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Article

Carney complex: the first 20 years.

Current opinion in oncology - 1 Jan 2007

Boikos Sosipatros A, Stratakis Constantine A

Abstract excerpt

PURPOSE OF REVIEW: The purpose of this review is to comment on the current findings on Carney complex, a dominantly inherited disease and a unique multiple endocrine neoplasia syndrome. RECENT FINDINGS: Sequencing of the PRKAR1A gene in more than 150 kindreds has revealed a number of pathogenic mutations; in more than 90% of the cases, the sequence change was predicted to lead to a premature stop codon and, thus,...

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Source

Identifiers

PMID: 17133108
DOI: 10.1097/CCO.0b013e32801195eb

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

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Carney complex: the first 20 years.PMID 17133108Read ↗

Carney Complex: Pathology and Molecular GeneticsSemantic proximity Read ↗

Carney complex: a curious case of a rare cancer syndrome caused by a novel pathogenic mutation in the PRKAR1A gene.Semantic proximity Read ↗

Clinical and molecular genetics of Carney complex.Semantic proximity Read ↗

A Novel Missense PRKAR1A Variant Causes Carney Complex.Semantic proximity Read ↗

Clinical and Molecular Features of the Carney Complex: Diagnostic Criteria and Recommendations for Patient EvaluationSemantic proximity Read ↗

Clinical and Molecular Features of the Carney Complex: Diagnostic Criteria and Recommendations for Patient EvaluationSemantic proximity Read ↗

MANAGEMENT OF ENDOCRINE DISEASE: Carney complex: clinical and genetic update 20 years after the identification of the CNC1 (PRKAR1A) gene.Semantic proximity Read ↗

Large Deletions of the <i>PRKAR1A</i> Gene in Carney ComplexSemantic proximity Read ↗

A deletion in the PRKAR1A gene is associated with Carney complex.Semantic proximity Read ↗

Mutations and polymorphisms in the gene encoding regulatory subunit type 1-alpha of protein kinase A (PRKAR1A): an update.Semantic proximity Read ↗

A novel PRKAR1A mutation resulting in a splicing variant in a case of Carney complex.Semantic proximity Read ↗

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 Carney complex.Semantic proximity Read ↗

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