-
2
-
-
77249169919
-
Two flavonolignans from milk thistle (Silybum marianum) inhibit CYP2C9-mediated warfarin metabolism at clinically achievable concentrations
-
Brantley SJ, Oberlies NH, Kroll DJ, and Paine MF (2010) Two flavonolignans from milk thistle (Silybum marianum) inhibit CYP2C9-mediated warfarin metabolism at clinically achievable concentrations. J Pharmacol Exp Ther 332:1081-1087.
-
(2010)
J Pharmacol Exp Ther
, vol.332
, pp. 1081-1087
-
-
Brantley, S.J.1
Oberlies, N.H.2
Kroll, D.J.3
Paine, M.F.4
-
3
-
-
0345490845
-
Effect of methanol, ethanol, dimethyl sulfoxide, and acetonitrile on in vitro activities of cDNA-expressed human cytochromes P-450
-
Busby WF Jr, Ackermann JM, and Crespi CL (1999) Effect of methanol, ethanol, dimethyl sulfoxide, and acetonitrile on in vitro activities of cDNA-expressed human cytochromes P-450. Drug Metab Dispos 27:246-249. (Pubitemid 29072079)
-
(1999)
Drug Metabolism and Disposition
, vol.27
, Issue.2
, pp. 246-249
-
-
Busby Jr., W.F.1
Ackermann, J.M.2
Crespi, C.L.3
-
4
-
-
0028228640
-
Disposition of warfarin enantiomers and metabolites in ptients during multiple dosing with rac-warfarin
-
Chan E, McLachlan AJ, Pegg M, MacKay AD, Cole RB, and Rowland M (1994) Disposition of warfarin enantiomers and metabolites in patients during multiple dosing with rac-warfarin. Br J Clin Pharmacol 37:563-569. (Pubitemid 24197150)
-
(1994)
British Journal of Clinical Pharmacology
, vol.37
, Issue.6
, pp. 563-569
-
-
Chan, E.1
McLachlan, A.J.2
Pegg, M.3
MacKay, A.D.4
Cole, R.B.5
Rowland, M.6
-
5
-
-
0031940804
-
Effect of common organic solvents on in vitro cytochrome P450-mediated metabolic activities in human liver microsomes
-
Chauret N, Gauthier A, and Nicoll-Griffith DA (1998) Effect of common organic solvents on in vitro cytochrome P450-mediated metabolic activities in human liver microsomes. Drug Metab Dispos 26:1-4. (Pubitemid 28071316)
-
(1998)
Drug Metabolism and Disposition
, vol.26
, Issue.1
, pp. 1-4
-
-
Chauret, N.1
Gauthier, A.2
Nicoll-Griffith, D.A.3
-
6
-
-
0031149716
-
Inhibition of coumarin 7-hydroxylase activity in human liver microsomes
-
DOI 10.1006/abbi.1997.9964
-
Draper AJ, Madan A, and Parkinson A (1997) Inhibition of coumarin 7-hydroxylase activity in human liver microsomes. Arch Biochem Biophys 341:47-61. (Pubitemid 27198030)
-
(1997)
Archives of Biochemistry and Biophysics
, vol.341
, Issue.1
, pp. 47-61
-
-
Draper, A.J.1
Madan, A.2
Parkinson, A.3
-
7
-
-
0035146956
-
Effects of organic solvents on the activities of cytochrome P450 isoforms, UDP-dependent glucuronyl transferase, and phenol sulfotransferase in human hepatocytes
-
Easterbrook J, Lu C, Sakai Y, and Li AP (2001) Effects of organic solvents on the activities of cytochrome P450 isoforms, UDP-dependent glucuronyl transferase, and phenol sulfotransferase in human hepatocytes. Drug Metab Dispos 29:141-144. (Pubitemid 32112927)
-
(2001)
Drug Metabolism and Disposition
, vol.29
, Issue.2
, pp. 141-144
-
-
Easterbrook, J.1
Lu, C.2
Sakai, Y.3
Li, A.P.4
-
8
-
-
0031696409
-
The contribution of intestinal and hepatic CYP3A to the interaction between midazolam and clarithromycin
-
DOI 10.1016/S0009-9236(98)90146-1
-
Gorski JC, Jones DR, Haehner-Daniels BD, Hamman MA, O'Mara EM Jr, and Hall SD (1998) The contribution of intestinal and hepatic CYP3A to the interaction between midazolam and clarithromycin. Clin Pharmacol Ther 64:133-143. (Pubitemid 28423848)
-
(1998)
Clinical Pharmacology and Therapeutics
, vol.64
, Issue.2
, pp. 133-143
-
-
Gorski, J.C.1
Jones, D.R.2
Haehner-Daniels, B.D.3
Hamman, M.A.4
O'Mara Jr., E.M.5
Hall, S.D.6
-
9
-
-
0026575955
-
The mechanism of the interaction between amiodarone and warfarin in humans
-
Heimark LD, Wienkers L, Kunze K, Gibaldi M, Eddy AC, Trager WF, O'Reilly RA, and Goulart DA (1992) The mechanism of the interaction between amiodarone and warfarin in humans. Clin Pharmacol Ther 51:398-407.
