DRD2 NM_000795.3:c.957C>T

Known as: NM_000795.3:c.957C>T, DRD2 957T Indel Mutation, DRD2 C957T Indel Mutation 
A nucleotide substitution at position 957 of the coding sequence of the DRD2 gene where cytosine has been mutated to thymine.
National Institutes of Health

Topic mentions per year

Topic mentions per year

2008-2017
01220082017

Papers overview

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2018
2018
BACKGROUND The dopamine receptor D2 receptor (DRD2) gene and lead exposure are both thought to contribute to the pathophysiology… (More)
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2017
2017
Small insertions and deletions (indels) have a significant influence in human disease and, in terms of frequency, they are second… (More)
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2015
2015
DEFB126 rs140685149 mutation was shown to cause sperm dysfunction and subfertility. Indel rs11467497 is another 4-nucleotide… (More)
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2014
2014
BACKGROUND Tumor necrosis factor alpha (TNF-α) plays a critical role in diverse cellular processes including ocular immune… (More)
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2014
2014
Background Multiple lines of evidence have implicated dysregulated immune processes in the pathogenesis of schizophrenia. Being… (More)
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2012
2012
Classical approaches to compute the genomic distance are usually limited to genomes with the same content and take into… (More)
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Review
2008
Review
2008
Somatostatin receptors (sst1–5) and dopamine receptor 2 (D2DR) are well expressed and co-localized in several human pituitary… (More)
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