-
1
-
-
0031826288
-
Hypothesis: comparisons of inter- and intra-individual variations can substitute for twin studies in drug research
-
Kalow W., Tang B.K., Endrenyi L. Hypothesis: comparisons of inter- and intra-individual variations can substitute for twin studies in drug research. Pharmacogenetics 1998, 8(4):283-289.
-
(1998)
Pharmacogenetics
, vol.8
, Issue.4
, pp. 283-289
-
-
Kalow, W.1
Tang, B.K.2
Endrenyi, L.3
-
2
-
-
77956930010
-
Germline genetic variation, cancer outcome, and pharmacogenetics
-
Coate L., Cuffe S., Horgan A., Hung R.J., Christiani D., Liu G. Germline genetic variation, cancer outcome, and pharmacogenetics. J Clin Oncol 2010, 28(26):4029-4037.
-
(2010)
J Clin Oncol
, vol.28
, Issue.26
, pp. 4029-4037
-
-
Coate, L.1
Cuffe, S.2
Horgan, A.3
Hung, R.J.4
Christiani, D.5
Liu, G.6
-
3
-
-
0037421590
-
Drug therapy-pharmacogenomics-drug disposition, drug targets, and side effects
-
Evans W.E., Mcleod H.L. Drug therapy-pharmacogenomics-drug disposition, drug targets, and side effects. N Engl J Med 2003, 348(6):538-549.
-
(2003)
N Engl J Med
, vol.348
, Issue.6
, pp. 538-549
-
-
Evans, W.E.1
Mcleod, H.L.2
-
4
-
-
0032212759
-
Thiopurine methyltransferase genotype predicts therapy-limiting severe toxicity from azathioprine
-
Black A.J., Mcleod H.L., Capell H.A., et al. Thiopurine methyltransferase genotype predicts therapy-limiting severe toxicity from azathioprine. Ann Intern Med 1998, 129(9):716-718.
-
(1998)
Ann Intern Med
, vol.129
, Issue.9
, pp. 716-718
-
-
Black, A.J.1
Mcleod, H.L.2
Capell, H.A.3
-
5
-
-
67649873216
-
Extent of MGMT promoter methylation correlates with outcome in glioblastomas given temozolomide and radiotherapy
-
Dunn J., Baborie A., Alam F., et al. Extent of MGMT promoter methylation correlates with outcome in glioblastomas given temozolomide and radiotherapy. Br J Cancer 2009, 101(1):124-131.
-
(2009)
Br J Cancer
, vol.101
, Issue.1
, pp. 124-131
-
-
Dunn, J.1
Baborie, A.2
Alam, F.3
-
6
-
-
34548385836
-
Translating pharmacogenomics: challenges on the road to the clinic
-
Swen J.J., Huizinga T.W., Gelderblom H., et al. Translating pharmacogenomics: challenges on the road to the clinic. PLoS Med 2007, 4(8):1317-1324.
-
(2007)
PLoS Med
, vol.4
, Issue.8
, pp. 1317-1324
-
-
Swen, J.J.1
Huizinga, T.W.2
Gelderblom, H.3
-
7
-
-
33845691198
-
Toward individualized treatment: prediction of anticancer drug disposition and toxicity with pharmacogenetics
-
Deeken J.F., Figg W.D., Bates S.E., Sparreboom A. Toward individualized treatment: prediction of anticancer drug disposition and toxicity with pharmacogenetics. Anticancer Drugs 2007, 18(2):111-126.
-
(2007)
Anticancer Drugs
, vol.18
, Issue.2
, pp. 111-126
-
-
Deeken, J.F.1
Figg, W.D.2
Bates, S.E.3
Sparreboom, A.4
-
8
-
-
77956938954
-
Impact of age, sex, and comorbidity on cancer therapy and disease progression
-
Pal S.K., Hurria A. Impact of age, sex, and comorbidity on cancer therapy and disease progression. J Clin Oncol 2010, 28(26):4086-4093.
-
(2010)
J Clin Oncol
, vol.28
, Issue.26
, pp. 4086-4093
-
-
Pal, S.K.1
Hurria, A.2
-
9
-
-
84861652799
-
Influence of gender on treatment outcome and toxicity in small cell lung cancer (SCLC)
-
Singh S., Parulekar W., Murray N., et al. Influence of gender on treatment outcome and toxicity in small cell lung cancer (SCLC). J Clin Oncol 2004, 22(14):626S.
-
(2004)
J Clin Oncol
, vol.22
, Issue.14
-
-
Singh, S.1
Parulekar, W.2
Murray, N.3
-
10
-
-
77950953973
-
Sex-dependent differences in cytochrome P450 3A activity as assessed by midazolam disposition in humans: a meta-analysis
-
Hu Z.Y., Zhao Y.S. Sex-dependent differences in cytochrome P450 3A activity as assessed by midazolam disposition in humans: a meta-analysis. Drug Metab Dispos 2010, 38(5):817-823.
-
(2010)
Drug Metab Dispos
, vol.38
, Issue.5
, pp. 817-823
-
-
Hu, Z.Y.1
Zhao, Y.S.2
-
11
-
-
68049140789
-
Cancer pharmacoethnicity: ethnic differences in susceptibility to the effects of chemotherapy
-
O'Donnell P.H., Dolan M.E. Cancer pharmacoethnicity: ethnic differences in susceptibility to the effects of chemotherapy. Clin Cancer Res 2009, 15(15):4806-4814.
-
(2009)
Clin Cancer Res
, vol.15
, Issue.15
, pp. 4806-4814
-
-
O'Donnell, P.H.1
Dolan, M.E.2
-
12
-
-
33749350447
-
Increased prevalence of dihydropyrimidine dehydrogenase deficiency in African-Americans compared with Caucasians
-
Mattison L.K., Fourie J., Desmond R.A., Modak A., Saif M.W., Diasio R.B. Increased prevalence of dihydropyrimidine dehydrogenase deficiency in African-Americans compared with Caucasians. Clin Cancer Res 2006, 12(18):5491-5495.
-
(2006)
Clin Cancer Res
, vol.12
, Issue.18
, pp. 5491-5495
-
-
Mattison, L.K.1
Fourie, J.2
Desmond, R.A.3
Modak, A.4
Saif, M.W.5
Diasio, R.B.6
-
13
-
-
0031938705
-
Pharmacokinetics of anticancer agents in patients with impaired liver function
-
Donelli M.G., Zucchetti M., Munzone E., D'Incalci M., Crosignani A. Pharmacokinetics of anticancer agents in patients with impaired liver function. Eur J Cancer 1998, 34(1):33-46.
-
(1998)
Eur J Cancer
, vol.34
, Issue.1
, pp. 33-46
-
-
Donelli, M.G.1
Zucchetti, M.2
Munzone, E.3
D'Incalci, M.4
Crosignani, A.5
-
14
-
-
75649093034
-
Activity of sulfotransferase 1A1 is dramatically upregulated in patients with hepatocellular carcinoma secondary to chronic hepatitis B virus infection
-
Wang X.R., Qu Z.Q., Li X.D., et al. Activity of sulfotransferase 1A1 is dramatically upregulated in patients with hepatocellular carcinoma secondary to chronic hepatitis B virus infection. Cancer Sci. 2010, 101(2):412-415.
-
(2010)
Cancer Sci.
, vol.101
, Issue.2
, pp. 412-415
-
-
Wang, X.R.1
Qu, Z.Q.2
Li, X.D.3
-
15
-
-
0037194409
-
Hepatic cytochrome P450 3A drug metabolism is reduced in cancer patients who have an acute-phase response
-
Rivory L.P., Slaviero K.A., Clarke S.J. Hepatic cytochrome P450 3A drug metabolism is reduced in cancer patients who have an acute-phase response. Br J Cancer 2002, 87(3):277-280.
-
(2002)
Br J Cancer
, vol.87
, Issue.3
, pp. 277-280
-
-
Rivory, L.P.1
Slaviero, K.A.2
Clarke, S.J.3
-
16
-
-
0041764982
-
CYP2E1 activity before and after weight loss in morbidly obese subjects with nonalcoholic fatty liver disease
-
Emery M.G., Fisher J.M., Chien J.Y., et al. CYP2E1 activity before and after weight loss in morbidly obese subjects with nonalcoholic fatty liver disease. Hepatology 2003, 38(2):428-435.
-
(2003)
Hepatology
, vol.38
, Issue.2
, pp. 428-435
-
-
Emery, M.G.1
Fisher, J.M.2
Chien, J.Y.3
-
17
-
-
0020569302
-
Enhanced glucuronide conjugation of drugs in obesity - studies of lorazepam, oxazepam, and acetaminophen
-
Abernethy D.R., Greenblatt D.J., Divoll M., Shader R.I. Enhanced glucuronide conjugation of drugs in obesity - studies of lorazepam, oxazepam, and acetaminophen. J Lab Clin Med 1983, 101(6):873-880.
-
(1983)
J Lab Clin Med
, vol.101
, Issue.6
, pp. 873-880
-
-
Abernethy, D.R.1
Greenblatt, D.J.2
Divoll, M.3
Shader, R.I.4
-
18
-
-
0033493296
-
Longitudinal study of weight, appetite, performance status, and inflammation in advanced gastrointestinal cancer
-
O'Gorman P., McMillan D.C., McArdle C.S. Longitudinal study of weight, appetite, performance status, and inflammation in advanced gastrointestinal cancer. Nutr Cancer 1999, 35(2):127-129.
