Skip to search formSkip to main contentSkip to account menu

PRKAR1A gene

Known as: TSE1, protein kinase cAMP-dependent type I regulatory subunit alpha, CNC1 
National Institutes of Health

Related topics

Related topics

5 relations
Carney Complex, Type 1PRKAR1A protein, humanPRKAR1A/RARA FUSION GENEPRKAR1B gene

Narrower (1)

PRKAR1A wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
Knockdown of PRKAR1A, the gene responsible for Carney complex, interferes with differentiation in osteoblastic cells.
PRKAR1A is the gene encoding the type 1A regulatory subunit of protein kinase A, and it is the cause of the inherited human tumor… 
2012
2012
In vitro studies of novel PRKAR1A mutants that extend the predicted RIα protein sequence into the 3'-untranslated open reading frame: proteasomal degradation leads to RIα haploinsufficiency and…
BACKGROUND Carney complex (CNC) is a multiple endocrine neoplasia syndrome due to inactivating mutations in the PRKAR1A gene that… 
2012
2012
A novel PRKAR1A mutation in Korean Carney complex family.
Carney complex (CNC) is an autosomal dominant hereditary or sporadic multiple neoplastic syndrome that shows variable clinical… 
Review
2009
Review
2009
Use of mouse models to understand the molecular basis of tissue‐specific tumorigenesis in the Carney complex
Carney complex (CNC) is an autosomal dominant, multiple endocrine neoplasia syndrome comprised of spotty skin pigmentation… 
Highly Cited
2008
Highly Cited
2008
Pituitary-specific knockout of the Carney complex gene Prkar1a leads to pituitary tumorigenesis.
Carney complex (CNC) is an inherited neoplasia syndrome characterized by spotty skin pigmentation, myxomas, endocrine tumors, and… 
2008
2008
A Deletion in the PRKARIA Gene is Associated with Carney Complex
Mutations of the PRKAR1A gene are an important cause of Carney complex (CC). The PRKAR1A gene encodes the type 1A regulatory… 
2006
2006
PRKAR1A inactivation leads to increased proliferation and decreased apoptosis in human B lymphocytes.
The multiple neoplasia syndrome Carney complex (CNC) is caused by heterozygote mutations in the gene, which codes for the RIalpha… 
2003
2003
Protein kinase-A activity in PRKAR 1 A-mutant cells , and regulation of mitogen-activated protein kinases ERK 1 / 2
Carney complex (CNC) is caused by PRKAR1A-inactivating mutations. PRKAR1A encodes the regulatory subunit type I-a (RIa) of the… 
Review
1995
Review
1995
Cushing’s Syndrome Due To Primary Pigmented Nodular Adrenocortical Disease
Primary pigmented nodular adrenocortical disease (PPNAD) is a rare cause of Cushing’s syndrome in infants, children and young… 
1990
1990
Regulation of chimeric phosphoenolpyruvate carboxykinase genes by the trans-dominant locus TSE1
Extinction of phosphoenolpyruvate carboxykinase (PCK) gene expression in hepatoma x fibroblast hybrids is mediated by a trans… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)