Mitochondrial content is preserved throughout disease progression in the mdx mouse model of Duchenne muscular dystrophy, regardless of taurine supplementation
Download
Download
DownloadExport
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
Dimensions Badge
Altmetric Badge
| Item type | Article |
| URI | https://vuir.vu.edu.au/id/eprint/37211 |
| DOI | 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 | 14 - View on Scopus |
| Download/View statistics | View download statistics for this item |
CORE (COnnecting REpositories)