Association analysis of TGFBR3 gene with Vogt-Koyanagi-Harada disease and Behcet's disease in the Chinese Han population. (Q54317946)

27 May 2018

title

Association analysis of TGFBR3 gene with Vogt-Koyanagi-Harada disease and Behcet's disease in the Chinese Han population. (English)

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27 May 2018

0 references

7

Aize Kijlstra

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27 May 2018

Yuanyuan Chen

1

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27 May 2018

Peizeng Yang

2

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27 May 2018

Fuzhen Li

3

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27 May 2018

Shengping Hou

4

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27 May 2018

Zhengxuan Jiang

5

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27 May 2018

Qinmeng Shu

6

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27 May 2018

publication date

1 April 2012

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27 May 2018

published in

Current Eye Research

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27 May 2018

volume

37

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27 May 2018

issue

4

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27 May 2018

page(s)

312-317

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27 May 2018

Clinical patterns and characteristics of uveitis in a tertiary center for uveitis in China.

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Tyrosinase family proteins are antigens specific to Vogt-Koyanagi-Harada disease.

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

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

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Upregulated IL-23 and IL-17 in Behçet patients with active uveitis.

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Transforming growth factor-beta induces development of the T(H)17 lineage

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The differentiation of human T(H)-17 cells requires transforming growth factor-beta and induction of the nuclear receptor RORgammat

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The type III transforming growth factor-beta receptor negatively regulates nuclear factor kappa B signaling through its interaction with beta-arrestin2.

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Genome-wide association and follow-up replication studies identified ADAMTS18 and TGFBR3 as bone mass candidate genes in different ethnic groups

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Association between genetic variations of the transforming growth factor ß receptor type III and asthma in a Korean population.

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Polymorphisms of IL23R and Vogt-Koyanagi-Harada syndrome in a Chinese Han population

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

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Differentiation of human TH-17 cells does require TGF-β!

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Association of the CTLA-4 gene with Vogt-Koyanagi-Harada syndrome

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10.3109/02713683.2011.635398

21 January 2018

Identifiers

DOI

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27 May 2018

1 reference

27 May 2018