Mice lacking COX10 in skeletal muscle recapitulate the phenotype of progressive mitochondrial myopathies associated with cytochrome c oxidase deficiency

Human Molecular Genetics

Volumn 14, Issue 18, 2005, Pages 2737-2748

  Diaz, Francisca ^a   Thomas, Christine K ^a   Garcia, Sofia ^a   Hernandez, Dayami ^a   Moraes, Carlos T ^a  

^a UNIVERSITY OF MIAMI MILLER SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CRE RECOMBINASE; CYTOCHROME C OXIDASE; HEMOPROTEIN; MYOSIN LIGHT CHAIN; PROTEIN COX10; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; CORRELATION ANALYSIS; CYTOCHROME C OXIDASE DEFICIENCY; DISEASE ASSOCIATION; DISEASE COURSE; DISEASE SEVERITY; ENZYME ACTIVITY; FATIGUE; FEMALE; HISTOPATHOLOGY; KNOCKOUT MOUSE; MALE; MISSENSE MUTATION; MITOCHONDRIAL MYOPATHY; MOUSE; MUSCLE CONTRACTION; MUSCLE FUNCTION; MUSCLE MITOCHONDRION; MUSCLE POTENTIAL; NONHUMAN; PHENOTYPE; PREDICTION; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN FUNCTION; SEX DIFFERENCE; TIME; TRANSGENIC MOUSE;

ANIMALS; CLONING, MOLECULAR; CROSSES, GENETIC; CYTOCHROME-C OXIDASE DEFICIENCY; DISEASE MODELS, ANIMAL; DISEASE PROGRESSION; ELECTRON TRANSPORT COMPLEX IV; GENE TRANSFER TECHNIQUES; IMMUNOHISTOCHEMISTRY; MICE; MICE, KNOCKOUT; MICROSCOPY, ELECTRON, TRANSMISSION; MITOCHONDRIAL MYOPATHIES; MOLECULAR PROBE TECHNIQUES; MUSCLE FATIGUE; MUSCLE, SKELETAL; MUTATION, MISSENSE;

ANIMALIA; MUS MUSCULUS;

EID: 24944447977     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/ddi307     Document Type: Article

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