Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Copy number variants and genetic polymorphisms in TBX21, GATA3, Rorc, Foxp3 and susceptibility to Behcet's disease and Vogt-Koyanagi-Harada syndrome.

Scientific reports - 15 Apr 2015

Liao Dan, Hou Shengping, Zhang Jun, Fang Jing, Liu Yunjia, Bai Lin, Cao Qingfeng, Kijlstra Aize, Yang Peizeng

Abstract excerpt

This study aimed to investigate the role of genetic variants including single nucleotide polymorphisms (SNPs) and copy number variants (CNVs) of TBX21, GATA3, Rorc and Foxp3 genes in Behcet's disease (BD) and Vogt-Koyanagi-Harada (VKH) syndrome in a Chinese Han population. Genotyping of 25 SNPs was performed by iPLEX system (Sequenom) or polymerase chain reaction-restriction fragment length polymorphism...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Behcet Syndrome
Share to DNA Copy Number Variations

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Forkhead Transcription Factors

Share to GABA Plasma Membrane Transport Proteins

Share to Nuclear Receptor Subfamily 1, Group F, Member 3

Share to T-bet Transcription Factor

Share to T-Box Domain Proteins

Share to Uveomeningoencephalitic Syndrome

Source

Open in PubMed Open full text

Identifiers

PMID: 25873156
DOI: 10.1038/srep09511
PMCID: PMC4397537

Genes

GATA3
TBX21

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Copy number variants and genetic polymorphisms in TBX21, GATA3, Rorc, Foxp3 and susceptibility to Behcet's disease and Vogt-Koyanagi-Harada syndrome.PMID 25873156Read ↗

Association analysis of TGFBR3 gene with Vogt-Koyanagi-Harada disease and Behcet's disease in the Chinese Han population.Semantic proximity Read ↗

Copy number variations and gene polymorphisms of complement components in ocular Behcet's disease and Vogt-Koyanagi-Harada syndrome.Semantic proximity Read ↗

Association of a TNIP1 polymorphism with Vogt-Koyanagi-Harada syndrome but not with ocular Behcet's disease in Han Chinese.Semantic proximity Read ↗

Genetic variations of IL17F and IL23A show associations with Behçet's disease and Vogt-Koyanagi-Harada syndrome.Semantic proximity Read ↗

The Association of Chemokine Gene Polymorphisms with VKH and Behcet's Disease in a Chinese Han Population.Semantic proximity Read ↗

miR-23a, miR-146a and miR-301a confer predisposition to Vogt-Koyanagi-Harada syndrome but not to Behcet's disease.Semantic proximity Read ↗

Genetic analysis of innate immunity in Behcet's disease identifies an association with IL-37 and IL-18RAP.Semantic proximity Read ↗

Genetic Variation in the REL Gene Increases Risk of Behcet's Disease in a Chinese Han Population but That of PRKCQ Does Not.Semantic proximity Read ↗

Interleukin-17 gene polymorphism is associated with Vogt-Koyanagi-Harada syndrome but not with Behçet's disease in a Chinese Han population.Semantic proximity Read ↗

RORC and Foxp3 axis in cerebrospinal fluid of patients with Neuro-Behçet's DiseaseSemantic proximity Read ↗

CD40 gene polymorphisms confer risk of Behcet's disease but not of Vogt-Koyanagi-Harada syndrome in a Han Chinese population.Semantic proximity Read ↗

Association of VPREB1 Gene Copy Number Variation and Rheumatoid Arthritis Susceptibility.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.