Early myopathy in Duchenne muscular dystrophy is associated with elevated mitochondrial H 2 O 2 emission during impaired oxidative phosphorylation-Reference-Cited by-同舟云学术

Early myopathy in Duchenne muscular dystrophy is associated with elevated mitochondrial H 2 O 2 emission during impaired oxidative phosphorylation

Published:2019-04-02 Issue:3 Volume:10 Page:643-661
ISSN:2190-5991
Container-title:Journal of Cachexia, Sarcopenia and Muscle
language:en
Short-container-title:Journal of Cachexia, Sarcopenia and Muscle

Author:

Hughes Meghan C.¹,Ramos Sofhia V.¹,Turnbull Patrick C.¹,Rebalka Irena A.²,Cao Andrew²,Monaco Cynthia M.F.²,Varah Nina E.²,Edgett Brittany A.³^ORCID,Huber Jason S.³^ORCID,Tadi Peyman¹,Delfinis Luca J.¹,Schlattner U.⁴,Simpson Jeremy A.³^ORCID,Hawke Thomas J.²,Perry Christopher G.R.¹^ORCID

Affiliation:

1. School of Kinesiology and Health Science, Muscle Health Research Centre, 344 Norman Bethune College York University Toronto ON Canada

2. Department of Pathology and Molecular Medicine McMaster University Hamilton ON Canada

3. Department of Human Health and Nutritional Sciences and Cardiovascular Research Group University of Guelph Guelph ON Canada

4. Laboratory of Fundamental and Applied Bioenergetics (LBFA) and SFR Environmental and Systems Biology (BEeSy) University Grenoble Alpes Grenoble France

Publisher

Wiley

Subject

Physiology (medical),Orthopedics and Sports Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jcsm.12405

Reference89 articles.

1. Duchenne muscular dystrophy—Meryon's disease

2. Molecular basis of muscular dystrophies

3. Genetic heterogeneity in Duchenne muscular dystrophy

4. Absence of Dystrophin Disrupts Skeletal Muscle Signaling: Roles of Ca2+, Reactive Oxygen Species, and Nitric Oxide in the Development of Muscular Dystrophy

5. The association of cardiac muscle necrosis and inflammation with the degenerative and persistent myopathy of MDX mice

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