MC1R Variants Increase Risk of Melanomas Harboring BRAF Mutations
- 1 October 2008
- journal article
- Published by Elsevier in Journal of Investigative Dermatology
- Vol. 128 (10), 2485-2490
- https://doi.org/10.1038/jid.2008.67
Abstract
No abstract availableKeywords
This publication has 19 references indexed in Scilit:
- Receptor function, dominant negative activity and phenotype correlations for MC1R variant allelesHuman Molecular Genetics, 2007
- The Genetics of Sun Sensitivity in HumansAmerican Journal of Human Genetics, 2004
- Does the Addition of Information on Genotype Improve Prediction of the Risk of Melanoma and Nonmelanoma Skin Cancer beyond That Obtained from Skin Phenotype?American Journal of Epidemiology, 2004
- Melanocortin 1 receptor (MC1R) gene variants may increase the risk of melanoma in France independently of clinical risk factors and UV exposureJournal of Medical Genetics, 2004
- Interactive effects of MC1R and OCA2 on melanoma risk phenotypesHuman Molecular Genetics, 2003
- Determinants of BRAF Mutations in Primary MelanomasJNCI Journal of the National Cancer Institute, 2003
- Mutations of the BRAF gene in human cancerNature, 2002
- Combined risk factors for melanoma in a Mediterranean populationBritish Journal of Cancer, 2001
- Melanocortin 1 Receptor (MC1R) Gene Variants are Associated with an Increased Risk for Cutaneous Melanoma Which is Largely Independent of Skin Type and Hair ColorJournal of Investigative Dermatology, 2001
- Melanocortin-1 Receptor Polymorphisms and Risk of Melanoma: Is the Association Explained Solely by Pigmentation Phenotype?American Journal of Human Genetics, 2000