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

Microsatellite genotyping of chromosome 14q13.2-14q13 in the vicinity of proteasomal gene PSMA6 and association with Graves' disease in the Latvian population.

Immunogenetics - 1 Jul 2004

Sjakste Tatjana, Eglite Jelena, Sochnevs Arturs, Marga Mara, Pirags Valdis, Collan Yrjö, Sjakste Nikolajs

Abstract excerpt

The 270-kb chromosome 14q13.2-14q13 region harboring the proteasomal alpha subunit 6 gene PSMA6 was analyzed for polymorphism of five microsatellite repeats in cases/controls and association with Graves' disease. Four novel microsatellite markers were localized to the 14q13.2 region upstream of PSMA6. Dinucleotide repeats HSMS801, HSMS702, HSMS701 were identified in two introns of the gene KIAA0391; the most...

Read the complete abstract on PubMed

Topics

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

Share to Chromosomes, Human, Pair 14
Share to Cysteine Endopeptidases

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Graves Disease

Share to Latvia

Share to Loss of Heterozygosity

Share to Multienzyme Complexes

Share to Proteasome Endopeptidase Complex

Share to RNA-Binding Proteins

Source

Identifiers

PMID: 15205934
DOI: 10.1007/s00251-004-0687-9

Genes

PSMA6

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

Microsatellite genotyping of chromosome 14q13.2-14q13 in the vicinity of proteasomal gene PSMA6 and association with Graves' disease in the Latvian population.PMID 15205934Read ↗

Association of microsatellite polymorphisms of the human 14q13.2 region with type 2 diabetes mellitus in Latvian and Finnish populations.Semantic proximity Read ↗

Association of 4p14 and 6q27 variation with Graves disease: a case-control study and a meta-analysis of available evidence.Semantic proximity Read ↗

The replication of the association of the rs6832151 within chromosomal band 4p14 with Graves' disease in a Polish Caucasian population.Semantic proximity Read ↗

Complex association analysis of graves disease using a set of polymorphic markers.Semantic proximity Read ↗

[Polymorphism of D6S2414 marker located in HLA (6p21.31) locus and genetic predisposition to Grave's disease in Moscow population].Semantic proximity Read ↗

Gender-dependent and age-of-onset-specific association of the rs11675434 single-nucleotide polymorphism near TPO with susceptibility to Graves' ophthalmopathy.Semantic proximity Read ↗

Association of single nucleotide polymorphism in CD28(C/T-I3 + 17) and CD40 (C/T-1) genes with the Graves' disease.Semantic proximity Read ↗

SNPs of PSMA6 gene--investigation of possible association with myocardial infarction and type 2 diabetes mellitus.Semantic proximity Read ↗

Polymorphisms of three new microsatellite sites of the dystrophin gene.Semantic proximity Read ↗

Association between the TAP1 gene codon 637 polymorphism and Graves' disease.Semantic proximity Read ↗

Association of the large multifunctional proteasome (LMP2) gene with Graves' disease is a result of linkage disequilibrium with the HLA haplotype DRB1*0304-DQB1*02-DQA1*0501.Semantic proximity Read ↗

Role of the CD40 locus in Graves' disease.Semantic proximity Read ↗

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