-
(1992)
Clin Pharmacol Ther
, vol.51
, pp. 398-407
-
-
Heimark, L.D.1
Wienkers, L.2
Kunze, K.3
Gibaldi, M.4
Eddy, A.C.5
Trager, W.F.6
O'Reilly, R.A.7
Goulart, D.A.8
-
10
-
-
0031921010
-
Evaluation of the selectivity of in vitro probes and suitability of organic solvents for the measurement of human cytochrome P450 monooxygenase activities
-
Hickman D, Wang JP, Wang Y, and Unadkat JD (1998) Evaluation of the selectivity of in vitro probes and suitability of organic solvents for the measurement of human cytochrome P450 monooxygenase activities. Drug Metab Dispos 26:207-215. (Pubitemid 28182395)
-
(1998)
Drug Metabolism and Disposition
, vol.26
, Issue.3
, pp. 207-215
-
-
Hickman, D.1
Wang, J.-P.2
Wang, Y.3
Unadkat, J.D.4
-
11
-
-
60749133620
-
Methods for predicting in vivo pharmacokinetics using data from in vitro assays
-
Houston JB and Galetin A (2008) Methods for predicting in vivo pharmacokinetics using data from in vitro assays. Curr Drug Metab 9:940-951.
-
(2008)
Curr Drug Metab
, vol.9
, pp. 940-951
-
-
Houston, J.B.A.1
Galetin, A.2
-
12
-
-
0347060621
-
Typical and atypical enzyme kinetics
-
Lee JS, Obach S, Fisher MB eds Fontis Media S.A., Lausanne, Switzerland and Marcel Dekker Inc., New York
-
Houston JB, Kenworthy KE, and Galetin A (2003) Typical and atypical enzyme kinetics, in Drug Metabolizing Enzymes: Cytochrome P450 and Other Enzymes in Drug Discovery and Development (Lee JS, Obach S, Fisher MB eds) pp 211-254, Fontis Media S.A., Lausanne, Switzerland and Marcel Dekker Inc., New York.
-
(2003)
Drug Metabolizing Enzymes: Cytochrome P450 and Other Enzymes in Drug Discovery and Development
, pp. 211-254
-
-
Houston, J.B.1
Kenworthy, K.E.2
Galetin, A.3
-
13
-
-
37549004394
-
The influence of CYP3A5 expression on the extent of hepatic CYP3A inhibition is substrate-dependent: An in vitro-in vivo evaluation
-
Isoherranen N, Ludington SR, Givens RC, Lamba JK, Pusek SN, Dees EC, Blough DK, Iwanaga K, Hawke RL, Schuetz EG, et al. (2008) The influence of CYP3A5 expression on the extent of hepatic CYP3A inhibition is substrate-dependent: an in vitro-in vivo evaluation. Drug Metab Dispos 36:146-154.
