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The Journal of Biological Chemistry|December 3, 2013
The two Na+ sites in the human serotonin transporter play distinct roles in the ion coupling and electrogenicity of transportBruce Felts, Akula Bala Pramod, Walter Sandtner, et al.
Neurochemistry International|November 26, 2013
Antagonist-induced conformational changes in dopamine transporter extracellular loop two involve residues in a potential salt bridgeJon D Gaffaney, Madhur Shetty, Bruce Felts, et al.
Neurochemistry International|August 21, 2018
Identification of the benztropine analog [125I]GA II 34 binding site on the human dopamine transporterMichael J Tomlinson, Danielle Krout, Akula Bala Pramod, et al.
The Journal of Biological Chemistry|November 8, 2005
Tyr-95 and Ile-172 in transmembrane segments 1 and 3 of human serotonin transporters interact to establish high affinity recognition of antidepressantsL Keith Henry, Julie R Field, Erika M Adkins, et al.
Nature Communications|January 26, 2016
Membrane potential shapes regulation of dopamine transporter trafficking at the plasma membraneBen D Richardson, Kaustuv Saha, Danielle Krout, et al.
ACS Chemical Neuroscience|January 23, 2019
Human Serotonin Transporter Coding Variation Establishes Conformational Bias with Functional ConsequencesMeagan A Quinlan, Danielle Krout, Rania M Katamish, et al.
Journal of Medicinal Chemistry|July 9, 2015
Novel Azido-Iodo Photoaffinity Ligands for the Human Serotonin Transporter Based on the Selective Serotonin Reuptake Inhibitor (S)-CitalopramVivek Kumar, Nageswari Yarravarapu, David J Lapinsky, et al.
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