MC1R Genotype Modifies Risk of Melanoma in Families Segregating CDKN2A Mutations
Top Cited Papers
- 1 October 2001
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 69 (4) , 765-773
- https://doi.org/10.1086/323412
Abstract
No abstract availableKeywords
This publication has 44 references indexed in Scilit:
- Melanocortin-1 Receptor Polymorphisms and Risk of Melanoma: Is the Association Explained Solely by Pigmentation Phenotype?American Journal of Human Genetics, 2000
- Participation of the Melanocortin-1 Receptor in the UV Control of PigmentationJournal of Investigative Dermatology Symposium Proceedings, 1999
- Prevalence of p16 and CDK4 germline mutations in 48 melanoma-prone families in France. The French Familial Melanoma Study Group [published erratum appears in Hum Mol Genet 1998 May;7(5):941]Human Molecular Genetics, 1998
- Analysis of the CDKN2A, CDKN2B and CDK4 genes in 48 Australian melanoma kindredsOncogene, 1997
- The Queensland Familial Melanoma ProjectMelanoma Research, 1996
- Mechanisms of Ultraviolet Light‐Induced PigmentationPhotochemistry and Photobiology, 1996
- Risk of cutaneous melanoma associated with pigmentation characteristics and freckling: Systematic overview of 10 case‐control studiesInternational Journal of Cancer, 1995
- A Cell Cycle Regulator Potentially Involved in Genesis of Many Tumor TypesScience, 1994
- A new regulatory motif in cell-cycle control causing specific inhibition of cyclin D/CDK4Nature, 1993
- Mutagenicity of melanin from human red hairCellular and Molecular Life Sciences, 1980