IRF4 variants have age-specific effects on nevus count and predispose to melanoma. - Wikidata - awgldk - TriplyDB

IRF4 variants have age-specific effects on nevus count and predispose to melanoma.

IRF4 variants have age-specific effects on nevus count and predispose to melanoma.

http://www.wikidata.org/entity/Q33960494

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Multiple common susceptibility variants near BMP pathway loci GREM1, BMP4, and BMP2 explain part of the missing heritability of colorectal cancer Cohort Profile: TwinsUK and healthy ageing twin study Cross-species models of human melanoma Melanoma. Shall we move away from the sun and focus more on embryogenesis, body weight and longevity?Human pigmentation genes under environmental selection A polymorphism in IRF4 affects human pigmentation through a tyrosinase-dependent MITF/TFAP2A pathway Confluence of genes, environment, development, and behavior in a post Genome-Wide Association Study world Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3 Genome-wide association study identifies three new melanoma susceptibility loci.The TERT variant rs2736100 is associated with colorectal cancer risk A customized pigmentation SNP array identifies a novel SNP associated with melanoma predisposition in the SLC45A2 gene.Genome-wide association studies and genetic architecture of common human diseases Genetic variants in PARP1 (rs3219090) and IRF4 (rs12203592) genes associated with melanoma susceptibility in a Spanish population Obesity gene NEGR1 associated with white matter integrity in healthy young adults Fine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regions Gene expression profiling identifies IRF4-associated molecular signatures in hematological malignancies A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma.Polymorphisms in nevus-associated genes MTAP, PLA2G6, and IRF4 and the risk of invasive cutaneous melanoma.High nevus counts confer a favorable prognosis in melanoma patients.Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma.Puzzling role of genetic risk factors in human longevity: "risk alleles" as pro-longevity variants.Evidence of CNIH3 involvement in opioid dependence.Association between functional polymorphisms in genes involved in the MAPK signaling pathways and cutaneous melanoma risk Update on the Epidemiology of Melanoma.Association of Interferon Regulatory Factor-4 Polymorphism rs12203592 With Divergent Melanoma Pathways.The UK Adult Twin Registry (TwinsUK Resource)Pigmentary traits, family history of melanoma and the risk of endometriosis: a cohort study of US women.Molecular alterations and tumor suppressive function of the DUSP22 (Dual Specificity Phosphatase 22) gene in peripheral T-cell lymphoma subtypes.Aetiology, genetics and prevention of secondary neoplasms in adult cancer survivors.Emerging trends in the epidemiology of melanoma.Sun-induced freckling: ephelides and solar lentigines.IRF4 and IRF8 Act in CD11c+ Cells To Regulate Terminal Differentiation of Lung Tissue Dendritic Cells.Endometriosis and the risk of skin cancer: a prospective cohort study.Further evidence for population specific differences in the effect of DNA markers and gender on eye colour prediction in forensics.Nevus count associations with pigmentary phenotype, histopathological melanoma characteristics and survival from melanoma Identification of Susceptibility Loci for Cutaneous Squamous Cell Carcinoma Heritability of naevus patterns in an adult twin cohort from the Brisbane Twin Registry: a cross-sectional study.Genetic variation in IRF4 expression modulates growth characteristics, tyrosinase expression and interferon-gamma response in melanocytic cells.Genetic variation at KIT locus may predispose to melanoma.Can genetic associations change with age? CFH and age-related macular degeneration.

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P2860

IRF4 variants have age-specific effects on nevus count and predispose to melanoma.

http://www.wikidata.org/entity/Q33960494

description

2010 nî lūn-bûn

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2010 թուականի Յունիսին հրատարակուած գիտական յօդուած

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2010 թվականի հունիսին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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name

IRF4 variants have age-specific effects on nevus count and predispose to melanoma.

@ast

IRF4 variants have age-specific effects on nevus count and predispose to melanoma.

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IRF4 variants have age-specific effects on nevus count and predispose to melanoma.

@en-gb

type

label

IRF4 variants have age-specific effects on nevus count and predispose to melanoma.

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IRF4 variants have age-specific effects on nevus count and predispose to melanoma.

@en

IRF4 variants have age-specific effects on nevus count and predispose to melanoma.

@en-gb

prefLabel

IRF4 variants have age-specific effects on nevus count and predispose to melanoma.

@ast

IRF4 variants have age-specific effects on nevus count and predispose to melanoma.

@en

IRF4 variants have age-specific effects on nevus count and predispose to melanoma.

@en-gb

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J.AJHG.2010.05.017

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American Journal of Human Genetics

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IRF4 variants have age-specific effects on nevus count and predispose to melanoma.

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Chris Hammond

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Dan Glass

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GenoMEL

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Gu Zhu

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Johan Hansson

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Julia A Newton-Bishop

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Mark M Iles

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Nicholas K Hayward

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Timothy D Spector

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Veronica Höiom

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P2860

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

Principal components analysis corrects for stratification in genome-wide association studies

Expression of the B-cell proliferation marker MUM1 by melanocytic lesions and comparison with S100, gp100 (HMB45), and MelanA

Molecular genetics of human pigmentation diversity

Genetic determinants of hair, eye and skin pigmentation in Europeans

Cloning of human lymphocyte-specific interferon regulatory factor (hLSIRF/hIRF4) and mapping of the gene to 6p23-p25

Personal genomes: The case of the missing heritability

KRAS variation and risk of endometriosis.

A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation.

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10.1016/J.AJHG.2010.05.017

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Massimo Mangino

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Richard A Sturm

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Grant W. Montgomery

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2010-06-17T00:00:00Z

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45093953

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20602913

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