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Melanoma molecular subtypes: unifying and paradoxical results.

Melanoma molecular subtypes: unifying and paradoxical results.

http://www.wikidata.org/entity/Q34179210

about

Genetic and morphologic features for melanoma classification Distribution of MC1R variants among melanoma subtypes: p.R163Q is associated with lentigo maligna melanoma in a Mediterranean population.Associations of MC1R genotype and patient phenotypes with BRAF and NRAS mutations in melanoma.

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P2860

Melanoma molecular subtypes: unifying and paradoxical results.

http://www.wikidata.org/entity/Q34179210

description

2010 nî lūn-bûn

@nan

2010 թուականի Յունուարին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի հունվարին հրատարակված գիտական հոդված

@hy

2010年の論文

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2010年論文

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2010年論文

@zh-hant

2010年論文

@zh-hk

2010年論文

@zh-mo

2010年論文

@zh-tw

2010年论文

@wuu

name

Melanoma molecular subtypes: unifying and paradoxical results.

@ast

Melanoma molecular subtypes: unifying and paradoxical results.

@en

Melanoma molecular subtypes: unifying and paradoxical results.

@nl

type

label

Melanoma molecular subtypes: unifying and paradoxical results.

@ast

Melanoma molecular subtypes: unifying and paradoxical results.

@en

Melanoma molecular subtypes: unifying and paradoxical results.

@nl

prefLabel

Melanoma molecular subtypes: unifying and paradoxical results.

@ast

Melanoma molecular subtypes: unifying and paradoxical results.

@en

Melanoma molecular subtypes: unifying and paradoxical results.

@nl

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Journal of Investigative Dermatology

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Melanoma molecular subtypes: unifying and paradoxical results

@en

P2093

Colin B Begg

http://www.w3.org/2001/XMLSchema#string

Kathleen Conway

http://www.w3.org/2001/XMLSchema#string

Nancy E Thomas

http://www.w3.org/2001/XMLSchema#string

Peter A Kanetsky

http://www.w3.org/2001/XMLSchema#string

P2860

Distinct sets of genetic alterations in melanoma

BRAF and NRAS mutations in melanoma and melanocytic nevi.

MC1R variants increase risk of melanomas harboring BRAF mutations.

Melanocortin-1 receptor polymorphisms and risk of melanoma: is the association explained solely by pigmentation phenotype?

Etiologic pathogenesis of melanoma: a unifying hypothesis for the missing attributable risk.

Interactive effects of MC1R and OCA2 on melanoma risk phenotypes.

Distinct clinical and pathological features are associated with the BRAF(T1799A(V600E)) mutation in primary melanoma.

The melanocortin 1 receptor and the UV response of human melanocytes--a shift in paradigm.

Amelanotic metastatic melanoma in a patient with oculocutaneous albinism.

Red hair is the null phenotype of MC1R.

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12-14

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scholarly article

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10.1038/JID.2009.332

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1

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Marianne Berwick

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2010-01-01T00:00:00Z

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