Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 222

1.

MC1R, ASIP, TYR, and TYRP1 gene variants in a population-based series of multiple primary melanomas.

Helsing P, Nymoen DA, Rootwelt H, Vårdal M, Akslen LA, Molven A, Andresen PA.

Genes Chromosomes Cancer. 2012 Jul;51(7):654-61. doi: 10.1002/gcc.21952. Epub 2012 Mar 23.

PMID:
22447455
2.

MC1R, ASIP, and DNA repair in sporadic and familial melanoma in a Mediterranean population.

Landi MT, Kanetsky PA, Tsang S, Gold B, Munroe D, Rebbeck T, Swoyer J, Ter-Minassian M, Hedayati M, Grossman L, Goldstein AM, Calista D, Pfeiffer RM.

J Natl Cancer Inst. 2005 Jul 6;97(13):998-1007. Erratum in: J Natl Cancer Inst. 2005 Sep 21;97(18):1385.

PMID:
15998953
3.

MC1R, SLC45A2 and TYR genetic variants involved in melanoma susceptibility in southern European populations: results from a meta-analysis.

Ibarrola-Villava M, Hu HH, Guedj M, Fernandez LP, Descamps V, Basset-Seguin N, Bagot M, Benssussan A, Saiag P, Fargnoli MC, Peris K, Aviles JA, Lluch A, Ribas G, Soufir N.

Eur J Cancer. 2012 Sep;48(14):2183-91. doi: 10.1016/j.ejca.2012.03.006. Epub 2012 Mar 28.

PMID:
22464347
4.

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.

Exp Dermatol. 2009 Feb;18(2):167-74. doi: 10.1111/j.1600-0625.2008.00760.x. Epub 2008 Jul 7.

PMID:
18637131
5.

Genetic variants in pigmentation genes, pigmentary phenotypes, and risk of skin cancer in Caucasians.

Nan H, Kraft P, Hunter DJ, Han J.

Int J Cancer. 2009 Aug 15;125(4):909-17. doi: 10.1002/ijc.24327.

6.

ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma.

Gudbjartsson DF, Sulem P, Stacey SN, Goldstein AM, Rafnar T, Sigurgeirsson B, Benediktsdottir KR, Thorisdottir K, Ragnarsson R, Sveinsdottir SG, Magnusson V, Lindblom A, Kostulas K, Botella-Estrada R, Soriano V, Juberías P, Grasa M, Saez B, Andres R, Scherer D, Rudnai P, Gurzau E, Koppova K, Kiemeney LA, Jakobsdottir M, Steinberg S, Helgason A, Gretarsdottir S, Tucker MA, Mayordomo JI, Nagore E, Kumar R, Hansson J, Olafsson JH, Gulcher J, Kong A, Thorsteinsdottir U, Stefansson K.

Nat Genet. 2008 Jul;40(7):886-91. doi: 10.1038/ng.161. Epub 2008 May 18. Erratum in: Nat Genet. 2008 Aug;40(8):1029.

PMID:
18488027
7.

CDKN2A mutations and MC1R variants in Italian patients with single or multiple primary melanoma.

Pastorino L, Bonelli L, Ghiorzo P, Queirolo P, Battistuzzi L, Balleari E, Nasti S, Gargiulo S, Gliori S, Savoia P, Abate Osella S, Bernengo MG, Bianchi Scarrà G.

Pigment Cell Melanoma Res. 2008 Dec;21(6):700-9. doi: 10.1111/j.1755-148X.2008.00512.x. Epub 2008 Oct 22.

PMID:
18983535
8.

Melanocortin-1 receptor gene variants determine the risk of nonmelanoma skin cancer independently of fair skin and red hair.

Bastiaens MT, ter Huurne JA, Kielich C, Gruis NA, Westendorp RG, Vermeer BJ, Bavinck JN; Leiden Skin Cancer Study Team.

