Mitochondrial DNA deletion mutations colocalize with segmental electron transport system abnormalities, muscle fiber atrophy, fiber splitting, and oxidative damage in sarcopenia-Reference-Cited by-同舟云学术

Mitochondrial DNA deletion mutations colocalize with segmental electron transport system abnormalities, muscle fiber atrophy, fiber splitting, and oxidative damage in sarcopenia

Published:2001-01 Issue:2 Volume:15 Page:322-332
ISSN:0892-6638
Container-title:The FASEB Journal
language:en
Short-container-title:FASEB j.

Author:

WANAGAT JONATHAN¹²,CAO ZHENGJIN²,PATHARE PRANALI²,AIKEN JUDD M.²

Affiliation:

1. Medical Scientist Training ProgramUniversity of Wisconsin Medical SchoolMadisonWisconsin53706USA

2. Department of Animal Health and Biomedical SciencesUniversity of Wisconsin‐MadisonMadisonWisconsin53706USA

Funder

National Institutes of Health

Publisher

Wiley

Subject

Genetics,Molecular Biology,Biochemistry,Biotechnology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1096/fj.00-0320com

Reference64 articles.

1. What Is Sarcopenia?

2. Sarcopenia: Origins and Clinical Relevance

3. Mechanisms of sarcopenia of aging;Short K. R.;J. Endocrinol. Invest.,1999

4. Aging: A Theory Based on Free Radical and Radiation Chemistry

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