Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Human tumors associated with Carney complex and germline PRKAR1A mutations: a protein kinase A disease!

FEBS letters - 3 Jul 2003

Stergiopoulos Sotirios G, Stratakis Constantine A

Abstract excerpt

Carney complex (CNC) is a multiple neoplasia syndrome that consists of endocrine (thyroid, pituitary, adrenocortical and gonadal), non-endocrine (myxomas, nevi and other cutaneous pigmented lesions), and neural (schwannomas) tumors. Primary pigmented nodular adrenocortical disease (PPNAD) is the...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Chromosomes, Human, Pair 17
Share to Cyclic AMP-Dependent Protein Kinase RIalpha Subunit
Share to Cyclic AMP-Dependent Protein Kinases

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genes, Tumor Suppressor

Share to Genetic Heterogeneity

Share to Models, Biological

Share to Multiple Endocrine Neoplasia

Share to Syndrome

Source

Identifiers

PMID: 12829237
DOI: 10.1016/s0014-5793(03)00452-6

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-12829237-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Human tumors associated with Carney complex and germline PRKAR1A mutations: a protein kinase A disease!PMID 12829237Read ↗

Protein kinase A and its role in human neoplasia: the Carney complex paradigm.Semantic proximity Read ↗

Carney complex: an update.Semantic 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 ↗

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

PRKACA: the catalytic subunit of protein kinase A and adrenocortical tumorsSemantic proximity Read ↗

Adrenal Pathophysiology: Lessons from the Carney ComplexSemantic proximity Read ↗

A Novel Mutation in the type Iα Regulatory Subunit of Protein Kinase A (PRKAR1A) in a Cushing's Syndrome Patient with Primary Pigmented Nodular Adrenocortical Disease.Semantic proximity Read ↗

Malignant psammomatous melanotic schwannoma in a patient with Carney complex associated with a novel variant in the PRKAR1A gene.Semantic proximity Read ↗

[Clinical features and pathogenesis of Carney complex, a rare form of multiple endocrine neoplasia syndromes].Semantic proximity Read ↗

Genetics of micronodular adrenal hyperplasia and Carney complex.Semantic proximity Read ↗

Carney Complex: Pathology and Molecular GeneticsSemantic proximity Read ↗

A Large Family with Carney Complex Caused by the S147G PRKAR1A Mutation Shows a Unique Spectrum of Disease Including Adrenocortical CancerSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.