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

Genetic Variations of NLR family genes in Behcet's Disease.

Scientific reports - 1 Feb 2016

Li Lin, Yu Hongsong, Jiang Yanni, Deng Bolin, Bai Lin, Kijlstra Aize, Yang Peizeng

Abstract excerpt

This study aimed to investigate whether single nucleotide polymorphisms (SNPs) of five NLR family genes (NOD1, NOD2, NLRP1, NLRP3 and CIITA) are associated with Behcet's disease (BD) in a Chinese Han population. The study was carried out in 950 BD patients and 1440 controls for 19 SNPs in the selected NLR genes. In the first-stage study, significantly decreased frequencies of the CIITA//rs12932187 C allele...

Read the complete abstract on PubMed

Topics

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

Share to Alleles
Share to Asian People

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Behcet Syndrome

Share to Gene Frequency

Share to NLRP1 gene

Share to Genotype

Share to Polymorphism, Single Nucleotide

Source

Open in PubMed Open full text

Identifiers

PMID: 26833430
DOI: 10.1038/srep20098
PMCID: PMC4735577

Genes

CIITA
NOD1
NLRP1
NLRP3
NOD2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genetic Variations of NLR family genes in Behcet's Disease.PMID 26833430Read ↗

Association of NOD1, NOD2, PYDC1 and PYDC2 genes with Behcet's disease susceptibility and clinical manifestations.Semantic proximity Read ↗

Genetic polymorphisms of C-type lectin receptors in Behcet's disease in a Chinese Han population.Semantic proximity Read ↗

Identification of genetic susceptibility loci for intestinal Behçet’s diseaseSemantic proximity Read ↗

Association of killer cell immunoglobulin-like receptor (KIR) genes and their HLA ligands with susceptibility to Behçet's‎ disease.Semantic proximity Read ↗

Identification of susceptibility SNPs in IL10 and IL23R-IL12RB2 for Behçet's disease in Han Chinese.Semantic proximity Read ↗

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

Mutational profile of rare variants in inflammasome-related genes in Behçet disease: A Next Generation Sequencing approach.Semantic proximity Read ↗

The genetics of Behçet's disease in a Chinese population.Semantic proximity Read ↗

Targeted resequencing implicates the familial Mediterranean fever gene MEFV and the toll-like receptor 4 gene TLR4 in Behçet disease.Semantic proximity Read ↗

PTPN2 rs1893217 single-nucleotide polymorphism is associated with risk of Behçet's disease in a Chinese Han population.Semantic proximity Read ↗

NOD2 exonic variations in Iranian Crohn's disease patients.Semantic proximity Read ↗

Association of Pre-miRNA-499 rs3746444 and Pre-miRNA-146a rs2910164 Polymorphisms and Susceptibility to Behcet's Disease.Semantic proximity Read ↗

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