"N-Methylaspartate" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
An amino acid that, as the D-isomer, is the defining agonist for the NMDA receptor subtype of glutamate receptors (RECEPTORS, NMDA).
| Descriptor ID |
D016202
|
| MeSH Number(s) |
D12.125.067.500.400 D12.125.119.170.400
|
| Concept/Terms |
N-Methylaspartate- N-Methylaspartate
- N Methylaspartate
- NMDA
- N-Methyl-D-aspartic Acid
- Acid, N-Methyl-D-aspartic
- N Methyl D aspartic Acid
- N-Methyl-D-aspartate
- N Methyl D aspartate
|
Below are MeSH descriptors whose meaning is more general than "N-Methylaspartate".
Below are MeSH descriptors whose meaning is more specific than "N-Methylaspartate".
This graph shows the total number of publications written about "N-Methylaspartate" by people in this website by year, and whether "N-Methylaspartate" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1995 | 1 | 0 | 1 |
| 2008 | 0 | 1 | 1 |
| 2017 | 1 | 0 | 1 |
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Below are the most recent publications written about "N-Methylaspartate" by people in Profiles.
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D-Cycloserine Augmentation of Exposure-Based Cognitive Behavior Therapy for Anxiety, Obsessive-Compulsive, and Posttraumatic Stress Disorders: A Systematic Review and Meta-analysis of Individual Participant Data. JAMA Psychiatry. 2017 05 01; 74(5):501-510.
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Fos expression following activation of the ventral pallidum in normal rats and in a model of Parkinson's Disease: implications for limbic system and basal ganglia interactions. Brain Struct Funct. 2008 Sep; 213(1-2):197-213.
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Basic fibroblast growth factor selectively increases AMPA-receptor subunit GluR1 protein level and differentially modulates Ca2+ responses to AMPA and NMDA in hippocampal neurons. J Neurochem. 1995 Dec; 65(6):2525-36.
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CPP, a selective N-methyl-D-aspartate (NMDA)-type receptor antagonist: characterization in vitro and in vivo. J Pharmacol Exp Ther. 1987 Mar; 240(3):737-46.