CD226 Gly307Ser association with multiple autoimmune diseases.
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Confirmation of the genetic association of CTLA4 and PTPN22 with ANCA-associated vasculitisRevealing 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 treatmentShared and distinct genetic variants in type 1 diabetes and celiac diseaseBeyond CTLA-4 and PD-1, the Generation Z of Negative Checkpoint RegulatorsHigh-density genotyping of immune-related loci identifies new SLE risk variants in individuals with Asian ancestryReassessment of the type I diabetes association of the OAS1 locusVstm3 is a member of the CD28 family and an important modulator of T-cell functionCutting edge: TIGIT has T cell-intrinsic inhibitory functionsRTL551 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 CNSA polymorphism in the HLA-DPB1 gene is associated with susceptibility to multiple sclerosisRare variants create synthetic genome-wide associationsrs2476601 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 populationThe 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 locusAnalyses 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 predictionAssociation of a rheumatoid arthritis susceptibility variant at the CCL21 locus with premature mortality in inflammatory polyarthritis patientsInvestigation of potential non-HLA rheumatoid arthritis susceptibility loci in a European cohort increases the evidence for nine markersInfluence 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 evolutionSample 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 sclerosisThe 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.
description
article científic
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article scientifique
@fr
articolo scientifico
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artigo científico
@pt
bilimsel makale
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scientific article published on 30 October 2008
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vedecký článok
@sk
vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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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
P2093
P2860
P50
P356
P1433
P1476
CD226 Gly307Ser association with multiple autoimmune diseases.
@en
P2093
H E Stevens
International Multiple Sclerosis Genetics Consortium (IMSGC)
J D Cooper
J M M Howson
J P Hafler
L S Wicker
P2860
P2888
P356
10.1038/GENE.2008.82
P577
2008-10-30T00:00:00Z
P5875
P6179
1035640821