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Current Opinion in Pharmacology|December 27, 2005
Glutamate-based therapeutic approaches: inhibitors of glycine transportSandra M LechnerNeuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|September 19, 2008
Drugability of extracellular targets: discovery of small molecule drugs targeting allosteric, functional, and subunit-selective sites on GPCRs and ion channelsDimitri E Grigoriadis, Samuel R J Hoare, Sandra M Lechner, et al.Neurogenetics|March 31, 2006
Gene expression analyses reveal molecular relationships among 20 regions of the human CNSRichard B Roth, Peter Hevezi, Jerry Lee, et al.The Journal of Comparative Neurology|September 1, 2005
Differential distribution of voltage-gated calcium channel alpha-2 delta (alpha2delta) subunit mRNA-containing cells in the rat central nervous system and the dorsal root gangliaRebecca L Cole, Sandra M Lechner, Mark E Williams, et al.Journal of Biomolecular Screening|June 6, 2006
A novel cell-based assay for G-protein-coupled receptor-mediated cyclic adenosine monophosphate response element binding protein phosphorylationJulie V Selkirk, Lisa M Nottebaum, Ian C Ford, et al.Journal of Neuroimmunology|November 23, 2005
Human class-I restricted T cell associated molecule is highly expressed in the cerebellum and is a marker for activated NKT and CD8+ T lymphocytesGenaro Patiño-Lopez, Peter Hevezi, Jerry Lee, et al.Pain and Therapy|January 8, 2025
Pharmacology and Mechanism of Action of Suzetrigine, a Potent and Selective NaV1.8 Pain Signal Inhibitor for the Treatment of Moderate to Severe PainJeremiah D Osteen, Swapna Immani, Tim L Tapley, et al.Brain Research|February 5, 2008
Distribution of metabotropic glutamate 2 and 3 receptors in the rat forebrain: Implication in emotional responses and central disinhibitionGuibao Gu, Daniel S Lorrain, Hongbing Wei, et al.The New England Journal of Medicine|August 2, 2023
Selective Inhibition of NaV1.8 with VX-548 for Acute PainJim Jones, Darin J Correll, Sandra M Lechner, et al.Bioorganic & Medicinal Chemistry Letters|October 7, 2008
2,6-Diaryl-4-acylaminopyrimidines as potent and selective adenosine A(2A) antagonists with improved solubility and metabolic stabilityManisha Moorjani, Zhiyong Luo, Emily Lin, et al.Pageof 2