pp. 142
-
-
Gaedigk, A.1
Spielberg, S.P.2
Grant, D.M.3
-
543
-
-
0028880593
-
Genetic analysis of microsomal epoxide hydrolase in patients with carbamazepine hypersensitivity
-
Green, V.J., Pirmohamed, M., Kitteringham, N.R., Gaedigk, A., Grant, D.M., Boxer, M., Burchell, B., and Park, B.K., Genetic analysis of microsomal epoxide hydrolase in patients with carbamazepine hypersensitivity. Biochem. Pharmacol. 50, 1353, 1995.
-
(1995)
Biochem. Pharmacol.
, vol.50
, pp. 1353
-
-
Green, V.J.1
Pirmohamed, M.2
Kitteringham, N.R.3
Gaedigk, A.4
Grant, D.M.5
Boxer, M.6
Burchell, B.7
Park, B.K.8
-
544
-
-
0030612534
-
Aflatoxin B1 8,9-epoxide hydrolysis in the presence of rat and human epoxide hydrolase Chem
-
Johnson, W.W., Yamazaki, H., Shimada, T., Ueng, Y.F., and Guengerich, F.P., Aflatoxin B1 8,9-epoxide hydrolysis in the presence of rat and human epoxide hydrolase Chem. Res. Toxicol. 10, 672, 1997.
-
(1997)
Res. Toxicol.
, vol.10
, pp. 672
-
-
Johnson, W.W.1
Yamazaki, H.2
Shimada, T.3
Ueng, Y.F.4
Guengerich, F.P.5
-
545
-
-
0029976725
-
Involvement of cytochrome P450, glutathione-S-transferase, and epoxide hydrolase in the metabolism of aflatoxin B1 and relevance to risk of human liver cancer
-
Guengerich, F.P., Johnson, W.W., Ueng, Y.-F., Yamazaki, H., and Shimada, T., Involvement of cytochrome P450, glutathione-S-transferase, and epoxide hydrolase in the metabolism of aflatoxin B1 and relevance to risk of human liver cancer. Environ. Health Perspect. 104(Suppl. 3), 557, 1996.
-
(1996)
Environ. Health Perspect.
, vol.104
, Issue.SUPPL. 3
, pp. 557
-
-
Guengerich, F.P.1
Johnson, W.W.2
Ueng, Y.-F.3
Yamazaki, H.4
Shimada, T.5
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