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

Copper toxicosis gene MURR1 is not changed in Wilson disease patients with normal blood ceruloplasmin levels.

World journal of gastroenterology - 14 Apr 2006

Weiss Karl Heinz, Merle Uta, Schaefer Mark, Ferenci Peter, Fullekrug Joachim, Stremmel Wolfgang

Abstract excerpt

AIM: To analyze our Wilson disease patient cohort (n=106) for alterations in the gene coding for MURR1. METHODS: Patients with an established diagnosis of Wilson disease but normal ceruloplasmin blood levels were chosen for our study (n = 14). Patients with two known disease-causing mutations in...

Read the complete abstract on PubMed

Topics

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

Share to Adaptor Proteins, Signal Transducing
Share to Aged
Share to Carrier Proteins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Ceruloplasmin

Share to Hepatolenticular Degeneration

Share to Mutation

Share to Proteins

Source

Open in PubMed Open full text

Identifiers

PMID: 16610028
DOI: 10.3748/wjg.v12.i14.2239
PMCID: PMC4087653

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-16610028-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Copper toxicosis gene MURR1 is not changed in Wilson disease patients with normal blood ceruloplasmin levels.PMID 16610028Read ↗

The canine copper toxicosis gene MURR1 is not implicated in the pathogenesis of Wilson disease.Semantic proximity Read ↗

Analysis of the human homologue of the canine copper toxicosis gene MURR1 in Wilson disease patients.Semantic proximity Read ↗

Mutation analysis of 218 Chinese patients with Wilson disease revealed no correlation between the canine copper toxicosis gene MURR1 and Wilson disease.Semantic proximity Read ↗

The Copper Toxicosis Gene Product Murr1 Directly Interacts with the Wilson Disease ProteinSemantic proximity Read ↗

Molecular regulation of copper excretion in the liver.Semantic proximity Read ↗

Analysis of the human Atox 1 homologue in Wilson patients.Semantic proximity Read ↗

Indirect molecular diagnosis of copper toxicosis in Bedlington terriers is complicated by haplotype diversity.Semantic proximity Read ↗

A novel COMMD1 mutation Thr174Met associated with elevated urinary copper and signs of enhanced apoptotic cell death in a Wilson Disease patient.Semantic proximity Read ↗

Mutation analysis of copper transporter genes in patients with ethylmalonic encephalopathy, mitochondriopathies and copper deficiency phenotypes.Semantic proximity Read ↗

Middle-aged heterozygous carriers of Wilson's disease do not present with significant phenotypic deviations related to copper metabolism.Semantic proximity Read ↗

Evaluation of haplotypes associated with copper toxicosis in Bedlington Terriers in Australia.Semantic proximity Read ↗

Not all absent serum ceruloplasmin is Wilson disease: a review of aceruloplasminemia.Semantic proximity Read ↗

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