Mechanistic Insight into NMDA Receptor Dysregulation by Rare Variants in the GluN2A and GluN2B Agonist Binding Domains-Reference-Cited by-同舟云学术

Mechanistic Insight into NMDA Receptor Dysregulation by Rare Variants in the GluN2A and GluN2B Agonist Binding Domains

Published:2016-12 Issue:6 Volume:99 Page:1261-1280
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Swanger Sharon A.,Chen Wenjuan,Wells Gordon,Burger Pieter B.,Tankovic Anel,Bhattacharya Subhrajit,Strong Katie L.,Hu Chun,Kusumoto Hirofumi,Zhang Jing,Adams David R.,Millichap John J.,Petrovski Slavé,Traynelis Stephen F.,Yuan Hongjie

Funder

Eunice Kennedy Shriver National Institute of Child Health & Human Development

National Center for Advancing Translational Sciences of the NIH

National Institute of Neurological Disorders and Stroke

Xiangya-Emory Medical Schools Visiting Student Program

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference101 articles.

1. NMDA receptors and brain development;Ewald,2009

2. Distinct spatio-temporal distributions of the NMDA receptor channel subunit mRNAs in the brain;Watanabe;Ann. N Y Acad. Sci.,1993

3. Developmental and regional expression in the rat brain and functional properties of four NMDA receptors;Monyer;Neuron,1994

4. Developmental expression of N-methyl-D-aspartate (NMDA) receptor subunits in human white and gray matter: potential mechanism of increased vulnerability in the immature brain;Jantzie;Cereb. Cortex,2015

5. Expression of NMDA receptor NR1, NR2A and NR2B subunit mRNAs during development of the human hippocampal formation;Law;Eur. J. Neurosci.,2003

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