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Volumn 146, Issue , 2009, Pages 213-223

New trends in the susceptibility to melanoma

Author keywords

[No Author keywords available]

Indexed keywords

B RAF KINASE; CYCLIN DEPENDENT KINASE 4; CYCLIN DEPENDENT KINASE INHIBITOR 2A; FAS ANTIGEN; FAS LIGAND; MELANOCORTIN 1 RECEPTOR; MEMBRANE PROTEIN; PROTEIN OCA2; UNCLASSIFIED DRUG; VITAMIN D RECEPTOR; CALCITRIOL RECEPTOR;

EID: 77953669670     PISSN: 09273042     EISSN: None     Source Type: Book Series    
DOI: 10.1007/978-0-387-78574-5_19     Document Type: Review
Times cited : (3)

References (57)
  • 1
    • 0033407455 scopus 로고    scopus 로고
    • The genetics of hereditary melanoma and nevi. 1998 update
    • GreeneMH. The genetics of hereditary melanoma and nevi. 1998 update. Cancer 1999; 86(11 Suppl):2464-77.
    • (1999) Cancer , vol.86 , Issue.11 SUPPL. , pp. 2464-2477
    • GreeneMH1
  • 3
    • 0028085975 scopus 로고
    • Analysis of the p16 gene (CDKN2) as a candidate for the chromosome 9p melanoma susceptibility locus
    • Kamb A, Shattuck-Eidens D, Eeles R, Liu Q, Gruis NA, Ding W, et al. Analysis of the p16 gene (CDKN2) as a candidate for the chromosome 9p melanoma susceptibility locus. Nat Genet 1994; 8(1):23-6.
    • (1994) Nat Genet , vol.8 , Issue.1 , pp. 23-26
    • Kamb, A.1    Shattuck-Eidens, D.2    Eeles, R.3    Liu, Q.4    Gruis, N.A.5    Ding, W.6
  • 4
    • 0029664339 scopus 로고    scopus 로고
    • Germline mutations in the p16INK4a binding domain of CDK4 in familial melanoma
    • Zuo L,Weger J, Yang Q, Goldstein AM, Tucker MA,Walker GJ, et al. Germline mutations in the p16INK4a binding domain of CDK4 in familial melanoma. Nat Genet 1996; 12(1):97-9.
    • (1996) Nat Genet , vol.12 , Issue.1 , pp. 97-99
    • Zuo, L.1    Weger, J.2    Yang, Q.3    Goldstein, A.M.4    Tucker, M.A.5    Walker, G.J.6
  • 5
    • 0035487104 scopus 로고    scopus 로고
    • The INK4a/ARF network in tumour suppression
    • Available from
    • Sherr CJ. The INK4a/ARF network in tumour suppression. Nat Rev Mol Cell Biol 2001; 2(10):731-7. Available from http://www.ncbi.nlmnih.gov/entrez/query. fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list uids=11584300.
    • (2001) Nat Rev Mol Cell Biol , vol.2 , Issue.10 , pp. 731-737
    • Sherr, C.J.1
  • 6
    • 0038795172 scopus 로고    scopus 로고
    • Genetics of melanoma predisposition
    • Available from
    • Hayward NK. Genetics of melanoma predisposition. Oncogene 2003; 22(20):3053-62. Available from http://www.ncbi.nlm.nih.gov/entrez/query.fcgi? cmd=Retrieve&db=PubMed&dopt=Citation&list uids=12789280.
    • (2003) Oncogene , vol.22 , Issue.20 , pp. 3053-3062
    • Hayward, N.K.1
  • 7
    • 18244366064 scopus 로고    scopus 로고
    • Newton Bishop JA, Bishop DT. The genetics of susceptibility to cutaneous melanoma. Drugs Today (Barc) 2005;41(3):193-203. Available from http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db= PubMed&dopt=Citation& list uids=15883616.
    • Newton Bishop JA, Bishop DT. The genetics of susceptibility to cutaneous melanoma. Drugs Today (Barc) 2005;41(3):193-203. Available from http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db= PubMed&dopt=Citation& list uids=15883616.
