Allelic effects on gene regulation at the autoimmunity-predisposing CTLA4 locus: a re-evaluation of the 3' +6230G>A polymorphism (Q56902801)

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Allelic effects on gene regulation at the autoimmunity-predisposing CTLA4 locus: a re-evaluation of the 3′ +6230G>A polymorphism

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English	Allelic effects on gene regulation at the autoimmunity-predisposing CTLA4 locus: a re-evaluation of the 3' +6230G>A polymorphism	article	Allelic effects on gene regulation at the autoimmunity-predisposing CTLA4 locus: a re-evaluation of the 3′ +6230G>A polymorphism

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scholarly article

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Allelic effects on gene regulation at the autoimmunity-predisposing CTLA4 locus: a re-evaluation of the 3' +6230G>A polymorphism (English)

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Constantin Polychronakos

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C Polychronakos

4

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author name string

S M Anjos

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W Shao

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L Marchand

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publication date

June 2005

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28 April 2005

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Genes and Immunity

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6

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4

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305-311

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The CTLA-4 gene region of chromosome 2q33 is linked to, and associated with, type 1 diabetes. Belgian Diabetes Registry

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

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Wnt signaling in the thymus

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A CTLA-4 gene polymorphism at position -318 in the promoter region affects the expression of protein

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Association of the cytotoxic T lymphocyte-associated antigen 4 gene with type 1 diabetes: evidence for independent effects of two polymorphisms on the same haplotype block

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Mechanisms of genetic susceptibility to type I diabetes: beyond HLA.

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CTLA-4 gene polymorphism at position 49 in exon 1 reduces the inhibitory function of CTLA-4 and contributes to the pathogenesis of Graves' disease

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A common autoimmunity predisposing signal peptide variant of the cytotoxic T-lymphocyte antigen 4 results in inefficient glycosylation of the susceptibility allele

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Allele-specific gene expression differences in humans

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Effects of a polymorphism in the human tumor necrosis factor alpha promoter on transcriptional activation

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Wanted: regulatory SNPs

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Evidence against GRB10 as the gene responsible for Silver-Russell syndrome

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10.1038/SJ.GENE.6364211

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