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

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

Molecular vision - 1 Jan 2008

Li Ke, Zhao Min, Hou Shengping, Du Liping, Kijlstra Aize, Yang Peizeng

Abstract excerpt

PURPOSE: Studies have shown a strong association of human leukocyte antigens-B51 (HLA-B51) with Behçet's disease (BD). However, little is known about the association of non-HLA genes with BD. The polymorphisms of the Fc receptor-like 3 gene (FCRL3), -169C/T, -110A/G, +358C/G, and +1381A/G, have been reported to be associated with several autoimmune diseases. This study was designed to determine whether the...

Read the complete abstract on PubMed

Topics

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

Share to Asian People
Share to Behcet Syndrome

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Eye Diseases

Share to Haplotypes

Share to HLA-B Antigens

Share to HLA-B51 Antigen

Share to Receptors, Immunologic

Share to Young Adult

Source

Open in PubMed Open full text

Identifiers

PMID: 19050767
PMCID: PMC2592528

Genes

FCRL3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Association between polymorphisms of FCRL3, a non-HLA gene, and Behçet's disease in a Chinese population with ophthalmic manifestations.PMID 19050767Read ↗

Analysis of the association between Fc receptor family gene polymorphisms and ocular Behçet's disease in Han Chinese.Semantic proximity Read ↗

Genetics of Behçet's DiseaseSemantic proximity Read ↗

HLA-B51 Carriers are Susceptible to Ocular Symptoms of Behçet Disease and the Association between the Two Becomes Stronger towards the East along the Silk Road: A Literature Survey.Semantic proximity Read ↗

Association of MICA polymorphism with HLA-B51 and disease severity in Korean patients with Behcet's disease.Semantic proximity Read ↗

HLA Alleles in a Behçet Disease Multiethnic Population With and Without Ophthalmic Manifestations.Semantic proximity Read ↗

Association of IL-23R and IL-10 variations with Behçet disease: a genetic analysis study.Semantic proximity Read ↗

Fc receptor like 3 in Chinese patients of Han nationality with Guillain-Barré syndrome.Semantic proximity Read ↗

HLA and non-HLA genes in Behçet's disease: a multicentric study in the Spanish population.Semantic proximity Read ↗

A weak association of HLA-B*2702 with Behçet's disease.Semantic proximity Read ↗

Genetic association of HLA-A*2601 with ocular Behçet's disease in Japanese patients.Semantic proximity Read ↗

Behçet's disease and genes within the major histocompatibility complex region.Semantic proximity Read ↗

Human leukocyte antigen serologic and DNA typing of Behçet's disease and its primary association with B51.Semantic proximity Read ↗

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