-
(1999)
Nutr Cancer
, vol.35
, Issue.2
, pp. 127-129
-
-
O'Gorman, P.1
McMillan, D.C.2
McArdle, C.S.3
-
19
-
-
4043179101
-
Drug interactions in oncology
-
Beijnen J.H., Schellens J.H.M. Drug interactions in oncology. Lancet Oncol 2004, 5(8):489-496.
-
(2004)
Lancet Oncol
, vol.5
, Issue.8
, pp. 489-496
-
-
Beijnen, J.H.1
Schellens, J.H.M.2
-
20
-
-
2042474777
-
Effect of cytochrome P450 3A4 inhibition on the pharmacokinetics of docetaxel
-
Engels F.K., ten Tije A.J., Baker S.D., et al. Effect of cytochrome P450 3A4 inhibition on the pharmacokinetics of docetaxel. Clin Pharmacol Ther 2004, 75(5):448-454.
-
(2004)
Clin Pharmacol Ther
, vol.75
, Issue.5
, pp. 448-454
-
-
Engels, F.K.1
ten Tije, A.J.2
Baker, S.D.3
-
21
-
-
0037151365
-
Effects of St. John's wort on irinotecan metabolism
-
Mathijssen R.H.J., Verweij J., de Bruijn P., Loos W.J., Sparreboom A. Effects of St. John's wort on irinotecan metabolism. J Natl Cancer Inst 2002, 94(16):1247-1249.
-
(2002)
J Natl Cancer Inst
, vol.94
, Issue.16
, pp. 1247-1249
-
-
Mathijssen, R.H.J.1
Verweij, J.2
de Bruijn, P.3
Loos, W.J.4
Sparreboom, A.5
-
22
-
-
0034007388
-
Phenotyping of drug-metabolizing enzymes in adults: a review of in-vivo cytochrome P450 phenotyping probes
-
Streetman D.S., Bertino J.S., Nafziger A.N. Phenotyping of drug-metabolizing enzymes in adults: a review of in-vivo cytochrome P450 phenotyping probes. Pharmacogenetics 2000, 10(3):187-216.
-
(2000)
Pharmacogenetics
, vol.10
, Issue.3
, pp. 187-216
-
-
Streetman, D.S.1
Bertino, J.S.2
Nafziger, A.N.3
-
23
-
-
13244298666
-
Individualised cancer chemotherapy: strategies and performance of prospective studies on therapeutic drug monitoring with dose adaptation: a review
-
de Jonge M.E., Huitema A.D., Schellens J.H., Rodenhuis S., Beijnen J.H. Individualised cancer chemotherapy: strategies and performance of prospective studies on therapeutic drug monitoring with dose adaptation: a review. Clin Pharmacokinet 2005, 44(2):147-173.
-
(2005)
Clin Pharmacokinet
, vol.44
, Issue.2
, pp. 147-173
-
-
de Jonge, M.E.1
Huitema, A.D.2
Schellens, J.H.3
Rodenhuis, S.4
Beijnen, J.H.5
-
24
-
-
79953193793
-
Mitotane has a strong and a durable inducing effect on CYP3A4 activity
-
van Erp N.P., Guchelaar H.J., Ploeger B.A., Romijn J.A., den Hartigh J., Gelderblom H. Mitotane has a strong and a durable inducing effect on CYP3A4 activity. Eur J Endocrinol 2011, 164(4):621-626.
-
(2011)
Eur J Endocrinol
, vol.164
, Issue.4
, pp. 621-626
-
-
van Erp, N.P.1
Guchelaar, H.J.2
Ploeger, B.A.3
Romijn, J.A.4
den Hartigh, J.5
Gelderblom, H.6
-
25
-
-
0036731724
-
Explaining interindividual variability of docetaxel pharmacokinetics and pharmacodynamics in Asians through phenotyping and genotyping strategies
-
Goh B.C., Lee S.C., Wang L.Z., et al. Explaining interindividual variability of docetaxel pharmacokinetics and pharmacodynamics in Asians through phenotyping and genotyping strategies. J Clin Oncol 2002, 20(17):3683-3690.
-
(2002)
J Clin Oncol
, vol.20
, Issue.17
, pp. 3683-3690
-
-
Goh, B.C.1
Lee, S.C.2
Wang, L.Z.3
-
26
-
-
33846607427
-
Appropriate phenotyping procedures for drug metabolizing enzymes and transporters in humans and their simultaneous use in the "cocktail" approach
-
Fuhr U., Jetter A., Kirchheiner J. Appropriate phenotyping procedures for drug metabolizing enzymes and transporters in humans and their simultaneous use in the "cocktail" approach. Clin Pharmacol Ther 2007, 81(2):270-283.
-
(2007)
Clin Pharmacol Ther
, vol.81
, Issue.2
, pp. 270-283
-
-
Fuhr, U.1
Jetter, A.2
Kirchheiner, J.3
-
27
-
-
70449640436
-
(13)C breath tests in personalized medicine: fiction or reality?
-
Modak A.S. (13)C breath tests in personalized medicine: fiction or reality?. Exp Rev Mol Diagn 2009, 9(8):805-815.
-
(2009)
Exp Rev Mol Diagn
, vol.9
, Issue.8
, pp. 805-815
-
-
Modak, A.S.1
-
28
-
-
3042676313
-
Oral administration of a low dose of midazolam (75μg) as an in vivo probe for CYP3A activity
-
Eap C.B., Buclin T., Cucchia G., et al. Oral administration of a low dose of midazolam (75μg) as an in vivo probe for CYP3A activity. Eur J Clin Pharmacol 2004, 60(4):237-246.
-
(2004)
Eur J Clin Pharmacol
, vol.60
, Issue.4
, pp. 237-246
-
-
Eap, C.B.1
Buclin, T.2
Cucchia, G.3
-
29
-
-
79956321178
-
Evaluation of 6 beta-hydroxycortisol, 6 beta-hydroxycortisone, and a combination of the two as endogenous probes for inhibition of CYP3A4 in vivo
-
Peng C.C., Templeton I., Thummel K.E., Davis C., Kunze K.L., Isoherranen N. Evaluation of 6 beta-hydroxycortisol, 6 beta-hydroxycortisone, and a combination of the two as endogenous probes for inhibition of CYP3A4 in vivo. Clin Pharmacol Ther 2011, 89(6):888-895.
-
(2011)
Clin Pharmacol Ther
, vol.89
, Issue.6
, pp. 888-895
-
-
Peng, C.C.1
Templeton, I.2
Thummel, K.E.3
Davis, C.4
Kunze, K.L.5
Isoherranen, N.6
-
30
-
-
78650982224
-
4 beta-hydroxycholesterol, an endogenous marker of CYP3A4/5 activity in humans
-
Diczfalusy U., Nylen H., Elander P., Bertilsson L. 4 beta-hydroxycholesterol, an endogenous marker of CYP3A4/5 activity in humans. Br J Clin Pharmacol 2011, 71(2):183-189.
-
(2011)
Br J Clin Pharmacol
, vol.71
, Issue.2
, pp. 183-189
-
-
Diczfalusy, U.1
Nylen, H.2
Elander, P.3
Bertilsson, L.4
-
31
-
-
0026750647
-
The Human Hepatic cytochromes-p450 involved in drug-metabolism
-
Wrighton S.A., Stevens J.C. The Human Hepatic cytochromes-p450 involved in drug-metabolism. Crit Rev Toxicol 1992, 22(1):1-21.
-
(1992)
Crit Rev Toxicol
, vol.22
, Issue.1
, pp. 1-21
-
-
Wrighton, S.A.1
Stevens, J.C.2
-
32
-
-
72949119743
-
Substrate specificity, regulation, and polymorphism of human cytochrome P450 2B6
-
Mo S.L., Liu Y.H., Duan W., Wei M.Q., Kanwar J.R., Zhou S.F. Substrate specificity, regulation, and polymorphism of human cytochrome P450 2B6. Curr Drug Metab 2009, 10(7):730-753.
-
(2009)
Curr Drug Metab
, vol.10
, Issue.7
, pp. 730-753
-
-
Mo, S.L.1
Liu, Y.H.2
Duan, W.3
Wei, M.Q.4
Kanwar, J.R.5
Zhou, S.F.6
-
33
-
-
26944481572
-
Clinical pharmacokinetics of cyclophosphamide
-
de Jonge M.E., Huitema A.D.R., Rodenhuis S., Beijnen J.H. Clinical pharmacokinetics of cyclophosphamide. Clin Pharmacokinet 2005, 44(11):1135-1164.
-
(2005)
Clin Pharmacokinet
, vol.44
, Issue.11
, pp. 1135-1164
-
-
de Jonge, M.E.1
Huitema, A.D.R.2
Rodenhuis, S.3
Beijnen, J.H.4
-
34
-
-
0038729519
-
Bioactivation of cyclophosphamide: the role of polymorphic CYP2C enzymes
-
Griskevicius L., Yasar U., Sandberg M., et al. Bioactivation of cyclophosphamide: the role of polymorphic CYP2C enzymes. Eur J Clin Pharmacol 2003, 59(2):103-109.
