P450 3A activity and cyclosporine dosing in kidney and heart transplant recipients
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P. Watkins | G. Deeb | R. Merion | D. Normolle | A. Leichtman | D. Turgeon | K. Lown | G. Deeb | Alan B Leichtman | Kenneth S Lown
[1] T. Annesley,et al. Erythromycin breath test predicts oral clearance of cyclosporine in kidney transplant recipients , 1992, Clinical pharmacology and therapeutics.
[2] J. Kolars,et al. Identification of rifampin-inducible P450IIIA4 (CYP3A4) in human small bowel enterocytes. , 1992, The Journal of clinical investigation.
[3] P. Watkins. Role of Cytochromes P45O in Drug Metabolism and Hepatotoxicity , 1990, Seminars in liver disease.
[4] P. Maurel,et al. Cyclosporin A drug interactions. Screening for inducers and inhibitors of cytochrome P-450 (cyclosporin A oxidase) in primary cultures of human hepatocytes and in liver microsomes. , 1990, Drug metabolism and disposition: the biological fate of chemicals.
[5] J. Kolars,et al. The erythromycin breath test as a predictor of cyclosporine blood levels , 1990, Clinical pharmacology and therapeutics.
[6] T. Aoyama,et al. Cytochrome P-450 hPCN3, a novel cytochrome P-450 IIIA gene product that is differentially expressed in adult human liver. cDNA and deduced amino acid sequence and distinct specificities of cDNA-expressed hPCN1 and hPCN3 for the metabolism of steroid hormones and cyclosporine. , 1989, The Journal of biological chemistry.
[7] J. Derancourt,et al. Metabolism of cyclosporin A. IV. Purification and identification of the rifampicin-inducible human liver cytochrome P-450 (cyclosporin A oxidase) as a product of P450IIIA gene subfamily. , 1989, Drug metabolism and disposition: the biological fate of chemicals.
[8] P. Watkins,et al. Erythromycin breath test as an assay of glucocorticoid-inducible liver cytochromes P-450. Studies in rats and patients. , 1989, The Journal of clinical investigation.
[9] B. Kahan,et al. Optimization of cyclosporine therapy in renal transplantation by a pharmacokinetic strategy. , 1988, Transplantation.
[10] T. Kronbach,et al. Cyclosporine metabolism in human liver: Identification of a cytochrome P‐450III gene family as the major cyclosporine‐metabolizing enzyme explains interactions of cyclosporine with other drugs , 1988, Clinical pharmacology and therapeutics.
[11] G. Forbes,et al. Central Nervous System Toxicity after Liver Transplantation , 1987 .
[12] P. Watkins,et al. Identification of glucocorticoid-inducible cytochromes P-450 in the intestinal mucosa of rats and man. , 1987, The Journal of clinical investigation.
[13] T. Annesley,et al. Liquid-chromatographic analysis for cyclosporine with use of a microbore column and small sample volume. , 1986, Clinical chemistry.
[14] D. Waxman,et al. Characterization of rat and human liver microsomal cytochrome P-450 forms involved in nifedipine oxidation, a prototype for genetic polymorphism in oxidative drug metabolism. , 1986, The Journal of biological chemistry.
[15] C. V. van Buren,et al. DEMOGRAPHIC FACTORS AFFECTING THE PHARMACOKINETICS OF CYCLOSPORINE ESTIMATED BY RADIOIMMUNOASSAY , 1986, Transplantation.
[16] P. Watkins,et al. Identification of an inducible form of cytochrome P-450 in human liver. , 1985, Proceedings of the National Academy of Sciences of the United States of America.
[17] J. D. Shoop,et al. Test for alcoholic cirrhosis by conversion of [14C]- or [13C]galactose to expired CO2. , 1976, Gastroenterology.
[18] M. J. Coon,et al. The P450 superfamily: update on new sequences, gene mapping, accession numbers, early trivial names of enzymes, and nomenclature. , 1993, DNA and cell biology.
[19] F. Guengerich. Characterization of human microsomal cytochrome P-450 enzymes. , 1989, Annual review of pharmacology and toxicology.