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

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
Uncontrolled Keywords: Duchenne muscular dystrophy; neuromuscular disorder; dystrophin; supplementation; muscle
Subjects: FOR Classification > 1116 Medical Physiology
Faculty/School/Research Centre/Department > Institute of Sport, Exercise and Active Living (ISEAL)
Depositing User: Symplectic Elements
Date Deposited: 08 Oct 2018 01:45
Last Modified: 30 Apr 2019 16:40
URI: http://vuir.vu.edu.au/id/eprint/37211
DOI: https://doi.org/10.1152/ajpcell.00046.2017
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Citations in Scopus: 2 - View on Scopus

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