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

A French CDK4-positive melanoma family with a co-inherited EDNRB mutation.

Journal of dermatological science - 1 Apr 2007

Soufir Nadem, Ollivaud Laurence, Bertrand Guylene, Lacapère Jean-Jacques, Descamps Vincent, Vitoux Dominique, Lebbe Céleste, Wolkenstein Pierre, Dupin Nicolas, Saiag Philippe, Basset-Seguin Nicole, Grandchamp Bernard

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Cyclin-Dependent Kinase 4
Share to France
Share to Melanoma

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation

Share to Pedigree

Share to Protein Structure, Tertiary

Share to Receptor, Endothelin B

Share to Skin Neoplasms

Source

Identifiers

PMID: 17223014
DOI: 10.1016/j.jdermsci.2006.11.016

Genes

CDK4
EDNRB

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A French CDK4-positive melanoma family with a co-inherited EDNRB mutation.PMID 17223014Read ↗

CDKN2 mutations in melanoma.Semantic proximity Read ↗

EDNRB gene variants and melanoma risk in two southern European populations.Semantic proximity Read ↗

Familial features affecting the melanoma risk in CDKN2A-negative melanoma families: a study based on the Swedish Cancer Registry.Semantic proximity Read ↗

Noncoding germline mutations in p16/CDKN2A in melanoma-prone families.Semantic proximity Read ↗

A large Norwegian family with inherited malignant melanoma, multiple atypical nevi, and CDK4 mutationSemantic proximity Read ↗

Novel CDKN2A mutations in Austrian melanoma patients.Semantic proximity Read ↗

Phenotypic and Histopathological Tumor Characteristics According to CDKN2A Mutation Status among Affected Members of Melanoma Families.Semantic proximity Read ↗

Rarity of CDK4 germline mutations in familial melanoma.Semantic proximity Read ↗

Inherited susceptibility to several cancers but absence of linkage between dysplastic nevus syndrome and CDKN2A in a melanoma family with a mutation in the CDKN2A ( P16INK4A ) geneSemantic proximity Read ↗

A step forward for patients with NRAS-mutant melanoma.Semantic proximity Read ↗

Germline mutations in the p16INK4a binding domain of CDK4 in familial melanomaSemantic proximity Read ↗

[CDKN2A gene in melanoma].Semantic proximity Read ↗

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