  • 8
    • 6844226190 scopus 로고    scopus 로고
    • Prevalence of p16 and CDK4 germline mutations in 48 melanoma-prone families in France. The French Familial Melanoma Study Group
    • Soufir N, Avril MF, Chompret A, Demenais F, Bombled J, Spatz A, et al. Prevalence of p16 and CDK4 germline mutations in 48 melanoma-prone families in France. The French Familial Melanoma Study Group. Hum Mol Genet 1998; 7(2):209-16.
    • (1998) Hum Mol Genet , vol.7 , Issue.2 , pp. 209-216
    • Soufir, N.1    Avril, M.F.2    Chompret, A.3    Demenais, F.4    Bombled, J.5    Spatz, A.6
  • 9
    • 0032784037 scopus 로고    scopus 로고
    • CDKN2A (P16(INK4a)) and CDK4 mutation analysis in 131 Australian melanoma probands: Effect of family history and multiple primary melanomas
    • Holland EA, Schmid H, Kefford RF, Mann GJ. CDKN2A (P16(INK4a)) and CDK4 mutation analysis in 131 Australian melanoma probands: effect of family history and multiple primary melanomas. Genes Chromosomes Cancer 1999; 25(4):339-48.
    • (1999) Genes Chromosomes Cancer , vol.25 , Issue.4 , pp. 339-348
    • Holland, E.A.1    Schmid, H.2    Kefford, R.F.3    Mann, G.J.4
  • 10
    • 33847282821 scopus 로고    scopus 로고
    • Goldstein AM, Chan M, Harland M, Hayward NK, Demenais F, Bishop DT, et al. Features associated with germline CDKN2A mutations: a GenoMEL study of melanoma-prone families from three continents. J Med Genet 2006. Available from http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db= PubMed&dopt=Citation& list uids=16905682.
    • Goldstein AM, Chan M, Harland M, Hayward NK, Demenais F, Bishop DT, et al. Features associated with germline CDKN2A mutations: a GenoMEL study of melanoma-prone families from three continents. J Med Genet 2006. Available from http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db= PubMed&dopt=Citation& list uids=16905682.
  • 11
    • 0029129816 scopus 로고
    • Increased risk of pancreatic cancer in melanoma-prone kindreds with p16INK4 mutations [see comments]
    • Goldstein AM, Fraser MC, Struewing JP, Hussussian CJ, Ranade K, Zametkin DP, et al. Increased risk of pancreatic cancer in melanoma-prone kindreds with p16INK4 mutations [see comments]. N Engl J Med 1995; 333(15):970-4.
    • (1995) N Engl J Med , vol.333 , Issue.15 , pp. 970-974
    • Goldstein, A.M.1    Fraser, M.C.2    Struewing, J.P.3    Hussussian, C.J.4    Ranade, K.5    Zametkin, D.P.6
  • 13
    • 0031879641 scopus 로고    scopus 로고
    • CDKN2A germline mutations in U.K. patients with familial melanoma and multiple primary melanomas
    • MacKie RM, Andrew N, Lanyon WG, Connor JM. CDKN2A germline mutations in U.K. patients with familial melanoma and multiple primary melanomas. J Invest Dermatol 1998; 111(2):269-72.
    • (1998) J Invest Dermatol , vol.111 , Issue.2 , pp. 269-272
    • MacKie, R.M.1    Andrew, N.2    Lanyon, W.G.3    Connor, J.M.4
  • 14
    • 0034671754 scopus 로고    scopus 로고
    • CDKN2A germ-line mutations in individuals with multiple cutaneous melanomas
    • Hashemi J, Platz A, Ueno T, Stierner U, Ringborg U, Hansson J. CDKN2A germ-line mutations in individuals with multiple cutaneous melanomas. Cancer Res 2000; 60(24):6864-7.
    • (2000) Cancer Res , vol.60 , Issue.24 , pp. 6864-6867
    • Hashemi, J.1    Platz, A.2    Ueno, T.3    Stierner, U.4    Ringborg, U.5    Hansson, J.6
  • 16
    • 0033518889 scopus 로고    scopus 로고
    • CDKN2A variants in a population-based sample of Queensland families with melanoma
    • Aitken J, Welch J, Duffy D, Milligan A, Green A, Martin N, et al. CDKN2A variants in a population-based sample of Queensland families with melanoma. J Natl Cancer Inst 1999; 91:446-52.