-
(2008)
Drug Metab Dispos
, vol.36
, pp. 146-154
-
-
Isoherranen, N.1
Ludington, S.R.2
Givens, R.C.3
Lamba, J.K.4
Pusek, S.N.5
Dees, E.C.6
Blough, D.K.7
Iwanaga, K.8
Hawke, R.L.9
Schuetz, E.G.10
-
14
-
-
33846244208
-
Evaluation of the effects of hydrophilic organic solvents on CYP3A-mediated drug-drug interaction in vitro
-
DOI 10.1177/0960327106071979
-
Iwase M, Kurata N, Ehana R, Nishimura Y, Masamoto T, and Yasuhara H (2006) Evaluation of the effects of hydrophilic organic solvents on CYP3A-mediated drug-drug interaction in vitro. Hum Exp Toxicol 25:715-721. (Pubitemid 46101697)
-
(2006)
Human and Experimental Toxicology
, vol.25
, Issue.12
, pp. 715-721
-
-
Iwase, M.1
Kurata, N.2
Ehana, R.3
Nishimura, Y.4
Masamoto, T.5
Yasuhara, H.6
-
15
-
-
0019180050
-
The effect of solvents on drug metabolism in vitro
-
Kawalek JC and Andrews AW (1980) The effect of solvents on drug metabolism in vitro. Drug Metab Dispos 8:380-384. (Pubitemid 11210385)
-
(1980)
Drug Metabolism and Disposition
, vol.8
, Issue.6
, pp. 380-384
-
-
Kawalek, J.C.1
Andrews, A.W.2
-
16
-
-
0032735988
-
CYP3A4 drug interactions: Correlation of 10 in vitro probe substrates
-
DOI 10.1046/j.1365-2125.1999.00073.x
-
Kenworthy KE, Bloomer JC, Clarke SE, and Houston JB (1999) CYP3A4 drug interactions: correlation of 10 in vitro probe substrates. Br J Clin Pharmacol 48:716-727. (Pubitemid 29520596)
-
(1999)
British Journal of Clinical Pharmacology
, vol.48
, Issue.5
, pp. 716-727
-
-
Kenworthy, K.E.1
Bloomer, J.C.2
Clarke, S.E.3
Houston, J.B.4
-
17
-
-
33751085910
-
Enzyme source effects on CYP2C9 kinetics and inhibition
-
DOI 10.1124/dmd.106.010249
-
Kumar V, Rock DA, Warren CJ, Tracy TS, and Wahlstrom JL (2006a) Enzyme source effects on CYP2C9 kinetics and inhibition. Drug Metab Dispos 34:1903-1908. (Pubitemid 44771720)
-
(2006)
Drug Metabolism and Disposition
, vol.34
, Issue.11
, pp. 1903-1908
-
-
Kumar, V.1
Rock, D.A.2
Warren, C.J.3
Tracy, T.S.4
Wahlstrom, J.L.5
-
18
-
-
33750547308
-
CYP2C9 inhibition: Impact of probe selection and pharmacogenetics on in vitro inhibition profiles
-
DOI 10.1124/dmd.106.010926
-
Kumar V, Wahlstrom JL, Rock DA, Warren CJ, Gorman LA, and Tracy TS (2006b) CYP2C9 inhibition: impact of probe selection and pharmacogenetics on in vitro inhibition profiles. Drug Metab Dispos 34:1966-1975. (Pubitemid 44837757)
-
(2006)
Drug Metabolism and Disposition
, vol.34
, Issue.12
, pp. 1966-1975
-
-
Kumar, V.1
Wahlstrom, J.L.2
Rock, D.A.3
Warren, C.J.4
Gorman, L.A.5
Tracy, T.S.6
-
19
-
-
0030888416
-
Steady-state clearance rates of warfarin and its enantiomers in therapeutically dosed patients
-
DOI 10.1002/(SICI)1520-636X(1997)9:1<13::AID-CHIR3>3.0.CO;2-H
-
McAleer SD, Foondun AS, Feely M, and Chrystyn H (1997) Steady-state clearance rates of warfarin and its enantiomers in therapeutically dosed patients. Chirality 9:13-16. (Pubitemid 27149065)
-
(1997)
Chirality
, vol.9
, Issue.1
, pp. 13-16
-
-
McAleer, S.D.1
Foondun, A.S.2
Feely, M.3
Chrystyn, H.4
-
20
-
-
61449104884
-
Identification of a cranberry juice product that inhibits enteric CYP3A-mediated first-pass metabolism in humans
-
Ngo N, Yan Z, Graf TN, Carrizosa DR, Kashuba AD, Dees EC, Oberlies NH, and Paine MF (2009) Identification of a cranberry juice product that inhibits enteric CYP3A-mediated first-pass metabolism in humans. Drug Metab Dispos 37:514-522.
