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

Two major histocompatibility complex haplotypes influence susceptibility to sporadic inclusion body myositis: critical evaluation of an association with HLA-DR3.

Tissue antigens - 1 Nov 2004

Price P, Santoso L, Mastaglia F, Garlepp M, Kok C C, Allcock R, Laing N

Abstract excerpt

Previous studies of sporadic inclusion body myositis (sIBM) have shown a strong association with HLA-DR3 and other components of the 8.1 ancestral haplotype (AH) (HLA-A1, B8, DR3), where the susceptibility locus has been mapped to the central major histocompatibility complex (MHC) region between HLA-DR and C4. Here, the association with HLA-DR3 and other genes in the central MHC and class II region was further...

Read the complete abstract on PubMed

Topics

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

Share to Butyrophilins
Share to Genetic Predisposition to Disease

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Haplotypes

Share to HLA-B8 Antigen

Share to HLA-DR3 Antigen

Share to Major Histocompatibility Complex

Share to Membrane Glycoproteins

Share to Myositis, Inclusion Body

Source

Identifiers

PMID: 15496200
DOI: 10.1111/j.1399-0039.2004.00310.x

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

Two major histocompatibility complex haplotypes influence susceptibility to sporadic inclusion body myositis: critical evaluation of an association with HLA-DR3.PMID 15496200Read ↗

Recombination mapping of the susceptibility region for sporadic inclusion body myositis within the major histocompatibility complex.Semantic proximity Read ↗

Sporadic inclusion body myositis: HLA-DRB1 allele interactions influence disease risk and clinical phenotype.Semantic proximity Read ↗

Sporadic inclusion body myositis: variability in prevalence and phenotype and influence of the MHC.Semantic proximity Read ↗

Analysis of HLA-DRB3 alleles and supertypical genotypes in the MHC Class II region in sporadic inclusion body myositis.Semantic proximity Read ↗

Sporadic inclusion body myositis in Japanese is associated with the MHC ancestral haplotype 52.1.Semantic proximity Read ↗

High-resolution HLA-DRB1 genotyping in an Australian inclusion body myositis (s-IBM) cohort: an analysis of disease-associated alleles and diplotypes.Semantic proximity Read ↗

Immune-Array Analysis in Sporadic Inclusion Body Myositis Reveals HLA-DRB1 Amino Acid Heterogeneity Across the Myositis Spectrum.Semantic proximity Read ↗

HLA associations with inclusion body myositisSemantic proximity Read ↗

Sporadic inclusion body myositis: phenotypic variability and influence of HLA-DR3 in a cohort of 57 Australian cases.Semantic proximity Read ↗

An update on the immunogenetics of idiopathic inflammatory myopathies: major histocompatibility complex and beyond.Semantic proximity Read ↗

High-resolution HLA genotyping in inclusion body myositis refines 8.1 ancestral haplotype association to DRB1*03:01:01 and highlights pathogenic role of arginine-74 of DRβ1 chain.Semantic proximity Read ↗

Immunogenetic risk and protective factors for the idiopathic inflammatory myopathies: distinct HLA-A, -B, -Cw, -DRB1 and -DQA1 allelic profiles and motifs define clinicopathologic groups in caucasians.Semantic proximity Read ↗

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