    • (1999) J Natl Cancer Inst , vol.91 , pp. 446-452
    • Aitken, J.1    Welch, J.2    Duffy, D.3    Milligan, A.4    Green, A.5    Martin, N.6
  • 17
    • 23044505848 scopus 로고    scopus 로고
    • A large Norwegian family with inherited malignant melanoma, multiple atypical nevi, and CDK4 mutation
    • Available from
    • Molven A, Grimstvedt MB, Steine SJ, HarlandM, Avril MF, Hayward NK, et al. A large Norwegian family with inherited malignant melanoma, multiple atypical nevi, and CDK4 mutation. Genes Chromosomes Cancer 2005; 44(1):10-8. Available from http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd= Retrieve&db=PubMed&dopt=Citation&list uids=15880589.
    • (2005) Genes Chromosomes Cancer , vol.44 , Issue.1 , pp. 10-18
    • Molven, A.1    Grimstvedt, M.B.2    Steine, S.J.3    Harland, M.4    Avril, M.F.5    Hayward, N.K.6
  • 18
    • 33847768225 scopus 로고    scopus 로고
    • A French CDK4-positive melanoma family with a co-inherited EDNRB mutation
    • Available from
    • Soufir N, Ollivaud L, Bertrand G, Lacapere JJ, Descamps V, Vitoux D, et al. A French CDK4-positive melanoma family with a co-inherited EDNRB mutation. J Dermatol Sci 2007; 46(1): 61-4. Available from http://www.ncbi.nlm.nih.gov/ entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list uids=17223014.
    • (2007) J Dermatol Sci , vol.46 , Issue.1 , pp. 61-64
    • Soufir, N.1    Ollivaud, L.2    Bertrand, G.3    Lacapere, J.J.4    Descamps, V.5    Vitoux, D.6
  • 19
    • 0028978274 scopus 로고
    • A p16INK4ainsensitive CDK4 mutant targeted by cytolytic T lymphocytes in a human melanoma
    • Wolfel T, HauerM, Schneider J, Serrano M,Wolfel C, Klehmann-Hieb E, et al. A p16INK4ainsensitive CDK4 mutant targeted by cytolytic T lymphocytes in a human melanoma. Science 1995; 269(5228):1281-4.
    • (1995) Science , vol.269 , Issue.5228 , pp. 1281-1284
    • Wolfel, T.1    Hauer, M.2    Schneider, J.3    Serrano, M.4    Wolfel, C.5    Klehmann-Hieb, E.6
  • 21
    • 0032549711 scopus 로고    scopus 로고
    • ARF promotes MDM2 degradation and stabilizes p53: ARF-INK4a locus deletion impairs both the Rb and p53 tumor suppression pathways
    • Zhang Y, Xiong Y, Yarbrough WG. ARF promotes MDM2 degradation and stabilizes p53: ARF-INK4a locus deletion impairs both the Rb and p53 tumor suppression pathways. Cell 1998; 92(6):725-34.
    • (1998) Cell , vol.92 , Issue.6 , pp. 725-734
    • Zhang, Y.1    Xiong, Y.2    Yarbrough, W.G.3
  • 22
    • 15444350658 scopus 로고    scopus 로고
    • Germ-line deletion involving the INK4 locus in familial proneness to melanoma and nervous system tumors
    • Bahuau M, Vidaud D, Jenkins RB, Bieche I, Kimmel DW, Assouline B, et al. Germ-line deletion involving the INK4 locus in familial proneness to melanoma and nervous system tumors. Cancer Res 1998; 58(11):2298-303.
