-
1
-
-
0027446505
-
The P450 superfamily: Update on new sequences, gene mapping, accession numbers, early trivial names of enzymes, and nomenclature
-
Nelson DR, Kamantaki T, Waxman DJ, et al. The P450 superfamily: update on new sequences, gene mapping, accession numbers, early trivial names of enzymes, and nomenclature. DNA Cell Biol 1993;12:1-51.
-
(1993)
DNA Cell Biol
, vol.12
, pp. 1-51
-
-
Nelson, D.R.1
Kamantaki, T.2
Waxman, D.J.3
-
2
-
-
0028237729
-
Interindividual variations in human liver cytochrome P-450 enzymes involved in the oxidation of drugs, carcinogens and toxic chemicals: Studies with human liver microsomes of 30 Japanese and 30 Caucasians
-
Shimada T, Yamazaki H, Mimura M, Inui Y, Guengerich FP. Interindividual variations in human liver cytochrome P-450 enzymes involved in the oxidation of drugs, carcinogens and toxic chemicals: studies with human liver microsomes of 30 Japanese and 30 Caucasians. J Pharmacol Exp Ther 1994;270:414-23.
-
(1994)
J Pharmacol Exp Ther
, vol.270
, pp. 414-423
-
-
Shimada, T.1
Yamazaki, H.2
Mimura, M.3
Inui, Y.4
Guengerich, F.P.5
-
3
-
-
0028095629
-
Assessment of liver metabolic function: Clinical implications
-
Brockmöller J, Roots I. Assessment of liver metabolic function: clinical implications. Clin Pharmacokinet 1994; 27:216-48.
-
(1994)
Clin Pharmacokinet
, vol.27
, pp. 216-248
-
-
Brockmöller, J.1
Roots, I.2
-
4
-
-
0027985726
-
Clozapine disposition covaries with the CYP1A2 activity determined by the caffeine test
-
Bertilsson L, Carrillo JA, Dahl ML, et al. Clozapine disposition covaries with the CYP1A2 activity determined by the caffeine test. Br J Clin Pharmacol 1994;38:471-3.
-
(1994)
Br J Clin Pharmacol
, vol.38
, pp. 471-473
-
-
Bertilsson, L.1
Carrillo, J.A.2
Dahl, M.L.3
-
5
-
-
0027383271
-
The pharmacogenetics of the selective serotonin reuptake inhibitors
-
Brøsen K. The pharmacogenetics of the selective serotonin reuptake inhibitors. Clin Invest 1993;71:1002-9.
-
(1993)
Clin Invest
, vol.71
, pp. 1002-1009
-
-
Brøsen, K.1
-
6
-
-
0028260641
-
The major genetic defect responsible for the polymorphism of S-mephenytoin metabolism in humans
-
deMorais SMF, Wilkinson GR, Blaisdell J, Nakamura K, Meyer UA, Goldstein JA. The major genetic defect responsible for the polymorphism of S-mephenytoin metabolism in humans. J Biol Chem 1994;269:15419-22.
-
(1994)
J Biol Chem
, vol.269
, pp. 15419-15422
-
-
DeMorais, S.M.F.1
Wilkinson, G.R.2
Blaisdell, J.3
Nakamura, K.4
Meyer, U.A.5
Goldstein, J.A.6
-
7
-
-
0028865992
-
A multifamily study on the relationship between CYP2C19 genotype and S-mephenytoin oxidation phenotype
-
Brøsen K, de Morais SMF, Meyer UA, Goldstein JA. A multifamily study on the relationship between CYP2C19 genotype and S-mephenytoin oxidation phenotype. Pharmaco-genetics 1995;5:312-7.
-
(1995)
Pharmacogenetics
, vol.5
, pp. 312-317
-
-
Brøsen, K.1
De Morais, S.M.F.2
Meyer, U.A.3
Goldstein, J.A.4
-
8
-
-
0025964524
-
The mephenytoin oxidation polymorphism is partially responsible for the Ndemethylation of imipramine
-
Skjelbo E, Brøsen K, Hallas J, Gram LF. The mephenytoin oxidation polymorphism is partially responsible for the Ndemethylation of imipramine. Clin Pharmacol Ther 1991; 49:18-23.
-
(1991)
Clin Pharmacol Ther
, vol.49
, pp. 18-23
-
-
Skjelbo, E.1
Brøsen, K.2
Hallas, J.3
Gram, L.F.4
-
9
-
-
0024359574
-
Clinical significance of the sparteine/ debrisoquine oxidation polymorphism
-
Brøsen K, Gram LF. Clinical significance of the sparteine/ debrisoquine oxidation polymorphism. Eur J Clin Pharmacol 1989;36:537-47.
-
(1989)
Eur J Clin Pharmacol
, vol.36
, pp. 537-547
-
-
Brøsen, K.1
Gram, L.F.2
-
10
-
-
0025080352
-
Genotyping of poor metabolisers of debrisoquine by allele-specific PCR amplification
-
Heim M, Meyer UA. Genotyping of poor metabolisers of debrisoquine by allele-specific PCR amplification. Lancet 1990;336:529-32.
-
(1990)
Lancet
, vol.336
, pp. 529-532
-
-
Heim, M.1
Meyer, U.A.2
-
11
-
-
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, Meyer UA. Debrisoquine/sparteine hydroxylation genotype and phenotype: analysis of common mutations and alleles of CYP2D6 in a European population. DNA Cell Biol 1991; 10:545-58.
-
(1991)
DNA Cell Biol
, vol.10
, pp. 545-558
-
-
Broly, F.1
Gaedigk, A.2
Heim, M.3
Eichelbaum, M.4
Morike, K.5
Meyer, U.A.6
-
12
-
-
0026610576
-
Analysis of the CYP2D6 gene in relation to debrisoquine and desipramine hydroxylation in a Swedish population
-
Dahl ML, Johansson I, Palmertz MP, Ingelman-Sundberg M, Sjöqvist F. Analysis of the CYP2D6 gene in relation to debrisoquine and desipramine hydroxylation in a Swedish population. Clin Pharmacol Ther 1992;51:12-7.
-
(1992)
Clin Pharmacol Ther
, vol.51
, pp. 12-17
-
-
Dahl, M.L.1
Johansson, I.2
Palmertz, M.P.3
Ingelman-Sundberg, M.4
Sjöqvist, F.5
-
13
-
-
0028007553
-
-
Brøsen K, Nielsen PN, Brusgaard K, Gram LF, Skjødt K. Eur J Clin Pharmacol 1994;47:221-5.
-
(1994)
Eur J Clin Pharmacol
, vol.47
, pp. 221-225
-
-
Brøsen, K.1
Nielsen, P.N.2
Brusgaard, K.3
Gram, L.F.4
Skjødt, K.5
-
14
-
-
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 ML, Sjöqvist F, Ingelman-Sundberg I. Inherited amplification of an active gene in the cytochrome P450 CYP2D locus as a cause of ultrarapid metabolism of debrisoquine. Proc Natl Acad Sci 1993;90:11825-9.
-
(1993)
Proc Natl Acad Sci
, vol.90
, pp. 11825-11829
-
-
Johansson, I.1
Lundqvist, E.2
Bertilsson, L.3
Dahl, M.L.4
Sjöqvist, F.5
Ingelman-Sundberg, I.6
-
15
-
-
0028071759
-
Noninvasive tests of CYP3A enzymes
-
Watkins PB. Noninvasive tests of CYP3A enzymes. Pharma-cogenetics 1994;4:171-84.
-
(1994)
Pharmacogenetics
, vol.4
, pp. 171-184
-
-
Watkins, P.B.1
|