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9. CDKN2A mutation in a non-FAMMM kindred with cancers at multiple sites results in a functionally abnormal protein. Sun S; Pollock PM; Liu L; Karimi S; Jothy S; Milner BJ; Renwick A; Lassam NJ; Hayward NK; Hogg D; Narod SA; Foulkes WD Int J Cancer; 1997 Nov; 73(4):531-6. PubMed ID: 9389568 [TBL] [Abstract][Full Text] [Related]
10. CDKN2A mutations in Spanish cutaneous malignant melanoma families and patients with multiple melanomas and other neoplasia. Ruiz A; Puig S; Malvehy J; Lázaro C; Lynch M; Gimenez-Arnau AM; Puig L; Sánchez-Conejo J; Estivill X; Castel T J Med Genet; 1999 Jun; 36(6):490-3. PubMed ID: 10874641 [TBL] [Abstract][Full Text] [Related]
11. The absence of multiple atypical nevi in germline CDKN2A mutations: Comment on "Hereditary melanoma: Update on syndromes and management: Genetics of familial atypical multiple mole melanoma syndrome". Ipenburg NA; Gruis NA; Bergman W; van Kester MS J Am Acad Dermatol; 2016 Oct; 75(4):e157. PubMed ID: 27646763 [No Abstract] [Full Text] [Related]
12. Swedish CDKN2A mutation carriers do not present the atypical mole syndrome phenotype. Nielsen K; Harbst K; Måsbäck A; Jönsson G; Borg A; Olsson H; Ingvar C Melanoma Res; 2010 Aug; 20(4):266-72. PubMed ID: 20526219 [TBL] [Abstract][Full Text] [Related]
13. A locus linked to p16 modifies melanoma risk in Dutch familial atypical multiple mole melanoma (FAMMM) syndrome families. van der Velden PA; Sandkuijl LA; Bergman W; Hille ET; Frants RR; Gruis NA Genome Res; 1999 Jun; 9(6):575-80. PubMed ID: 10400925 [TBL] [Abstract][Full Text] [Related]
14. Multiple melanomas after treatment for Hodgkin lymphoma in a non-Dutch p16-Leiden mutation carrier with 2 MC1R high-risk variants. Figl A; Thirumaran RK; Ugurel S; Gast A; Hemminki K; Kumar R; Schadendorf D Arch Dermatol; 2007 Apr; 143(4):495-9. PubMed ID: 17438182 [TBL] [Abstract][Full Text] [Related]
15. Frequency of UV-inducible NRAS mutations in melanomas of patients with germline CDKN2A mutations. Eskandarpour M; Hashemi J; Kanter L; Ringborg U; Platz A; Hansson J J Natl Cancer Inst; 2003 Jun; 95(11):790-8. PubMed ID: 12783933 [TBL] [Abstract][Full Text] [Related]
16. Associations of 9p21 variants with cutaneous malignant melanoma, nevi, and pigmentation phenotypes in melanoma-prone families with and without CDKN2A mutations. Yang XR; Liang X; Pfeiffer RM; Wheeler W; Maeder D; Burdette L; Yeager M; Chanock S; Tucker MA; Goldstein AM Fam Cancer; 2010 Dec; 9(4):625-33. PubMed ID: 20574843 [TBL] [Abstract][Full Text] [Related]
17. Detection of a rare CDKN2A intronic mutation in a Hungarian melanoma-prone family and its role in splicing regulation. Balogh K; Széll M; Polyánka H; Pagani F; Bussani E; Kemény L; Oláh J Br J Dermatol; 2012 Jul; 167(1):131-3. PubMed ID: 22292911 [TBL] [Abstract][Full Text] [Related]
18. CDKN2A/p16 is inactivated in most melanoma cell lines. Castellano M; Pollock PM; Walters MK; Sparrow LE; Down LM; Gabrielli BG; Parsons PG; Hayward NK Cancer Res; 1997 Nov; 57(21):4868-75. PubMed ID: 9354451 [TBL] [Abstract][Full Text] [Related]
19. Analysis of mutations in the p16/CDKN2A gene in sporadic and familial melanoma in the Polish population. Lamperska K; Karezewska A; Kwiatkowska E; Mackiewicz A Acta Biochim Pol; 2002; 49(2):369-76. PubMed ID: 12362978 [TBL] [Abstract][Full Text] [Related]
20. A single nucleotide polymorphism in the 3'untranslated region of the CDKN2A gene is common in sporadic primary melanomas but mutations in the CDKN2B, CDKN2C, CDK4 and p53 genes are rare. Kumar R; Smeds J; Berggren P; Straume O; Rozell BL; Akslen LA; Hemminki K Int J Cancer; 2001 Nov; 95(6):388-93. PubMed ID: 11668523 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]