    • (1998) Cancer Res , vol.58 , Issue.11 , pp. 2298-2303
    • Bahuau, M.1    Vidaud, D.2    Jenkins, R.B.3    Bieche, I.4    Kimmel, D.W.5    Assouline, B.6
  • 23
    • 0035170850 scopus 로고    scopus 로고
    • Randerson-Moor JA, Harland M, Williams S, Cuthbert-Heavens D, Sheridan E, Aveyard J, t al. A germline deletion of p14(ARF) but not CDKN2A in a melanoma-neural system tumour syndrome family. Hum Mol Genet 2001; 10(1):55-62.
    • Randerson-Moor JA, Harland M, Williams S, Cuthbert-Heavens D, Sheridan E, Aveyard J, t al. A germline deletion of p14(ARF) but not CDKN2A in a melanoma-neural system tumour syndrome family. Hum Mol Genet 2001; 10(1):55-62.
  • 24
    • 17644384830 scopus 로고    scopus 로고
    • Intronic sequence variants of the CDKN2A gene in melanoma pedigrees
    • Available from
    • Harland M, Taylor CF, Bass S, Churchman M, Randerson-Moor JA, Holland EA, et al. Intronic sequence variants of the CDKN2A gene in melanoma pedigrees. Genes Chromosomes Cancer 2005; 43(2):128-36. Available from http://www.ncbi.nlm. nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list uids=15761864.
    • (2005) Genes Chromosomes Cancer , vol.43 , Issue.2 , pp. 128-136
    • Harland, M.1    Taylor, C.F.2    Bass, S.3    Churchman, M.4    Randerson-Moor, J.A.5    Holland, E.A.6
  • 25
    • 30744446941 scopus 로고    scopus 로고
    • Comprehensive analysis of CDKN2A (p16INK4A/p14ARF) and CDKN2B genes in 53 melanoma index cases considered to be at heightened risk of melanoma
    • Available from
    • Laud K, Marian C, Avril MF, Barrois M, Chompret A, Goldstein AM, et al. Comprehensive analysis of CDKN2A (p16INK4A/p14ARF) and CDKN2B genes in 53 melanoma index cases considered to be at heightened risk of melanoma. J Med Genet 2006;43(1): 39-47. Available from http://www.ncbi.nlm.nih.gov/entrez/ query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list uids=15937071.
    • (2006) J Med Genet , vol.43 , Issue.1 , pp. 39-47
    • Laud, K.1    Marian, C.2    Avril, M.F.3    Barrois, M.4    Chompret, A.5    Goldstein, A.M.6
  • 26
    • 0035798659 scopus 로고    scopus 로고
    • Mutations in the INK4a/ARF melanoma susceptibility locus functionally impair p14ARF
    • Rizos H, Darmanian AP, Holland EA, Mann GJ, Kefford RF. Mutations in the INK4a/ARF melanoma susceptibility locus functionally impair p14ARF. J Biol Chem 2001; 276(44):41424-34.
    • (2001) J Biol Chem , vol.276 , Issue.44 , pp. 41424-41434
    • Rizos, H.1    Darmanian, A.P.2    Holland, E.A.3    Mann, G.J.4    Kefford, R.F.5
  • 28
    • 0033796298 scopus 로고    scopus 로고
    • Gene-covariate interaction between dysplastic nevi and the CDKN2A gene in American melanoma-prone families
    • Goldstein AM, Martinez M, Tucker MA, Demenais F. Gene-covariate interaction between dysplastic nevi and the CDKN2A gene in American melanoma-prone families. Cancer Epidemiol Biomarkers Prev 2000; 9(9):889-94.
    • (2000) Cancer Epidemiol Biomarkers Prev , vol.9 , Issue.9 , pp. 889-894
    • Goldstein, A.M.1    Martinez, M.2    Tucker, M.A.3    Demenais, F.4
  • 29
    • 2942683037 scopus 로고    scopus 로고
    • Influence of genes, nevi, and sun sensitivity on melanoma risk in a family sample unselected by family history and in melanoma-prone families
    • Available from
    • Chaudru V, Chompret A, Bressac-de Paillerets B, Spatz A, Avril MF, Demenais F. Influence of genes, nevi, and sun sensitivity on melanoma risk in a family sample unselected by family history and in melanoma-prone families. J Natl Cancer Inst 2004; 96(10):785-95. Available from http://www.ncbi.nlm.nih. gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list uids=15150307.
