Muscular Dystrophy, Animal
"Muscular Dystrophy, Animal" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
MUSCULAR DYSTROPHY that occurs in VERTEBRATE animals.
Descriptor ID |
D009137
|
MeSH Number(s) |
C22.595
|
Concept/Terms |
Muscular Dystrophy, Animal- Muscular Dystrophy, Animal
- Animal Muscular Dystrophies
- Animal Muscular Dystrophy
- Dystrophies, Animal Muscular
- Dystrophy, Animal Muscular
- Muscular Dystrophies, Animal
|
Below are MeSH descriptors whose meaning is more general than "Muscular Dystrophy, Animal".
Below are MeSH descriptors whose meaning is more specific than "Muscular Dystrophy, Animal".
This graph shows the total number of publications written about "Muscular Dystrophy, Animal" by people in this website by year, and whether "Muscular Dystrophy, Animal" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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1997 | 1 | 0 | 1 |
2008 | 1 | 0 | 1 |
2010 | 0 | 1 | 1 |
2014 | 1 | 0 | 1 |
2018 | 1 | 1 | 2 |
2024 | 0 | 1 | 1 |
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Below are the most recent publications written about "Muscular Dystrophy, Animal" by people in Profiles.
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ANKRD1 expression is aberrantly upregulated in the mdm mouse model of muscular dystrophy and induced by stretch through NF?B. J Muscle Res Cell Motil. 2024 Dec; 45(4):191-200.
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Inhibition of Rev-erba ameliorates muscular dystrophy. Exp Cell Res. 2021 09 15; 406(2):112766.
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Cycles of myofiber degeneration and regeneration lead to remodeling of the neuromuscular junction in two mammalian models of Duchenne muscular dystrophy. PLoS One. 2018; 13(10):e0205926.
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Direct Reprogramming of Mouse Fibroblasts into Functional Skeletal Muscle Progenitors. Stem Cell Reports. 2018 05 08; 10(5):1505-1521.
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Telomere shortening and metabolic compromise underlie dystrophic cardiomyopathy. Proc Natl Acad Sci U S A. 2016 11 15; 113(46):13120-13125.
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Src-dependent impairment of autophagy by oxidative stress in a mouse model of Duchenne muscular dystrophy. Nat Commun. 2014 Jul 16; 5:4425.
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Disruption of Nrf2/ARE signaling impairs antioxidant mechanisms and promotes cell degradation pathways in aged skeletal muscle. Biochim Biophys Acta. 2012 Jun; 1822(6):1038-50.
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Anisotropic regulation of Ankrd2 gene expression in skeletal muscle by mechanical stretch. FASEB J. 2010 Sep; 24(9):3330-40.
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Early mechanical dysfunction of the diaphragm in the muscular dystrophy with myositis (Ttnmdm) model. Am J Physiol Cell Physiol. 2008 Nov; 295(5):C1092-102.
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SIK1 is a class II HDAC kinase that promotes survival of skeletal myocytes. Nat Med. 2007 May; 13(5):597-603.