Dihydrorhodamine 123 identifies impaired mitochondrial respiratory chain function in cultured cells harboring mitochondrial DNA mutations

Journal of Histochemistry and Cytochemistry

Volumn 44, Issue 6, 1996, Pages 571-579

  Sobreira, Cláudia ^a,b   Davidson, Mercy ^a   King, Michael P ^a   Miranda, Armand F ^a  

^a Columbia University ^*  (United States)

^b UNIVERSITY OF SÃO PAULO   (Brazil)

Author keywords

Cybrid and hybrid cultures; Cytochrome c oxidase; Dihydrorhodamine 123; Fluorescence microscopy; Human mitochondrial encephalomyopathies; Mitochondrial DNA mutations; Respiratory chain; Rhodamine 123

Indexed keywords

FLUORESCENT DYE; MITOCHONDRIAL DNA; RHODAMINE 123;

ARTICLE; CONTROLLED STUDY; FLUORESCENCE MICROSCOPY; GENE DOSAGE; HELA CELL; HUMAN; HUMAN CELL; HYBRID CELL; MELAS SYNDROME; MERRF SYNDROME; MITOCHONDRIAL MYOPATHY; MITOCHONDRIAL RESPIRATION; MUTATION; OXIDATIVE PHOSPHORYLATION; OXYGEN CONSUMPTION; PRIORITY JOURNAL; RESPIRATORY CHAIN;

EID: 0029886977     PISSN: 00221554     EISSN: None     Source Type: Journal    
DOI: 10.1177/44.6.8666742     Document Type: Article

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