Am J Hum Genet. 2001 Apr;68(4):884-94. Epub 2001 Mar 16.

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;16(2):175-82.

PMID:
16567973
10.

Genotype versus phenotype: human pigmentation.

Tully G.

Forensic Sci Int Genet. 2007 Jun;1(2):105-10. doi: 10.1016/j.fsigen.2007.01.005. Epub 2007 Mar 1.

PMID:
19083738
11.

Potential association of single nucleotide polymorphisms in pigmentation genes with the development of basal cell carcinoma.

Kosiniak-Kamysz A, Pośpiech E, Wojas-Pelc A, Marcińska M, Branicki W.

J Dermatol. 2012 Aug;39(8):693-8. doi: 10.1111/j.1346-8138.2012.01559.x. Epub 2012 Apr 18.

PMID:
22512251
12.

MC1R variants increase melanoma risk in families with CDKN2A mutations: a meta-analysis.

Fargnoli MC, Gandini S, Peris K, Maisonneuve P, Raimondi S.

Eur J Cancer. 2010 May;46(8):1413-20. doi: 10.1016/j.ejca.2010.01.027. Epub 2010 Feb 26. Review.

PMID:
20189796
13.

Dermoscopic features of melanomas associated with MC1R variants in Spanish CDKN2A mutation carriers.

Cuéllar F, Puig S, Kolm I, Puig-Butille J, Zaballos P, Martí-Laborda R, Badenas C, Malvehy J.

Br J Dermatol. 2009 Jan;160(1):48-53. doi: 10.1111/j.1365-2133.2008.08826.x. Epub 2008 Sep 15.

PMID:
18795926
14.

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.

Kennedy C, ter Huurne J, Berkhout M, Gruis N, Bastiaens M, Bergman W, Willemze R, Bavinck JN.

J Invest Dermatol. 2001 Aug;117(2):294-300.

15.

Population-based study of natural variation in the melanocortin-1 receptor gene and melanoma.

Kanetsky PA, Rebbeck TR, Hummer AJ, Panossian S, Armstrong BK, Kricker A, Marrett LD, Millikan RC, Gruber SB, Culver HA, Zanetti R, Gallagher RP, Dwyer T, Busam K, From L, Mujumdar U, Wilcox H, Begg CB, Berwick M.

Cancer Res. 2006 Sep 15;66(18):9330-7.

16.

Inherited variation at MC1R and ASIP and association with melanoma-specific survival.

Taylor NJ, Reiner AS, Begg CB, Cust AE, Busam KJ, Anton-Culver H, Dwyer T, From L, Gallagher RP, Gruber SB, Rosso S, White KA, Zanetti R, Orlow I, Thomas NE, Rebbeck TR, Berwick M, Kanetsky PA; GEM Study Group.

Int J Cancer. 2015 Jun 1;136(11):2659-67. doi: 10.1002/ijc.29317. Epub 2014 Nov 26.

17.

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;14(9):2208-12.

18.

Variants at chromosome 20 (ASIP locus) and melanoma risk.

Maccioni L, Rachakonda PS, Scherer D, Bermejo JL, Planelles D, Requena C, Hemminki K, Nagore E, Kumar R.

Int J Cancer. 2013 Jan 1;132(1):42-54. doi: 10.1002/ijc.27648. Epub 2012 Jun 13.

19.

MC1R variation and melanoma risk in the Swedish population in relation to clinical and pathological parameters.

Höiom V, Tuominen R, Käller M, Lindén D, Ahmadian A, Månsson-Brahme E, Egyhazi S, Sjöberg K, Lundeberg J, Hansson J.

Pigment Cell Melanoma Res. 2009 Apr;22(2):196-204. doi: 10.1111/j.1755-148X.2008.00526.x. Epub 2008 Dec 9.

PMID:
19077144
20.

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;156(2):357-62.

PMID:
17223878

Supplemental Content

Support Center