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Clinical Pharmacology and Therapeutics|March 1, 1992
The erythromycin breath test selectively measures P450IIIA in patients with severe liver diseaseK Lown, J Kolars, K Turgeon, et al.Journal of Pharmacological and Toxicological Methods|March 29, 2001
Present and future in vitro approaches for drug metabolismS Ekins, B J Ring, J Grace, et al.Biochemical Pharmacology|October 25, 1996
Studies of flurbiprofen 4'-hydroxylation. Additional evidence suggesting the sole involvement of cytochrome P450 2C9T S Tracy, C Marra, S A Wrighton, et al.Biochemical Pharmacology|April 29, 1994
Regioselective biotransformation of midazolam by members of the human cytochrome P450 3A (CYP3A) subfamilyJ C Gorski, S D Hall, D R Jones, et al.Pharmacogenetics|February 18, 1999
Human cytochrome P450 3A (CYP3A) mediated midazolam metabolism: the effect of assay conditions and regioselective stimulation by alpha-naphthoflavone, terfenadine and testosteroneJ Mäenpää, S D Hall, B J Ring, et al.The Journal of Biological Chemistry|May 15, 1986
Macrolide antibiotics inhibit the degradation of the glucocorticoid-responsive cytochrome P-450p in rat hepatocytes in vivo and in primary monolayer cultureP B Watkins, S A Wrighton, E G Schuetz, et al.Carcinogenesis|November 1, 1984
Binding and metabolism of benzo[a]pyrene and 7,12-dimethylbenz[a]anthracene by seven purified forms of cytochrome P-450N M Wilson, M Christou, C R Turner, et al.Archives of Biochemistry and Biophysics|May 1, 1992
Differential apoprotein loss of rat liver cytochromes P450 after their inactivation by 3,5-dicarbethoxy-2,6-dimethyl-4-ethyl-1,4-dihydropyridine: a case for distinct proteolytic mechanisms?M A Correia, K Yao, S A Wrighton, et al.Archives of Biochemistry and Biophysics|March 10, 1995
Interactions of peroxyquinols with cytochromes P450 2B1, 3A1, and 3A5: influence of the apoprotein on heterolytic versus homolytic O-O bond cleavageM A Correia, K Yao, A J Allentoff, et al.Drug Metabolism and Disposition: the Biological Fate of Chemicals|September 1, 1993
Comparison of human and rhesus monkey in vitro phase I and phase II hepatic drug metabolism activitiesJ C Stevens, L A Shipley, J R Cashman, et al.Pageof 12