-
(2009)
Drug Metab Dispos
, vol.37
, pp. 514-522
-
-
Ngo, N.1
Yan, Z.2
Graf, T.N.3
Carrizosa, D.R.4
Kashuba, A.D.5
Dees, E.C.6
Oberlies, N.H.7
Paine, M.F.8
-
21
-
-
84866321358
-
The warfarin-cranberry juice interaction revisited: A systematic in vitro-in vivo evaluation
-
Ngo N, Brantley SJ, Carrizosa DR, Kashuba AD, Dees EC, Kroll DJ, Oberlies NH, and Paine MF (2010) The warfarin-cranberry juice interaction revisited: a systematic in vitro-in vivo evaluation. J Exp Pharmacol 2010:83-91.
-
(2010)
J Exp Pharmacol
, vol.2010
, pp. 83-91
-
-
Ngo, N.1
Brantley, S.J.2
Carrizosa, D.R.3
Kashuba, A.D.4
Dees, E.C.5
Kroll, D.J.6
Oberlies, N.H.7
Paine, M.F.8
-
22
-
-
0032733974
-
Prediction of human clearance of twenty-nine drugs from hepatic microsomal intrinsic clearance data: An examination of in vitro half-life approach and nonspecific binding to microsomes
-
Obach RS (1999) Prediction of human clearance of twenty-nine drugs from hepatic microsomal intrinsic clearance data: an examination of in vitro half-life approach and nonspecific binding to microsomes. Drug Metab Dispos 27:1350-1359.
-
(1999)
Drug Metab Dispos
, vol.27
, pp. 1350-1359
-
-
Obach, R.S.1
-
23
-
-
0030799001
-
The prediction of human pharmacokinetic parameters from preclinical and in vitro metabolism data
-
Obach RS, Baxter JG, Liston TE, Silber BM, Jones BC, MacIntyre F, Rance DJ, and Wastall P (1997) The prediction of human pharmacokinetic parameters from preclinical and in vitro metabolism data. J Pharmacol Exp Ther 283:46-58. (Pubitemid 27438945)
-
(1997)
Journal of Pharmacology and Experimental Therapeutics
, vol.283
, Issue.1
, pp. 46-58
-
-
Obach, R.S.1
Baxter, J.G.2
Liston, T.E.3
Silber, B.M.4
Jones, B.C.5
Macintyre, F.6
Rance, D.J.7
Wastall, P.8
-
24
-
-
0015451733
-
Sodium warfarin
-
O'Reilly RA (1972) Sodium warfarin. Pharmacology 8:181-190.
-
(1972)
Pharmacology
, vol.8
, pp. 181-190
-
-
O'Reilly, R.A.1
-
25
-
-
84857569031
-
Is there a relationship between the substrate preferences and structural flexibility of cytochromes P450?
-
Otyepka M, Berka K, and Anzenbacher P (2012) Is there a relationship between the substrate preferences and structural flexibility of cytochromes P450? Curr Drug Metab 13:130-142.
-
(2012)
Curr Drug Metab
, vol.13
, pp. 130-142
-
-
Otyepka, M.1
Berka, K.2
Anzenbacher, P.3
-
26
-
-
33645809139
-
The human intestinal cytochrome P450 "pie."
-
Paine MF, Hart HL, Ludington SS, Haining RL, Rettie AE, and Zeldin DC (2006) The human intestinal cytochrome P450 "pie." Drug Metab Dispos 34:880-886.
-
(2006)
Drug Metab Dispos
, vol.34
, pp. 880-886
-
-
Paine, M.F.1
Hart, H.L.2
Ludington, S.S.3
Haining, R.L.4
Rettie, A.E.5
Zeldin, D.C.6
-
27
-
-
0023697057
-
Cytochrome P-450-catalyzed desaturation of valproic acid in vitro. Species differences, induction effects, and mechanistic studies
-
Rettie AE, Boberg M, Rettenmeier AW, and Baillie TA (1988) Cytochrome P-450-catalyzed desaturation of valproic acid in vitro. Species differences, induction effects, and mechanistic studies. J Biol Chem 263:13733-13738.
