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

[Role of perlecan in neuromuscular function: studies in knockout mice and human disorders].

Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme - 1 Nov 2004

Hirasawa Eri

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Acetylcholine
Share to Acetylcholinesterase
Share to Chondrogenesis
Share to Heparan Sulfate Proteoglycans

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Morphogenesis

Share to Neuromuscular Diseases

Share to Neuromuscular Junction

Share to Osteochondrodysplasias

Source

Identifiers

PMID: 15552996

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Role of perlecan in neuromuscular function: studies in knockout mice and human disorders].PMID 15552996Read ↗

[Roles of perlecan in development and disease: studies in knockout mice and human disorders].Semantic proximity Read ↗

Role of perlecan in skeletal development and diseases.Semantic proximity Read ↗

Perlecan, A Multi-Functional, Cell-Instructive, Matrix-Stabilizing Proteoglycan With Roles in Tissue Development Has Relevance to Connective Tissue Repair and RegenerationSemantic proximity Read ↗

A mouse model of Schwartz-Jampel syndrome reveals myelinating Schwann cell dysfunction with persistent axonal depolarization in vitro and distal peripheral nerve hyperexcitability when perlecan is lacking.Semantic proximity Read ↗

Structural and functional mutations of the perlecan gene cause Schwartz-Jampel syndrome, with myotonic myopathy and chondrodysplasia.Semantic proximity Read ↗

Sleuthing molecular targets for neurological diseases at the neuromuscular junction.Semantic proximity Read ↗

Novel interactions of perlecan: Unraveling perlecan's role in angiogenesisSemantic proximity Read ↗

Perlecan, the major proteoglycan of basement membranes, is altered in patients with Schwartz-Jampel syndrome (chondrodystrophic myotonia).Semantic proximity Read ↗

Reduced perlecan in mice results in chondrodysplasia resembling Schwartz-Jampel syndrome.Semantic proximity Read ↗

A central function for perlecan in skeletal muscle and cardiovascular developmentSemantic proximity Read ↗

Heparan sulfate: lessons from knockout mice.Semantic proximity Read ↗

Dyssegmental dysplasia, Silverman-Handmaker type, is caused by functional null mutations of the perlecan gene.Semantic proximity Read ↗

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