-
(2003)
Eur J Clin Pharmacol
, vol.59
, Issue.2
, pp. 103-109
-
-
Griskevicius, L.1
Yasar, U.2
Sandberg, M.3
-
35
-
-
14144254437
-
Effects of co-medicated drugs on cyclophosphamide bioactivation in human liver microsomes
-
de Jonge M.E., Huitema A.D.R., van Dam S.M., Rodenhuis S., Beijnen J.H. Effects of co-medicated drugs on cyclophosphamide bioactivation in human liver microsomes. Anticancer Drugs 2005, 16(3):331-336.
-
(2005)
Anticancer Drugs
, vol.16
, Issue.3
, pp. 331-336
-
-
de Jonge, M.E.1
Huitema, A.D.R.2
van Dam, S.M.3
Rodenhuis, S.4
Beijnen, J.H.5
-
36
-
-
84861689385
-
-
Draft FDA guidance for industry. September Available from:
-
Draft FDA guidance for industry. September 2006. Available from: http://www.fda.gov/downloads/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/ucm072101.pdf.
-
(2006)
-
-
-
37
-
-
0142188754
-
Bupropion and 4-OH-bupropion pharmacokinetics in relation to genetic polymorphisms in CYP2B6
-
Kirchheiner J., Klein C., Meineke I., et al. Bupropion and 4-OH-bupropion pharmacokinetics in relation to genetic polymorphisms in CYP2B6. Pharmacogenetics 2003, 13(10):619-626.
-
(2003)
Pharmacogenetics
, vol.13
, Issue.10
, pp. 619-626
-
-
Kirchheiner, J.1
Klein, C.2
Meineke, I.3
-
38
-
-
40749104678
-
Stereoselective bupropion hydroxylation as an in vivo phenotypic probe for cytochrome P4502B6 (CYP2B6) activity
-
Kharasch E.D., Mitchell D., Coles R. Stereoselective bupropion hydroxylation as an in vivo phenotypic probe for cytochrome P4502B6 (CYP2B6) activity. J Clin Pharmacol 2008, 48(4):464-474.
-
(2008)
J Clin Pharmacol
, vol.48
, Issue.4
, pp. 464-474
-
-
Kharasch, E.D.1
Mitchell, D.2
Coles, R.3
-
39
-
-
70649100416
-
Cytochrome P450 2C8 pharmacogenetics: a review of clinical studies
-
Daily E.B., Aquilante C.L. Cytochrome P450 2C8 pharmacogenetics: a review of clinical studies. Pharmacogenomics 2009, 10(9):1489-1510.
-
(2009)
Pharmacogenomics
, vol.10
, Issue.9
, pp. 1489-1510
-
-
Daily, E.B.1
Aquilante, C.L.2
-
40
-
-
28144461394
-
Association of Cyp2C8, Cyp3A4, Cyp3A5, and Abcb1 polymorphisms with the pharmacokinetics of paclitaxel
-
Henningsson A., Marsh S., Loos W.J., et al. Association of Cyp2C8, Cyp3A4, Cyp3A5, and Abcb1 polymorphisms with the pharmacokinetics of paclitaxel. Clin Cancer Res 2005, 11(22):8097-8104.
-
(2005)
Clin Cancer Res
, vol.11
, Issue.22
, pp. 8097-8104
-
-
Henningsson, A.1
Marsh, S.2
Loos, W.J.3
-
41
-
-
0030758131
-
Identification of the polymorphically expressed CYP2C19 and the wild-type CYP2C9-ILE359 allele as low-K-m catalysts of cyclophosphamide and ifosfamide activation
-
Chang T.K.H., Yu L., Goldstein J.A., Waxman D.J. Identification of the polymorphically expressed CYP2C19 and the wild-type CYP2C9-ILE359 allele as low-K-m catalysts of cyclophosphamide and ifosfamide activation. Pharmacogenetics 1997, 7(3):211-221.
-
(1997)
Pharmacogenetics
, vol.7
, Issue.3
, pp. 211-221
-
-
Chang, T.K.H.1
Yu, L.2
Goldstein, J.A.3
Waxman, D.J.4
-
42
-
-
18544389188
-
The influence of CYP2B6, CYP2C9 and CYP2D6 genotypes on the formation of the potent antioestrogen Z-4-hydroxy-tamoxifen in human liver
-
Coller J.K., Krebsfaenger N., Klein K., et al. The influence of CYP2B6, CYP2C9 and CYP2D6 genotypes on the formation of the potent antioestrogen Z-4-hydroxy-tamoxifen in human liver. Br J Clin Pharmacol 2002, 54(2):157-167.
-
(2002)
Br J Clin Pharmacol
, vol.54
, Issue.2
, pp. 157-167
-
-
Coller, J.K.1
Krebsfaenger, N.2
Klein, K.3
-
43
-
-
78149470864
-
Polymorphisms of human cytochrome P450 2C9 and the functional relevance
-
Zhou S.F., Zhou Z.W., Huang M. Polymorphisms of human cytochrome P450 2C9 and the functional relevance. Toxicology 2010, 278(2):165-188.
-
(2010)
Toxicology
, vol.278
, Issue.2
, pp. 165-188
-
-
Zhou, S.F.1
Zhou, Z.W.2
Huang, M.3
-
44
-
-
44449142319
-
Influence of polymorphisms of drug metabolizing enzymes (CYP2136, CYP2C9, CYPX19, CYP3A4, CYP3A5, GSTA1, GSTP1, ALDH1A1 and ALDH3A1) on the pharmacokinetics of cyclophosphamide and 4-hydroxycyclophosphamide
-
Ekhart C., Doodeman V.D., Rodenhuis S., Smits P.H.M., Beijnen J.H., Huitema A.D.R. Influence of polymorphisms of drug metabolizing enzymes (CYP2136, CYP2C9, CYPX19, CYP3A4, CYP3A5, GSTA1, GSTP1, ALDH1A1 and ALDH3A1) on the pharmacokinetics of cyclophosphamide and 4-hydroxycyclophosphamide. Pharmacogenet Genomics 2008, 18(6):515-523.
-
(2008)
Pharmacogenet Genomics
, vol.18
, Issue.6
, pp. 515-523
-
-
Ekhart, C.1
Doodeman, V.D.2
Rodenhuis, S.3
Smits, P.H.M.4
Beijnen, J.H.5
Huitema, A.D.R.6
-
45
-
-
78149487509
-
Cyclophosphamide-metabolizing enzyme polymorphisms and survival outcomes after adjuvant chemotherapy for node-positive breast cancer: a retrospective cohort study
-
Gor P.P., Su H.I., Gray R.J., et al. Cyclophosphamide-metabolizing enzyme polymorphisms and survival outcomes after adjuvant chemotherapy for node-positive breast cancer: a retrospective cohort study. Breast Cancer Res 2010, 12(3).
-
(2010)
Breast Cancer Res
, vol.12
, Issue.3
-
-
Gor, P.P.1
Su, H.I.2
Gray, R.J.3
-
46
-
-
67650602114
-
Relative impact of genotype and enzyme induction on the metabolic capacity of CYP2C9 in healthy volunteers
-
Vormfelde S.V., Brockmoller J., Bauer S., et al. Relative impact of genotype and enzyme induction on the metabolic capacity of CYP2C9 in healthy volunteers. Clin Pharmacol Ther 2009, 86(1):54-61.
-
(2009)
Clin Pharmacol Ther
, vol.86
, Issue.1
, pp. 54-61
-
-
Vormfelde, S.V.1
Brockmoller, J.2
Bauer, S.3
-
47
-
-
47549105549
-
Cytochrome P4502C9 mediated metabolism in people with and without cancer
-
Shord S.S., Cavallari L.H., Viana M.A.G., et al. Cytochrome P4502C9 mediated metabolism in people with and without cancer. Int J Clin Pharmacol Ther 2008, 46(7):365-374.
-
(2008)
Int J Clin Pharmacol Ther
, vol.46
, Issue.7
, pp. 365-374
-
-
Shord, S.S.1
Cavallari, L.H.2
Viana, M.A.G.3
-
48
-
-
0036285336
-
Thalidomide metabolism by the CYP2C subfamily
-
Ando Y., Fuse E., Figg W.D. Thalidomide metabolism by the CYP2C subfamily. Clin Cancer Res 2002, 8(6):1964-1973.
-
(2002)
Clin Cancer Res
, vol.8
, Issue.6
, pp. 1964-1973
-
-
Ando, Y.1
Fuse, E.2
Figg, W.D.3
-
49
-
-
0031031421
-
Variable contribution of cytochromes P450 2D6, 2C9 and 3A4 to the 4-hydroxylation of tamoxifen by human liver microsomes
-
Crewe H.K., Ellis S.W., Lennard M.S., Tucker G.T. Variable contribution of cytochromes P450 2D6, 2C9 and 3A4 to the 4-hydroxylation of tamoxifen by human liver microsomes. Biochem Pharmacol 1997, 53(2):171-178.
-
(1997)
Biochem Pharmacol
, vol.53
, Issue.2
, pp. 171-178
-
-
Crewe, H.K.1
Ellis, S.W.2
Lennard, M.S.3
Tucker, G.T.4
-
50
-
-
53849083819
-
CYP2C19 pharmacogenetics in advanced cancer: compromised function independent of genotype
-
Helsby N.A., Lo W.Y., Sharples K., et al. CYP2C19 pharmacogenetics in advanced cancer: compromised function independent of genotype. Br J Cancer 2008, 99(8):1251-1255.
