Showing results (1-10 of 35) with videos related to

Sort By:
Pageof 4
Trends in Pharmacological Sciences|April 30, 2005
A renaissance in trace amines inspired by a novel GPCR familyLothar Lindemann, Marius C Hoener
Trends in Pharmacological Sciences|October 23, 2012
Synapse dysfunction in autism: a molecular medicine approach to drug discovery in neurodevelopmental disordersWill Spooren, Lothar Lindemann, Anirvan Ghosh, et al.
Nature Reviews. Drug Discovery|October 2, 2013
Drug discovery for autism spectrum disorder: challenges and opportunitiesAnirvan Ghosh, Aubin Michalon, Lothar Lindemann, et al.
Current Opinion in Pharmacology|December 10, 2014
Metabotropic glutamate receptor 5 as drug target for Fragile X syndromeSebastian H Scharf, Georg Jaeschke, Joseph G Wettstein, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 30, 2015
Metabotropic glutamate receptor signaling is required for NMDA receptor-dependent ocular dominance plasticity and LTD in visual cortexMichael S Sidorov, Eitan S Kaplan, Emily K Osterweil, et al.
Cellular and Molecular Neurobiology|July 9, 2010
Darkness reduces BDNF expression in the visual cortex and induces repressive chromatin remodeling at the BDNF gene in both hippocampus and visual cortexNina N Karpova, Tomi Rantamäki, Antonio Di Lieto, et al.
Genomics|February 19, 2005
Trace amine-associated receptors form structurally and functionally distinct subfamilies of novel G protein-coupled receptorsLothar Lindemann, Martin Ebeling, Nicole A Kratochwil, et al.
Human Molecular Genetics|February 12, 2013
Astroglial FMRP-dependent translational down-regulation of mGluR5 underlies glutamate transporter GLT1 dysregulation in the fragile X mouseHaruki Higashimori, Lydie Morel, James Huth, et al.
Neuropharmacology|August 9, 2011
Acetylcholinesterase inhibitors rapidly activate Trk neurotrophin receptors in the mouse hippocampusHenri Autio, Kert Mätlik, Tomi Rantamäki, et al.
Nature Neuroscience|January 13, 2015
Contribution of mGluR5 to pathophysiology in a mouse model of human chromosome 16p11.2 microdeletionDi Tian, Laura J Stoppel, Arnold J Heynen, et al.
Pageof 4