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

Characterization of the human nebulette gene: a polymorphism in an actin-binding motif is associated with nonfamilial idiopathic dilated cardiomyopathy.

Human genetics - 1 Nov 2000

Arimura T, Nakamura T, Hiroi S, Satoh M, Takahashi M, Ohbuchi N, Ueda K, Nouchi T, Yamaguchi N, Akai J, Matsumori A, Sasayama S, Kimura A

Abstract excerpt

Idiopathic dilated cardiomyopathy (IDC) is characterized by a thin-walled heart with systolic dysfunction of unknown etiology. Because abnormalities in genes for cytoskeletal proteins related to Z-disc function have recently been reported to cause IDC, genomic organization of the gene for nebulet...

Read the complete abstract on PubMed

Topics

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

Share to Cardiomyopathy, Dilated
Share to Cytoskeletal Proteins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Gene Library

Share to LIM Domain Proteins

Share to Microfilament Proteins

Share to Muscle Proteins

Share to Myocardium

Share to Reference Values

Source

Identifiers

PMID: 11140941
DOI: 10.1007/s004390000389

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-11140941-2026-09-02.2. 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

Characterization of the human nebulette gene: a polymorphism in an actin-binding motif is associated with nonfamilial idiopathic dilated cardiomyopathy.PMID 11140941Read ↗

Mutations in NEBL encoding the cardiac Z-disk protein nebulette are associated with various cardiomyopathiesSemantic proximity Read ↗

Mutations in NEXN, a Z-disc gene, are associated with hypertrophic cardiomyopathy.Semantic proximity Read ↗

The Role of Z-disc Proteins in Myopathy and Cardiomyopathy.Semantic proximity Read ↗

Roles of Nebulin Family Members in the Heart.Semantic proximity Read ↗

Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutations.Semantic proximity Read ↗

Characterization of nebulette and nebulin and emerging concepts of their roles for vertebrate Z-discs.Semantic proximity Read ↗

Nebulette mutations are associated with dilated cardiomyopathy and endocardial fibroelastosis.Semantic proximity Read ↗

Identification and functional characterization of <i>LDB3</i> gene variants in DCM patients from Indian PopulationSemantic proximity Read ↗

Mutations in the Z-band protein myopalladin gene and idiopathic dilated cardiomyopathy.Semantic proximity Read ↗

A Cypher/ZASP mutation associated with dilated cardiomyopathy alters the binding affinity to protein kinase C.Semantic proximity Read ↗

Myozenin 2 is a novel gene for human hypertrophic cardiomyopathy.Semantic proximity Read ↗

Novel mutations in the sarcomeric protein myopalladin in patients with dilated cardiomyopathy.Semantic proximity Read ↗

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