The CDKN2A tumour suppressor gene
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Cancer Research,Dermatology,Oncology
Reference15 articles.
1. Molecular genetics of familial cutaneous melanoma.
2. CDKN2AMutations in Multiple Primary Melanomas
3. A single nucleotide polymorphism in the 3?untranslated region of theCDKN2A gene is common in sporadic primary melanomas but mutations in theCDKN2B,CDKN2C,CDK4 andp53 genes are rare
4. High Frequency of Multiple Melanomas and Breast and Pancreas Carcinomas in CDKN2A Mutation-Positive Melanoma Families
5. Increased Risk of Pancreatic Cancer in Melanoma-Prone Kindreds withp16INK4Mutations
Cited by 7 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Malignant Melanoma–a Genetic Overview;Actas Dermo-Sifiliográficas;2009-11
2. Selection criteria for genetic assessment of patients with familial melanoma;Journal of the American Academy of Dermatology;2009-10
3. Predisposición genética en el melanoma cutáneo;Actas Dermo-Sifiliográficas;2006-05
4. Search for germline alterations in CDKN2A/ARF and CDK4 of 42 Jewish melanoma families with or without neural system tumours;British Journal of Cancer;2005-05-31
5. A familial syndromic association between cutaneous malignant melanoma and neural system tumours;British Journal of Dermatology;2004-12
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