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Journal of Pharmaceutical Sciences|March 5, 2013
Chlorothiazide is a substrate for the human uptake transporters OAT1 and OAT3Viktória Juhász, Erzsébet Beéry, Zoltán Nagy, et al.
Toxicology in Vitro : an International Journal Published in Association with BIBRA|October 13, 2017
Kinetic characterization of bile salt transport by human NTCP (SLC10A1)Márton Jani, Erzsébet Beéry, Teresa Heslop, et al.
Toxicology in Vitro : an International Journal Published in Association with BIBRA|June 23, 2018
Human OATP1B1 (SLCO1B1) transports sulfated bile acids and bile salts with particular efficiencyBeáta Tóth, Márton Jani, Erzsébet Beéry, et al.
European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences|May 21, 2013
A P-gp vesicular transport inhibition assay - optimization and validation for drug-drug interaction testingKrisztina Herédi-Szabó, Johan E Palm, Tommy B Andersson, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|May 5, 2007
Interaction of positional isomers of quercetin glucuronides with the transporter ABCC2 (cMOAT, MRP2)Gary Williamson, Isabelle Aeberli, Laurence Miguet, et al.
The Journal of Membrane Biology|May 1, 2015
Membrane Assays to Characterize Interaction of Drugs with ABCB1Zsolt Fekete, Zsuzsanna Rajnai, Tünde Nagy, et al.
Xenobiotica; the Fate of Foreign Compounds in Biological Systems|July 20, 2018
Inhibitor selectivity of CNTs and ENTsBalázs Vaskó, Viktória Juhász, Beáta Tóth, et al.
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