-
1
-
-
0038122762
-
Genetic epidemiology of melanoma
-
Bataille V. Genetic epidemiology of melanoma. Eur J Cancer 2003: 39: 1341-1347.
-
(2003)
Eur J Cancer
, vol.39
, pp. 1341-1347
-
-
Bataille, V.1
-
4
-
-
0038795172
-
Genetics of melanoma predisposition
-
Hayward N K. Genetics of melanoma predisposition. Oncogene 2003: 22: 3053-3062.
-
(2003)
Oncogene
, vol.22
, pp. 3053-3062
-
-
Hayward, N.K.1
-
5
-
-
33847188116
-
Melanocyte biology and skin pigmentation
-
Lin J Y, Fisher D E. Melanocyte biology and skin pigmentation. Nature 2007: 445: 843-850.
-
(2007)
Nature
, vol.445
, pp. 843-850
-
-
Lin, J.Y.1
Fisher, D.E.2
-
6
-
-
33745881916
-
Contribution of melanocortin-1 receptor gene variants to sporadic cutaneous melanoma risk in a population in central Italy: A case-control study
-
Fargnoli M. Contribution of melanocortin-1 receptor gene variants to sporadic cutaneous melanoma risk in a population in central Italy: A case-control study. Melanoma Res 2006: 16: 175-182.
-
(2006)
Melanoma Res
, vol.16
, pp. 175-182
-
-
Fargnoli, M.1
-
7
-
-
17644432720
-
Melanocortin 1 receptor (MC1R) gene variants may increase the risk of melanoma in France independently of clinical risk factors and UV exposure
-
Matichard E, Verpillat P, Meziani R 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: e13.
-
(2004)
J Med Genet
, vol.41
-
-
Matichard, E.1
Verpillat, P.2
Meziani, R.3
-
8
-
-
34548135234
-
MC1R: Three novel variants identified in a malignant melanoma association study in the Spanish population
-
Fernandez L, Milne R L, Bravo J et.al. MC1R: Three novel variants identified in a malignant melanoma association study in the Spanish population. Carcinogenesis 2007: 28: 1659-1664.
-
(2007)
Carcinogenesis
, vol.28
, pp. 1659-1664
-
-
Fernandez, L.1
Milne, R.L.2
Bravo, J.3
-
9
-
-
0028786945
-
Variants of the melanocyte-stimulating hormone receptor gene are associated with red hair and fair skin in humans
-
[see comment]
-
Valverde P, Healy E, Jackson I, Rees J L, Thody A J. Variants of the melanocyte-stimulating hormone receptor gene are associated with red hair and fair skin in humans [see comment]. Nat Genet 1995: 11: 328-330.
-
(1995)
Nat Genet
, vol.11
, pp. 328-330
-
-
Valverde, P.1
Healy, E.2
Jackson, I.3
Rees, J.L.4
Thody, A.J.5
-
10
-
-
34247647905
-
Comprehensive evaluation of allele frequency differences of MC1R variants across populations
-
Gerstenblith M R, Goldstein A M, Fargnoli M C, Peris K, Landi M T. Comprehensive evaluation of allele frequency differences of MC1R variants across populations. Hum Mutat 2007: 28: 495-505.
-
(2007)
Hum Mutat
, vol.28
, pp. 495-505
-
-
Gerstenblith, M.R.1
Goldstein, A.M.2
Fargnoli, M.C.3
Peris, K.4
Landi, M.T.5
-
11
-
-
6344290128
-
The genetics of sun sensitivity in humans
-
Rees J L. The genetics of sun sensitivity in humans. Am J Hum Genet 2004: 75: 739-751.
-
(2004)
Am J Hum Genet
, vol.75
, pp. 739-751
-
-
Rees, J.L.1
-
12
-
-
28944447769
-
Evidence for recent positive selection at the human AIM1 locus in a European population
-
Soejima M, Tachida H, Ishida T, Sano A, Koda Y. Evidence for recent positive selection at the human AIM1 locus in a European population. Mol Biol Evol 2006: 23: 179-188.
-
(2006)
Mol Biol Evol
, vol.23
, pp. 179-188
-
-
Soejima, M.1
Tachida, H.2
Ishida, T.3
Sano, A.4
Koda, Y.5
-
13
-
-
14944367557
-
Single nucleotide polymorphisms in the MATP gene are associated with normal human pigmentation variation
-
Graf J, Hodgson R, van Daal A. Single nucleotide polymorphisms in the MATP gene are associated with normal human pigmentation variation. Hum Mutat 2005: 25: 278-284.
-
(2005)
Hum Mutat
, vol.25
, pp. 278-284
-
-
Graf, J.1
Hodgson, R.2
van Daal, A.3
-
14
-
-
51549094379
-
SLC45A2: A novel malignant melanoma-associated gene
-
Fernandez L P, Milne R L, Pita G et al. SLC45A2: A novel malignant melanoma-associated gene. Hum Mutat 2008: 29: 1161-1167.