    • (2004) J Natl Cancer Inst , vol.96 , Issue.10 , pp. 785-795
    • Chaudru, V.1    Chompret, A.2    Bressac-de Paillerets, B.3    Spatz, A.4    Avril, M.F.5    Demenais, F.6
  • 31
  • 32
    • 26444597589 scopus 로고    scopus 로고
    • Melanocortin-1 receptor (MC1R) gene variants and dysplastic nevi modify penetrance of CDKN2A mutations in French melanoma-prone pedigrees
    • Available from
    • Chaudru V, Laud K, Avril MF, Miniere A, Chompret A, Bressac-de Paillerets B, et al. Melanocortin-1 receptor (MC1R) gene variants and dysplastic nevi modify penetrance of CDKN2A mutations in French melanoma-prone pedigrees. Cancer Epidemiol Biomarkers Prev 2005; 14(10):2384-90. Available from http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db= PubMed&dopt=Citation&list uids=16214921.
    • (2005) Cancer Epidemiol Biomarkers Prev , vol.14 , Issue.10 , pp. 2384-2390
    • Chaudru, V.1    Laud, K.2    Avril, M.F.3    Miniere, A.4    Chompret, A.5    Bressac-de Paillerets, B.6
  • 33
    • 0029848043 scopus 로고    scopus 로고
    • Distribution of cDNA for melanocortin receptor subtypes in human tissues
    • Chhajlani V. Distribution of cDNA for melanocortin receptor subtypes in human tissues. Biochem Mol Biol Int 1996; 38(1):73-80.
    • (1996) Biochem Mol Biol Int , vol.38 , Issue.1 , pp. 73-80
    • Chhajlani, V.1
  • 34
    • 0345084470 scopus 로고    scopus 로고
    • Human pigmentation phenotype: A point mutation generates nonfunctional MSH receptor
    • Frandberg PA, Doufexis M, Kapas S, Chhajlani V. Human pigmentation phenotype: a point mutation generates nonfunctional MSH receptor. Biochem Biophys Res Commun 1998; 245(2):490-2.
    • (1998) Biochem Biophys Res Commun , vol.245 , Issue.2 , pp. 490-492
    • Frandberg, P.A.1    Doufexis, M.2    Kapas, S.3    Chhajlani, V.4
  • 36
  • 39
    • 6344275551 scopus 로고    scopus 로고
    • Pharmacological characterization of loss of function mutations of the human melanocortin 1 receptor that are associated with red hair
    • Available from
    • Ringholm A, Klovins J, Rudzish R, Phillips S, Rees JL, Schioth HB. Pharmacological characterization of loss of function mutations of the human melanocortin 1 receptor that are associated with red hair. J Invest Dermatol 2004; 123(5):917-23. Available from http://www.ncbi.nlm.nih.gov/entrez/query. fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list uids=15482480.
    • (2004) J Invest Dermatol , vol.123 , Issue.5 , pp. 917-923
    • Ringholm, A.1    Klovins, J.2    Rudzish, R.3    Phillips, S.4    Rees, J.L.5    Schioth, H.B.6
  • 40
    • 0036753176 scopus 로고    scopus 로고
    • Skin colour and skin cancer: MC1R, the genetic link
    • Sturm RA. Skin colour and skin cancer: MC1R, the genetic link. Melanoma Res 2002; 12(5):405-16.
    • (2002) Melanoma Res , vol.12 , Issue.5 , pp. 405-416
    • Sturm, R.A.1
  • 41
    • 6344290128 scopus 로고    scopus 로고
    • The genetics of sun sensitivity in humans
    • Available from
    • Rees JL. The genetics of sun sensitivity in humans. Am J Hum Genet 2004; 75(5):739-51. Available from http://www.ncbi.nlm.nih.gov/entrez/query fcgi?cmd=Retrieve& db=PubMed&dopt=Citation&list uids=15372380.
