Ozgun Gokce, PhD

Affiliations: 
2004-2009 Brain Mind Institute, EPFL, Lausanne, Vaud, Switzerland 
 2009-2016 mcp Stanford University, Palo Alto, CA 
 2016- Institut für Schlaganfall- und Demenzforschung (ISD) Ludwig-Maximilians-Universität München, München, Bayern, Germany 
Area:
Neuroscience
Website:
http://research.isd-muc.de/Systemsneuroscience.html
Google:
"Ozgun Gokce"
Mean distance: 14.79 (cluster 11)
 
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Publications

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Stanley G, Gokce O, Malenka RC, et al. (2019) Continuous and Discrete Neuron Types of the Adult Murine Striatum. Neuron
Zhang B, Gokce O, Hale WD, et al. (2018) Autism-associated neuroligin-4 mutation selectively impairs glycinergic synaptic transmission in mouse brainstem synapses. The Journal of Experimental Medicine
Chen LY, Jiang M, Zhang B, et al. (2017) Conditional Deletion of All Neurexins Defines Diversity of Essential Synaptic Organizer Functions for Neurexins. Neuron. 94: 611-625.e4
Zhang B, Seigneur E, Wei P, et al. (2016) Developmental plasticity shapes synaptic phenotypes of autism-associated neuroligin-3 mutations in the calyx of Held. Molecular Psychiatry
Gokce O, Stanley GM, Treutlein B, et al. (2016) Cellular Taxonomy of the Mouse Striatum as Revealed by Single-Cell RNA-Seq. Cell Reports. 16: 1126-37
Zhang B, Chen LY, Liu X, et al. (2015) Neuroligins Sculpt Cerebellar Purkinje-Cell Circuits by Differential Control of Distinct Classes of Synapses. Neuron. 87: 781-96
Fuccillo MV, Földy C, Gökce Ö, et al. (2015) Single-Cell mRNA Profiling Reveals Cell-Type-Specific Expression of Neurexin Isoforms. Neuron. 87: 326-40
Rothwell PE, Fuccillo MV, Maxeiner S, et al. (2014) Autism-associated neuroligin-3 mutations commonly impair striatal circuits to boost repetitive behaviors. Cell. 158: 198-212
Treutlein B, Gokce O, Quake SR, et al. (2014) Cartography of neurexin alternative splicing mapped by single-molecule long-read mRNA sequencing. Proceedings of the National Academy of Sciences of the United States of America. 111: E1291-9
Smith MR, Syed A, Lukacsovich T, et al. (2014) A potent and selective Sirtuin 1 inhibitor alleviates pathology in multiple animal and cell models of Huntington's disease. Human Molecular Genetics. 23: 2995-3007
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