-
(2008)
Br J Cancer
, vol.99
, Issue.8
, pp. 1251-1255
-
-
Helsby, N.A.1
Lo, W.Y.2
Sharples, K.3
-
51
-
-
70449704111
-
Clinical pharmacokinetics of tyrosine kinase inhibitors
-
van Erp N.P., Gelderblom H., Guchelaar H.J. Clinical pharmacokinetics of tyrosine kinase inhibitors. Cancer Treat Rev 2009, 35(8):692-706.
-
(2009)
Cancer Treat Rev
, vol.35
, Issue.8
, pp. 692-706
-
-
van Erp, N.P.1
Gelderblom, H.2
Guchelaar, H.J.3
-
52
-
-
0030812209
-
CYP2D6 catalyzes tamoxifen 4-hydroxylation in human liver
-
Dehal S.S., Kupfer D. CYP2D6 catalyzes tamoxifen 4-hydroxylation in human liver. Cancer Res 1997, 57(16):3402-3406.
-
(1997)
Cancer Res
, vol.57
, Issue.16
, pp. 3402-3406
-
-
Dehal, S.S.1
Kupfer, D.2
-
53
-
-
79955485361
-
Tamoxifen metabolite concentrations, CYP2D6 genotype, and breast cancer outcomes
-
Madlensky L., Natarajan L., Tchu S., et al. Tamoxifen metabolite concentrations, CYP2D6 genotype, and breast cancer outcomes. Clin Pharmacol Ther 2011, 89(5):718-725.
-
(2011)
Clin Pharmacol Ther
, vol.89
, Issue.5
, pp. 718-725
-
-
Madlensky, L.1
Natarajan, L.2
Tchu, S.3
-
54
-
-
19944434201
-
CYP2D6 genotype, antidepressant use, and tamoxifen metabolism during adjuvant breast cancer treatment
-
Jin Y., Desta Z., Stearns V., et al. CYP2D6 genotype, antidepressant use, and tamoxifen metabolism during adjuvant breast cancer treatment. J Natl Cancer Inst 2005, 97(1):30-39.
-
(2005)
J Natl Cancer Inst
, vol.97
, Issue.1
, pp. 30-39
-
-
Jin, Y.1
Desta, Z.2
Stearns, V.3
-
55
-
-
33947180388
-
Evaluation of probe drugs and pharmacokinetic metrics for CYP2D6 phenotyping
-
Frank D., Jaehde U., Fuhr U. Evaluation of probe drugs and pharmacokinetic metrics for CYP2D6 phenotyping. Eur J Clin Pharmacol 2007, 63(4):321-333.
-
(2007)
Eur J Clin Pharmacol
, vol.63
, Issue.4
, pp. 321-333
-
-
Frank, D.1
Jaehde, U.2
Fuhr, U.3
-
56
-
-
0034782996
-
Comparative contribution to dextromethorphan metabolism by cytochrome P450 isoforms in vitro: can dextromethorphan be used as a dual probe for both CYP2D6 and CYP3A activities?
-
Yu A.M., Haining R.L. Comparative contribution to dextromethorphan metabolism by cytochrome P450 isoforms in vitro: can dextromethorphan be used as a dual probe for both CYP2D6 and CYP3A activities?. Drug Metab Dispos 2001, 29(11):1514-1520.
-
(2001)
Drug Metab Dispos
, vol.29
, Issue.11
, pp. 1514-1520
-
-
Yu, A.M.1
Haining, R.L.2
-
57
-
-
80052009180
-
Dextromethorphan As a Phenotyping Test to Predict Endoxifen Exposure in Patients on Tamoxifen Treatment
-
de Graan A.J., Teunissen S.F., de Vos F.Y., et al. Dextromethorphan As a Phenotyping Test to Predict Endoxifen Exposure in Patients on Tamoxifen Treatment. J Clin Oncol 2011, 29(24):3240-3246.
-
(2011)
J Clin Oncol
, vol.29
, Issue.24
, pp. 3240-3246
-
-
de Graan, A.J.1
Teunissen, S.F.2
de Vos, F.Y.3
-
58
-
-
34249078591
-
Assessment of ifosfamide pharmacokinetics, toxicity, and relation to CYP3A4 activity as measured by the erythromycin breath test in patients with sarcoma
-
Chugh R., Wagner T., Griffith K.A., et al. Assessment of ifosfamide pharmacokinetics, toxicity, and relation to CYP3A4 activity as measured by the erythromycin breath test in patients with sarcoma. Cancer 2007, 109(11):2315-2322.
-
(2007)
Cancer
, vol.109
, Issue.11
, pp. 2315-2322
-
-
Chugh, R.1
Wagner, T.2
Griffith, K.A.3
-
59
-
-
0031716724
-
Role of human cytochrome P450 3A4 and 3A5 in the metabolism of taxotere and its derivatives: enzyme specificity, interindividual distribution and metabolic contribution in human liver
-
Shou M., Martinet M., Korzekwa K.R., Krausz K.W., Gonzalez F.J., Gelboin H.V. Role of human cytochrome P450 3A4 and 3A5 in the metabolism of taxotere and its derivatives: enzyme specificity, interindividual distribution and metabolic contribution in human liver. Pharmacogenetics 1998, 8(5):391-401.
-
(1998)
Pharmacogenetics
, vol.8
, Issue.5
, pp. 391-401
-
-
Shou, M.1
Martinet, M.2
Korzekwa, K.R.3
Krausz, K.W.4
Gonzalez, F.J.5
Gelboin, H.V.6
-
60
-
-
0033840446
-
CYP3A4 is mainly responsibile for the metabolism of a new vinca alkaloid, vinorelbine, in human liver microsomes
-
Kajita J., Kuwabara T., Kobayashi H., Kobayashi S. CYP3A4 is mainly responsibile for the metabolism of a new vinca alkaloid, vinorelbine, in human liver microsomes. Drug Metab Dispos 2000, 28(9):1121-1127.
-
(2000)
Drug Metab Dispos
, vol.28
, Issue.9
, pp. 1121-1127
-
-
Kajita, J.1
Kuwabara, T.2
Kobayashi, H.3
Kobayashi, S.4
-
61
-
-
0037099535
-
Modulation of irinotecan metabolism by ketoconazole
-
Kehrer D.F.S., Mathijssen R.H.J., Verweij J., de Bruijn P., Sparreboom A. Modulation of irinotecan metabolism by ketoconazole. J Clin Oncol 2002, 20(14):3122-3129.
-
(2002)
J Clin Oncol
, vol.20
, Issue.14
, pp. 3122-3129
-
-
Kehrer, D.F.S.1
Mathijssen, R.H.J.2
Verweij, J.3
de Bruijn, P.4
Sparreboom, A.5
-
62
-
-
0035071598
-
Sequence diversity in CYP3A promoters and characterization of the genetic basis of polymorphic CYP3A5 expression
-
Kuehl P., Zhang J., Lin Y., et al. Sequence diversity in CYP3A promoters and characterization of the genetic basis of polymorphic CYP3A5 expression. Nat Genet 2001, 27(4):383-391.
-
(2001)
Nat Genet
, vol.27
, Issue.4
, pp. 383-391
-
-
Kuehl, P.1
Zhang, J.2
Lin, Y.3
-
63
-
-
0037131879
-
Genetic contribution to variable human CYP3A-mediated metabolism
-
Lamba J.K., Lin Y.S., Schuetz E.G., Thummel K.E. Genetic contribution to variable human CYP3A-mediated metabolism. Adv Drug Deliv Rev 2002, 54(10):1271-1294.
-
(2002)
Adv Drug Deliv Rev
, vol.54
, Issue.10
, pp. 1271-1294
-
-
Lamba, J.K.1
Lin, Y.S.2
Schuetz, E.G.3
Thummel, K.E.4
-
64
-
-
0024556650
-
Erythromycin breath test as an assay of glucocorticoid-inducible liver cytochromes P-450. Studies in rats and patients
-
Watkins P.B., Murray S.A., Winkelman L.G., Heuman D.M., Wrighton S.A., Guzelian P.S. Erythromycin breath test as an assay of glucocorticoid-inducible liver cytochromes P-450. Studies in rats and patients. J Clin Invest 1989, 83(2):688-697.
-
(1989)
J Clin Invest
, vol.83
, Issue.2
, pp. 688-697
-
-
Watkins, P.B.1
Murray, S.A.2
Winkelman, L.G.3
Heuman, D.M.4
Wrighton, S.A.5
Guzelian, P.S.6
-
65
-
-
0029937721
-
Hepatic biotransformation of docetaxel (taxotere) in vitro: involvement of the CYP3A subfamily in humans
-
Marre F., Sanderink G.J., de S.G., Gaillard C., Martinet M., Rahmani R. Hepatic biotransformation of docetaxel (taxotere) in vitro: involvement of the CYP3A subfamily in humans. Cancer Res 1996, 56(6):1296-1302.
