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Journal Abstract Search

337 related items for PubMed ID: 17397031

  • 1. Cutaneous phenotype and MC1R variants as modifying factors for the development of melanoma in CDKN2A G101W mutation carriers from 4 countries.
    Goldstein AM, Chaudru V, Ghiorzo P, Badenas C, Malvehy J, Pastorino L, Laud K, Hulley B, Avril MF, Puig-Butille JA, Miniere A, Marti R, Chompret A, Cuellar F, Kolm I, Mila M, Tucker MA, Demenais F, Bianchi-Scarra G, Puig S, de-Paillerets BB.
    Int J Cancer; 2007 Aug 15; 121(4):825-31. PubMed ID: 17397031
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  • 2. Association of MC1R variants and host phenotypes with melanoma risk in CDKN2A mutation carriers: a GenoMEL study.
    Demenais F, Mohamdi H, Chaudru V, Goldstein AM, Newton Bishop JA, Bishop DT, Kanetsky PA, Hayward NK, Gillanders E, Elder DE, Avril MF, Azizi E, van Belle P, Bergman W, Bianchi-Scarrà G, Bressac-de Paillerets B, Calista D, Carrera C, Hansson J, Harland M, Hogg D, Höiom V, Holland EA, Ingvar C, Landi MT, Lang JM, Mackie RM, Mann GJ, Ming ME, Njauw CJ, Olsson H, Palmer J, Pastorino L, Puig S, Randerson-Moor J, Stark M, Tsao H, Tucker MA, van der Velden P, Yang XR, Gruis N, Melanoma Genetics Consortium.
    J Natl Cancer Inst; 2010 Oct 20; 102(20):1568-83. PubMed ID: 20876876
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  • 6. Melanocortin-1 receptor (MC1R) gene variants and dysplastic nevi modify penetrance of CDKN2A mutations in French melanoma-prone pedigrees.
    Chaudru V, Laud K, Avril MF, Minière A, Chompret A, Bressac-de Paillerets B, Demenais F.
    Cancer Epidemiol Biomarkers Prev; 2005 Oct 20; 14(10):2384-90. PubMed ID: 16214921
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  • 9. Contribution of melanocortin-1 receptor gene variants to sporadic cutaneous melanoma risk in a population in central Italy: a case-control study.
    Fargnoli MC, Altobelli E, Keller G, Chimenti S, Höfler H, Peris K.
    Melanoma Res; 2006 Apr 20; 16(2):175-82. PubMed ID: 16567973
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  • 12. Association of MC1R variants and risk of melanoma in melanoma-prone families with CDKN2A mutations.
    Goldstein AM, Landi MT, Tsang S, Fraser MC, Munroe DJ, Tucker MA.
    Cancer Epidemiol Biomarkers Prev; 2005 Sep 20; 14(9):2208-12. PubMed ID: 16172233
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  • 17. High naevus count and MC1R red hair alleles contribute synergistically to increased melanoma risk.
    Duffy DL, Lee KJ, Jagirdar K, Pflugfelder A, Stark MS, McMeniman EK, Soyer HP, Sturm RA.
    Br J Dermatol; 2019 Nov 20; 181(5):1009-1016. PubMed ID: 30820946
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  • 18. p53 codon 72 Pro homozygosity increases the risk of cutaneous melanoma in individuals with dark skin complexion and among noncarriers of melanocortin 1 receptor red hair variants.
    Stefanaki I, Stratigos AJ, Dimisianos G, Nikolaou V, Papadopoulos O, Polydorou D, Gogas H, Tsoutsos D, Panagiotou P, Kanavakis E, Antoniou C, Katsambas AD.
    Br J Dermatol; 2007 Feb 20; 156(2):357-62. PubMed ID: 17223878
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  • 19. Assessment of polymorphic variants in the melanocortin-1 receptor gene with cutaneous pigmentation using an evolutionary approach.
    Kanetsky PA, Ge F, Najarian D, Swoyer J, Panossian S, Schuchter L, Holmes R, Guerry D, Rebbeck TR.
    Cancer Epidemiol Biomarkers Prev; 2004 May 20; 13(5):808-19. PubMed ID: 15159314
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  • 20. Melanocortin receptor 1 variants and melanoma risk: a study of 2 European populations.
    Scherer D, Nagore E, Bermejo JL, Figl A, Botella-Estrada R, Thirumaran RK, Angelini S, Hemminki K, Schadendorf D, Kumar R.
    Int J Cancer; 2009 Oct 15; 125(8):1868-75. PubMed ID: 19585506
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