GRIN3B Antibody

1. GRIN3B missense mutation is an inherited risk factor for schizophrenia. PMID: 28132660
2. Authors investigated the significance of a common human genetic variation of the NMDAR NR3B subunit PMID: 25768306
3. Rs2240158 of GRIN3B was significantly associated with mismatch negativity in healthy subjects. PMID: 24814139
4. our findings suggest that the over-expression of NR3B subunit of NMDA receptor is a long lasting result of chronic opioid abuse. PMID: 20153313
5. These observations suggest that the genetic variation of the NR3B subunit of the NMDA receptor is not a risk factor for Alzheimer's dis pathogenesis PMID: 20016182
6. NR3B mRNA expression in the human hippocampal formation (CA1-CA4 and dentate gyrus) and adjacent neocortex may have implications for understanding the role of NMDA receptors for physiological and pathological processes in these forebrain regions. PMID: 15722182
7. cross-talk between NR3B and NR4A receptors is a mechanism modulating the transcriptional activities of these orphan nuclear receptors PMID: 17543277
8. We tested whether genetic dysfunction of GRIN3B is implicated in the pathogenesis of amyotrophic lateral sclerosis (ALS). PMID: 17687115

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HGNC: 16768

OMIM: 606651

KEGG: hsa:116444

STRING: 9606.ENSP00000234389

UniGene: Hs.660378