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Yurong Lai

Showing results (91-100 of 136) with videos related to

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Pharmacology & Therapeutics|August 24, 2022
The next frontier in ADME science: Predicting transporter-based drug disposition, tissue concentrations and drug-drug interactions in humansFlavia Storelli, Mengyue Yin, Aditya R Kumar, et al.
Molecular Pharmaceutics|February 25, 2016
Disruption of BSEP Function in HepaRG Cells Alters Bile Acid Disposition and Is a Susceptive Factor to Drug-Induced Cholestatic InjuryXi Qiu, Yueping Zhang, Tongtong Liu, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|June 10, 2010
Novel metabolic bioactivation mechanism for a series of anti-inflammatory agents (2,5-diaminothiophene derivatives) mediated by cytochrome p450 enzymesYiding Hu, Shengtian Yang, F Barclay Shilliday, et al.
The AAPS Journal|March 12, 2026
Application of a Modified In Situ Perfusion Model to Quantify Intestinal Drug Excretion and Transporter-Mediated Interactions after Intravenous AdministrationRongjin Sun, Li Li, Lu Wang, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|February 9, 2013
Quantitative prediction of repaglinide-rifampicin complex drug interactions using dynamic and static mechanistic models: delineating differential CYP3A4 induction and OATP1B1 inhibition potential of rifampicinManthena V S Varma, Jian Lin, Yi-An Bi, et al.
European Journal of Medicinal Chemistry|July 31, 2012
Mechanistic insights from comparing intrinsic clearance values between human liver microsomes and hepatocytes to guide drug designLi Di, Christopher Keefer, Dennis O Scott, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|January 10, 2019
A Comparison of Total and Plasma Membrane Abundance of Transporters in Suspended, Plated, Sandwich-Cultured Human Hepatocytes Versus Human Liver Tissue Using Quantitative Targeted Proteomics and Cell Surface BiotinylationVineet Kumar, Laurent Salphati, Cornelis E C A Hop, et al.
Acta Pharmaceutica Sinica. B|June 27, 2022
Recent advances in the translation of drug metabolism and pharmacokinetics science for drug discovery and developmentYurong Lai, Xiaoyan Chu, Li Di, et al.
Drug Metabolism and Pharmacokinetics|February 28, 2026
Applications of in vitro transporter assays for mechanistic characterization and prediction of clinical drug-drug interactionsKrisztina Herédi-Szabó, Sumito Ito, Xiaomin Liang, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|June 4, 2017
Comparative Evaluation of Plasma Bile Acids, Dehydroepiandrosterone Sulfate, Hexadecanedioate, and Tetradecanedioate with Coproporphyrins I and III as Markers of OATP Inhibition in Healthy SubjectsHong Shen, Weiqi Chen, Dieter M Drexler, et al.
Pageof 14

Showing results (91-100 of 136) with videos related to

Sort By:
Pageof 14
Pharmacology & Therapeutics|August 24, 2022
The next frontier in ADME science: Predicting transporter-based drug disposition, tissue concentrations and drug-drug interactions in humansFlavia Storelli, Mengyue Yin, Aditya R Kumar, et al.
Molecular Pharmaceutics|February 25, 2016
Disruption of BSEP Function in HepaRG Cells Alters Bile Acid Disposition and Is a Susceptive Factor to Drug-Induced Cholestatic InjuryXi Qiu, Yueping Zhang, Tongtong Liu, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|June 10, 2010
Novel metabolic bioactivation mechanism for a series of anti-inflammatory agents (2,5-diaminothiophene derivatives) mediated by cytochrome p450 enzymesYiding Hu, Shengtian Yang, F Barclay Shilliday, et al.
The AAPS Journal|March 12, 2026
Application of a Modified In Situ Perfusion Model to Quantify Intestinal Drug Excretion and Transporter-Mediated Interactions after Intravenous AdministrationRongjin Sun, Li Li, Lu Wang, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|February 9, 2013
Quantitative prediction of repaglinide-rifampicin complex drug interactions using dynamic and static mechanistic models: delineating differential CYP3A4 induction and OATP1B1 inhibition potential of rifampicinManthena V S Varma, Jian Lin, Yi-An Bi, et al.
European Journal of Medicinal Chemistry|July 31, 2012
Mechanistic insights from comparing intrinsic clearance values between human liver microsomes and hepatocytes to guide drug designLi Di, Christopher Keefer, Dennis O Scott, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|January 10, 2019
A Comparison of Total and Plasma Membrane Abundance of Transporters in Suspended, Plated, Sandwich-Cultured Human Hepatocytes Versus Human Liver Tissue Using Quantitative Targeted Proteomics and Cell Surface BiotinylationVineet Kumar, Laurent Salphati, Cornelis E C A Hop, et al.
Acta Pharmaceutica Sinica. B|June 27, 2022
Recent advances in the translation of drug metabolism and pharmacokinetics science for drug discovery and developmentYurong Lai, Xiaoyan Chu, Li Di, et al.
Drug Metabolism and Pharmacokinetics|February 28, 2026
Applications of in vitro transporter assays for mechanistic characterization and prediction of clinical drug-drug interactionsKrisztina Herédi-Szabó, Sumito Ito, Xiaomin Liang, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|June 4, 2017
Comparative Evaluation of Plasma Bile Acids, Dehydroepiandrosterone Sulfate, Hexadecanedioate, and Tetradecanedioate with Coproporphyrins I and III as Markers of OATP Inhibition in Healthy SubjectsHong Shen, Weiqi Chen, Dieter M Drexler, et al.
Pageof 14