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Drug Metabolism and Disposition: the Biological Fate of Chemicals|April 1, 1995
Catalytic role of cytochrome P4503A4 in multiple pathways of alfentanil metabolismR B Labroo, K E Thummel, K L Kunze, et al.Biochemical and Biophysical Research Communications|February 15, 1985
Stereoselective and regioselective hydroxylation of warfarin and selective O-dealkylation of phenoxazone ethers in human placentaA E Rettie, L Heimark, R T Mayer, et al.Biochemistry|July 18, 2001
Active site characteristics of CYP4B1 probed with aromatic ligandsK R Henne, M B Fisher, K R Iyer, et al.Clinical Pharmacology and Therapeutics|November 24, 2001
Fluvoxamine-theophylline interaction: gap between in vitro and in vivo inhibition constants toward cytochrome P4501A2C Yao, K L Kunze, E D Kharasch, et al.Biochemistry|April 12, 2000
Mechanism-based inactivation of cytochrome P450 3A4 by L-754,394L K Lightning, J P Jones, T Friedberg, et al.Clinical Pharmacology and Therapeutics|May 1, 1994
Disposition of drugs in cystic fibrosis. VI. In vivo activity of cytochrome P450 isoforms involved in the metabolism of (R)-warfarin (including P450 3A4) is not enhanced in cystic fibrosisJ P Wang, J D Unadkat, S McNamara, et al.Clinical Pharmacology and Therapeutics|January 1, 1986
The warfarin-sulfinpyrazone interaction: stereochemical considerationsS Toon, L K Low, M Gibaldi, et al.Clinical Pharmacology and Therapeutics|June 1, 1992
Mechanisms of the stereoselective interaction between miconazole and racemic warfarin in human subjectsR A O'Reilly, D A Goulart, K L Kunze, et al.Chemical Research in Toxicology|May 5, 1998
Oxidation of acetaminophen to its toxic quinone imine and nontoxic catechol metabolites by baculovirus-expressed and purified human cytochromes P450 2E1 and 2A6W Chen, L L Koenigs, S J Thompson, et al.Pharmacogenetics|November 14, 1997
Genetic association between sensitivity to warfarin and expression of CYP2C9*3D J Steward, R L Haining, K R Henne, et al.Pageof 9