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PPP1R3A gene

Known as: PPP1R3, PROTEIN PHOSPHATASE 1, REGULATORY SUBUNIT 3, GM 
 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
BACKGROUND Abnormal calcium (Ca2+) release from the sarcoplasmic reticulum (SR) contributes to the pathogenesis of atrial… Expand
2019
2019
Heart failure is a leading cause of mortality, yet our understanding of the genetic interactions underlying this disease remains… Expand
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2018
2018
It has been presumed that increased susceptibility in Mexicans to type 2 diabetes (T2D) is attributed to the Native American… Expand
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2016
2016
AIMS To identify the role of copy number variations (CNVs) on disease risk genes and its effect on disease phenotypes in type 2… Expand
2014
2014
Background Lung cancers are classified as squamous cell carcinoma (SQ), adenocarcinoma (AC) and small cell lung carcinoma (SCLC… Expand
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Highly Cited
2012
Highly Cited
2012
Disruptions in FOXP2, a transcription factor, are the only known monogenic cause of speech and language impairment. We report on… Expand
2011
2011
BackgroundPPP1R6 is a protein phosphatase 1 glycogen-targeting subunit (PP1-GTS) abundant in skeletal muscle with an undefined… Expand
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2008
2008
Background Stored glycogen is an important source of energy for skeletal muscle. Human genetic disorders primarily affecting… Expand
2003
2003
BackgroundThe ARE insertion/deletion polymorphism of PPP1R3A has been associated with variation in glycaemic parameters and… Expand
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1999
1999
Recently, the PTEN/MMAC1 gene encoding a protein phosphatase (PP) and the PPP2R1B gene encoding a regulatory subunit of PP2A have… Expand
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