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

A CTLA‐4 gene polymorphism is associated with both Graves' disease and autoimmune hypothyroidism

1 May 1997

Abstract excerpt

OBJECTIVE: The autoimmune thyroid diseases, Graves disease and autoimmune hypothyroidism, result from a complex interaction between genetic, environmental and endogenous factors. The genetic loci conferring susceptibility remain unclear. A recent report has demonstrated an association between a microsatellite polymorphism of the CTLA-4 gene (allele 106) on chromosome 2q33 and Graves' disease in Caucasian patients...

Read the complete abstract on PubMed

Topics

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

Share to Diabetes and associated disorders
Share to Ophthalmology and Eye Disorders
Share to Thyroid Disorders and Treatments

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 9231050
DOI: 10.1046/j.1365-2265.1997.1710996.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A CTLA‐4 gene polymorphism is associated with both Graves' disease and autoimmune hypothyroidismPMID 9231050Read ↗

The development of Graves' disease and the CTLA-4 gene on chromosome 2q33.Semantic proximity Read ↗

The Development of Graves' Disease and the CTLA-4 Gene on Chromosome 2q33Semantic proximity Read ↗

CTLA-4 gene polymorphism associated with Graves' disease in a Caucasian population.Semantic proximity Read ↗

CTLA4 gene and Graves’ disease: association of Graves’ disease with the CTLA4 exon 1 and intron 1 polymorphisms, but not with the promoter polymorphismSemantic proximity Read ↗

A cytotoxic T lymphocyte antigen-4 (CTLA-4) gene polymorphism is associated with autoimmune Addison's disease in English patients.Semantic proximity Read ↗

Soluble CTLA-4 receptor an immunological marker of Graves' disease and severity of ophthalmopathy is associated with CTLA-4 Jo31 and CT60 gene polymorphisms.Semantic proximity Read ↗

A significant association of the CTLA4 gene variants with the risk of autoimmune Graves' disease in ethnic Kashmiri population.Semantic proximity Read ↗

Clinical associations of the genetic variants of CTLA-4, Tg, TSHR, PTPN22, PTPN12 and FCRL3 in patients with Graves' disease.Semantic proximity Read ↗

CTLA-4 gene polymorphisms in Tunisian patients with Graves' disease.Semantic proximity Read ↗

Analysis of a microsatellite polymorphism of the cytotoxic T-lymphocyte antigen-4 gene in patients with vitiligo.Semantic proximity Read ↗

CTLA-4 gene polymorphism and its association with Graves' disease in the Lebanese population.Semantic proximity Read ↗

Association of CTLA-4 gene polymorphism with Graves' disease and ophthalmopathy in Iranian patients.Semantic proximity Read ↗

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