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Association study of the g.8818A>G polymorphism of the human agouti gene with melanoma risk and pigmentary characteristics in a French population.

作者信息

Meziani R, Descamps V, Gérard B, Matichard E, Bertrand G, Archimbaud A, Ollivaud L, Saiag P, Lebbé C, Basset-Seguin N, Alberti C, Crickx B, Grandchamp B, Soufir N

出版信息

J Dermatol Sci. 2005 Nov;40(2):133-6. doi: 10.1016/j.jdermsci.2005.08.001. Epub 2005 Sep 23.

DOI:10.1016/j.jdermsci.2005.08.001
PMID:16183259
Abstract
摘要

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Association study of the g.8818A>G polymorphism of the human agouti gene with melanoma risk and pigmentary characteristics in a French population.人类刺鼠基因g.8818A>G多态性与法国人群黑色素瘤风险及色素沉着特征的关联研究。
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Re: MC1R, ASIP, and DNA repair in sporadic and familial melanoma in a Mediterranean population.关于：地中海人群散发性和家族性黑色素瘤中的MC1R、ASIP与DNA修复
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Main pigmentary features and melanocortin 1 receptor (MC1R) gene polymorphisms in the population of the Canary Islands.加那利群岛人群的主要色素沉着特征及黑皮质素1受体（MC1R）基因多态性
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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.p53基因第72位密码子的脯氨酸纯合性增加了肤色较深个体以及黑皮质素1受体红发变异非携带者患皮肤黑色素瘤的风险。
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Hum Mol Genet. 2019 Jun 15;28(12):2093-2106. doi: 10.1093/hmg/ddz018.
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MC1R, the cAMP pathway, and the response to solar UV: extending the horizon beyond pigmentation.黑素皮质素受体1（MC1R）、环磷酸腺苷（cAMP）信号通路与对太阳紫外线的反应：拓展色素沉着以外的研究范畴
Pigment Cell Melanoma Res. 2014 Sep;27(5):699-720. doi: 10.1111/pcmr.12257. Epub 2014 May 30.
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Genetic variants in pigmentation genes, pigmentary phenotypes, and risk of skin cancer in Caucasians.
白种人中色素沉着基因的遗传变异、色素沉着表型与皮肤癌风险
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Regulation of eumelanin/pheomelanin synthesis and visible pigmentation in melanocytes by ligands of the melanocortin 1 receptor.黑皮质素1受体配体对黑素细胞中真黑素/褐黑素合成及可见色素沉着的调节
Pigment Cell Melanoma Res. 2008 Aug;21(4):477-86. doi: 10.1111/j.1755-148X.2008.00479.x. Epub 2008 Jun 27.
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Common sequence variants on 20q11.22 confer melanoma susceptibility.20号染色体长臂11.22区域的常见序列变异赋予黑色素瘤易感性。
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