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

Breeding of the gad-mdx mouse: influence of genetically induced denervation on dystrophic muscle fibers.

Laboratory animal science - 1 Feb 1994

Suh J G, Yamazaki A, Tomita T

Abstract excerpt

A new double mutant mouse strain, gad-mdx, was established. The transmission of mdx and gad genes was monitored by determining their chemical markers, creative kinase activity and phosphoglucomutase-1 isoenzyme, respectively, in blood samples. This new strain was characterized by high creatine kinase activity in the plasma, lack of dystrophin in the muscle, and the presence of axonal swellings in the neural...

Read the complete abstract on PubMed

Topics

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

Share to Breeding
Share to Dystrophin
Share to Mice

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Mice, Inbred C57BL

Share to Mice, Mutant Strains

Share to Muscles

Share to Mutation

Share to Phosphoglucomutase

Source

Identifiers

PMID: 8007658

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Breeding of the gad-mdx mouse: influence of genetically induced denervation on dystrophic muscle fibers.PMID 8007658Read ↗

Animal models for genetic neuromuscular diseases.Semantic proximity Read ↗

Animal models of muscular dystrophy – what can they teach us?Semantic proximity Read ↗

Effect of genetic background on the dystrophic phenotype in mdx mice.Semantic proximity Read ↗

Myotonic ADR-MDX mutant mice show less severe muscular dystrophy than MDX mice.Semantic proximity Read ↗

Major clinical and histopathological characteristics of canine X-linked muscular dystrophy in Japan, CXMDJ.Semantic proximity Read ↗

Autonomic, locomotor and cardiac abnormalities in a mouse model of muscular dystrophy: targeting the renin-angiotensin system.Semantic proximity Read ↗

Effects of the compact mutant myostatin allele Mstn (Cmpt-dl1Abc) introgressed into a high growth mouse line on skeletal muscle cellularity.Semantic proximity Read ↗

Abnormal myotonic dystrophy protein kinase levels produce only mild myopathy in mice.Semantic proximity Read ↗

Pathological analysis of muscle hypertrophy and degeneration in muscular dystrophy in gamma-sarcoglycan-deficient mice.Semantic proximity Read ↗

Overexpression of myogenin in muscles of transgenic mice: interaction with Id-1, negative crossregulation of myogenic factors, and induction of extrasynaptic acetylcholine receptor expression.Semantic proximity Read ↗

Variable phenotypes of knockin mice carrying the M712T Gne mutation.Semantic proximity Read ↗

Duchenne-like myopathy in double-mutant mdx mice expressing exaggerated mast cell activity.Semantic proximity Read ↗

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