The failure to extend lifespan via disruption of complex II is linked to preservation of dynamic control of energy metabolism

Mitochondrion

Volumn 12, Issue 2, 2012, Pages 280-287

  Kuang, Jujiao ^a   Ebert, Paul R ^a  

^a UNIVERSITY OF QUEENSLAND   (Australia)

Author keywords

Longevity; Metabolism; Mitochondria; Succinate dehydrogenase

Indexed keywords

ARTICLE; CAENORHABDITIS ELEGANS; COMPLEX I GENE; COMPLEX II GENE; COMPLEX III GENE; COMPLEX IV GENE; CONTROLLED STUDY; ELECTRON TRANSPORT; ENERGY METABOLISM; ENERGY RESOURCE; GENE CONTROL; GENE DISRUPTION; GENE INACTIVATION; GENE REPRESSION; GENE SILENCING; GENETIC LINKAGE; LIFE EXTENSION; LINKAGE ANALYSIS; LONGEVITY; METABOLIC STRESS; MITOCHONDRIAL ENERGY TRANSFER; MITOCHONDRIAL GENE; MITOCHONDRIAL GENETICS; MITOCHONDRIAL MEMBRANE POTENTIAL; NONHUMAN; PRIORITY JOURNAL;

ADENOSINE TRIPHOSPHATE; ANIMALS; CAENORHABDITIS ELEGANS; ELECTRON TRANSPORT COMPLEX I; ELECTRON TRANSPORT COMPLEX II; ELECTRON TRANSPORT COMPLEX III; ELECTRON TRANSPORT COMPLEX IV; ENERGY METABOLISM; GENE EXPRESSION REGULATION; GENE SILENCING; LIFE SUPPORT CARE; MEMBRANE POTENTIAL, MITOCHONDRIAL; STRESS, PHYSIOLOGICAL;

ANIMALIA; CAENORHABDITIS ELEGANS;

EID: 84858007124     PISSN: 15677249     EISSN: 18728278     Source Type: Journal    
DOI: 10.1016/j.mito.2011.10.003     Document Type: Article

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