-
(2008)
Hum Mutat
, vol.29
, pp. 1161-1167
-
-
Fernandez, L.P.1
Milne, R.L.2
Pita, G.3
-
15
-
-
58249125574
-
The contribution of melanocortin 1 receptor gene polymorphisms and the agouti signalling protein gene 8818A>G polymorphism to cutaneous melanoma and basal cell carcinoma in a Polish population
-
Brudnik U, Branicki W, Wojas-Pelc A, Kanas P. The contribution of melanocortin 1 receptor gene polymorphisms and the agouti signalling protein gene 8818A>G polymorphism to cutaneous melanoma and basal cell carcinoma in a Polish population. Exp Dermatol 2009: 18: 167-174.
-
(2009)
Exp Dermatol
, vol.18
, pp. 167-174
-
-
Brudnik, U.1
Branicki, W.2
Wojas-Pelc, A.3
Kanas, P.4
-
17
-
-
24744455058
-
Association between endothelin receptor B nonsynonymous variants and melanoma risk
-
[see comment]
-
Soufir N, Meziani R, Lacapere J J et al. Association between endothelin receptor B nonsynonymous variants and melanoma risk [see comment]. J Natl Cancer Inst 2005: 97: 1297-1301.
-
(2005)
J Natl Cancer Inst
, vol.97
, pp. 1297-1301
-
-
Soufir, N.1
Meziani, R.2
Lacapere, J.J.3
-
18
-
-
0035904403
-
Human pigmentation genes: Identification, structure and consequences of polymorphic variation
-
Sturm R A, Teasdale R D, Box N F. Human pigmentation genes: identification, structure and consequences of polymorphic variation. Gene 2001: 277: 49-62.
-
(2001)
Gene
, vol.277
, pp. 49-62
-
-
Sturm, R.A.1
Teasdale, R.D.2
Box, N.F.3
-
19
-
-
13444262174
-
Role of myosin VIIa and Rab27a in the motility and localization of RPE melanosomes
-
Gibbs D, Azarian S M, Lillo C et al. Role of myosin VIIa and Rab27a in the motility and localization of RPE melanosomes. J Cell Sci 2004: 117: 6473-6483.
-
(2004)
J Cell Sci
, vol.117
, pp. 6473-6483
-
-
Gibbs, D.1
Azarian, S.M.2
Lillo, C.3
-
20
-
-
0036854790
-
The mouse mahoganoid coat color mutation disrupts a novel C3HC4 RING domain protein
-
Phan L K, Lin F, LeDuc C A, Chung W K, Leibel R L. The mouse mahoganoid coat color mutation disrupts a novel C3HC4 RING domain protein. J Clin Invest 2002: 110: 1449-1459.
-
(2002)
J Clin Invest
, vol.110
, pp. 1449-1459
-
-
Phan, L.K.1
Lin, F.2
LeDuc, C.A.3
Chung, W.K.4
Leibel, R.L.5
-
21
-
-
0030742789
-
Genetic studies of the mouse mutations mahogany and mahoganoid
-
Miller K A, Gunn T M, Carrasquillo M M, Lamoreux M L, Galbraith D B, Barsh G S. Genetic studies of the mouse mutations mahogany and mahoganoid. Genetics 1997: 146: 1407-1415.
-
(1997)
Genetics
, vol.146
, pp. 1407-1415
-
-
Miller, K.A.1
Gunn, T.M.2
Carrasquillo, M.M.3
Lamoreux, M.L.4
Galbraith, D.B.5
Barsh, G.S.6
-
22
-
-
0038727501
-
Accessory proteins for melanocortin signaling: Attractin and mahogunin
-
He L, Eldridge A G, Jackson P K, Gunn T M, Barsh G S. Accessory proteins for melanocortin signaling: Attractin and mahogunin. Ann NY Acad Sci 2003: 994: 288-298.
-
(2003)
Ann NY Acad Sci
, vol.994
, pp. 288-298
-
-
He, L.1
Eldridge, A.G.2
Jackson, P.K.3
Gunn, T.M.4
Barsh, G.S.5
-
23
-
-
0037968710
-
MLANA/MART1 and SILV/PMEL17/GP100 are transcriptionally regulated by MITF in melanocytes and melanoma
-
Du J, Miller A J, Widlund H R, Horstmann M A, Ramaswamy S, Fisher D E. MLANA/MART1 and SILV/PMEL17/GP100 are transcriptionally regulated by MITF in melanocytes and melanoma. Am J Pathol 2003: 163: 333-343.
-
(2003)
Am J Pathol
, vol.163
, pp. 333-343
-
-
Du, J.1
Miller, A.J.2
Widlund, H.R.3
Horstmann, M.A.4
Ramaswamy, S.5
Fisher, D.E.6
-
24
-
-
0038457509
-
Melanoma etiology: Where are we?
-
Tucker M A, Goldstein A M. Melanoma etiology: Where are we? Oncogene 2003: 22: 3042-3052.
-
(2003)
Oncogene
, vol.22
, pp. 3042-3052
-
-
Tucker, M.A.1
Goldstein, A.M.2
-
25
-
-
1242307966
-
Interactive effects of MC1R and OCA2 on melanoma risk phenotypes
-
Duffy D L, Box N F, Chen W et al. Interactive effects of MC1R and OCA2 on melanoma risk phenotypes. Hum Mol Genet 2004: 13: 447-461.
