From bedside‐to‐bench: What disease‐associated variants are teaching us about the NMDA receptor-Reference-Cited by-同舟云学术

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From bedside‐to‐bench: What disease‐associated variants are teaching us about the NMDA receptor

Published:2020-04-09 Issue:2 Volume:599 Page:397-416
ISSN:0022-3751
Container-title:The Journal of Physiology
language:en
Short-container-title:J Physiol

Author:

Amin Johansen B.¹²,Moody Gabrielle R.²,Wollmuth Lonnie P.³⁴⁵^ORCID

Affiliation:

1. Medical Scientist Training Program (MSTP) Stony Brook University Stony Brook NY 11794‐5230

2. Graduate Program in Molecular and Cellular Pharmacology Stony Brook University Stony Brook NY 11794‐5230

3. Department of Neurobiology & Behavior Stony Brook University Stony Brook NY 11794‐5230

4. Department of Biochemistry & Cell Biology Stony Brook University Stony Brook NY 11794‐5230

5. Center for Nervous System Disorders Stony Brook University Stony Brook NY 11794‐5230

Funder

National Institutes of Health

Publisher

Wiley

Subject

Physiology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1113/JP278705

Reference132 articles.

1. Epilepsy-associated GRIN2A mutations reduce NMDA receptor trafficking and agonist potency – molecular profiling and functional rescue

2. A Molecular Determinant of Subtype-Specific Desensitization in Ionotropic Glutamate Receptors

3. Separate Intramolecular Targets for Protein Kinase A Control N-Methyl-d-aspartate Receptor Gating and Ca2+ Permeability

4. A conserved glycine harboring disease-associated mutations permits NMDA receptor slow deactivation and high Ca2+ permeability

5. Divergent roles of a peripheral transmembrane segment in AMPA and NMDA receptors

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1. Disease-Associated Variants in GRIN1, GRIN2A and GRIN2B genes: Insights into NMDA Receptor Structure, Function, and Pathophysiology;Physiological Research;2024-08-31

2. Characterization of 13 Novel Genetic Variants in Genes Associated with Epilepsy: Implications for Targeted Therapeutic Strategies;Molecular Diagnosis & Therapy;2024-07-14

3. Characterization of Mice Carrying a Neurodevelopmental Disease-Associated GluN2B(L825V) Variant;The Journal of Neuroscience;2024-06-26

4. Discovery of GluN2A subtype-selective N-methyl-d-aspartate (NMDA) receptor ligands;Acta Pharmaceutica Sinica B;2024-05

5. Integrated network pharmacology and phosphoproteomic analyses of Baichanting in Parkinson's disease model mice;Heliyon;2024-03

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