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Physiology & Behavior|April 1, 1990
Analysis of spontaneous alcohol drinking in rhesus monkeysM Kornet, C Goosen, L G Ribbens, et al.Journal of Clinical Pharmacology|September 21, 2023
Physiologically Based Pharmacokinetic Modeling of the Drug-Drug Interaction Between CYP3A4 Substrate Glasdegib and Moderate CYP3A4 Inducers in Lieu of a Clinical StudyErnesto Callegari, Susanna Tse, Angela C Doran, et al.European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology|March 1, 1992
Low doses of morphine reduce voluntary alcohol consumption in rhesus monkeysM Kornet, J A van Vlaardingen, C Goosen, et al.Journal of Proteome Research|August 28, 2013
Targeted quantitative proteomics for the analysis of 14 UGT1As and -2Bs in human liver using NanoUPLC-MS/MS with selected reaction monitoringJohn K Fallon, Hendrik Neubert, Ruth Hyland, et al.Pharmacology & Therapeutics|September 27, 2020
Evidence-based strategies for the characterisation of human drug and chemical glucuronidation in vitro and UDP-glucuronosyltransferase reaction phenotypingJohn O Miners, Andrew Rowland, Jonathan J Novak, et al.Drug Metabolism and Disposition: the Biological Fate of Chemicals|April 3, 2021
Cytochrome P450 3A Time-Dependent Inhibition Assays Are Too Sensitive for Identification of Drugs Causing Clinically Significant Drug-Drug Interactions: A Comparison of Human Liver Microsomes and Hepatocytes and Definition of Boundaries for Inactivation Rate ConstantsHeather Eng, Elaine Tseng, Matthew A Cerny, et al.Drug Metabolism and Disposition: the Biological Fate of Chemicals|May 25, 2004
Silybin inactivates cytochromes P450 3A4 and 2C9 and inhibits major hepatic glucuronosyltransferasesChitra Sridar, Theunis C Goosen, Ute M Kent, et al.The AAPS Journal|February 4, 2025
Development of a PBPK Model for Lamotrigine which Incorporates Metabolism by UGT2B10: Impact of UGT2B10 Poor Metabolizer Phenotype and PregnancyIain Gardner, Aki T Heikkinen, Lloyd Wei Tat Tang, et al.International Journal of Pharmaceutics|December 22, 1999
The influence of the physicochemical characteristics and pharmacokinetic properties of selected NSAID's on their transdermal absorptionE Beetge, J du Plessis, D G Müller, et al.International Journal of Pharmaceutics|July 6, 2004
Percutaneous delivery of carbamazepine and selected N-alkyl and N-hydroxyalkyl analoguesL Fourie, J C Breytenbach, J Du Plessis, et al.Pageof 9