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GRIN2B gene
Known as:
glutamate ionotropic receptor NMDA type subunit 2B
, N-METHYL-D-ASPARTATE RECEPTOR CHANNEL, SUBUNIT EPSILON-2
, GluN2B
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This gene plays a role in both neurotransmitter binding and ion transport.
National Institutes of Health
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Related topics
Related topics
7 relations
GRIN2B protein, human
Homo sapiens
Ionophore activity
Ligand Binding
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2019
Highly Cited
2019
l-Serine dietary supplementation is associated with clinical improvement of loss-of-function GRIN2B-related pediatric encephalopathy
David Soto
,
M. Olivella
,
+18 authors
X. Altafaj
Science Signaling
2019
Corpus ID: 195066421
Dietary l-serine supplements correct NMDAR deficiency and neurodevelopmental defects in a pediatric patient. Treating NMDA…
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Review
2017
Review
2017
Genetics of Alzheimer’s Disease: the Importance of Polygenic and Epistatic Components
Neha S. Raghavan
,
G. Tosto
Current Neurology and Neuroscience Reports
2017
Corpus ID: 4580608
Purpose of ReviewWe aimed to summarize the recent advances in genetic findings of Alzheimer’s disease (AD), focusing on…
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Highly Cited
2016
Highly Cited
2016
A Novel Binding Mode Reveals Two Distinct Classes of NMDA Receptor GluN2B-selective Antagonists
David Stroebel
,
D. Buhl
,
+6 authors
J. Pandit
Molecular Pharmacology
2016
Corpus ID: 2996602
N-methyl-d-aspartate receptors (NMDARs) are glutamate-gated ion channels that play key roles in brain physiology and pathology…
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Highly Cited
2015
Highly Cited
2015
DRD and GRIN2B polymorphisms and their association with the development of impulse control behaviour among Malaysian Parkinson’s disease patients
Shahidee Zainal Abidin
,
E. Tan
,
+11 authors
Norlinah Mohamed Ibrahim
BMC Neurology
2015
Corpus ID: 10235393
BackgroundImpulse control disorder (ICD) and behaviours (ICB) represent a group of behavioural disorders that have become…
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Highly Cited
2014
Highly Cited
2014
Three rare diseases in one Sib pair: RAI1, PCK1, GRIN2B mutations associated with Smith-Magenis Syndrome, cytosolic PEPCK deficiency and NMDA receptor glutamate insensitivity.
D. Adams
,
Hongjie Yuan
,
+22 authors
W. Gahl
Molecular Genetics and Metabolism
2014
Corpus ID: 23059112
Highly Cited
2013
Highly Cited
2013
Status epilepticus triggers early and late alterations in brain-derived neurotrophic factor and NMDA glutamate receptor Grin2b DNA methylation levels in the hippocampus
R. R. Parrish
,
Asher J. Albertson
,
+4 authors
Farah D. Lubin
Neuroscience
2013
Corpus ID: 23457282
Highly Cited
2009
Highly Cited
2009
Structural Basis of NR2B-Selective Antagonist Recognition by N-Methyl-d-aspartate Receptors
Laetitia Mony
,
Lucie Krzaczkowski
,
+6 authors
P. Paoletti
Molecular Pharmacology
2009
Corpus ID: 28154965
N-Methyl-d-aspartate receptors (NMDARs) are ionotropic glutamate receptors endowed with unique pharmacological and functional…
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Highly Cited
2007
Highly Cited
2007
Association of the glutamate receptor subunit gene GRIN2B with attention‐deficit/hyperactivity disorder
Kimberley M. Dorval
,
K. Wigg
,
+7 authors
C. Barr
Genes, Brain and Behavior
2007
Corpus ID: 3958410
The glutamatergic signaling pathway represents an ideal candidate susceptibility system for attention‐deficit/hyperactivity…
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Highly Cited
2005
Highly Cited
2005
An association study of the N-methyl-D-aspartate receptor NR1 subunit gene (GRIN1) and NR2B subunit gene (GRIN2B) in schizophrenia with universal DNA microarray
Shengying Qin
,
Xunchao Zhao
,
+6 authors
Lin He
European Journal of Human Genetics
2005
Corpus ID: 22483678
Dysfunction of the N-methyl-D-aspartate (NMDA) receptors has been implicated in the etiology of schizophrenia based on…
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Highly Cited
2001
Highly Cited
2001
Association analysis for NMDA receptor subunit 2B (GRIN2B) genetic variants and psychopathology and clozapine response in schizophrenia
C. Hong
,
Y. W. Yu
,
Ching-hua Lin
,
Chih-ya Cheng
,
S. Tsai
Psychiatric Genetics
2001
Corpus ID: 35087626
It is known that a syndrome resembling schizophrenia is produced by the N-methyl-d-aspartate receptor antagonists. It has also…
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