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

Sporadic inclusion body myositis in Japanese is associated with the MHC ancestral haplotype 52.1.

Neuromuscular disorders : NMD - 1 May 2006

Scott Adrian Phillip, Allcock Richard James Nigel, Mastaglia Frank, Nishino Ichizo, Nonaka Ikuya, Laing Nigel

Abstract excerpt

In Caucasians, sporadic inclusion body myositis has been associated with the MHC ancestral haplotypes; HLA-A1, B8, DR3 (8.1AH) and HLA-B35, DR1 (35.2AH). It is not known whether these haplotypes carry susceptibility for the disease in other ethnic groups. We report here the results of HLA-B and -DRB1 typing using a high-resolution sequence-based technique in a cohort of 31 Japanese patients with definite sIBM....

Read the complete abstract on PubMed

Topics

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

Share to Asian People
Share to Cohort Studies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to DNA Mutational Analysis

Share to Genetic Testing

Share to Haplotypes

Share to Histocompatibility Antigens

Share to Inheritance Patterns

Share to Myositis, Inclusion Body

Source

Identifiers

PMID: 16564169
DOI: 10.1016/j.nmd.2006.02.002

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

Sporadic inclusion body myositis in Japanese is associated with the MHC ancestral haplotype 52.1.PMID 16564169Read ↗

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

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

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

HLA allele distribution distinguishes sporadic inclusion body myositis from hereditary inclusion body myopathies.Semantic proximity Read ↗

The association of sporadic inclusion body myositis and Sjögren's syndrome in carriers of HLA-DR3 and the 8.1 MHC ancestral haplotype.Semantic proximity Read ↗

Familial inclusion body myositis: a report on two Japanese sisters.Semantic proximity Read ↗

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

HLA-DRB1 allele and autoantibody profiles in Japanese patients with inclusion body myositis.Semantic proximity Read ↗

Genetics of inclusion-body myositis.Semantic proximity Read ↗

Mapping of a candidate region for susceptibility to inclusion body myositis in the human major histocompatibility complex.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 ↗

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

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