-
(1996)
Cancer Res
, vol.56
, Issue.6
, pp. 1296-1302
-
-
Marre, F.1
Sanderink, G.J.2
de, S.G.3
Gaillard, C.4
Martinet, M.5
Rahmani, R.6
-
66
-
-
0034047560
-
The effect of an individual's cytochrome CYP3A4 activity on docetaxel clearance
-
Hirth J., Watkins P.B., Strawderman M., Schott A., Bruno R., Baker L.H. The effect of an individual's cytochrome CYP3A4 activity on docetaxel clearance. Clin Cancer Res 2000, 6(4):1255-1258.
-
(2000)
Clin Cancer Res
, vol.6
, Issue.4
, pp. 1255-1258
-
-
Hirth, J.1
Watkins, P.B.2
Strawderman, M.3
Schott, A.4
Bruno, R.5
Baker, L.H.6
-
67
-
-
33750682345
-
Pharmacokinetics and toxicity of weekly docetaxel in older patients
-
Hurria A., Fleming M.T., Baker S.D., et al. Pharmacokinetics and toxicity of weekly docetaxel in older patients. Clin Cancer Res 2006, 12(20):6100-6105.
-
(2006)
Clin Cancer Res
, vol.12
, Issue.20
, pp. 6100-6105
-
-
Hurria, A.1
Fleming, M.T.2
Baker, S.D.3
-
68
-
-
33645958840
-
Combination vinorelbine and capecitabine for metastatic breast cancer using a non-body surface area dosing scheme
-
Schott A.F., Rae J.M., Griffith K.A., Hayes D.F., Sterns V., Baker L.H. Combination vinorelbine and capecitabine for metastatic breast cancer using a non-body surface area dosing scheme. Cancer Chemother Pharmacol 2006, 58(1):129-135.
-
(2006)
Cancer Chemother Pharmacol
, vol.58
, Issue.1
, pp. 129-135
-
-
Schott, A.F.1
Rae, J.M.2
Griffith, K.A.3
Hayes, D.F.4
Sterns, V.5
Baker, L.H.6
-
69
-
-
33748051705
-
The erythromycin breath test reflects P-glycoprotein function independently of cytochrome P450 3A activity
-
Kurnik D., Wood A.J.J., Wilkinson G.R. The erythromycin breath test reflects P-glycoprotein function independently of cytochrome P450 3A activity. Clin Pharmacol Ther 2006, 80(3):228-234.
-
(2006)
Clin Pharmacol Ther
, vol.80
, Issue.3
, pp. 228-234
-
-
Kurnik, D.1
Wood, A.J.J.2
Wilkinson, G.R.3
-
70
-
-
0025161416
-
Studies on the expression and metabolic capabilities of human liver cytochrome P450IIIA5 (HLp3)
-
Wrighton S.A., Brian W.R., Sari M.A., et al. Studies on the expression and metabolic capabilities of human liver cytochrome P450IIIA5 (HLp3). Mol Pharmacol 1990, 38(2):207-213.
-
(1990)
Mol Pharmacol
, vol.38
, Issue.2
, pp. 207-213
-
-
Wrighton, S.A.1
Brian, W.R.2
Sari, M.A.3
-
71
-
-
0024427759
-
The Increase in urinary-excretion of 6-beta-hydroxycortisol as a marker of human hepatic cytochrome-P450Iiia induction
-
Ged C., Rouillon J.M., Pichard L., et al. The Increase in urinary-excretion of 6-beta-hydroxycortisol as a marker of human hepatic cytochrome-P450Iiia induction. Br J Clin Pharmacol 1989, 28(4):373-387.
-
(1989)
Br J Clin Pharmacol
, vol.28
, Issue.4
, pp. 373-387
-
-
Ged, C.1
Rouillon, J.M.2
Pichard, L.3
-
72
-
-
0036210193
-
The effects of rifampicin on the pharmacokinetics and pharmacodynamics of orally administered nilvadipine to healthy subjects
-
Saima S., Furuie K., Yoshimoto H., Fukuda J., Hayashi T., Echizen H. The effects of rifampicin on the pharmacokinetics and pharmacodynamics of orally administered nilvadipine to healthy subjects. Br J Clin Pharmacol 2002, 53(2):203-206.
-
(2002)
Br J Clin Pharmacol
, vol.53
, Issue.2
, pp. 203-206
-
-
Saima, S.1
Furuie, K.2
Yoshimoto, H.3
Fukuda, J.4
Hayashi, T.5
Echizen, H.6
-
73
-
-
78649304183
-
Effects of rifampin and ketoconazole on the pharmacokinetics of nilotinib in healthy participants
-
Tanaka C., Yin O.Q.P., Smith T., et al. Effects of rifampin and ketoconazole on the pharmacokinetics of nilotinib in healthy participants. J Clin Pharmacol 2011, 51(1):75-83.
-
(2011)
J Clin Pharmacol
, vol.51
, Issue.1
, pp. 75-83
-
-
Tanaka, C.1
Yin, O.Q.P.2
Smith, T.3
-
74
-
-
20044369878
-
Randomized pharmacokinetic and pharmacodynamic study of docetaxel: dosing based on body-surface area compared with individualized dosing based on cytochrome P450 activity estimated using a urinary metabolite of exogenous cortisol
-
Yamamoto N., Tamura T., Murakami H., et al. Randomized pharmacokinetic and pharmacodynamic study of docetaxel: dosing based on body-surface area compared with individualized dosing based on cytochrome P450 activity estimated using a urinary metabolite of exogenous cortisol. J Clin Oncol 2005, 23(6):1061-1069.
-
(2005)
J Clin Oncol
, vol.23
, Issue.6
, pp. 1061-1069
-
-
Yamamoto, N.1
Tamura, T.2
Murakami, H.3
-
75
-
-
0030435332
-
Dexamethasone metabolism by human liver in vitro. Metabolite identification and inhibition of 6-hydroxylation
-
Gentile D.M., Tomlinson E.S., Maggs J.L., Park B.K., Back D.J. Dexamethasone metabolism by human liver in vitro. Metabolite identification and inhibition of 6-hydroxylation. J Pharmacol Exp Ther 1996, 277(1):105-112.
-
(1996)
J Pharmacol Exp Ther
, vol.277
, Issue.1
, pp. 105-112
-
-
Gentile, D.M.1
Tomlinson, E.S.2
Maggs, J.L.3
Park, B.K.4
Back, D.J.5
-
76
-
-
21744454394
-
Dexamethasone as a probe for vinorelbine clearance
-
Puisset F., Dalenc F., Chatelut E., et al. Dexamethasone as a probe for vinorelbine clearance. Br J Clin Pharmacol 2005, 60(1):45-53.
-
(2005)
Br J Clin Pharmacol
, vol.60
, Issue.1
, pp. 45-53
-
-
Puisset, F.1
Dalenc, F.2
Chatelut, E.3
-
77
-
-
4344599828
-
Dexamethasone as a probe for docetaxel clearance
-
Puisset F., Chatelut E., Dalenc F., et al. Dexamethasone as a probe for docetaxel clearance. Cancer Chemother Pharmacol 2004, 54(3):265-272.
-
(2004)
Cancer Chemother Pharmacol
, vol.54
, Issue.3
, pp. 265-272
-
-
Puisset, F.1
Chatelut, E.2
Dalenc, F.3
-
78
-
-
0036908935
-
Application of semisimultaneous midazolam administration for hepatic and intestinal cytochrome P450 3A phenotyping
-
Lee J.I., Chaves-Gnecco D., Amico J.A., Kroboth P.D., Wilson J.W., Frye R.F. Application of semisimultaneous midazolam administration for hepatic and intestinal cytochrome P450 3A phenotyping. Clin Pharmacol Ther 2002, 72(6):718-728.
-
(2002)
Clin Pharmacol Ther
, vol.72
, Issue.6
, pp. 718-728
-
-
Lee, J.I.1
Chaves-Gnecco, D.2
Amico, J.A.3
Kroboth, P.D.4
Wilson, J.W.5
Frye, R.F.6
-
79
-
-
4644263308
-
CYP3A5 Contributes significantly to CYP3A-mediated drug oxidations in liver microsomes from Japanese subjects
-
Yamaori S., Yamazaki H., Iwano S., et al. CYP3A5 Contributes significantly to CYP3A-mediated drug oxidations in liver microsomes from Japanese subjects. Drug Metab Pharmacokinet 2004, 19(2):120-129.
-
(2004)
Drug Metab Pharmacokinet
, vol.19
, Issue.2
, pp. 120-129
-
-
Yamaori, S.1
Yamazaki, H.2
Iwano, S.3
-
80
-
-
0032903499
-
First-pass midazolam metabolism catalyzed by 1alpha, 25-dihydroxy vitamin D3-modified Caco-2 cell monolayers
-
Fisher J.M., Wrighton S.A., Watkins P.B., et al. First-pass midazolam metabolism catalyzed by 1alpha, 25-dihydroxy vitamin D3-modified Caco-2 cell monolayers. J Pharmacol Exp Ther 1999, 289(2):1134-1142.
-
(1999)
J Pharmacol Exp Ther
, vol.289
, Issue.2
, pp. 1134-1142
-
-
Fisher, J.M.1
Wrighton, S.A.2
Watkins, P.B.3
-
81
-
-
0007204117
-
Failure of erythromycin breath test to correlate with midazolam clearance as a probe of cytochrome P4503A
-
Kinirons M.T., O'Shea D., Kim R.B., et al. Failure of erythromycin breath test to correlate with midazolam clearance as a probe of cytochrome P4503A. Clin Pharmacol Ther 1999, 66(3):224-231.
