Subcomplexes of mitochondrial complex V reveal mutations in mitochondrial DNA

Electrophoresis

Volumn 30, Issue 20, 2009, Pages 3565-3572

  Smet, Joél ^a   Seneca, Sara ^b   De Paepe, Boel ^a   Meulemans, Ann ^b   Verhelst, Helene ^a   Leroy, Jules ^a   De Meirleir, Linda ^b   Lissens, Willy ^b   Van Coster, Rudy ^a  

^a GHENT UNIVERSITY HOSPITAL   (Belgium)

^b FREE UNIVERSITY OF BRUSSELS   (Belgium)

Author keywords

Blue Native PAGE; Complex V subcomplexes; mtDNA depletion; mtDNA point mutation; Oxidative phosphorylation

Indexed keywords

CELL CULTURE; CELL MEMBRANES; DNA; MITOCHONDRIA; PHOSPHORYLATION; TISSUE;

BLUE NATIVE PAGE; COMPLEX V SUBCOMPLEX; MITOCHONDRIAL COMPLEX; MITOCHONDRIAL DNA; MITOCHONDRIAL DNA DEPLETION; MITOCHONDRIAL DNA POINT MUTATION; OXIDATIVE PHOSPHORYLATION; POINT MUTATIONS; SUBCOMPLEXES;

DEFECTS;

ADENOSINE TRIPHOSPHATE; MITOCHONDRIAL COMPLEX 5; MITOCHONDRIAL DNA; OXIDOREDUCTASE; TRANSFER RNA; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; CONTROLLED STUDY; ENZYME ACTIVITY; FEMALE; GENE DELETION; GENE MUTATION; HUMAN; HUMAN TISSUE; MAJOR CLINICAL STUDY; MALE; MITOCHONDRIAL DNA DISORDER; OXIDATIVE PHOSPHORYLATION; POINT MUTATION; POLYACRYLAMIDE GEL ELECTROPHORESIS; PROTEIN DOMAIN; SKIN FIBROBLAST; SPECTROPHOTOMETRY; TISSUE CULTURE;

EID: 70649092386     PISSN: 01730835     EISSN: 15222683     Source Type: Journal    
DOI: 10.1002/elps.200900213     Document Type: Article

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