Structured Summary
Abstract
A strain of mice arising from a spontaneous MUTATION (mdx) in inbred C57BL mice. This mutation is X chromosome-linked and produces viable homozygous animals that lack the muscle protein DYSTROPHIN, have high serum levels of muscle ENZYMES, and possess histological lesions similar to human MUSCULAR DYSTROPHY. The histological features, linkage, and map position of mdx make these mice a worthy animal model of DUCHENNE MUSCULAR DYSTROPHY.
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Synonyms
7 entry terms
- Mice, Inbred mdx
- Mice, mdx
- Mouse, Inbred mdx
- Mouse, mdx
- Inbred mdx Mouse
- mdx Mice
- mdx Mouse
MeSH Record
Aspects Covered
18 allowable subheadings
Indexed with the subheadings abnormalities, anatomy & histology, blood, cerebrospinal fluid, classification, embryology, genetics, growth & development, immunology, injuries, metabolism, microbiology, parasitology, physiology, psychology, surgery, urine, virology.
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Indexing Annotation
NIM with no qualifiers when experimental animal
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History Note
94
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Previous Indexing
- Mice, Inbred C57BL (1984-1993)
- Mice, Mutant Strains (1984-1993)
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AMA Style
References
- National Library of Medicine. Inbred mdx Mice. Medical Subject Headings (MeSH). 2026. Unique ID D018101. http://id.nlm.nih.gov/mesh/2026/D018101
- Inbred mdx Mice. In: Wikidata. https://www.wikidata.org/wiki/Q69466189