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PPP2R1A wt Allele

Known as: PR65A, Protein Phosphatase 2 (Formerly 2A), Regulatory Subunit A (PR 65), Alpha Isoform Gene, Protein Phosphatase 2, 65kDa Regulatory Subunit A Gene 
Human PPP2R1A wild-type allele is located in the vicinity of 19q13.41 and is approximately 37 kb in length. This allele, which encodes serine… 
National Institutes of Health

Related topics

Related topics

13 relations
19q13.41ApoptosisCanonical Wnt Signaling PathwayCell Proliferation Regulatory Process

Broader (1)

PPP2R1A gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2010
2010
Inherited dysfibrinogenemia: clinical phenotypes associated with five different fibrinogen structure defects
Hereditary dysfibrinogenemia is a rare clotting disorder, which results from mutations in at least one of the three fibrinogen… 
2007
2007
Homophenotypic Aalpha R16H fibrinogen (Kingsport): uniquely altered polymerization associated with slower fibrinopeptide A than fibrinopeptide B release.
We detail for the first time the uniquely altered fibrin polymerization of homophenotypic Aalpha R16H dysfibrinogen. By… 
2007
2007
Fibrinogen Nový Jicín and Praha II: cases of hereditary Aalpha 16 Arg-->Cys and Aalpha 16 Arg-->His dysfibrinogenemia.
INTRODUCTION Various dysfibrinogenemias have been described worldwide. This paper describes two new cases of dysfibrinogenemia… 
2001
2001
Fibrinogen Milano XII: a dysfunctional variant containing 2 amino acid substitutions, Aalpha R16C and gamma G165R.
Fibrinogen Milano XII was detected in an asymptomatic Italian woman, whose routine coagulation test results revealed a prolonged… 
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