Multiple pigmentation gene polymorphisms account for a substantial proportion of risk of cutaneous malignant melanoma.
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A partial gene deletion of SLC45A2 causes oculocutaneous albinism in Doberman pinscher dogsGenome-wide association studies of quantitatively measured skin, hair, and eye pigmentation in four European populationsHuman pigmentation genes under environmental selectionThe Pathophysiological Impact of HLA Class Ia and HLA-G Expression and Regulatory T Cells in Malignant Melanoma: A ReviewGenome-wide association studies of pigmentation and skin cancer: a review and meta-analysisGenome-wide association study identifies three new melanoma susceptibility loci.Identification of a melanoma susceptibility locus and somatic mutation in TET2.Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.Genome-wide association study identifies novel loci predisposing to cutaneous melanomaTwo-stage genome-wide association study identifies a novel susceptibility locus associated with melanomaReplication of associations between GWAS SNPs and melanoma risk in the Population Architecture Using Genomics and Epidemiology (PAGE) Study.Global skin colour prediction from DNAEvaluating phecodes, clinical classification software, and ICD-9-CM codes for phenome-wide association studies in the electronic health record.A customized pigmentation SNP array identifies a novel SNP associated with melanoma predisposition in the SLC45A2 gene.CXCR4 pathway associated with family history of melanoma.Genome-wide association studies and genetic architecture of common human diseasesIRF4 variants have age-specific effects on nevus count and predispose to melanoma.Molecular analysis of common polymorphisms within the human Tyrosinase locus and genetic association with pigmentation traitsMelanoma genetics.GWAS findings for human iris patterns: associations with variants in genes that influence normal neuronal pattern development.Comprehensive candidate gene study highlights UGT1A and BNC2 as new genes determining continuous skin color variation in Europeans.Melanocortin-1 receptor, skin cancer and phenotypic characteristics (M-SKIP) project: study design and methods for pooling results of genetic epidemiological studiesThe role of alpha-synuclein in melanin synthesis in melanoma and dopaminergic neuronal cells.MC1R genotype may modify the effect of sun exposure on melanoma risk in the GEM studyReplication and predictive value of SNPs associated with melanoma and pigmentation traits in a Southern European case-control studyGenetic variants in PARP1 (rs3219090) and IRF4 (rs12203592) genes associated with melanoma susceptibility in a Spanish populationA melanin-independent interaction between Mc1r and Met signaling pathways is required for HGF-dependent melanomaSystematic identification of DNA variants associated with ultraviolet radiation using a novel Geographic-Wide Association Study (GeoWAS)A germline variant in the interferon regulatory factor 4 gene as a novel skin cancer risk locus.Melanocortin MC₁ receptor in human genetics and model systems.Joint effect of multiple common SNPs predicts melanoma susceptibilityFine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regionsGenetic factors associated with naevus count and dermoscopic patterns: preliminary results from the Study of Nevi in Children (SONIC)Variants of SCARB1 and VDR Involved in Complex Genetic Interactions May Be Implicated in the Genetic Susceptibility to Clear Cell Renal Cell CarcinomaSkin transcriptome profiles associated with skin color in chickens.Polymorphisms in nevus-associated genes MTAP, PLA2G6, and IRF4 and the risk of invasive cutaneous melanoma.Genetics of skin color variation in Europeans: genome-wide association studies with functional follow-up.Pigmentary Markers in Danes--Associations with Quantitative Skin Colour, Nevi Count, Familial Atypical Multiple-Mole, and Melanoma SyndromeComprehensive field synopsis and systematic meta-analyses of genetic association studies in cutaneous melanomaReport of a novel OCA2 gene mutation and an investigation of OCA2 variants on melanoma risk in a familial melanoma pedigree.
P2860
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P2860
Multiple pigmentation gene polymorphisms account for a substantial proportion of risk of cutaneous malignant melanoma.
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
2009年论文
@zh
2009年论文
@zh-cn
name
Multiple pigmentation gene pol ...... cutaneous malignant melanoma.
@en
type
label
Multiple pigmentation gene pol ...... cutaneous malignant melanoma.
@en
prefLabel
Multiple pigmentation gene pol ...... cutaneous malignant melanoma.
@en
P2860
P50
P356
P1476
Multiple pigmentation gene pol ...... cutaneous malignant melanoma.
@en
P2093
Nicholas K Hayward
Zhen Z Zhao
P2860
P2888
P304
P356
10.1038/JID.2009.258
P407
P577
2009-08-27T00:00:00Z