-
(1999)
Clin Pharmacol Ther
, vol.66
, Issue.3
, pp. 224-231
-
-
Kinirons, M.T.1
O'Shea, D.2
Kim, R.B.3
-
82
-
-
0028847788
-
The erythromycin breath test predicts the clearance of midazolam
-
Lown K.S., Thummel K.E., Benedict P.E., et al. The erythromycin breath test predicts the clearance of midazolam. Clin Pharmacol Ther 1995, 57(1):16-24.
-
(1995)
Clin Pharmacol Ther
, vol.57
, Issue.1
, pp. 16-24
-
-
Lown, K.S.1
Thummel, K.E.2
Benedict, P.E.3
-
83
-
-
7944233687
-
Prediction of irinotecan pharmacokinetics by use of cytochrome p450 3A4 phenotyping probes
-
Mathijssen R.H.J., de Jong F.A., van Schaik R.H.N., et al. Prediction of irinotecan pharmacokinetics by use of cytochrome p450 3A4 phenotyping probes. J Natl Cancer Inst 2004, 96(21):1585-1592.
-
(2004)
J Natl Cancer Inst
, vol.96
, Issue.21
, pp. 1585-1592
-
-
Mathijssen, R.H.J.1
de Jong, F.A.2
van Schaik, R.H.N.3
-
84
-
-
74549205743
-
A CYP3A4 phenotype-based dosing algorithm for individualized treatment of irinotecan
-
van der Bol J.M., Mathijssen R.H.J., Creemers G.J.M., et al. A CYP3A4 phenotype-based dosing algorithm for individualized treatment of irinotecan. Clin Cancer Res 2010, 16(2):736-742.
-
(2010)
Clin Cancer Res
, vol.16
, Issue.2
, pp. 736-742
-
-
van der Bol, J.M.1
Mathijssen, R.H.J.2
Creemers, G.J.M.3
-
85
-
-
82455175240
-
Pharmacologic and phenotypic study of docetaxel in patients with ovarian or primary peritoneal cancer
-
Zamboni W.C., Combest A.J., Deloia J.A., et al. Pharmacologic and phenotypic study of docetaxel in patients with ovarian or primary peritoneal cancer. Cancer Chemother Pharmacol 2011, 68(5):1255-1262.
-
(2011)
Cancer Chemother Pharmacol
, vol.68
, Issue.5
, pp. 1255-1262
-
-
Zamboni, W.C.1
Combest, A.J.2
Deloia, J.A.3
-
86
-
-
33845680787
-
CYP3A phenotyping approach to predict systemic exposure to EGFR tyrosine kinase inhibitors
-
Li J., Karlsson M.O., Brahmer J., et al. CYP3A phenotyping approach to predict systemic exposure to EGFR tyrosine kinase inhibitors. J Natl Cancer Inst 2006, 98(23):1714-1723.
-
(2006)
J Natl Cancer Inst
, vol.98
, Issue.23
, pp. 1714-1723
-
-
Li, J.1
Karlsson, M.O.2
Brahmer, J.3
-
87
-
-
34250676807
-
Imatinib disposition and ABCB1 (MDR1, p-glycoprotein) genotype
-
Gurney H., Wong M., Balleine R.L., et al. Imatinib disposition and ABCB1 (MDR1, p-glycoprotein) genotype. Clin Pharmacol Ther 2007, 82(1):33-40.
-
(2007)
Clin Pharmacol Ther
, vol.82
, Issue.1
, pp. 33-40
-
-
Gurney, H.1
Wong, M.2
Balleine, R.L.3
-
88
-
-
77953934202
-
CYP3A activity influences imatinib response in patients with chronic myeloid leukemia: a pilot study on in vivo CYP3A activity
-
Green H., Skoglund K., Rommel F., Mirghani R.A., Lotfi K. CYP3A activity influences imatinib response in patients with chronic myeloid leukemia: a pilot study on in vivo CYP3A activity. Eur J Clin Pharmacol 2010, 66(4):383-386.
-
(2010)
Eur J Clin Pharmacol
, vol.66
, Issue.4
, pp. 383-386
-
-
Green, H.1
Skoglund, K.2
Rommel, F.3
Mirghani, R.A.4
Lotfi, K.5
-
89
-
-
0023187085
-
Clinical pharmacokinetics of 5-fluorouracil and its metabolites in plasma, urine, and bile
-
Heggie G.D., Sommadossi J.P., Cross D.S., Huster W.J., Diasio R.B. Clinical pharmacokinetics of 5-fluorouracil and its metabolites in plasma, urine, and bile. Cancer Res 1987, 47(8):2203-2206.
-
(1987)
Cancer Res
, vol.47
, Issue.8
, pp. 2203-2206
-
-
Heggie, G.D.1
Sommadossi, J.P.2
Cross, D.S.3
Huster, W.J.4
Diasio, R.B.5
-
90
-
-
79955998006
-
Relationship between single nucleotide polymorphisms and haplotypes in DPYD and toxicity and efficacy of capecitabine in advanced colorectal cancer
-
Deenen M.J., Tol J., Burylo A.M., et al. Relationship between single nucleotide polymorphisms and haplotypes in DPYD and toxicity and efficacy of capecitabine in advanced colorectal cancer. Clin Cancer Res 2011, 17(10):3455-3468.
-
(2011)
Clin Cancer Res
, vol.17
, Issue.10
, pp. 3455-3468
-
-
Deenen, M.J.1
Tol, J.2
Burylo, A.M.3
-
91
-
-
0026753035
-
Correlation between dihydropyrimidine dehydrogenase-activity in peripheral mononuclear-cells and systemic clearance of fluorouracil in cancer-patients
-
Fleming R.A., Milano G., Thyss A., et al. Correlation between dihydropyrimidine dehydrogenase-activity in peripheral mononuclear-cells and systemic clearance of fluorouracil in cancer-patients. Cancer Res 1992, 52(10):2899-2902.
-
(1992)
Cancer Res
, vol.52
, Issue.10
, pp. 2899-2902
-
-
Fleming, R.A.1
Milano, G.2
Thyss, A.3
-
92
-
-
28244441304
-
Physiologically based pharmacokinetic modelling of the three-step metabolism of pyrimidine using C-13-uracil as an in vivo probe
-
Ito S., Kawamura T., Inada M., et al. Physiologically based pharmacokinetic modelling of the three-step metabolism of pyrimidine using C-13-uracil as an in vivo probe. Br J Clin Pharmacol 2005, 60(6):584-593.
-
(2005)
Br J Clin Pharmacol
, vol.60
, Issue.6
, pp. 584-593
-
-
Ito, S.1
Kawamura, T.2
Inada, M.3
-
93
-
-
82455209056
-
Pharmacokinetics of orally administered uracil in healthy volunteers and in DPD-deficient patients, a possible tool for screening of DPD deficiency
-
van Staveren M.C., Theeuwes-Oonk B., Guchelaar H.J., van Kuilenburg A.B., Maring J.G. Pharmacokinetics of orally administered uracil in healthy volunteers and in DPD-deficient patients, a possible tool for screening of DPD deficiency. Cancer Chemother Pharmacol 2011, 68(6):1611-1617.
-
(2011)
Cancer Chemother Pharmacol
, vol.68
, Issue.6
, pp. 1611-1617
-
-
van Staveren, M.C.1
Theeuwes-Oonk, B.2
Guchelaar, H.J.3
van Kuilenburg, A.B.4
Maring, J.G.5
-
94
-
-
77957732473
-
The value of dihydrouracil/uracil plasma ratios in predicting 5-fluorouracil-related toxicity in colorectal cancer patients
-
Kristensen M.H., Pedersen P., Mejer J. The value of dihydrouracil/uracil plasma ratios in predicting 5-fluorouracil-related toxicity in colorectal cancer patients. J Int Med Res 2010, 38(4):1313-1323.
-
(2010)
J Int Med Res
, vol.38
, Issue.4
, pp. 1313-1323
-
-
Kristensen, M.H.1
Pedersen, P.2
Mejer, J.3
-
95
-
-
0032940053
-
Correlation between uracil and dihydrouracil plasma ratio, fluorouracil (5-FU) pharmacokinetic parameters, and tolerance in patients with advanced colorectal cancer: a potential interest for predicting 5-FU toxicity and determining optimal 5-FU dosage
-
Gamelin E., Boissdron-Celle M., Guerin-Meyer V., et al. Correlation between uracil and dihydrouracil plasma ratio, fluorouracil (5-FU) pharmacokinetic parameters, and tolerance in patients with advanced colorectal cancer: a potential interest for predicting 5-FU toxicity and determining optimal 5-FU dosage. J Clin Oncol 1999, 17(4):1105-1110.
-
(1999)
J Clin Oncol
, vol.17
, Issue.4
, pp. 1105-1110
-
-
Gamelin, E.1
Boissdron-Celle, M.2
Guerin-Meyer, V.3
-
96
-
-
33847721425
-
The dihydrouracil/uracil ratios in plasma and toxicities of 5-fluorouracil-based adjuvant chemotherapy in colorectal cancer patients
-
Zhou Z.W., Wang G.Q., Wan D.S., et al. The dihydrouracil/uracil ratios in plasma and toxicities of 5-fluorouracil-based adjuvant chemotherapy in colorectal cancer patients. Chemotherapy 2007, 53(2):127-131.