-
(2004)
Hum Mol Genet
, vol.13
, pp. 447-461
-
-
Duffy, D.L.1
Box, N.F.2
Chen, W.3
-
26
-
-
33846617194
-
A three-single-nucleotide polymorphism haplotype in intron 1 of OCA2 explains most human eye-color variation
-
Duffy D L, Montgomery G W, Chen W et al. A three-single-nucleotide polymorphism haplotype in intron 1 of OCA2 explains most human eye-color variation. Am J Hum Genet 2007: 80: 241-252.
-
(2007)
Am J Hum Genet
, vol.80
, pp. 241-252
-
-
Duffy, D.L.1
Montgomery, G.W.2
Chen, W.3
-
27
-
-
23644448602
-
Allele variations in the OCA2 gene (pink-eyed-dilution locus) are associated with genetic susceptibility to melanoma
-
Jannot A S, Meziani R, Bertrand G et al. Allele variations in the OCA2 gene (pink-eyed-dilution locus) are associated with genetic susceptibility to melanoma. Eur J Hum Genet 2005: 13: 913-920.
-
(2005)
Eur J Hum Genet
, vol.13
, pp. 913-920
-
-
Jannot, A.S.1
Meziani, R.2
Bertrand, G.3
-
28
-
-
0034653681
-
Genetics of risk factors for melanoma: An adult twin study of nevi and freckles
-
Bataille V, Snieder H, MacGregor A J, Sasieni P, Spector T D. Genetics of risk factors for melanoma: An adult twin study of nevi and freckles. J Natl Cancer Inst 2000: 92: 457-463.
-
(2000)
J Natl Cancer Inst
, vol.92
, pp. 457-463
-
-
Bataille, V.1
Snieder, H.2
MacGregor, A.J.3
Sasieni, P.4
Spector, T.D.5
-
29
-
-
40749158014
-
A single SNP in an evolutionary conserved region within intron 86 of the HERC2 gene determines human blue-brown eye color
-
Sturm R, Duffy D, Zhao Z Z et al. A single SNP in an evolutionary conserved region within intron 86 of the HERC2 gene determines human blue-brown eye color. Am J Hum Genet 2008: 82: 424-431.
-
(2008)
Am J Hum Genet
, vol.82
, pp. 424-431
-
-
Sturm, R.1
Duffy, D.2
Zhao, Z.Z.3
-
30
-
-
39549097952
-
Blue eye color in humans may be caused by a perfectly associated founder mutation in a regulatory element located within the HERC2 gene inhibiting OCA2 expression
-
Eiberg H, Troelsen J, Nielsen M et al. Blue eye color in humans may be caused by a perfectly associated founder mutation in a regulatory element located within the HERC2 gene inhibiting OCA2 expression. Hum Genet 2008: 123: 177-187.
-
(2008)
Hum Genet
, vol.123
, pp. 177-187
-
-
Eiberg, H.1
Troelsen, J.2
Nielsen, M.3
-
31
-
-
40749148586
-
Three genome-wide association studies and a linkage analysis identify HERC2 as a human iris color gene
-
Kayser M, Liu F, Janssens A et al. Three genome-wide association studies and a linkage analysis identify HERC2 as a human iris color gene. Am J Hum Genet 2008: 82: 411-423.
-
(2008)
Am J Hum Genet
, vol.82
, pp. 411-423
-
-
Kayser, M.1
Liu, F.2
Janssens, A.3
-
32
-
-
34248667614
-
Myosins in melanocytes: To move or not to move?
-
Coudrier E. Myosins in melanocytes: To move or not to move? Pigment Cell Res 2007: 20: 153-160.
-
(2007)
Pigment Cell Res
, vol.20
, pp. 153-160
-
-
Coudrier, E.1
-
33
-
-
34147187315
-
MYO7A mutation screening in Usher syndrome type I patients from diverse origins
-
Jaijo T, Aller E, Beneyto M et al. MYO7A mutation screening in Usher syndrome type I patients from diverse origins. J Med Genet 2007: 44: e71.
-
(2007)
J Med Genet
, vol.44
-
-
Jaijo, T.1
Aller, E.2
Beneyto, M.3
-
34
-
-
0347361675
-
Sequences associated with human iris pigmentation
-
Frudakis T, Thomas M, Gaskin Z et al. Sequences associated with human iris pigmentation. Genetics 2003: 165: 2071-2083.
-
(2003)
Genetics
, vol.165
, pp. 2071-2083
-
-
Frudakis, T.1
Thomas, M.2
Gaskin, Z.3
-
35
-
-
0034844162
-
Molecular and phenotypic analysis of Attractin mutant mice
-
Gunn T M, Inui T, Kitada K et al. Molecular and phenotypic analysis of Attractin mutant mice. Genetics 2001: 158: 1683-1695.
-
(2001)
Genetics
, vol.158
, pp. 1683-1695
-
-
Gunn, T.M.1
Inui, T.2
Kitada, K.3
|