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

Analysing regenerative potential in zebrafish models of congenital muscular dystrophy.

The international journal of biochemistry & cell biology - 1 Nov 2014

Wood A J, Currie P D

Abstract excerpt

The congenital muscular dystrophies (CMDs) are a clinically and genetically heterogeneous group of muscle disorders. Clinically hypotonia is present from birth, with progressive muscle weakness and wasting through development. For the most part, CMDs can mechanistically be attributed to failure o...

Read the complete abstract on PubMed

Topics

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

Share to Disease Models, Animal
Share to Dystroglycans
Share to Laminin

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Muscular Dystrophies

Share to Muscular Dystrophy, Animal

Share to Regenerative Medicine

Share to Zebrafish

Share to Zebrafish Proteins

Source

Identifiers

PMID: 25449259
DOI: 10.1016/j.biocel.2014.10.021

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-25449259-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Analysing regenerative potential in zebrafish models of congenital muscular dystrophy.PMID 25449259Read ↗

Muscular dystrophy modeling in zebrafish.Semantic proximity Read ↗

Modeling Human Muscular Dystrophies in Zebrafish: Mutant Lines, Transgenic Fluorescent Biosensors, and Phenotyping AssaysSemantic proximity Read ↗

Dystrophin-deficient zebrafish feature aspects of the Duchenne muscular dystrophy pathology.Semantic proximity Read ↗

Removal of dystroglycan causes severe muscular dystrophy in zebrafish embryosSemantic proximity Read ↗

Zebrafish models flex their muscles to shed light on muscular dystrophiesSemantic proximity Read ↗

A splice site mutation in laminin-α2 results in a severe muscular dystrophy and growth abnormalities in zebrafish.Semantic proximity Read ↗

Laminin-α2 Chain-Deficient Congenital Muscular Dystrophy: Pathophysiology and Development of Treatment.Semantic proximity Read ↗

Deregulation of multiple mechanisms shapes the onset of <i>LAMA2</i> -congenital muscular dystrophySemantic proximity Read ↗

A Family of Laminin α2 Chain-Deficient Mouse Mutants: Advancing the Research on LAMA2-CMDSemantic proximity Read ↗

The zebrafish dystrophic mutant softy maintains muscle fibre viability despite basement membrane rupture and muscle detachment.Semantic proximity Read ↗

Laminin-deficient muscular dystrophy: Molecular pathogenesis and structural repair strategies.Semantic proximity Read ↗

Skeletal muscle laminin and MDC1A: pathogenesis and treatment strategiesSemantic proximity Read ↗

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