Mitochondrial content is preserved throughout disease progression in the mdx mouse model of Duchenne muscular dystrophy, regardless of taurine supplementation

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Barker, RG, Wyckelsma, Victoria ORCID: 0000-0001-6921-4638, Xu, H and Murphy, RM (2018) Mitochondrial content is preserved throughout disease progression in the mdx mouse model of Duchenne muscular dystrophy, regardless of taurine supplementation. American Journal of Physiology - Cell Physiology, 314 (4). 483 - 491. ISSN 0363-6143

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Item type Article
URI https://vuir.vu.edu.au/id/eprint/37211
DOI https://doi.org/10.1152/ajpcell.00046.2017
Official URL https://www.physiology.org/doi/abs/10.1152/ajpcell...
Subjects Historical > FOR Classification > 1116 Medical Physiology
Historical > Faculty/School/Research Centre/Department > Institute of Sport, Exercise and Active Living (ISEAL)
Keywords Duchenne muscular dystrophy; neuromuscular disorder; dystrophin; supplementation; muscle
Citations in Scopus 9 - View on Scopus
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