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The Journal of Pharmacology and Experimental Therapeutics|February 15, 2018
Establishing Transcriptional Signatures to Differentiate PXR-, CAR-, and AhR-Mediated Regulation of Drug Metabolism and Transport Genes in Cryopreserved Human HepatocytesJamie E Moscovitz, Amit S Kalgutkar, Kelly Nulick, et al.
Pharmaceutical Research|January 12, 2013
Mechanistic modeling to predict the transporter- and enzyme-mediated drug-drug interactions of repaglinideManthena V S Varma, Yurong Lai, Emi Kimoto, et al.
Pharmaceutical Research|September 21, 2002
Chemical stabilities and biological activities of thalidomide and its N-alkyl analogsColleen Goosen, Timothy J Laing, Jeanetta du Plessis, et al.
Pharmaceutical Research|May 30, 2002
Percutaneous delivery of thalidomide and its N-alkyl analogsColleen Goosen, Timothy J Laing, Jeanetta du Plessis, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|September 26, 2013
A perspective on the prediction of drug pharmacokinetics and disposition in drug research and developmentLi Di, Bo Feng, Theunis C Goosen, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|October 6, 2020
In Vitro Characterization of Ertugliflozin Metabolism by UDP-Glucuronosyltransferase and Cytochrome P450 EnzymesKimberly Lapham, Ernesto Callegari, Julie Cianfrogna, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|July 30, 2021
Static and Dynamic Projections of Drug-Drug Interactions Caused by Cytochrome P450 3A Time-Dependent Inhibitors Measured in Human Liver Microsomes and HepatocytesElaine Tseng, Heather Eng, Jian Lin, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|May 15, 2012
Physicochemical property space of hepatobiliary transport and computational models for predicting rat biliary excretionManthena V S Varma, George Chang, Yurong Lai, et al.
Psychopharmacology|April 1, 1995
Morphine and naltrexone modulate D2 but not D1 receptor induced motor behavior in MPTP-lesioned monkeysR J Vermeulen, B Drukarch, M C Sahadat, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|May 2, 2007
Atorvastatin glucuronidation is minimally and nonselectively inhibited by the fibrates gemfibrozil, fenofibrate, and fenofibric acidTheunis C Goosen, Jonathan N Bauman, John A Davis, et al.
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