(Q56902801)

4

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author name string

S M Anjos

1

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W Shao

2

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L Marchand

https://scigraph.springernature.com/pub.10.1038/sj.gene.6364211

3

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language of work or name

English

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publication date

June 2005

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28 April 2005

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published in

Genes and Immunity

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volume

6

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issue

4

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page(s)

305-311

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exact match

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cites work

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

1 reference

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

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The emerging role of the CTLA-4 gene in autoimmune endocrinopathies

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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

21 January 2018

1 reference

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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

21 January 2018

1 reference

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

21 January 2018

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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

21 January 2018

1 reference

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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

21 January 2018

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Allele-specific gene expression differences in humans

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Cis-acting regulatory variation in the human genome

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

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Genomic imprinting: parental influence on the genome

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Genetic analysis of genome-wide variation in human gene expression

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Insulin-dependent diabetes mellitus (IDDM) is associated with CTLA4 polymorphisms in multiple ethnic groups

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Genetic and physical mapping of a type 1 diabetes susceptibility gene (IDDM12) to a 100-kb phagemid artificial chromosome clone containing D2S72-CTLA4-D2S105 on chromosome 2q33

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Allele-specific quantification of tumor necrosis factor alpha (TNF) transcription and the role of promoter polymorphisms in rheumatoid arthritis patients and healthy individuals

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Wanted: regulatory SNPs

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Parental genomic imprinting of the human IGF2 gene

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

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Cis-acting variation in the expression of a high proportion of genes in human brain

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