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

TIM-3 genetic variants and risk of Behçet disease in the Iranian population.

Anais brasileiros de dermatologia - 1 Jan 2019

Ataei Mitra, Behfarjam Farinaz, Jadali Zohreh

Abstract excerpt

BACKGROUND: Behçet disease is a prototypical systemic autoimmune disease, caused by a complex interplay between environmental and genetic factors. The transmembrane immunoglobulin and mucin domain-3 (TIM-3) is a distinct member of the TIM family that is preferentially expressed on Th1 cells and plays a role in Th1-mediated autoimmune or inflammatory diseases, such as Behçet disease. OBJECTIVE: The aim of this...

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 Case-Control Studies
Share to Genetic Association Studies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hepatitis A Virus Cellular Receptor 2

Share to Logistic Models

Share to Multiplex Polymerase Chain Reaction

Share to Risk Assessment

Source

Open in PubMed Open full text

Identifiers

PMID: 31644615
DOI: 10.1590/abd1806-4841.20198022
PMCID: PMC7007023

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

TIM-3 genetic variants and risk of Behçet disease in the Iranian population.PMID 31644615Read ↗

TIM-3 rs1036199 polymorphism increases susceptibility to autoimmune diseases: evidence based on 4200 subjectsSemantic proximity Read ↗

Investigation of T-cell immunoglobulin- and mucin-domain-containing molecule-3 (TIM-3) polymorphisms in essential thrombocythaemia (ET).Semantic proximity Read ↗

The +4259A>C polymorphism of TIM-3 but not -1637C>T polymorphism of TIM-1 is associated with Multiple sclerosis in Isfahan population.Semantic proximity Read ↗

A comprehensive overview on the genetics of Behçet's disease.Semantic proximity Read ↗

Molecular variations in Th1-specific cell surface gene Tim-3.Semantic proximity Read ↗

Polymorphisms of the T-cell immunoglobulin and mucin domain molecule-3 are not associated with autoimmune Graves' disease in a Chinese Han Population.Semantic proximity Read ↗

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

[Linkage disequilibrium analysis of -1516, -574 and 4259 single nucleotide polymorphisms in TIM-3 gene].Semantic proximity Read ↗

The immunogenetics of Behçet's disease: A comprehensive review.Semantic proximity Read ↗

Association between Functional MICA-TM and Behcet's Disease: A Systematic Review and Meta-analysis.Semantic proximity Read ↗

The polymorphisms of Th1 cell surface gene Tim-3 are associated in a Korean population with rheumatoid arthritis.Semantic proximity Read ↗

The Immunogenetics of Behcet's Disease.Semantic proximity Read ↗

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