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

Adaptations of cytoarchitecture in human dilated cardiomyopathy

10 Dec 2014

Abstract excerpt

Hypertrophic cardiomyopathy is characterised by a histological phenotype of myocyte disarray, but heart tissue samples from patients with dilated cardiomyopathy (DCM) often look comparatively similar to those from healthy individuals apart from conspicuous regions of fibrosis and necrosis. We have previously investigated subcellular alterations in the cytoarchitecture of mouse models of dilated cardiomyopathy and...

Read the complete abstract on PubMed

Topics

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

Share to Cardiomyopathy and Myosin Studies
Share to Cardiovascular Effects of Exercise
Share to Viral Infections and Immunology Research

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 28509975
DOI: 10.1007/s12551-014-0146-2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Adaptations of cytoarchitecture in human dilated cardiomyopathyPMID 28509975Read ↗

Cardiac cytoarchitecture — why the “hardware” is important for heart function!Semantic proximity Read ↗

Disorganization of Intercalated Discs in Dilated CardiomyopathySemantic proximity Read ↗

EH-myomesin splice isoform is a novel marker for dilated cardiomyopathySemantic proximity Read ↗

Disturbed Desmoglein-2 in the intercalated disc of pediatric patients with dilated cardiomyopathy.Semantic proximity Read ↗

HSBP7 Rescue of a Titin Cardiomyopathy Identified by Morphological ProfilingSemantic proximity Read ↗

Towards a re-definition of 'cardiac hypertrophy' through a rational characterization of left ventricular phenotypes: a position paper of the Working Group 'Myocardial Function' of the ESC.Semantic proximity Read ↗

Molecular composition of the intercalated disc in a spontaneous canine animal model of arrhythmogenic right ventricular dysplasia/cardiomyopathy.Semantic proximity Read ↗

Mechanosensitive Gene Regulation by Myocardin-Related Transcription Factors Is Required for Cardiomyocyte Integrity in Load-Induced Ventricular HypertrophySemantic proximity Read ↗

Ultrastructural evidence of intercalated disc remodelling in arrhythmogenic right ventricular cardiomyopathy: an electron microscopy investigation on endomyocardial biopsies.Semantic proximity Read ↗

Myoarchitectural disarray of hypertrophic cardiomyopathy begins pre‐birthSemantic proximity Read ↗

MLP-deficient mice exhibit a disruption of cardiac cytoarchitectural organization, dilated cardiomyopathy, and heart failure.Semantic proximity Read ↗

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

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