-
(1988)
J Biol Chem
, vol.263
, pp. 13733-13738
-
-
Rettie, A.E.1
Boberg, M.2
Rettenmeier, A.W.3
Baillie, T.A.4
-
28
-
-
0035148967
-
Triazolam substrate inhibition: Evidence of competition for heme-bound reactive oxygen within the CYP3A4 active site
-
Schrag ML and Wienkers LC (2001) Triazolam substrate inhibition: evidence of competition for heme-bound reactive oxygen within the CYP3A4 active site. Drug Metab Dispos 29:70-75. (Pubitemid 32041682)
-
(2001)
Drug Metabolism and Disposition
, vol.29
, Issue.1
, pp. 70-75
-
-
Schrag, M.L.1
Wienkers, L.C.2
-
29
-
-
33744803155
-
Multiple molecular dynamics simulations of human P450 monooxygenase CYP2C9: The molecular basis of substrate binding and regioselectivity toward warfarin
-
DOI 10.1002/prot.20951
-
Seifert A, Tatzel S, Schmid RD, and Pleiss J (2006) Multiple molecular dynamics simulations of human p450 monooxygenase CYP2C9: the molecular basis of substrate binding and regioselectivity toward warfarin. Proteins 64:147-155. (Pubitemid 43830993)
-
(2006)
Proteins: Structure, Function and Genetics
, vol.64
, Issue.1
, pp. 147-155
-
-
Seifert, A.1
Tatzel, S.2
Schmid, R.B.3
Pleiss, J.4
-
30
-
-
0033373389
-
Potentiation of anticoagulant effect of warfarin caused by enantioselective metabolic inhibition by the uricosuric agent benzbromarone
-
Takahashi H, Sato T, Shimoyama Y, Shioda N, Shimizu T, Kubo S, Tamura N, Tainaka H, Yasumori T, and Echizen H (1999) Potentiation of anticoagulant effect of warfarin caused by enantioselective metabolic inhibition by the uricosuric agent benzbromarone. Clin Pharmacol Ther 66:569-581. (Pubitemid 30014082)
-
(1999)
Clinical Pharmacology and Therapeutics
, vol.66
, Issue.6
, pp. 569-581
-
-
Takahashi, H.1
Sato, T.2
Shimoyama, Y.3
Shioda, N.4
Shimizu, T.5
Kubo, S.6
Tamura, N.7
Tainaka, H.8
Yasumori, T.9
Echizen, H.10
-
31
-
-
0034007499
-
Substrate-dependent effect of acetonitrile on human liver microsomal cytochrome P450 2C9 (CYP2C9) activity
-
Tang C, Shou M, and Rodrigues AD (2000) Substrate-dependent effect of acetonitrile on human liver microsomal cytochrome P450 2C9 (CYP2C9) activity. Drug Metab Dispos 28:567-572. (Pubitemid 30238516)
-
(2000)
Drug Metabolism and Disposition
, vol.28
, Issue.5
, pp. 567-572
-
-
Tang, C.1
Shou, M.2
Rodrigues, A.D.3
-
32
-
-
0030015297
-
Oral first-pass elimination of midazolam involves both gastrointestinal and hepatic CYP3A-mediated metabolism
-
DOI 10.1016/S0009-9236(96)90177-0
-
Thummel KE, O'Shea D, Paine MF, Shen DD, Kunze KL, Perkins JD, and Wilkinson GR (1996) Oral first-pass elimination of midazolam involves both gastrointestinal and hepatic CYP3A-mediated metabolism. Clin Pharmacol Ther 59:491-502. (Pubitemid 26193889)
-
(1996)
Clinical Pharmacology and Therapeutics
, vol.59
, Issue.5
, pp. 491-502
-
-
Thummel, K.E.1
O'Shea, D.2
Paine, M.F.3
Shen, D.D.4
Kunze, K.L.5
Perkins, J.D.6
Wilkinson, G.R.7
-
33
-
-
0032700543
-
Differentiation of intestinal and hepatic cytochrome P450 3A activity with use of midazolam as an in vivo probe: Effect of ketoconazole
-
Tsunoda SM, Velez RL, von Moltke LL, and Greenblatt DJ (1999) Differentiation of intestinal and hepatic cytochrome P450 3A activity with use of midazolam as an in vivo probe: effect of ketoconazole. Clin Pharmacol Ther 66:461-471.
