(Q54283225)

27 May 2018

title

TNFAIP3 gene polymorphisms confer risk for Behcet's disease in a Chinese Han population. (English)

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27 May 2018

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7

Aize Kijlstra

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27 May 2018

Hong Li

1

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27 May 2018

Qing Liu

2

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27 May 2018

Shengping Hou

3

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27 May 2018

Liping Du

4

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27 May 2018

Qingyun Zhou

5

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27 May 2018

Yan Zhou

6

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27 May 2018

Zheng Li

8

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27 May 2018

Peizeng Yang

9

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27 May 2018

publication date

18 November 2012

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27 May 2018

published in

Human Genetics

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27 May 2018

volume

132

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27 May 2018

issue

3

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27 May 2018

page(s)

293-300

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27 May 2018

https://scigraph.springernature.com/pub.10.1007/s00439-012-1250-7

exact match

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cites work

Association of a functional variant downstream of TNFAIP3 with systemic lupus erythematosus

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1250-7

Anti-TNF agents for Behçet's disease: analysis of published data on 369 patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1250-7

The ubiquitin-modifying enzyme A20 is required for termination of Toll-like receptor responses

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1250-7

Rare variation at the TNFAIP3 locus and susceptibility to rheumatoid arthritis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1250-7

Confirmation of TNIP1 and IL23A as susceptibility loci for psoriatic arthritis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1250-7

B cells lacking the tumor suppressor TNFAIP3/A20 display impaired differentiation and hyperactivation and cause inflammation and autoimmunity in aged mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1250-7

Association of the MIC-A gene and HLA-B51 with Behçet's disease in Arabs and non-Ashkenazi Jews in Israel

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1250-7

Multiple common variants for celiac disease influencing immune gene expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1250-7

Identification of novel genetic susceptibility loci for Behçet's disease using a genome-wide association study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1250-7

Analysis of 17 autoimmune disease-associated variants in type 1 diabetes identifies 6q23/TNFAIP3 as a susceptibility locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1250-7

Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1250-7

Expression of A20 by dendritic cells preserves immune homeostasis and prevents colitis and spondyloarthritis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1250-7

The ubiquitin-editing enzyme A20 restricts nucleotide-binding oligomerization domain containing 2-triggered signals

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1250-7

SUMO4 gene polymorphisms in Chinese Han patients with Behcet's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1250-7

Monocyte chemoattractant protein-1 -2518 A/G single nucleotide polymorphism in Chinese Han patients with ocular Behçet's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1250-7

Replication study confirms the association between UBAC2 and Behçet's disease in two independent Chinese sets of patients and controls

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1250-7

Two-stage association study in Chinese Han identifies two independent associations in CCR1/CCR3 locus as candidate for Behçet's disease susceptibility.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1250-7

Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1250-7

STAT4 polymorphism in a Chinese Han population with Vogt-Koyanagi-Harada syndrome and Behçet's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1250-7

Behçet's disease: global epidemiology of an Old Silk Road disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1250-7

The ubiquitin-editing protein A20 prevents dendritic cell activation, recognition of apoptotic cells, and systemic autoimmunity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1250-7

Failure to regulate TNF-induced NF-kappaB and cell death responses in A20-deficient mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1250-7

A20 (TNFAIP3) deficiency in myeloid cells triggers erosive polyarthritis resembling rheumatoid arthritis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1250-7

Genome-wide association studies identify IL23R-IL12RB2 and IL10 as Behçet's disease susceptibility loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1250-7

Multiple polymorphisms in the TNFAIP3 region are independently associated with systemic lupus erythematosus

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1250-7

Sequencing of TNFAIP3 and association of variants with multiple autoimmune diseases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1250-7

Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1250-7

Two independent alleles at 6q23 associated with risk of rheumatoid arthritis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1250-7

Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behçet's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1250-7

The tumor necrosis factor-inducible zinc finger protein A20 interacts with TRAF1/TRAF2 and inhibits NF-kappaB activation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1250-7

The ubiquitin modifying enzyme A20 restricts B cell survival and prevents autoimmunity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1250-7

TNFAIP3 gene polymorphisms are associated with response to TNF blockade in psoriasis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1250-7

Rheumatoid arthritis association at 6q23.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1250-7

Coeliac disease-associated risk variants in TNFAIP3 and REL implicate altered NF-kappaB signalling

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1250-7

Enterocyte-specific A20 deficiency sensitizes to tumor necrosis factor-induced toxicity and experimental colitis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1250-7

Comparative genetic analysis of inflammatory bowel disease and type 1 diabetes implicates multiple loci with opposite effects

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1250-7

Clinical characteristics of Behçet's disease in China.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1250-7

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1250-7

Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1250-7

Association of the TNFAIP3 rs5029939 variant with systemic sclerosis in the European Caucasian population

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-012-1250-7

Criteria for diagnosis of Behçet's disease. International Study Group for Behçet's Disease

21 January 2018

1 reference

12 December 2020

Evidence for linkage of the HLA-B locus in Behçet's disease, obtained using the transmission disequilibrium test

1 reference

12 December 2020

Clinical features of chinese patients with Behçet's disease

1 reference

12 December 2020

A20 zinc finger protein inhibits TNF and IL-1 signaling

1 reference

12 December 2020

Functional evaluation of TNFAIP3 (A20) in rheumatoid arthritis

1 reference

12 December 2020

Intercellular adhesion molecule-1 gene polymorphisms in Behçet's disease

1 reference

12 December 2020

IL-23R gene confers susceptibility to Behcet's disease in a Chinese Han population

1 reference

12 December 2020

Association between polymorphisms of FCRL3, a non-HLA gene, and Behçet's disease in a Chinese population with ophthalmic manifestations

1 reference

12 December 2020

The association of a nonsynonymous single-nucleotide polymorphism in TNFAIP3 with systemic lupus erythematosus and rheumatoid arthritis in the Japanese population

1 reference

12 December 2020

10.1007/S00439-012-1250-7

Identifiers

DOI

1 reference

27 May 2018

PubMed ID

23161053

1 reference

27 May 2018