Mitochondrial reactive oxygen species generation by the SDHC V69E mutation causes low birth weight and neonatal growth retardation

Mitochondrion

Volumn 11, Issue 1, 2011, Pages 155-165

  Ishii, Takamasa ^a,b   Miyazawa, Masaki ^a   Onodera, Akira ^a   Yasuda, Kayo ^a   Kawabe, Noboru ^a   Kirinashizawa, Mika ^a   Yoshimura, Shinichi ^a   Maruyama, Naoki ^c   Hartman, Philip S ^d   Ishii, Naoaki ^a  

^a TOKAI UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^b UNIVERSITY OF COLORADO   (United States)

^c TOKYO METROPOLITAN INSTITUTE OF GERONTOLOGY   (Japan)

^d TEXAS CHRISTIAN UNIVERSITY   (United States)

Author keywords

Apoptosis; Development; Mitochondria; Oxidative stress; Reactive oxygen species; SDHC

Indexed keywords

MITOCHONDRIAL PROTEIN; REACTIVE OXYGEN METABOLITE; SUCCINATE DEHYDROGENASE;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; APOPTOSIS; ARTICLE; CONTROLLED STUDY; ENZYME ACTIVITY; GENE OVEREXPRESSION; GROWTH RETARDATION; LOW BIRTH WEIGHT; MITOCHONDRIAL RESPIRATION; MOUSE; NEWBORN; NONHUMAN; OXIDATIVE STRESS; PRIORITY JOURNAL; TRANSGENE; TRANSGENIC MOUSE;

CAENORHABDITIS ELEGANS; MUS; MUS MUSCULUS;

EID: 78650018619     PISSN: 15677249     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.mito.2010.09.006     Document Type: Article

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