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

FASEB Journal

Volumn 15, Issue 2, 2001, Pages 322-332

  Wanagat, Jonathan ^a,b   Cao, Zhengjin ^b   Pathare, Pranali ^b   Aiken, Judd M ^b  

^a UNIVERSITY OF WISCONSIN SCHOOL OF MEDICINE AND PUBLIC HEALTH   (United States)

^b UNIVERSITY OF WISCONSIN MADISON   (United States)

Author keywords

Aging; Laser capture microdissection; Skeletal muscle

Indexed keywords

MITOCHONDRIAL DNA;

ANIMAL TISSUE; ARTICLE; ELECTRON TRANSPORT; GENE AMPLIFICATION; GENE DELETION; MUSCLE ATROPHY; NONHUMAN; OXIDATION; PRIORITY JOURNAL; RAT;

AGING; ANIMALS; ATROPHY; BASE SEQUENCE; DNA DAMAGE; DNA, MITOCHONDRIAL; ELECTRON TRANSPORT; ELECTRON TRANSPORT COMPLEX IV; HYBRIDIZATION, GENETIC; MALE; MITOCHONDRIA, MUSCLE; MUSCLE DEVELOPMENT; MUSCLE FIBERS; MUSCLE, SKELETAL; MUSCULAR DISEASES; RATS; RATS, INBRED BN; RATS, INBRED F344; SEQUENCE DELETION; SUCCINATE DEHYDROGENASE;

ANIMALIA; RECTUS; RODENTIA;

EID: 0035127889     PISSN: 08926638     EISSN: None     Source Type: Journal    
DOI: 10.1096/fj.00-0320com     Document Type: Article

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