CD226 Gly307Ser association with multiple autoimmune diseases. - Wikidata - wikimedia - TriplyDB

CD226 Gly307Ser association with multiple autoimmune diseases.

CD226 Gly307Ser association with multiple autoimmune diseases.

http://www.wikidata.org/entity/Q37083069

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Confirmation of the genetic association of CTLA4 and PTPN22 with ANCA-associated vasculitis Revealing the genetic basis of multiple sclerosis: are we there yet?Investigation of rheumatoid arthritis susceptibility genes identifies association of AFF3 and CD226 variants with response to anti-tumour necrosis factor treatment Shared and distinct genetic variants in type 1 diabetes and celiac disease Beyond CTLA-4 and PD-1, the Generation Z of Negative Checkpoint Regulators High-density genotyping of immune-related loci identifies new SLE risk variants in individuals with Asian ancestry Reassessment of the type I diabetes association of the OAS1 locus Vstm3 is a member of the CD28 family and an important modulator of T-cell function Cutting edge: TIGIT has T cell-intrinsic inhibitory functions RTL551 treatment of EAE reduces CD226 and T-bet+ CD4 T cells in periphery and prevents infiltration of T-bet+ IL-17, IFN-γ producing T cells into CNS A polymorphism in the HLA-DPB1 gene is associated with susceptibility to multiple sclerosis Rare variants create synthetic genome-wide associations rs2476601 T allele (R620W) defines high-risk PTPN22 type I diabetes-associated haplotypes with preliminary evidence for an additional protective haplotype.Overview of the Type I Diabetes Genetics Consortium.The Type I Diabetes Genetics Consortium 'Rapid Response' family-based candidate gene study: strategy, genes selection, and main outcome.Alternative splicing and transcriptome profiling of experimental autoimmune encephalomyelitis using genome-wide exon arrays.Evaluation of IL12B as a candidate type I diabetes susceptibility gene using data from the Type I Diabetes Genetics Consortium.Autoimmune disease classification by inverse association with SNP alleles.Allelic variants in the PHTF1-PTPN22, C12orf30 and CD226 regions as candidate susceptibility factors for the type 1 diabetes in the Estonian population The effect of single nucleotide polymorphisms from genome wide association studies in multiple sclerosis on gene expression.A powerful association test of multiple genetic variants using a random-effects model.No association of the IRS1 and PAX4 genes with type I diabetes.Evidence for association of the TCF7 locus with type I diabetes.The type I diabetes association of the IL2RA locus.Remapping the type I diabetes association of the CTLA4 locus Analyses of multiple single-nucleotide polymorphisms in the SUMO4/IDDM5 region in affected sib-pair families with type I diabetes.Analysis of 19 genes for association with type I diabetes in the Type I Diabetes Genetics Consortium families.CD226 rs763361 is associated with the susceptibility to type 1 diabetes and greater frequency of GAD65 autoantibody in a Brazilian cohort.The genetic aspects of multiple sclerosis.Cancer immunotherapy by targeting immune checkpoints: mechanism of T cell dysfunction in cancer immunity and new therapeutic targets.Non-synonymous variant (Gly307Ser) in CD226 is associated with susceptibility to multiple autoimmune diseases.Perspectives on the use of multiple sclerosis risk genes for prediction Association of a rheumatoid arthritis susceptibility variant at the CCL21 locus with premature mortality in inflammatory polyarthritis patients Investigation of potential non-HLA rheumatoid arthritis susceptibility loci in a European cohort increases the evidence for nine markers Influence of MIF, CD40, and CD226 polymorphisms on risk of rheumatoid arthritis.A ChIP-seq defined genome-wide map of vitamin D receptor binding: associations with disease and evolution Sample reproducibility of genetic association using different multimarker TDTs in genome-wide association studies: characterization and a new approach.Hexose-6-phosphate dehydrogenase: a new risk gene for multiple sclerosis.Identity-by-descent mapping to detect rare variants conferring susceptibility to multiple sclerosis The role of rheumatoid arthritis genetic susceptibility markers in the prediction of erosive disease in patients with early inflammatory polyarthritis: results from the Norfolk Arthritis Register.

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CD226 Gly307Ser association with multiple autoimmune diseases.

http://www.wikidata.org/entity/Q37083069

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

@tr

scientific article published on 30 October 2008

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

CD226 Gly307Ser association with multiple autoimmune diseases.

@en

CD226 Gly307Ser association with multiple autoimmune diseases.

@nl

type

label

CD226 Gly307Ser association with multiple autoimmune diseases.

@en

CD226 Gly307Ser association with multiple autoimmune diseases.

@nl

prefLabel

CD226 Gly307Ser association with multiple autoimmune diseases.

@en

CD226 Gly307Ser association with multiple autoimmune diseases.

@nl

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Genes and Immunity

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CD226 Gly307Ser association with multiple autoimmune diseases.

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B Healy

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G Coleman

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H E Stevens

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International Multiple Sclerosis Genetics Consortium (IMSGC)

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J A Todd

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J D Cooper

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J M M Howson

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J P Hafler

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L M Maier

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L S Wicker

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Recommended diagnostic criteria for multiple sclerosis: Guidelines from the international panel on the diagnosis of multiple sclerosis

DNAM-1, a novel adhesion molecule involved in the cytolytic function of T lymphocytes

The Interaction of Selection and Linkage. I. General Considerations; Heterotic Models.

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

A second generation human haplotype map of over 3.1 million SNPs

Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes

Physical and functional association of LFA-1 with DNAM-1 adhesion molecule

Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease

Risk alleles for multiple sclerosis identified by a genomewide study

Population structure, differential bias and genomic control in a large-scale, case-control association study

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5-10

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scholarly article

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10.1038/GENE.2008.82

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1

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10

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Vincent Plagnol

Jane Worthington

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2008-10-30T00:00:00Z

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23439563

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1035640821

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multiple sclerosis

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