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Volumn 12, Issue 1, 2014, Pages

Prevalence and predictors of germline CDKN2A mutations for melanoma cases from Australia, Spain and the United Kingdom

(32)  Harland, Mark a   Cust, Anne E b   Badenas, Celia c,d   Chang, Yu Mei a   Holland, Elizabeth A e   Aguilera, Paula c,d   Aitken, Joanne F f   Armstrong, Bruce K b   Barrett, Jennifer H a   Carrera, Cristina c,d   Chan, May a   Gascoyne, Joanne a   Giles, Graham G g,h   Agha Hamilton, Chantelle e   Hopper, John L g   Jenkins, Mark A g   Kanetsky, Peter A i   Kefford, Richard F e   Kolm, Isabel e   Lowery, Johanna j   more..


Author keywords

CDKN2A; Family history; Melanoma; Multiple primaries; Population based

Indexed keywords

CYCLIN DEPENDENT KINASE INHIBITOR 2A;

EID: 84928727401     PISSN: 17312302     EISSN: 18974287     Source Type: Journal    
DOI: 10.1186/1897-4287-12-20     Document Type: Article
Times cited : (51)

References (34)
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    • Mutation scanning using high-resolution melting
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  • 24
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    • 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: 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. Int J Cancer 2001, 95:388-393. 10.1002/1097-0215(20011120)95:6<388::AID-IJC1069>3.0.CO;2-6
    • (2001) Int J Cancer , vol.95 , pp. 388-393
    • Kumar, R.1    Smeds, J.2    Berggren, P.3    Straume, O.4    Rozell, B.L.5    Akslen, L.A.6    Hemminki, K.7
  • 25
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    • The CDKN2a common variants: 148 Ala/Thr and 500 C/G in 3'UTR, and their association with clinical course of melanoma
    • Lamperska KM, Przybyla A, Kycler W, Mackiewicz A: The CDKN2a common variants: 148 Ala/Thr and 500 C/G in 3'UTR, and their association with clinical course of melanoma. Acta Biochim Pol 2007, 54:119-124.
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    • Lamperska, K.M.1    Przybyla, A.2    Kycler, W.3    Mackiewicz, A.4
  • 30
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    • A deep intronic mutation in CDKN2A is associated with disease in a subset of melanoma pedigrees
    • Harland M, Mistry S, Bishop DT, Newton Bishop JA: A deep intronic mutation in CDKN2A is associated with disease in a subset of melanoma pedigrees. Hum Mol Genet 2001, 10:2679-2686. 10.1093/hmg/10.23.2679
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    • Harland, M.1    Mistry, S.2    Bishop, D.T.3    Newton Bishop, J.A.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.