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Drug Metabolism and Disposition: the Biological Fate of Chemicals|April 1, 1996
Warfarin-fluconazole. I. Inhibition of the human cytochrome P450-dependent metabolism of warfarin by fluconazole: in vitro studiesK L Kunze, L C Wienkers, K E Thummel, et al.Clinical Pharmacology and Therapeutics|September 1, 1987
Interaction of amiodarone with racemic warfarin and its separated enantiomorphs in humansR A O'Reilly, W F Trager, A E Rettie, et al.Drug Metabolism and Disposition: the Biological Fate of Chemicals|November 1, 1990
Isotope effect studies on the mechanism of the cytochrome P-450IIA1-catalyzed formation of delta 6-testosterone from testosteroneK R Korzekwa, W F Trager, K Nagata, et al.American Journal of Hospital Pharmacy|April 1, 1986
Variation in light transmission properties of amber oral syringesW R Porter, S F BauwensJournal of Chromatography|September 9, 1983
Resolution of valproic acid from deuterated analogues and their quantitation in plasma using capillary gas chromatographyD J Hoffman, W R PorterArchives of Biochemistry and Biophysics|November 24, 1999
Structural forms of phenprocoumon and warfarin that are metabolized at the active site of CYP2C9M He, K R Korzekwa, J P Jones, et al.Clinical Pharmacology and Therapeutics|October 1, 1987
The mechanism of the warfarin-rifampin drug interaction in humansL D Heimark, M Gibaldi, W F Trager, et al.Journal of Medicinal Chemistry|August 24, 2000
A refined 3-dimensional QSAR of cytochrome P450 2C9: computational predictions of drug interactionsS Rao, R Aoyama, M Schrag, et al.Drug Metabolism and Disposition: the Biological Fate of Chemicals|November 26, 1999
Characterization of the in vitro biotransformation of the HIV-1 reverse transcriptase inhibitor nevirapine by human hepatic cytochromes P-450D A Erickson, G Mather, W F Trager, et al.Biochemistry|June 25, 1991
Theoretical studies on the mechanism of conversion of androgens to estrogens by aromataseK R Korzekwa, W F Trager, S J Smith, et al.Pageof 11