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

Mapping modifiers affecting muscularity of the myostatin mutant (Mstn(Cmpt-dl1Abc)) compact mouse.

Genetics - 1 Sept 2003

Varga László, Müller Géza, Szabó Gyula, Pinke Orsolya, Korom Edit, Kovács Balázs, Patthy László, Soller Morris

Abstract excerpt

The hypermuscular Compact phenotype was first noted in a line of mice selected for high body weight and protein content. A new line, based on mice showing the Compact phenotype, was formed and selected for maximum expression of the Compact phenotype. Previously we mapped and identified a 12-bp deletion in the myostatin gene, denoted Mstn(Cmpt-dl1Abc), which can be considered as a major gene responsible for the...

Read the complete abstract on PubMed

Topics

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

Share to Chromosome Mapping
Share to Crosses, Genetic

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genes, Regulator

Share to Genetic Markers

Share to Genotype

Share to Muscles

Share to Transforming Growth Factor beta

Source

Open in PubMed Open full text

Identifiers

PMID: 14504233
DOI: 10.1093/genetics/165.1.257
PMCID: PMC1462759

Genes

CAST

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

Mapping modifiers affecting muscularity of the myostatin mutant (Mstn(Cmpt-dl1Abc)) compact mouse.PMID 14504233Read ↗

Mapping a syntenic modifier on mouse chromosome 1 influencing the expressivity of the compact phenotype in the myostatin mutant (MstnCmpt-dl1Abc) compact mouse.Semantic proximity Read ↗

Inheritance and mapping of Compact (Cmpt), a new mutation causing hypermuscularity in mice.Semantic proximity Read ↗

Marker-assisted introgression of the Compact mutant myostatin allele MstnCmpt-dl1Abc into a mouse line with extreme growth effects on body composition and muscularity.Semantic proximity Read ↗

Myostatin propeptide mutation of the hypermuscular Compact mice decreases the formation of myostatin and improves insulin sensitivity.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 ↗

A deletion in the myostatin gene causes the compact ( Cmpt ) hypermuscular mutation in miceSemantic proximity Read ↗

Genome-wide associations reveal human-mouse genetic convergence and modifiers of myogenesis, <i>CPNE1</i> and <i>STC2</i>Semantic proximity Read ↗

Fine mapping of "mini-muscle," a recessive mutation causing reduced hindlimb muscle mass in mice.Semantic proximity Read ↗

The compact mutation of myostatin causes a glycolytic shift in the phenotype of fast skeletal muscles.Semantic proximity Read ↗

Genetic and genomic analyses of musculoskeletal differences between BEH and BEL strains.Semantic proximity Read ↗

Effect of the myostatin locus on muscle mass and intramuscular fat content in a cross between mouse lines selected for hypermuscularity.Semantic proximity Read ↗

An EM algorithm for mapping binary disease loci: application to fibrosarcoma in a four-way cross mouse family.Semantic proximity Read ↗

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