    • (2004) Am J Hum Genet , vol.75 , Issue.5 , pp. 739-751
    • Rees, J.L.1
  • 42
    • 0037902558 scopus 로고    scopus 로고
    • The role of melanocortin-1 receptor polymorphism in skin cancer risk phenotypes
    • Sturm RA, Duffy DL, Box NF, Chen W, Smit DJ, Brown DL, et al. The role of melanocortin-1 receptor polymorphism in skin cancer risk phenotypes. Pigment Cell Res 2003; 16(3):266-72.
    • (2003) Pigment Cell Res , vol.16 , Issue.3 , pp. 266-272
    • Sturm, R.A.1    Duffy, D.L.2    Box, N.F.3    Chen, W.4    Smit, D.J.5    Brown, D.L.6
  • 43
    • 0033910271 scopus 로고    scopus 로고
    • Melanocortin-1receptor polymorphisms and risk of melanoma: Is the association explained solely by pigmentation phenotype?
    • Palmer JS, Duffy DL, Box NF, Aitken JF, O'Gorman LE, Green AC, et al. Melanocortin-1receptor polymorphisms and risk of melanoma: is the association explained solely by pigmentation phenotype? Am J Hum Genet 2000; 66(1):176-86.
    • (2000) Am J Hum Genet , vol.66 , Issue.1 , pp. 176-186
    • Palmer, J.S.1    Duffy, D.L.2    Box, N.F.3    Aitken, J.F.4    O'Gorman, L.E.5    Green, A.C.6
  • 44
    • 0035722059 scopus 로고    scopus 로고
    • Melanocortin 1 receptor (MC1R) gene variants are associated with an increased risk for cutaneous melanoma which is largely independent of skin type and hair color
    • Available from
    • Kennedy C, ter Huurne J, Berkhout M, Gruis N, Bastiaens M, Bergman W, et al. Melanocortin 1 receptor (MC1R) gene variants are associated with an increased risk for cutaneous melanoma which is largely independent of skin type and hair color. J Invest Dermatol 2001; 117(2):294-300. Available from http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db= PubMed&dopt=Citation&list uids=11511307.
    • (2001) J Invest Dermatol , vol.117 , Issue.2 , pp. 294-300
    • Kennedy, C.1    ter Huurne, J.2    Berkhout, M.3    Gruis, N.4    Bastiaens, M.5    Bergman, W.6
  • 45
    • 17644432720 scopus 로고    scopus 로고
    • Melanocortin 1 receptor (MC1R) gene variants may increase the risk of melanoma in France independently of clinical risk factors and UV exposure
    • Available from
    • Matichard E, Verpillat P, Meziani R, Gerard B, Descamps V, Legroux E, et al. Melanocortin 1 receptor (MC1R) gene variants may increase the risk of melanoma in France independently of clinical risk factors and UV exposure. J Med Genet 2004; 41(2):e13. Available from http://www.ncbi.nlm.nih.gov/entrez/query. fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list uids=14757863.
    • (2004) J Med Genet , vol.41 , Issue.2
    • Matichard, E.1    Verpillat, P.2    Meziani, R.3    Gerard, B.4    Descamps, V.5    Legroux, E.6
  • 46
    • 33746121511 scopus 로고    scopus 로고
    • Melanocortin receptor-1 gene polymorphisms and the risk of cutaneous melanoma in a low-risk southern European population
    • Available from
    • Stratigos AJ, Dimisianos G, Nikolaou V, Poulou M, Sypsa V, Stefanaki I, et al.Melanocortin receptor-1 gene polymorphisms and the risk of cutaneous melanoma in a low-risk southern European population. J Invest Dermatol 2006; 126: 1842-1849. Available from http://www.ncbi.nlm.nih.gov/entrez/query.fcgi? cmd=Retrieve&db=PubMed&dopt=Citation&list uids=16601669.
    • (2006) J Invest Dermatol , vol.126 , pp. 1842-1849
    • Stratigos, A.J.1    Dimisianos, G.2    Nikolaou, V.3    Poulou, M.4    Sypsa, V.5    Stefanaki, I.6
  • 47
    • 21244446712 scopus 로고    scopus 로고
    • MC1R, ASIP, and DNA repair in sporadic and familial melanoma in a Mediterranean population
    • Available from
    • Landi MT, Kanetsky PA, Tsang S, Gold B, Munroe D, Rebbeck T, et al. MC1R, ASIP, and DNA repair in sporadic and familial melanoma in a Mediterranean population. J Natl Cancer Inst 2005; 97(13):998-1007. Available from http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db= PubMed&dopt=Citation&list uids=15998953.
