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Investigating Potential Biomarkers in Autism Spectrum Disorder.
The duper mutation reveals previously unsuspected functions of Cryptochrome 1 in circadian entrainment and heart disease.
Liver-directed SERPINA1 gene therapy attenuates progression of spontaneous and tobacco smoke-induced emphysema in a1-antitrypsin null mice.
Tannic acid-fortified zein-pectin nanoparticles: Stability, properties, antioxidant activity, and in vitro digestion.
Motor axonopathies in a mouse model of Duchenne muscular dystrophy.
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Motor axonopathies in a mouse model of Duchenne muscular dystrophy.
Dhindsa JS, McCall AL, Strickland LM, Fusco AF, Kahn AF, ElMallah MK. Motor axonopathies in a mouse model of Duchenne muscular dystrophy. Sci Rep. 2020 06 02; 10(1):8967.
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PubMed
subject areas
Animals
Axons
Diaphragm
Disease Models, Animal
Dystrophin
Hypoglossal Nerve
Loss of Function Mutation
Mice, Inbred mdx
Muscular Dystrophy, Duchenne
Phrenic Nerve
Respiratory Insufficiency