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

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

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

http://www.wikidata.org/entity/Q28201947

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The interferon induced with helicase domain 1 A946T polymorphism is not associated with rheumatoid arthritis Confirmation of the genetic association of CTLA4 and PTPN22 with ANCA-associated vasculitis Methods for high-density admixture mapping of disease genes Assessing the impact of population stratification on genetic association studies A functional variant in FCRL3, encoding Fc receptor-like 3, is associated with rheumatoid arthritis and several autoimmunities.Replication of putative candidate-gene associations with rheumatoid arthritis in >4,000 samples from North America and Sweden: association of susceptibility with PTPN22, CTLA4, and PADI4 Immunogenetics of Hashimoto's thyroiditis Autoimmune thyroid disorders-An update Follow-up of potential novel Graves' disease susceptibility loci, identified in the UK WTCCC genome-wide nonsynonymous SNP study A candidate gene study of CLEC16A does not provide evidence of association with risk for anti-CCP-positive rheumatoid arthritis A human type 1 diabetes susceptibility locus maps to chromosome 21q22.3 Central role of defective interleukin-2 production in the triggering of islet autoimmune destruction Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes The CD40, CTLA-4, thyroglobulin, TSH receptor, and PTPN22 gene quintet and its contribution to thyroid autoimmunity: back to the future A haplotype map of the human genome Multiple functions for CD28 and cytotoxic T lymphocyte antigen-4 during different phases of T cell responses: implications for arthritis and autoimmune diseases T1DBase, a community web-based resource for type 1 diabetes research Emerging mechanisms of immune regulation: the extended B7 family and regulatory T cells Genome wide in silico SNP-tumor association analysis Construction and analysis of tag single nucleotide polymorphism maps for six human-mouse orthologous candidate genes in type 1 diabetes Complex genetic predisposition in adult and juvenile rheumatoid arthritis Investigating the utility of combining phi29 whole genome amplification and highly multiplexed single nucleotide polymorphism BeadArray genotyping HLA DR phenotypic frequencies and genetic risk of Type 1 diabetes in west region of Algeria, Tlemcen Lack of correlation between the levels of soluble cytotoxic T-lymphocyte associated antigen-4 (CTLA-4) and the CT-60 genotypes Polymorphism discovery and association analyses of the interferon genes in type 1 diabetes Molecular Genetic of Atopic dermatitis: An Update The Role of Alternative Splicing in the Control of Immune Homeostasis and Cellular Differentiation MECHANISMS IN ENDOCRINOLOGY: Alternative splicing: the new frontier in diabetes research Association of genetic polymorphisms with osteosarcoma risk: a meta-analysis New approaches for predicting T cell-mediated drug reactions: A role for inducible and potentially preventable autoimmunity Cytotoxic T lymphocyte-associated antigen 4 gene polymorphisms and autoimmune thyroid diseases: an updated systematic review and cumulative meta-analysis From genetics of inflammatory bowel disease towards mechanistic insights Mechanisms of autoimmune thyroid diseases: from genetics to epigenetics Association between CTLA-4 exon-1 +49A/G polymorphism and asthma: an updated meta-analysis Genetic variation of pre-mRNA alternative splicing in human populations Insights into type 1 diabetes from the autoimmune polyendocrine syndromes Rethinking mechanisms of autoimmune pathogenesis A bispecific protein capable of engaging CTLA-4 and MHCII protects non-obese diabetic mice from autoimmune diabetes HCV E2 protein binds directly to thyroid cells and induces IL-8 production: A new mechanism for HCV induced thyroid autoimmunity What Unrelated Hematopoietic Stem Cell Transplantation in Thalassemia Taught us about Transplant Immunogenetics

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P2860

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

http://www.wikidata.org/entity/Q28201947

description

2003 nî lūn-bûn

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2003 թուականի Մայիսին հրատարակուած գիտական յօդուած

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2003 թվականի մայիսին հրատարակված գիտական հոդված

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2003年の論文

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2003年論文

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2003年論文

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2003年論文

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2003年論文

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2003年論文

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2003年论文

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name

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

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

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

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type

label

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

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

@en

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

@nl

prefLabel

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

@ast

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

@en

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

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

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Amit Allahabadia

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Annabel N Smith

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Barry Healy

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Chris C Patterson

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Constantin Ionescu-Tîrgovişte

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Costantino Motzo

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Cristian Guja

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Cristina Bordin

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P2860

Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease

CD4+CD25+ T(R) cells suppress innate immune pathology through cytokine-dependent mechanisms

Hay fever, hygiene, and household size

The structure of haplotype blocks in the human genome

A native soluble form of CTLA-4

A soluble form of CTLA-4 generated by alternative splicing is expressed by nonstimulated human T cells

A unified stepwise regression procedure for evaluating the relative effects of polymorphisms within a gene using case/control or family data: application to HLA in type 1 diabetes

High-throughput genotyping of single nucleotide polymorphisms using new biplex invader technology.

CTLA-4 in autoimmune diseases--a general susceptibility gene to autoimmunity?

Organ-specific autoimmune disease: a deficiency of tolerogenic stimulation

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