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Canadian Journal of Physiology and Pharmacology|April 1, 1991
Porphyrinogenic effects in chick embryo liver cell culture of chloramphenicol analogues that are mechanism-based inactivators of cytochrome P-450R P Green-Thompson, D S Riddick, J E Mackie, et al.
Biochemistry|October 14, 2011
The structural basis for homotropic and heterotropic cooperativity of midazolam metabolism by human cytochrome P450 3A4Arthur G Roberts, Jing Yang, James R Halpert, et al.
The Journal of Pharmacology and Experimental Therapeutics|July 20, 1999
Use of the steroid derivative RPR 106541 in combination with site-directed mutagenesis for enhanced cytochrome P-450 3A4 structure/function analysisJ C Stevens, T L Domanski, G R Harlow, et al.
Radiology|April 1, 1983
Work in progress: radioisotopic evaluation of gastroplasty patientsW E Drane, D S Marks, S M Simms, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|November 14, 1997
Inactivation of cytochrome P450s 2B1, 2B4, 2B6, and 2B11 by arylalkynesE S Roberts, N E Hopkins, M Foroozesh, et al.
The Journal of Pharmacology and Experimental Therapeutics|January 1, 1996
Suppression of rat hepatic microsomal cytochromes P450 by cyclophosphamide is correlated with plasma thyroid hormone levels and displays differential strain sensitivityJ C Kraner, E T Morgan, T S Poet, et al.
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