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

Genomic instability in scleroderma.

Asian Pacific journal of allergy and immunology - 1 Jan 2000

Roberts-Thomson P J, Male D A, Walker J G, Cox S R, Shen X, Smith M D, Ahern M J, Turner D R

Abstract excerpt

Scleroderma is an enigmatic rheumatic disorder of uncertain etio-pathogenesis. Cancer has an approximately two-fold higher incidence in scleroderma patients than in the general population. There are preliminary data of acquired genetic damage in scleroderma but the significance of these observati...

Read the complete abstract on PubMed

Topics

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

Share to Mutation
Share to Scleroderma, Systemic
Share to Genomic Instability

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Glycophorins

Share to Adolescent

Share to Alleles

Share to Flow Cytometry

Source

Identifiers

PMID: 15565952

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-15565952-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genomic instability in scleroderma.PMID 15565952Read ↗

In vivo somatic mutation and segregation at the human glycophorin A (GPA) locus: phenotypic variation encompassing both gene-specific and chromosomal mechanisms.Semantic proximity Read ↗

HLA-DRB1*0407 and *1304 are risk factors for scleroderma renal crisis.Semantic proximity Read ↗

Chromosome aberrations in Raynaud's phenomenon.Semantic proximity Read ↗

Autoantibodies and scleroderma phenotype define subgroups at high-risk and low-risk for cancer.Semantic proximity Read ↗

Molecular genetics of glycophorin MNS variants.Semantic proximity Read ↗

The GPA in vivo somatic mutation assay.Semantic proximity Read ↗

Epidemiology of Wegener's granulomatosis: Lessons from descriptive studies and analyses of genetic and environmental risk determinants.Semantic proximity Read ↗

Use of the glycophorin A somatic mutation assay for rapid, unambiguous identification of Fanconi anemia homozygotes regardless of GPA genotype.Semantic proximity Read ↗

DNA allelic alterations within VNTR loci of scleroderma families.Semantic proximity Read ↗

Diagnosis of ataxia telangiectasia with the glycophorin A somatic mutation assay.Semantic proximity Read ↗

Genomic alterations in abnormal neutrophils isolated from adult patients with systemic lupus erythematosusSemantic proximity Read ↗

Genetic instability and hematologic disease risk in Werner syndrome patients and heterozygotes.Semantic proximity Read ↗

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