    • (2005) J Natl Cancer Inst , vol.97 , Issue.13 , pp. 998-1007
    • Landi, M.T.1    Kanetsky, P.A.2    Tsang, S.3    Gold, B.4    Munroe, D.5    Rebbeck, T.6
  • 48
    • 33746589029 scopus 로고    scopus 로고
    • MC1R germline variants confer risk for BRAF-mutant melanoma
    • Available from
    • Landi MT, Bauer J, Pfeiffer RM, Elder DE, Hulley B, Minghetti P, et al. MC1R germline variants confer risk for BRAF-mutant melanoma. Science 2006; 313(5786):521-2. Available from http://www.ncbi.nlm.nih.gov/entrez/query.fcgi? cmd=Retrieve&db=PubMed&dopt=Citation&list uids=16809487.
    • (2006) Science , vol.313 , Issue.5786 , pp. 521-522
    • Landi, M.T.1    Bauer, J.2    Pfeiffer, R.M.3    Elder, D.E.4    Hulley, B.5    Minghetti, P.6
  • 49
    • 0028014593 scopus 로고
    • Mutations of the P gene in oculocutaneous albinism, ocular albinism, and Prader-Willi syndrome plus albinism
    • Lee ST, Nicholls RD, Bundey S, Laxova R, Musarella M, Spritz RA. Mutations of the P gene in oculocutaneous albinism, ocular albinism, and Prader-Willi syndrome plus albinism. N Engl J Med 1994; 330(8):529-34.
    • (1994) N Engl J Med , vol.330 , Issue.8 , pp. 529-534
    • Lee, S.T.1    Nicholls, R.D.2    Bundey, S.3    Laxova, R.4    Musarella, M.5    Spritz, R.A.6
  • 50
    • 33747877809 scopus 로고    scopus 로고
    • Genetic variants of the ADPRT, XRCC1, and APE1 genes and risk of cutaneous melanoma
    • Available from
    • Li C, Liu Z, Wang LE, Strom SS, Lee JE, Gershenwald JE, et al. Genetic variants of the ADPRT, XRCC1, and APE1 genes and risk of cutaneous melanoma. Carcinogenesis 2006;27(9):1894-901. Available from http://www.ncbi.nlm.nih.gov/ entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list uids=16621887.
    • (2006) Carcinogenesis , vol.27 , Issue.9 , pp. 1894-1901
    • Li, C.1    Liu, Z.2    Wang, L.E.3    Strom, S.S.4    Lee, J.E.5    Gershenwald, J.E.6
  • 51
    • 10744233034 scopus 로고    scopus 로고
    • XPD gene polymorphism and host characteristics in the association with cutaneous malignant melanoma risk
    • Available from
    • Baccarelli A, Calista D, Minghetti P, Marinelli B, Albetti B, Tseng T, et al. XPD gene polymorphism and host characteristics in the association with cutaneous malignant melanoma risk. Br J Cancer 2004; 90(2):497-502. Available from http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db= PubMed&dopt=Citation&list uids=14735199.
    • (2004) Br J Cancer , vol.90 , Issue.2 , pp. 497-502
    • Baccarelli, A.1    Calista, D.2    Minghetti, P.3    Marinelli, B.4    Albetti, B.5    Tseng, T.6
  • 52
    • 20444400600 scopus 로고    scopus 로고
    • Genetic variation in XPD, sun exposure, and risk of skin cancer
    • Available from
    • Han J, Colditz GA, Liu JS, Hunter DJ. Genetic variation in XPD, sun exposure, and risk of skin cancer. Cancer Epidemiol Biomarkers Prev 2005; 14(6):1539-44. Available from http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd= Retrieve&db=PubMed&dopt=Citation&list uids=15941969.
