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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

Papers overview

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2019
2019
Mutations in FMS-like tyrosine kinase 3 (FLT3) gene occur frequently in acute myeloid leukemia (AML) and are rare in acute… 
2018
2018
Autogenous proteolytic enzymes of the calpain family are implicated in myofibrillar protein degradation. As a result, the… 
2017
2017
BackgroundSmall insertions and deletions (indels) have a significant influence in human disease and, in terms of frequency, they… 
2015
2015
DEFB126 rs140685149 mutation was shown to cause sperm dysfunction and subfertility. Indel rs11467497 is another 4‐nucleotide… 
2013
2013
BackgroundClassical approaches to compute the genomic distance are usually limited to genomes with the same content and take into… 
2010
2010
The aim of this investigation was to study the influence of genetic polymorphisms of biotransformation enzymes and dopamine… 
Review
2008
Review
2008
Somatostatin receptors (sst1–5) and dopamine receptor 2 (D2DR) are well expressed and co-localized in several human pituitary… 
2005
2005
  • Dr. K. Yamagiwa
  • Archiv für Pathologische Anatomie und Physiologie…
  • 2005
  • Corpus ID: 13385052
ration der Geschwulst des Oberschenkelknochens, wie der des Rectum, endlich das Bevorzugtsein des letzteren f/it die primi~re…