-
(2007)
Chemotherapy
, vol.53
, Issue.2
, pp. 127-131
-
-
Zhou, Z.W.1
Wang, G.Q.2
Wan, D.S.3
-
98
-
-
33846261196
-
The role of drug-metabolising enzymes in clinical responses to chemotherapy
-
Scripture C.D., Figg W.D., Sparreboom A. The role of drug-metabolising enzymes in clinical responses to chemotherapy. Expert Opin Drug Metab Toxicol 2006, 2(1):17-25.
-
(2006)
Expert Opin Drug Metab Toxicol
, vol.2
, Issue.1
, pp. 17-25
-
-
Scripture, C.D.1
Figg, W.D.2
Sparreboom, A.3
-
99
-
-
0033569516
-
Pharmacogenomics: translating functional genomics into rational therapeutics
-
Evans W.E., Relling M.V. Pharmacogenomics: translating functional genomics into rational therapeutics. Science 1999, 286(5439):487-491.
-
(1999)
Science
, vol.286
, Issue.5439
, pp. 487-491
-
-
Evans, W.E.1
Relling, M.V.2
-
100
-
-
15244342411
-
UDP-glucuronosyltransferases and clinical drug-drug interactions
-
Kiang T.K., Ensom M.H., Chang T.K. UDP-glucuronosyltransferases and clinical drug-drug interactions. Pharmacol Ther 2005, 106(1):97-132.
-
(2005)
Pharmacol Ther
, vol.106
, Issue.1
, pp. 97-132
-
-
Kiang, T.K.1
Ensom, M.H.2
Chang, T.K.3
-
101
-
-
0026323763
-
Drug glucuronidation in humans
-
Miners J.O., Mackenzie P.I. Drug glucuronidation in humans. Pharmacol Ther 1991, 51(3):347-369.
-
(1991)
Pharmacol Ther
, vol.51
, Issue.3
, pp. 347-369
-
-
Miners, J.O.1
Mackenzie, P.I.2
-
102
-
-
74549132748
-
Interindividual variability in hepatic drug glucuronidation: studies into the role of age, sex, enzyme inducers, and genetic polymorphism using the human liver bank as a model system
-
Court M.H. Interindividual variability in hepatic drug glucuronidation: studies into the role of age, sex, enzyme inducers, and genetic polymorphism using the human liver bank as a model system. Drug Metab Rev 2010, 42(1):209-224.
-
(2010)
Drug Metab Rev
, vol.42
, Issue.1
, pp. 209-224
-
-
Court, M.H.1
-
103
-
-
0032519431
-
Genetic predisposition to the metabolism of irinotecan (CPT-11) - role of uridine diphosphate glucuronosyltransferase isoform 1A1 in the glucuronidation of its active metabolite (SN-38) in human liver microsomes
-
Iyer L., King C.D., Whitington P.F., et al. Genetic predisposition to the metabolism of irinotecan (CPT-11) - role of uridine diphosphate glucuronosyltransferase isoform 1A1 in the glucuronidation of its active metabolite (SN-38) in human liver microsomes. J Clin Invest 1998, 101(4):847-854.
-
(1998)
J Clin Invest
, vol.101
, Issue.4
, pp. 847-854
-
-
Iyer, L.1
King, C.D.2
Whitington, P.F.3
-
104
-
-
33847358669
-
UDP-glucuronosyltransferase 1A1 is the principal enzyme responsible for etoposide glucuronidation in human liver and intestinal microsomes: structural characterization of phenolic and alcoholic glucuronides of etoposide and estimation of enzyme kinetics
-
Wen Z.M., Tallman M.N., Ali S.Y., Smith P.C. UDP-glucuronosyltransferase 1A1 is the principal enzyme responsible for etoposide glucuronidation in human liver and intestinal microsomes: structural characterization of phenolic and alcoholic glucuronides of etoposide and estimation of enzyme kinetics. Drug Metab Dispos 2007, 35(3):371-380.
-
(2007)
Drug Metab Dispos
, vol.35
, Issue.3
, pp. 371-380
-
-
Wen, Z.M.1
Tallman, M.N.2
Ali, S.Y.3
Smith, P.C.4
-
105
-
-
0028276410
-
Bilirubin UDP-glucuronosyltransferase-1 is the only relevant bilirubin glucuronidating isoform in man
-
Bosma P.J., Seppen J., Goldhoorn B., et al. Bilirubin UDP-glucuronosyltransferase-1 is the only relevant bilirubin glucuronidating isoform in man. J Biol Chem 1994, 269(27):17960-17964.
-
(1994)
J Biol Chem
, vol.269
, Issue.27
, pp. 17960-17964
-
-
Bosma, P.J.1
Seppen, J.2
Goldhoorn, B.3
-
106
-
-
0023112104
-
Paracetamol as a test drug to determine glucuronide formation in man - effects of inducers and of smoking
-
Bock K.W., Wiltfang J., Blume R., Ullrich D., Bircher J. Paracetamol as a test drug to determine glucuronide formation in man - effects of inducers and of smoking. Eur J Clin Pharmacol 1987, 31(6):677-683.
-
(1987)
Eur J Clin Pharmacol
, vol.31
, Issue.6
, pp. 677-683
-
-
Bock, K.W.1
Wiltfang, J.2
Blume, R.3
Ullrich, D.4
Bircher, J.5
-
107
-
-
0030958098
-
Pharmacokinetic and pharmacodynamic evaluation of the topoisomerase inhibitor irinotecan in cancer patients
-
Gupta E., Mick R., Ramirez J., et al. Pharmacokinetic and pharmacodynamic evaluation of the topoisomerase inhibitor irinotecan in cancer patients. J Clin Oncol 1997, 15(4):1502-1510.
-
(1997)
J Clin Oncol
, vol.15
, Issue.4
, pp. 1502-1510
-
-
Gupta, E.1
Mick, R.2
Ramirez, J.3
-
108
-
-
0027454954
-
Characterization of glutathione conjugation in humans - stereoselectivity in plasma elimination pharmacokinetics and urinary-excretion of (R)-2-bromoisovalerylurea and (S)-2-bromoisovalerylurea in healthy-volunteers
-
Mulders T.M.T., Venizelos V., Schoemaker R., Cohen A.F., Breimer D.D., Mulder G.J. Characterization of glutathione conjugation in humans - stereoselectivity in plasma elimination pharmacokinetics and urinary-excretion of (R)-2-bromoisovalerylurea and (S)-2-bromoisovalerylurea in healthy-volunteers. Clin Pharmacol Ther 1993, 53(1):49-58.
-
(1993)
Clin Pharmacol Ther
, vol.53
, Issue.1
, pp. 49-58
-
-
Mulders, T.M.T.1
Venizelos, V.2
Schoemaker, R.3
Cohen, A.F.4
Breimer, D.D.5
Mulder, G.J.6
-
109
-
-
79959652551
-
Assessment of thiopurine S-methyltransferase activity in patients prescribed thiopurines: a systematic review
-
Booth R.A., Ansari M.T., Loit E., et al. Assessment of thiopurine S-methyltransferase activity in patients prescribed thiopurines: a systematic review. Ann Intern Med 2011, 154(12):U814-U872.
-
(2011)
Ann Intern Med
, vol.154
, Issue.12
-
-
Booth, R.A.1
Ansari, M.T.2
Loit, E.3
-
110
-
-
0034814792
-
Determination of thiopurine methyltransferase activity in human erythrocytes by high-performance liquid chromatography: comparison with the radiochemical method
-
Menor C., Fueyo J.A., Escribano O., et al. Determination of thiopurine methyltransferase activity in human erythrocytes by high-performance liquid chromatography: comparison with the radiochemical method. Ther Drug Monit 2001, 23(5):536-541.
-
(2001)
Ther Drug Monit
, vol.23
, Issue.5
, pp. 536-541
-
-
Menor, C.1
Fueyo, J.A.2
Escribano, O.3
-
111
-
-
49949089862
-
Genetic variation in drug transporters in ethnic populations
-
Cropp C.D., Yee S.W., Giacomini K.M. Genetic variation in drug transporters in ethnic populations. Clin Pharmacol Ther 2008, 84(3):412-416.
-
(2008)
Clin Pharmacol Ther
, vol.84
, Issue.3
, pp. 412-416
-
-
Cropp, C.D.1
Yee, S.W.2
Giacomini, K.M.3
-
112
-
-
58549112368
-
An overview of the relations between polymorphisms in drug metabolising enzymes and drug transporters and survival after cancer drug treatment
-
Ekhart C., Rodenhuis S., Smits P.H.M., Beijnen J.H., Huitema A.D.R. An overview of the relations between polymorphisms in drug metabolising enzymes and drug transporters and survival after cancer drug treatment. Cancer Treat Rev 2009, 35(1):18-31.
-
(2009)
Cancer Treat Rev
, vol.35
, Issue.1
, pp. 18-31
-
-
Ekhart, C.1
Rodenhuis, S.2
Smits, P.H.M.3
Beijnen, J.H.4
Huitema, A.D.R.5
-
113
-
-
77949392921
-
Evaluation of in vivo P-glycoprotein phenotyping probes a need for validation
-
Ma J.D., Tsunoda S.M., Bertino J.S., Trivedi M., Beale K.K., Nafziger A.N. Evaluation of in vivo P-glycoprotein phenotyping probes a need for validation. Clin Pharmacokinet 2010, 49(4):223-237.
