CDKN2a/p16INK4a Mutations and Lack of p19ARF Involvement in Familial Melanoma Kindreds
- 31 December 1998
- journal article
- Published by Elsevier in Journal of Investigative Dermatology
- Vol. 111 (6) , 1202-1206
- https://doi.org/10.1046/j.1523-1747.1998.00412.x
Abstract
No abstract availableKeywords
This publication has 28 references indexed in Scilit:
- Germline Mutations of the CDKN2 Gene in UK Melanoma FamiliesHuman Molecular Genetics, 1997
- Prevalence of germ-line mutations in p16, p19ARF, and CDK4 in familial melanoma: analysis of a clinic-based population.Proceedings of the National Academy of Sciences, 1996
- Increased Risk of Pancreatic Cancer in Melanoma-Prone Kindreds withp16INK4MutationsNew England Journal of Medicine, 1995
- Homozygotes for CDKN2 (p16) germline mutation in Dutch familial melanoma kindredsNature Genetics, 1995
- Frequent somatic mutations and homozygous deletions of the p16 (MTS1) gene in pancreatic adenocarcinomaNature Genetics, 1994
- Germline p16 mutations in familial melanomaNature Genetics, 1994
- pl5INK4B is a potentia| effector of TGF-β-induced cell cycle arrestNature, 1994
- Analysis of the p16 gene (CDKN2) as a candidate for the chromosome 9p melanoma susceptibility locusNature Genetics, 1994
- A Cell Cycle Regulator Potentially Involved in Genesis of Many Tumor TypesScience, 1994
- Assignment of a Locus for Familial Melanoma, MLM, to Chromosome 9p13-p22Science, 1992