Sharon Swanger, PhD
Affiliations: | Emory University, Atlanta, GA |
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"Sharon Swanger"Mean distance: 15.15 (cluster 11) | S | N | B | C | P |
Cross-listing: Chemistry Tree
Parents
Sign in to add mentorItzhak Fischer | research assistant | 2002-2005 | |
Gary J. Bassell | grad student | Emory | |
Stephen F. Traynelis | post-doc | Emory |
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Publications
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D'Erasmo MP, Akins NS, Ma P, et al. (2023) Development of a Dihydroquinoline-Pyrazoline GluN2C/2D-Selective Negative Allosteric Modulator of the -Methyl-d-aspartate Receptor. Acs Chemical Neuroscience |
Hansen KB, Wollmuth LP, Bowie D, et al. (2021) Structure, Function, and Pharmacology of Glutamate Receptor Ion Channels. Pharmacological Reviews. 73: 298-487 |
Perszyk RE, Swanger SA, Shelley C, et al. (2020) Biased modulators of NMDA receptors control channel opening and ion selectivity. Nature Chemical Biology |
Li J, Zhang J, Tang W, et al. (2019) De Novo GRIN Variants in NMDA Receptor M2 Channel Pore-Forming Loop Are Associated with Neurological Diseases. Human Mutation |
Hanson E, Armbruster M, Lau LA, et al. (2019) Tonic activation of GluN2C/GluN2D-containing NMDA receptors by ambient glutamate facilitates cortical interneuron maturation. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience |
Bhattacharya S, Khatri A, Swanger SA, et al. (2018) Triheteromeric GluN1/GluN2A/GluN2C NMDARs with Unique Single-Channel Properties Are the Dominant Receptor Population in Cerebellar Granule Cells. Neuron. 99: 315-328.e5 |
Swanger SA, Traynelis SF. (2018) Synaptic Receptor Diversity Revealed Across Space and Time. Trends in Neurosciences. 41: 486-488 |
Fry AE, Fawcett KA, Zelnik N, et al. (2018) De novo mutations in GRIN1 cause extensive bilateral polymicrogyria. Brain : a Journal of Neurology |
Swanger SA, Vance KM, Acker TM, et al. (2017) A novel negative allosteric modulator selective for GluN2C/2D-containing NMDA receptors inhibits synaptic transmission in hippocampal interneurons. Acs Chemical Neuroscience |
Chen W, Shieh C, Swanger SA, et al. (2017) GRIN1 mutation associated with intellectual disability alters NMDA receptor trafficking and function. Journal of Human Genetics |