Reduced mitochondrial respiration and increased calcium deposits in the EDL muscle, but not in soleus, from 12-week-old dystrophic mdx mice-Reference-Cited by-同舟云学术

Reduced mitochondrial respiration and increased calcium deposits in the EDL muscle, but not in soleus, from 12-week-old dystrophic mdx mice

Published:2019-02-13 Issue:1 Volume:9 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Gaglianone Rhayanna B.,Santos Anderson Teixeira,Bloise Flavia Fonseca^ORCID,Ortiga-Carvalho Tania Maria,Costa Manoel Luis,Quirico-Santos Thereza,da Silva Wagner Seixas,Mermelstein Claudia^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/s41598-019-38609-4.pdf

Reference45 articles.

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2. Allen, D. G., Whitehead, N. P. & Froehner, S. C. Absence of dystrophin disrupts skeletal muscle signaling: roles of Ca2+, reactive oxygen species, and nitric oxide in the development of muscular dystrophy. Physiol. Rev. 96, 253–305 (2016).

3. Rodrigues, M., Echigoya, Y., Fukada, S.-I. & Yokota, T. Current translational research and murine models for Duchenne muscular dystrophy. J Neuromuscul Dis. 3, 29–48 (2016).

4. Yucel, N., Chang, A. C., Day, J. W., Rosenthal, N. & Blau, H. M. Humanizing the mdx mouse model of DMD: the long and the short of it. NPJ Regen Med. 3, 4 (2018).

5. McGreevy, J. W., Hakim, C. H., McIntosh, M. A. & Duan, D. Animal models of Duchenne muscular dystrophy: from basic mechanisms to gene therapy. Dis. Model Mech. 8, 195–213 (2015).

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