-
(1999)
Clin Pharmacol Ther
, vol.66
, pp. 461-471
-
-
Tsunoda, S.M.1
Velez, R.L.2
Von Moltke, L.L.3
Greenblatt, D.J.4
-
34
-
-
0029743080
-
Midazolam hydroxylation by human liver microsomes in vitro: Inhibition by fluoxetine, norfluoxetine, and by azole antifungal agents
-
von Moltke LL, Greenblatt DJ, Schmider J, Duan SX, Wright CE, Harmatz JS, and Shader RI (1996) Midazolam hydroxylation by human liver microsomes in vitro: inhibition by fluoxetine, norfluoxetine, and by azole antifungal agents. J Clin Pharmacol 36:783-791. (Pubitemid 26329500)
-
(1996)
Journal of Clinical Pharmacology
, vol.36
, Issue.9
, pp. 783-791
-
-
Von Moltke, L.L.1
Greenblatt, D.J.2
Schmider, J.3
Duan, S.X.4
Wright, C.E.5
Harmatz, J.S.6
Shader, R.I.7
-
35
-
-
35548936928
-
Human enteric microsomal CYP4F enzymes O-demethylate the antiparasitic prodrug pafuramidine
-
DOI 10.1124/dmd.107.016428
-
Wang MZ, Wu JQ, Bridges AS, Zeldin DC, Kornbluth S, Tidwell RR, Hall JE, and Paine MF (2007) Human enteric microsomal CYP4F enzymes O-demethylate the antiparasitic prodrug pafuramidine. Drug Metab Dispos 35:2067-2075. (Pubitemid 350005197)
-
(2007)
Drug Metabolism and Disposition
, vol.35
, Issue.11
, pp. 2067-2075
-
-
Wang, M.Z.1
Wu, J.Q.2
Bridges, A.S.3
Zeldin, D.C.4
Kornbluth, S.5
Tidwell, R.R.6
Hall, J.E.7
Paine, M.F.8
-
36
-
-
27644596457
-
Predicting in vivo drug interactions from in vitro drug discovery data
-
DOI 10.1038/nrd1851, PII N1851
-
Wienkers LC and Heath TG (2005) Predicting in vivo drug interactions from in vitro drug discovery data. Nat Rev Drug Discov 4:825-833. (Pubitemid 41553963)
-
(2005)
Nature Reviews Drug Discovery
, vol.4
, Issue.10
, pp. 825-833
-
-
Wienkers, L.C.1
Heath, T.G.2
-
37
-
-
0042265520
-
Crystal structure of human cytochrome P450 2C9 with bound warfarin
-
DOI 10.1038/nature01862
-
Williams PA, Cosme J, Ward A, Angove HC, Matak Vinković D, and Jhoti H (2003) Crystal structure of human cytochrome P450 2C9 with bound warfarin. Nature 424:464-468. (Pubitemid 36917499)
-
(2003)
Nature
, vol.424
, Issue.6947
, pp. 464-468
-
-
Williams, P.A.1
Cosme, J.2
Ward, A.3
Angove, H.C.4
Vinkovic, D.M.5
Jhoti, H.6
-
38
-
-
33847411025
-
Misuse of the well-stirred model of hepatic drug clearance
-
DOI 10.1124/dmd.106.013359
-
Yang J, Jamei M, Yeo KR, Rostami-Hodjegan A, and Tucker GT (2007) Misuse of the well-stirred model of hepatic drug clearance. Drug Metab Dispos 35:501-502. (Pubitemid 46333921)
-
(2007)
Drug Metabolism and Disposition
, vol.35
, Issue.3
, pp. 501-502
-
-
Yang, J.1
Jamei, M.2
Yeo, K.R.3
Rostami-Hodjegan, A.4
Tucker, G.T.5
-
39
-
-
0036893593
-
Evaluation of cytochrome p450 probe substrates commonly used by the pharmaceutical industry to study in vitro drug interactions
-
DOI 10.1124/dmd.30.12.1311
-
Yuan R, Madani S, Wei XX, Reynolds K, and Huang SM (2002) Evaluation of cytochrome P450 probe substrates commonly used by the pharmaceutical industry to study in vitro drug interactions. Drug Metab Dispos 30:1311-1319. (Pubitemid 35397032)
-
(2002)
Drug Metabolism and Disposition
, vol.30
, Issue.12
, pp. 1311-1319
-
-
Yuan, R.1
Madani, S.2
Wei, X.-X.3
Reynolds, K.4
Huang, S.-M.5
-
40
-
-
54949144309
-
Functional pharmacogenetics/genomics of human cytochromes P450 involved in drug biotransformation
-
Zanger UM, Turpeinen M, Klein K, and Schwab M (2008) Functional pharmacogenetics/genomics of human cytochromes P450 involved in drug biotransformation. Anal Bioanal Chem 392:1093-1108.
-
(2008)
Anal Bioanal Chem
, vol.392
, pp. 1093-1108
-
-
Zanger, U.M.1
Turpeinen, M.2
Klein, K.3
Schwab, M.4
|