Showing results (271-280 of 424) with videos related to
Sort By:
Pageof 43
The Journal of Pharmacology and Experimental Therapeutics|September 5, 2003
In vitro characterization of ephedrine-related stereoisomers at biogenic amine transporters and the receptorome reveals selective actions as norepinephrine transporter substratesRichard B Rothman, Nga Vu, John S Partilla, et al.The Journal of Clinical Investigation|March 3, 2011
Rapid, reversible activation of AgRP neurons drives feeding behavior in miceMichael J Krashes, Shuichi Koda, ChianPing Ye, et al.Nature Medicine|December 27, 2016
Targeting the histone methyltransferase G9a activates imprinted genes and improves survival of a mouse model of Prader-Willi syndromeYuna Kim, Hyeong-Min Lee, Yan Xiong, et al.Journal of Medicinal Chemistry|February 3, 2006
Synthesis and structure-activity relationships of 3-[(2-methyl-1,3-thiazol-4-yl)ethynyl]pyridine analogues as potent, noncompetitive metabotropic glutamate receptor subtype 5 antagonists; search for cocaine medicationsYasuyoshi Iso, Ewa Grajkowska, Jarda T Wroblewski, et al.Nature|May 3, 2013
Structure of the human smoothened receptor bound to an antitumour agentChong Wang, Huixian Wu, Vsevolod Katritch, et al.Neuron|March 26, 2013
Inhibition of mediodorsal thalamus disrupts thalamofrontal connectivity and cognitionSebastien Parnaudeau, Pia-Kelsey O'Neill, Scott S Bolkan, et al.ACS Chemical Neuroscience|May 6, 2014
Synthesis, pharmacological characterization, and structure-activity relationship studies of small molecular agonists for the orphan GPR88 receptorChunyang Jin, Ann M Decker, Xi-Ping Huang, et al.Journal of Medicinal Chemistry|June 15, 2012
Life beyond kinases: structure-based discovery of sorafenib as nanomolar antagonist of 5-HT receptorsXingyu Lin, Xi-Ping Huang, Gang Chen, et al.Cell|July 9, 2019
VEGAS as a Platform for Facile Directed Evolution in Mammalian CellsJustin G English, Reid H J Olsen, Katherine Lansu, et al.The Journal of Pharmacology and Experimental Therapeutics|October 17, 2014
The G protein-biased κ-opioid receptor agonist RB-64 is analgesic with a unique spectrum of activities in vivoKate L White, J Elliott Robinson, Hu Zhu, et al.Pageof 43