PRKAR1A gene

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

Topic mentions per year

Topic mentions per year

2000-2018
0520002018

Papers overview

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2013
2013
Acrodysostosis is characterized by a peripheral dysostosis that is accompanied by short stature, midface hypoplasia, and… (More)
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2008
2008
PURPOSE Since the identification of PRKAR1A mutations in Carney complex, substitutions and small insertions/deletions have been… (More)
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2007
2007
We report the molecular and cytogenetic characterization of a novel variant of acute promyelocytic leukemia (APL). The bone… (More)
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2006
2006
CONTEXT Primary pigmented nodular adrenocortical disease (PPNAD), a rare cause of corticotropin-independent Cushing syndrome, can… (More)
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2005
2005
BACKGROUND PRKAR1A gene encodes the type 1A regulatory subunit of protein kinase A. The mutation of this gene causes Carney… (More)
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2003
2003
Carney complex (CNC) is caused by PRKAR1A-inactivating mutations. PRKAR1A encodes the regulatory subunit type I-alpha (RIalpha… (More)
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2002
2002
Primary pigmented nodular adrenocortical disease (PPNAD) is a cause of ACTH-independent Cushing's syndrome. This condition can be… (More)
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2002
2002
OBJECTIVE Carney complex (CNC) is an autosomal dominant multiple neoplasia syndrome featuring cardiac, endocrine, cutaneous and… (More)
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2002
2002
The tumor-suppressor gene encoding the cyclic AMP-dependent protein kinase A type I-alpha regulatory subunit PRKAR1A has been… (More)
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Highly Cited
2000
Highly Cited
2000
Carney complex (CNC) is an autosomal dominant multiple neoplasia syndrome, which has been linked to loci on 2p16 and 17q22-24. We… (More)
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