-
(2010)
Clin Pharmacokinet
, vol.49
, Issue.4
, pp. 223-237
-
-
Ma, J.D.1
Tsunoda, S.M.2
Bertino, J.S.3
Trivedi, M.4
Beale, K.K.5
Nafziger, A.N.6
-
114
-
-
11344272181
-
Hepatic technetium Tc 99m-labeled sestamibi elimination rate and ABCB1 (MDR1) genotype as indicators of ABCB1 (P-glycoprotein) activity in patients with cancer
-
Wong M., Evans S., Rivory L.P., et al. Hepatic technetium Tc 99m-labeled sestamibi elimination rate and ABCB1 (MDR1) genotype as indicators of ABCB1 (P-glycoprotein) activity in patients with cancer. Clin Pharmacol Ther 2005, 77(1):33-42.
-
(2005)
Clin Pharmacol Ther
, vol.77
, Issue.1
, pp. 33-42
-
-
Wong, M.1
Evans, S.2
Rivory, L.P.3
-
115
-
-
33744995028
-
Predictors of vinorelbine pharmacokinetics and pharmacodynamics in patients with cancer
-
Wong M., Balleine R.L., Blair E.Y.L., et al. Predictors of vinorelbine pharmacokinetics and pharmacodynamics in patients with cancer. J Clin Oncol 2006, 24(16):2448-2455.
-
(2006)
J Clin Oncol
, vol.24
, Issue.16
, pp. 2448-2455
-
-
Wong, M.1
Balleine, R.L.2
Blair, E.Y.L.3
-
116
-
-
0037132703
-
Role of body surface area in dosing of investigational anticancer agents in adults, 1991-2001
-
Baker S.D., Verweij J., Rowinsky E.K., et al. Role of body surface area in dosing of investigational anticancer agents in adults, 1991-2001. J Natl Cancer Inst 2002, 94(24):1883-1888.
-
(2002)
J Natl Cancer Inst
, vol.94
, Issue.24
, pp. 1883-1888
-
-
Baker, S.D.1
Verweij, J.2
Rowinsky, E.K.3
-
117
-
-
0029743058
-
Dose calculation of anticancer drugs: a review of the current practice and introduction of an alternative
-
Gurney H. Dose calculation of anticancer drugs: a review of the current practice and introduction of an alternative. J Clin Oncol 1996, 14(9):2590-2611.
-
(1996)
J Clin Oncol
, vol.14
, Issue.9
, pp. 2590-2611
-
-
Gurney, H.1
-
118
-
-
80052020634
-
Genotype-guided tamoxifen dosing increases active metabolite exposure in women with reduced CYP2D6 metabolism: a multicenter study
-
Irvin W.J., Walko C.M., Weck K.E., et al. Genotype-guided tamoxifen dosing increases active metabolite exposure in women with reduced CYP2D6 metabolism: a multicenter study. J Clin Oncol 2011, 29(24):3232-3239.
-
(2011)
J Clin Oncol
, vol.29
, Issue.24
, pp. 3232-3239
-
-
Irvin, W.J.1
Walko, C.M.2
Weck, K.E.3
-
119
-
-
33745347897
-
Quantitative effect of CYP2D6 genotype and inhibitors on tamoxifen metabolism: implication for optimization of breast cancer treatment
-
Borges S., Desta Z., Li L., et al. Quantitative effect of CYP2D6 genotype and inhibitors on tamoxifen metabolism: implication for optimization of breast cancer treatment. Clin Pharmacol Ther 2006, 80(1):61-74.
-
(2006)
Clin Pharmacol Ther
, vol.80
, Issue.1
, pp. 61-74
-
-
Borges, S.1
Desta, Z.2
Li, L.3
-
120
-
-
77956255908
-
Composite functional genetic and comedication CYP2D6 activity score in predicting tamoxifen drug exposure among breast cancer patients
-
Borges S., Desta Z., Jin Y., et al. Composite functional genetic and comedication CYP2D6 activity score in predicting tamoxifen drug exposure among breast cancer patients. J Clin Pharmacol 2010, 50(4):450-458.
-
(2010)
J Clin Pharmacol
, vol.50
, Issue.4
, pp. 450-458
-
-
Borges, S.1
Desta, Z.2
Jin, Y.3
-
121
-
-
0031460481
-
Individualization of cancer therapy based on cytochrome P450 polymorphism: a pharmacogenetic approach
-
Vermes A., Guchelaar H.J., Koopmans R.P. Individualization of cancer therapy based on cytochrome P450 polymorphism: a pharmacogenetic approach. Cancer Treat Rev 1997, 23(5-6):321-339.
-
(1997)
Cancer Treat Rev
, vol.23
, Issue.5-6
, pp. 321-339
-
-
Vermes, A.1
Guchelaar, H.J.2
Koopmans, R.P.3
-
122
-
-
0032946502
-
Role of CYP2B6 and CYP3A4 in the in vitro N-dechloroethylation of (R)- and (S)-ifosfamide in human liver microsomes
-
Granvil C.P., Madan A., Sharkawi M., Parkinson A., Wainer I.W. Role of CYP2B6 and CYP3A4 in the in vitro N-dechloroethylation of (R)- and (S)-ifosfamide in human liver microsomes. Drug Metab Dispos 1999, 27(4):533-541.
-
(1999)
Drug Metab Dispos
, vol.27
, Issue.4
, pp. 533-541
-
-
Granvil, C.P.1
Madan, A.2
Sharkawi, M.3
Parkinson, A.4
Wainer, I.W.5
-
123
-
-
0032900953
-
Biochemical, cellular, and pharmacological aspects of the multidrug transporter
-
Ambudkar S.V., Dey S., Hrycyna C.A., Ramachandra M., Pastan I., Gottesman M.M. Biochemical, cellular, and pharmacological aspects of the multidrug transporter. Annu Rev Pharmacol Toxicol 1999, 39:361-398.
-
(1999)
Annu Rev Pharmacol Toxicol
, vol.39
, pp. 361-398
-
-
Ambudkar, S.V.1
Dey, S.2
Hrycyna, C.A.3
Ramachandra, M.4
Pastan, I.5
Gottesman, M.M.6
-
124
-
-
84856723269
-
Docetaxel pharmacokinetics and its correlation with two in vivo probes for cytochrome P450 enzymes: the C(14)-erythromycin breath test and the antipyrine clearance test
-
Michael M., Cullinane C., Hatzimihalis A., et al. Docetaxel pharmacokinetics and its correlation with two in vivo probes for cytochrome P450 enzymes: the C(14)-erythromycin breath test and the antipyrine clearance test. Cancer Chemother Pharmacol 2011.
-
(2011)
Cancer Chemother Pharmacol
-
-
Michael, M.1
Cullinane, C.2
Hatzimihalis, A.3
-
125
-
-
70449403286
-
Evidence for oxazepam as an in vivo probe of UGT2B15: oxazepam clearance is reduced by UGT2B15 D85Y polymorphism but unaffected by UGT2B17 deletion
-
He X., Hesse L.M., Hazarika S., et al. Evidence for oxazepam as an in vivo probe of UGT2B15: oxazepam clearance is reduced by UGT2B15 D85Y polymorphism but unaffected by UGT2B17 deletion. Br J Clin Pharmacol 2009, 68(5):721-730.
-
(2009)
Br J Clin Pharmacol
, vol.68
, Issue.5
, pp. 721-730
-
-
He, X.1
Hesse, L.M.2
Hazarika, S.3
-
126
-
-
45549101956
-
Population pharmacokinetic model for docetaxel in patients with varying degrees of liver function: incorporating cytochrome P450 3A activity measurements
-
Hooker A.C., ten Tije A.J., Carducci M.A., et al. Population pharmacokinetic model for docetaxel in patients with varying degrees of liver function: incorporating cytochrome P450 3A activity measurements. Clin Pharmacol Ther 2008, 84(1):111-118.
-
(2008)
Clin Pharmacol Ther
, vol.84
, Issue.1
, pp. 111-118
-
-
Hooker, A.C.1
ten Tije, A.J.2
Carducci, M.A.3
-
127
-
-
0346057807
-
Population pharmacokinetics of weekly docetaxel in patients with advanced cancer
-
Slaviero K.A., Clarke S.J., McLachlan A.J., Blair E.Y.L., Rivory L.P. Population pharmacokinetics of weekly docetaxel in patients with advanced cancer. Br J Clin Pharmacol 2004, 57(1):44-53.
-
(2004)
Br J Clin Pharmacol
, vol.57
, Issue.1
, pp. 44-53
-
-
Slaviero, K.A.1
Clarke, S.J.2
McLachlan, A.J.3
Blair, E.Y.L.4
Rivory, L.P.5
-
128
-
-
84861689378
-
-
Predictive value of drug elimination gene polymorphisms on clearance and dose adjustment of sunitinib in cancer patients (CLEARSUN). Available from:
-
Predictive value of drug elimination gene polymorphisms on clearance and dose adjustment of sunitinib in cancer patients (CLEARSUN). Available from: http://www.clinicaltrials.gov/ct2/show/NCT01098903?term=01098903&rank=1.
-
-
-
|