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

Characterization of a Dmd (EGFP) reporter mouse as a tool to investigate dystrophin expression.

Skeletal muscle - 1 Jan 2016

Petkova Mina V, Morales-Gonzales Susanne, Relizani Karima, Gill Esther, Seifert Franziska, Radke Josefine, Stenzel Werner, Garcia Luis, Amthor Helge, Schuelke Markus

Abstract excerpt

BACKGROUND: Dystrophin is a rod-shaped cytoplasmic protein that provides sarcolemmal stability as a structural link between the cytoskeleton and the extracellular matrix via the dystrophin-associated protein complex (DAPC). Mutations in the dystrophin-encoding DMD gene cause X-linked dystrophinopathies with variable phenotypes, the most severe being Duchenne muscular dystrophy (DMD) characterized by progressive...

Read the complete abstract on PubMed

Topics

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

Share to 3' Untranslated Regions
Share to Dystrophin

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genes, Reporter

Share to Green Fluorescent Proteins

Share to Mice, Transgenic

Share to Microscopy, Fluorescence

Share to Recombinant Fusion Proteins

Share to Satellite Cells, Skeletal Muscle

Source

Open in PubMed Open full text

Identifiers

PMID: 27382459
DOI: 10.1186/s13395-016-0095-5
PMCID: PMC4932663

Genes

DMD

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Characterization of a Dmd (EGFP) reporter mouse as a tool to investigate dystrophin expression.PMID 27382459Read ↗

Live-imaging of revertant and therapeutically restored dystrophin in the DmdEGFP-mdx mouse model for Duchenne muscular dystrophy.Semantic proximity Read ↗

Dmdmdx/Largemyd: a new mouse model of neuromuscular diseases useful for studying physiopathological mechanisms and testing therapies.Semantic proximity Read ↗

The Multi-System Roles of Dp71 Dystrophin Isoforms in Duchenne Muscular DystrophySemantic proximity Read ↗

Muscle-specific increased expression of JAG1 improves the skeletal muscle phenotype in dystrophin-deficient mice.Semantic proximity Read ↗

Conditional <i>Dystrophin</i> ablation in the skeletal muscle and brain causes profound effects on muscle function, neurobehavior, and extracellular matrix pathwaysSemantic proximity Read ↗

Muscle-specific increased expression of <i>JAG1</i> improves skeletal muscle phenotype in dystrophin-deficient miceSemantic proximity Read ↗

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

Muscle-specific CRISPR/Cas9 dystrophin gene editing ameliorates pathophysiology in a mouse model for Duchenne muscular dystrophy.Semantic proximity Read ↗

In vivo genome editing in mouse restores dystrophin expression in Duchenne muscular dystrophy patient muscle fibers.Semantic proximity Read ↗

A comprehensive spatiotemporal map of dystrophin isoform expression in the developing and adult human brainSemantic proximity Read ↗

Prevention of dystrophic pathology in mdx mice by a truncated dystrophin isoform.Semantic proximity Read ↗

Dystrophin and utrophin: genetic analyses of their role in skeletal muscle.Semantic proximity Read ↗

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