Stephen F. Traynelis
Affiliations: | Rollins Research Center | Emory University, Atlanta, GA |
Area:
NMDA receptors, Rare Mutations, Epilepsy, StrokeGoogle:
"Stephen Traynelis"Mean distance: 13.11 (cluster 11) | S | N | B | C | P |
Parents
Sign in to add mentorRay Dingledine | grad student | 1984-1988 | UNC Chapel Hill |
Stuart G. Cull-Candy | post-doc | UCL | |
Steve F. Heinemann | post-doc | Salk Institute |
Children
Sign in to add traineeCollaborators
Sign in to add collaboratorDavid R. Adams | collaborator | National Human Genome Research Institute | |
Hiro Furukawa | collaborator | (Chemistry Tree) | |
David Goldstein | collaborator | Institute for Genomic Medicine, Columbia University (FlyTree) | |
Randy A. Hall | collaborator | Emory | |
Michael Hollmann | collaborator | ||
Richard L. Huganir | collaborator | HHMI | |
Denise C. Liotta | collaborator | Emory | |
John J. Millichap | collaborator | Northwestern School of Medicine | |
Slovay Petrovski | collaborator | University of Melbourne | |
David Weinshenker | collaborator | Emory |
BETA: Related publications
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Publications
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Montanucci L, Brünger T, Bhattarai N, et al. (2024) Distances from ligands as main predictive features for pathogenicity and functional effect of variants in NMDA receptors. Medrxiv : the Preprint Server For Health Sciences |
Xu Y, Song R, Perszyk RE, et al. (2024) De novo GRIN variants in M3 helix associated with neurological disorders control channel gating of NMDA receptor. Cellular and Molecular Life Sciences : Cmls. 81: 153 |
Banke TG, Traynelis SF, Barria A. (2024) Early Expression of GluN2A-Containing NMDA Receptors in A Model of Fragile X Syndrome. Journal of Neurophysiology |
Romero CA, Lim J, Wang H, et al. (2023) Epithelial N-methyl-D-aspartate (NMDA) receptors mediate renal vasodilation by affecting kidney autoregulation. Biorxiv : the Preprint Server For Biology |
Allen JP, Garber KB, Perszyk R, et al. (2023) Clinical features, functional consequences, and rescue pharmacology of missense GRID1 and GRID2 human variants. Human Molecular Genetics |
XiangWei W, Perszyk RE, Liu N, et al. (2023) Clinical and functional consequences of GRIA variants in patients with neurological diseases. Cellular and Molecular Life Sciences : Cmls. 80: 345 |
Camp CR, Vlachos A, Klöckner C, et al. (2023) Loss of Grin2a causes a transient delay in the electrophysiological maturation of hippocampal parvalbumin interneurons. Communications Biology. 6: 952 |
Song R, Zhang J, Perszyk RE, et al. (2023) Differential responses of disease-related GRIN variants located in pore-forming M2 domain of N-methyl-D-aspartate receptor to FDA-approved inhibitors. Journal of Neurochemistry |
Liu N, Li J, Gao K, et al. (2023) De novo CLPTM1 variants with reduced GABA R current response in patients with epilepsy. Epilepsia |
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 |