    • (2005) Cancer Epidemiol Biomarkers Prev , vol.14 , Issue.6 , pp. 1539-1544
    • Han, J.1    Colditz, G.A.2    Liu, J.S.3    Hunter, D.J.4
  • 53
    • 33644928341 scopus 로고    scopus 로고
    • Polymorphisms in nucleotide excision repair genes and risk of multiple primary melanoma: The Genes Environment and Melanoma Study
    • Available from
    • Millikan RC, Hummer A, Begg C, Player J, de Cotret AR, Winkel S, et al. Polymorphisms in nucleotide excision repair genes and risk of multiple primary melanoma: the Genes Environment and Melanoma Study. Carcinogenesis 2006; 27(3):610-8. Available from http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd= Retrieve&db=PubMed&dopt=Citation&list uids=16258177.
    • (2006) Carcinogenesis , vol.27 , Issue.3 , pp. 610-618
    • Millikan, R.C.1    Hummer, A.2    Begg, C.3    Player, J.4    de Cotret, A.R.5    Winkel, S.6
  • 54
    • 22344450281 scopus 로고    scopus 로고
    • Assessment of 3 xeroderma pigmentosum group C gene polymorphisms and risk of cutaneous melanoma: A case-control study
    • Available from
    • Blankenburg S, Konig IR, Moessner R, Laspe P, Thoms KM, Krueger U, et al. Assessment of 3 xeroderma pigmentosum group C gene polymorphisms and risk of cutaneous melanoma: a case-control study. Carcinogenesis 2005; 26(6):1085-90. Available from http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd= Retrieve&db=PubMed&dopt=Citation&list uids=15731165.
    • (2005) Carcinogenesis , vol.26 , Issue.6 , pp. 1085-1090
    • Blankenburg, S.1    Konig, I.R.2    Moessner, R.3    Laspe, P.4    Thoms, K.M.5    Krueger, U.6
  • 55
    • 2342512130 scopus 로고    scopus 로고
    • Polymorphisms in DNA double-strand break repair genes and skin cancer risk
    • Available from
    • Han J, Colditz GA, Samson LD, Hunter DJ. Polymorphisms in DNA double-strand break repair genes and skin cancer risk. Cancer Res 2004; 64(9):3009-13. Available from http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd= Retrieve&db=PubMed&dopt=Citation&list uids=15126335.
    • (2004) Cancer Res , vol.64 , Issue.9 , pp. 3009-3013
    • Han, J.1    Colditz, G.A.2    Samson, L.D.3    Hunter, D.J.4
  • 56
    • 17544392528 scopus 로고    scopus 로고
    • Vitamin D receptor polymorphisms are associated with altered prognosis in patients with malignant melanoma
    • Available from
    • Hutchinson PE, Osborne JE, Lear JT, Smith AG, Bowers PW, Morris PN, et al. Vitamin D receptor polymorphisms are associated with altered prognosis in patients with malignant melanoma. Clin Cancer Res 2000; 6(2):498-504. Available from http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db= PubMed&dopt=Citation&list uids=10690530.
    • (2000) Clin Cancer Res , vol.6 , Issue.2 , pp. 498-504
    • Hutchinson, P.E.1    Osborne, J.E.2    Lear, J.T.3    Smith, A.G.4    Bowers, P.W.5    Morris, P.N.6
  • 57
    • 33645074700 scopus 로고    scopus 로고
    • Polymorphisms of the FAS and FAS ligand genes associated with risk of cutaneous malignant melanoma
    • Available from
    • Li C, Larson D, Zhang Z, Liu Z, Strom SS, Gershenwald JE, et al. Polymorphisms of the FAS and FAS ligand genes associated with risk of cutaneous malignant melanoma. Pharmacogenet Genomics 2006; 16(4):253-63. Available from http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db= PubMed&dopt=Citation&list uids=16538172.
    • (2006) Pharmacogenet Genomics , vol.16 , Issue.4 , pp. 253-263
    • Li, C.1    Larson, D.2    Zhang, Z.3    Liu, Z.4    Strom, S.S.5    Gershenwald, J.E.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.