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The Journal of Biological Chemistry|June 14, 2013
Analysis of the structural and molecular basis of voltage-sensitive sodium channel inhibition by the spider toxin huwentoxin-IV (μ-TRTX-Hh2a)Natali A Minassian, Alan Gibbs, Amy Y Shih, et al.Annals of Surgery|July 28, 2023
Perfusate Proteomes Provide Biological Insight Into Oxygenated Versus Standard Hypothermic Machine Perfusion in Kidney TransplantationJohn F Mulvey, Sadr Ul Shaheed, Philip D Charles, et al.ACS Medicinal Chemistry Letters|April 17, 2024
Structure-Based Optimization of Selective and Brain Penetrant CK1δ Inhibitors for the Treatment of Circadian DisruptionsStefan McCarver, Luke Hanna, Andrew Samant, et al.Journal of Lipid Research|April 6, 2015
Global deletion of MGL in mice delays lipid absorption and alters energy homeostasis and diet-induced obesityJohn D Douglass, Yin Xiu Zhou, Amy Wu, et al.Molecular Pharmacology|September 10, 2015
GPR139, an Orphan Receptor Highly Enriched in the Habenula and Septum, Is Activated by the Essential Amino Acids L-Tryptophan and L-PhenylalanineChanglu Liu, Pascal Bonaventure, Grace Lee, et al.Psychopharmacology|December 3, 2009
In vitro and in vivo characterization of JNJ-31020028 (N-(4-{4-[2-(diethylamino)-2-oxo-1-phenylethyl]piperazin-1-yl}-3-fluorophenyl)-2-pyridin-3-ylbenzamide), a selective brain penetrant small molecule antagonist of the neuropeptide Y Y(2) receptorJames R Shoblock, Natalie Welty, Diane Nepomuceno, et al.Annals of the New York Academy of Sciences|May 7, 2009
Relaxin family peptides and receptors in mammalian brainAndrew L Gundlach, Sherie Ma, Qian Sang, et al.Cancers|May 4, 2026
Ex Vivo Characterization Studies Identify Candidate Therapies for the Individualized Care of NF2-Related SchwannomatosisEthan W Hass, Anna Nagel, Alexandra J Scott, et al.Proceedings of the National Academy of Sciences of the United States of America|August 6, 2014
Oxysterols are agonist ligands of RORγt and drive Th17 cell differentiationPejman Soroosh, Jiejun Wu, Xiaohua Xue, et al.Pageof 17