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Molecular Pharmacology|December 25, 2013
Pore-exposed tyrosine residues of P-glycoprotein are important hydrogen-bonding partners for drugsYaprak Dönmez Cakil, Narakorn Khunweeraphong, Zahida Parveen, et al.
Cells|January 8, 2025
Inhibition of Neural Crest Cell Migration by Strobilurin Fungicides and Other Mitochondrial ToxicantsViktoria Magel, Jonathan Blum, Xenia Dolde, et al.
European Journal of Pharmaceutics and Biopharmaceutics : Official Journal of Arbeitsgemeinschaft Fur Pharmazeutische Verfahrenstechnik E.V|May 18, 2022
Structure-based peptide ligand design for improved epidermal growth factor receptor targeted gene deliverySimon Decker, Alexander Taschauer, Emanuela Geppl, et al.
Molecular Informatics|January 8, 2013
Annotating Human P-Glycoprotein Bioassay DataBarbara Zdrazil, Marta Pinto, Poongavanam Vasanthanathan, et al.
Bioorganic & Medicinal Chemistry|April 18, 2015
Structure activity relationship of selective GABA uptake inhibitorsStine B Vogensen, Lars Jørgensen, Karsten K Madsen, et al.
Journal of Medicinal Chemistry|April 28, 2018
Ligand Desolvation Steers On-Rate and Impacts Drug Residence Time of Heat Shock Protein 90 (Hsp90) InhibitorsDoris A Schuetz, Lars Richter, Marta Amaral, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|December 16, 2014
'Second-generation' mephedrone analogs, 4-MEC and 4-MePPP, differentially affect monoamine transporter functionKusumika Saha, John S Partilla, Kurt R Lehner, et al.
Nature Reviews. Drug Discovery|July 31, 2010
Coexistence of passive and carrier-mediated processes in drug transportKiyohiko Sugano, Manfred Kansy, Per Artursson, et al.
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