PUIG S

Last name: PUIG S

2007 (v1)

Publication

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Cutaneous phenotype and MC1R variants as modifying factors for the development of melanoma in CDKN2A G101W mutation carriers from 4 countries.

Goldstein AM Chaudru V GHIORZO, PAOLA

The G101W founder mutation is the most common CDKN2A mutation in Italy, Spain, and France. As the background of modifying genes, environmental exposures, and sun behavior vary across countries, studying G101W carriers from distinct countries offers a unique opportunity to evaluate possible modifying factors in melanoma development. We evaluated...

Uploaded on: October 11, 2023
2012 (v1)

Publication

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Duplication of CXC chemokine genes on chromosome 4q13 in a melanoma-prone family.

Yang XR Brown K Landi MT

No description

Uploaded on: April 14, 2023
2013 (v1)

Publication

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Somatic BRAF and NRAS Mutations in Familial Melanomas with Known Germline CDKN2A Status: A GenoMEL Study.

Zebary A Omholt K van Doorn R

No description

Uploaded on: April 14, 2023
2016 (v1)

Publication

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Association of Melanocortin-1 Receptor Variants with Pigmentary Traits in Humans: A Pooled Analysis from the M-Skip Project

Tagliabue E Gandini S García Borrón JC

BACKGROUND: The melanocortin-1-receptor (MC1R) gene regulates human pigmentation and is highly polymorphic in populations of European origins. The aims of this study were to evaluate the association between MC1R variants and the risk of non-melanoma skin cancer (NMSC), and to investigate whether risk estimates differed by phenotypic...

Uploaded on: April 14, 2023

PUIG S

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