Common variants in FOXP1 are associated with generalized vitiligo. - Wikidata - wikimedia - TriplyDB

Common variants in FOXP1 are associated with generalized vitiligo.

Common variants in FOXP1 are associated with generalized vitiligo.

http://www.wikidata.org/entity/Q33945522

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De novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairment Genetic advances in the study of speech and language disorders Modern vitiligo genetics sheds new light on an ancient disease The distinct and overlapping phenotypic spectra of FOXP1 and FOXP2 in cognitive disorders Genetic Susceptibility to Vitiligo: GWAS Approaches for Identifying Vitiligo Susceptibility Genes and Loci Concise review of recent studies in vitiligo Melanocytes and their diseases Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo Genetics of Vitiligo.Transcriptomics of morphological color change in polychromatic Midas cichlids.Psoriasis regression analysis of MHC loci identifies shared genetic variants with vitiligo.Shared genetic relationships underlying generalized vitiligo and autoimmune thyroid disease.The genetics of generalized vitiligo: autoimmune pathways and an inverse relationship with malignant melanoma MHC class II super-enhancer increases surface expression of HLA-DR and HLA-DQ and affects cytokine production in autoimmune vitiligo.Genome-wide analysis identifies a quantitative trait locus in the MHC class II region associated with generalized vitiligo age of onset Comprehensive association analysis of candidate genes for generalized vitiligo supports XBP1, FOXP3, and TSLP.RNASET2 tag SNP but not CCR6 polymorphisms is associated with autoimmune thyroid diseases in the Chinese Han population Six decades of vitiligo genetics: genome-wide studies provide insights into autoimmune pathogenesis.FOXP3 is a promising and potential candidate gene in generalised vitiligo susceptibility.Psoriasis and other complex trait dermatoses: from Loci to functional pathways.Next-generation DNA re-sequencing identifies common variants of TYR and HLA-A that modulate the risk of generalized vitiligo via antigen presentation.Recent progress in the genetics of generalized vitiligo.Polymorphisms of the centrosomal gene (FGFR1OP) and lung cancer risk: a meta-analysis of 14,463 cases and 44,188 controls.Genome-wide association studies of autoimmune vitiligo identify 23 new risk loci and highlight key pathways and regulatory variants.Vitiligo as an inflammatory skin disorder: a therapeutic perspective.Potential role of neurogenic inflammatory factors in the pathogenesis of vitiligo.The prevalence of thyroid disease in patients with vitiligo: a systematic review.The association between tumor necrosis factor-α-308 G/A polymorphism and risk for vitiligo: a meta-analysis.Association analysis revealed one susceptibility locus for vitiligo with immune-related diseases in the Chinese Han population.Nonsegmental vitiligo and autoimmune mechanism.Pre- vs. post-pubertal onset of vitiligo: multivariate analysis indicates atopic diathesis association in pre-pubertal onset vitiligo.No evidence for rare pathological SIAE coding variants in patients with vitiligo.The replication of the association of the rs9355610 within 6p27 with Graves' disease.Data analysis in the post-genome-wide association study era.FOXP1mutations cause intellectual disability and a recognizable phenotype

P2860

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P2860

Common variants in FOXP1 are associated with generalized vitiligo.

http://www.wikidata.org/entity/Q33945522

description

2010 nî lūn-bûn

@nan

2010 թուականի Յունիսին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի հունիսին հրատարակված գիտական հոդված

@hy

2010年の論文

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2010年論文

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2010年論文

@zh-hant

2010年論文

@zh-hk

2010年論文

@zh-mo

2010年論文

@zh-tw

2010年论文

@wuu

name

Common variants in FOXP1 are associated with generalized vitiligo.

@ast

Common variants in FOXP1 are associated with generalized vitiligo.

@en

type

label

Common variants in FOXP1 are associated with generalized vitiligo.

@ast

Common variants in FOXP1 are associated with generalized vitiligo.

@en

prefLabel

Common variants in FOXP1 are associated with generalized vitiligo.

@ast

Common variants in FOXP1 are associated with generalized vitiligo.

@en

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Nature Genetics

P1476

Common variants in FOXP1 are associated with generalized vitiligo

@en

P2093

Alain Taïeb

http://www.w3.org/2001/XMLSchema#string

Andreas Overbeck

http://www.w3.org/2001/XMLSchema#string

Anthony P Weetman

http://www.w3.org/2001/XMLSchema#string

Christina M Mailloux

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David J Gawkrodger

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Giovanni Leone

http://www.w3.org/2001/XMLSchema#string

Jo Lambert

http://www.w3.org/2001/XMLSchema#string

Katherine Gowan

http://www.w3.org/2001/XMLSchema#string

Margaret R Wallace

http://www.w3.org/2001/XMLSchema#string

Nanny van Geel

http://www.w3.org/2001/XMLSchema#string

P2860

Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease

Down-regulation of the forkhead transcription factor Foxp1 is required for monocyte differentiation and macrophage function

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

PLINK: a tool set for whole-genome association and population-based linkage analyses

Foxp1 is an essential transcriptional regulator of B cell development

Genome-wide association study of generalized vitiligo in an isolated European founder population identifies SMOC2, in close proximity to IDDM8

Family-based tests for associating haplotypes with general phenotype data: application to asthma genetics.

Foxp1 is an essential transcriptional regulator for the generation of quiescent naive T cells during thymocyte development.

CCR6-mediated dendritic cell activation of pathogen-specific T cells in Peyer's patches.

IPEX, FOXP3 and regulatory T-cells: a model for autoimmunity.

P2888

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576-578

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10.1038/NG.602

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7

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42

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Khaled Ezzedine

Dorothy C Bennett

Wayne T McCormack

Elizabeth Helen Kemp

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2010-06-06T00:00:00Z

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44652228

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20526340

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2893242

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