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

FOXP3/Scurfin gene polymorphism is associated with adult onset type 1 diabetes in Japanese, especially in women and slowly progressive-type patients.

Autoimmunity - 1 Feb 2009

Iwase Kyoko, Shimada Akira, Kawai Toshihide, Okubo Yoshiaki, Kanazawa Yasuhiko, Irie Junichiro, Oikawa Yoichi, Hirose Hiroshi, Maruyama Taro, Itoh Hiroshi

Abstract excerpt

PURPOSE: Some reports have shown that the cause of type 1 diabetes is associated with dysfunction of regulatory T cells (Tregs). The FOXP3/Scurfin gene is known to be a master gene of Tregs. Therefore, we tried to analyze the relation between the gene polymorphism and adult onset type 1 diabetes...

Read the complete abstract on PubMed

Topics

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

Share to Age of Onset
Share to Autoantibodies
Share to Diabetes Mellitus, Type 1

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Forkhead Transcription Factors

Share to Gene Frequency

Share to Microsatellite Repeats

Share to Sex Factors

Source

Identifiers

PMID: 19085184
DOI: 10.1080/08916930802488258

Genes

FOXP3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19085184-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

FOXP3/Scurfin gene polymorphism is associated with adult onset type 1 diabetes in Japanese, especially in women and slowly progressive-type patients.PMID 19085184Read ↗

A functional polymorphism in the promoter/enhancer region of the FOXP3/Scurfin gene associated with type 1 diabetes.Semantic proximity Read ↗

Forkhead box P3 gene polymorphisms predispose to type 2 diabetes and diabetic nephropathy in the Han Chinese populations: a genetic-association and gender-based evaluation study.Semantic proximity Read ↗

Gender bias in the genetic vulnerability towards type 2 diabetes and diabetic nephropathy: Role of forkhead box Protein3 transcription factor gene variants.Semantic proximity Read ↗

Forkhead box P3 gene polymorphisms predispose to type 2 diabetes and diabetic nephropathy in the Han Chinese populations: a genetic-associated and gender-based evaluation studySemantic proximity Read ↗

Association of genetic variations in FoxP3 gene with Graves' disease in a Southwest Chinese Han population.Semantic proximity Read ↗

FOXP3 gene polymorphisms increase the risk of systemic lupus erythematosus in a Han Chinese population.Semantic proximity Read ↗

Foxp3 gene polymorphisms and haplotypes associate with susceptibility of Graves' disease in Chinese Han population.Semantic proximity Read ↗

Haplotypes of FOXP3 genetic variants are associated with susceptibility, autoantibodies, and TGF-β1 in patients with systemic lupus erythematosus.Semantic proximity Read ↗

Association of single-nucleotide polymorphisms in FOXP3 gene with systemic lupus erythematosus susceptibility: a case-control study.Semantic proximity Read ↗

Sex and FOXP3 gene rs2232365 polymorphism may be associated with the clinical and pathological aspects of chronic viral diseasesSemantic proximity Read ↗

SOX2 has gender-specific genetic effects on diabetic nephropathy in samples from patients with type 1 diabetes mellitus in the GoKinD study.Semantic proximity Read ↗

HLA-DQB1 Allele Polymorphism Associated with Oral Submucous Fibrosis in Hunan, China.Semantic proximity Read ↗

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