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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
SPEF2 (sperm flagella 2 gene), also known as KPL2, plays important roles in germ cell development. The aim of this study was to… Expand
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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… Expand
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2018
2018
Autogenous proteolytic enzymes of the calpain family are implicated in myofibrillar protein degradation. As a result, the… Expand
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2017
2017
BackgroundSmall insertions and deletions (indels) have a significant influence in human disease and, in terms of frequency, they… Expand
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2015
2015
DEFB126 rs140685149 mutation was shown to cause sperm dysfunction and subfertility. Indel rs11467497 is another 4-nucleotide… Expand
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2014
2014
BACKGROUND Tumor necrosis factor alpha (TNF-α) plays a critical role in diverse cellular processes including ocular immune… Expand
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2012
2012
BackgroundClassical approaches to compute the genomic distance are usually limited to genomes with the same content and take into… Expand
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2009
2009
The aim of this investigation was to study the influence of genetic polymorphisms of biotransformation enzymes and dopamine… Expand
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2005
2005
ration der Geschwulst des Oberschenkelknochens, wie der des Rectum, endlich das Bevorzugtsein des letzteren f/it die primi~re… Expand
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