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Basic & Clinical Pharmacology & Toxicology|December 17, 2009
Predicting drug disposition via application of a Biopharmaceutics Drug Disposition Classification SystemLeslie Z BenetMolecular Interventions|April 12, 2005
There are no useful CYP3A probes that quantitatively predict the in vivo kinetics of other CYP3A substrates and no expectation that one will be foundLeslie Z BenetPharmaceutical Research|May 30, 2002
Can the enhanced renal clearance of antibiotics in cystic fibrosis patients be explained by P-glycoprotein transport?Miki Susanto, Leslie Z BenetJournal of Pharmacokinetics and Pharmacodynamics|April 19, 2011
Intermittent drug dosing intervals guided by the operational multiple dosing half lives for predictable plasma accumulation and fluctuationAnita Grover, Leslie Z BenetPharmaceutical Research|July 2, 2009
The role of transporters in the pharmacokinetics of orally administered drugsSarah Shugarts, Leslie Z BenetJournal of Pharmaceutical Sciences|May 28, 2011
Effects of uremic toxins on transport and metabolism of different biopharmaceutics drug disposition classification system xenobioticsMaribel Reyes, Leslie Z BenetChemical Research in Toxicology|February 14, 2013
Characterization of the acyl-adenylate linked metabolite of mefenamic AcidHoward Horng, Leslie Z BenetDrug Metabolism and Disposition: the Biological Fate of Chemicals|August 27, 2013
The nonenzymatic reactivity of the acyl-linked metabolites of mefenamic acid toward amino and thiol functional group bionucleophilesHoward Horng, Leslie Z BenetPharmacology|January 8, 2020
Late-Stage Failures of Monoclonal Antibody Drugs: A Retrospective Case Study AnalysisAmy Sun, Leslie Z BenetThe AAPS Journal|April 29, 2009
Effects of drug transporters on volume of distributionAnita Grover, Leslie Z BenetPageof 18