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Pharmaceutical Research|November 10, 2006
Transport of poly(amidoamine) dendrimers across Caco-2 cell monolayers: Influence of size, charge and fluorescent labelingKelly M Kitchens, Rohit B Kolhatkar, Peter W Swaan, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|August 20, 2015
Potent and Selective Inhibition of Plasma Membrane Monoamine Transporter by HIV Protease InhibitorsHaichuan Duan, Tao Hu, Robert S Foti, et al.
Pharmaceutical Research|October 5, 2013
Microfluidic preparation of liposomes to determine particle size influence on cellular uptake mechanismsAbhay U Andar, Renee R Hood, Wyatt N Vreeland, et al.
The Journal of Biological Chemistry|June 8, 2011
Transmembrane helix 1 contributes to substrate translocation and protein stability of bile acid transporter SLC10A2Tatiana Claro da Silva, Naissan Hussainzada, Chandra M Khantwal, et al.
Clinical Pharmacology and Therapeutics|July 8, 2018
Molecular Modeling of Drug-Transporter Interactions-An International Transporter Consortium PerspectiveAvner Schlessinger, Matthew A Welch, Herman van Vlijmen, et al.
Pharmaceutical Research|September 12, 2007
Computational models to assign biopharmaceutics drug disposition classification from molecular structureAkash Khandelwal, Praveen M Bahadduri, Cheng Chang, et al.
The Journal of Pharmacology and Experimental Therapeutics|August 6, 2011
Molecular analysis and structure-activity relationship modeling of the substrate/inhibitor interaction site of plasma membrane monoamine transporterHorace T B Ho, Yongmei Pan, Zhiyi Cui, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|March 5, 2015
Toward predicting drug-induced liver injury: parallel computational approaches to identify multidrug resistance protein 4 and bile salt export pump inhibitorsMatthew A Welch, Kathleen Köck, Thomas J Urban, et al.
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