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Drug Metabolism and Disposition: the Biological Fate of Chemicals|June 27, 2007
Dehydroepiandrosterone induces human CYP2B6 through the constitutive androstane receptorKrisztina Kohalmy, Viola Tamási, László Kóbori, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|October 19, 2010
Inhibition of human sterol Δ7-reductase and other postlanosterol enzymes by LK-980, a novel inhibitor of cholesterol synthesisJure Acimovic, Tina Korosec, Matej Seliskar, et al.
British Journal of Clinical Pharmacology|September 28, 2020
Clinical significance of personalized tacrolimus dosing by adjusting to donor CYP3A-status in liver transplant recipientsNóra Csikány, Ádám Kiss, Máté Déri, et al.
Circulation Research|April 30, 2013
ABCC6 is a basolateral plasma membrane proteinViola Pomozi, Olivier Le Saux, Christopher Brampton, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|October 31, 2008
Drug interaction potential of 2-((3,4-dichlorophenethyl)(propyl)amino)-1-(pyridin-3-yl)ethanol (LK-935), the novel nonstatin-type cholesterol-lowering agentKatalin Monostory, Jean-Marc Pascussi, Pál Szabó, et al.
Scientific Reports|July 18, 2024
PK/PD investigation of antiviral host matriptase/TMPRSS2 inhibitors in cell modelsDávid Gamba, Nicholas van Eijk, Katalin Lányi, et al.
Bioorganic & Medicinal Chemistry|February 24, 2018
Discovery of isatin and 1H-indazol-3-ol derivatives as d-amino acid oxidase (DAAO) inhibitorsBence Szilágyi, Péter Kovács, György G Ferenczy, et al.
European Journal of Hospital Pharmacy : Science and Practice|July 8, 2025
How to manage the overwhelming amount of database-detected interactions? A focus group meeting study on the management of database-detected risks of drug interactionsDénes Kleiner, Faraz Haghverdi, Orsolya Szépe, et al.
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