Analysis of mouse models of cytochrome c oxidase deficiency owing to mutations in Sco2

Human Molecular Genetics

Volumn 19, Issue 1, 2009, Pages 170-180

  Yang, Hua ^a   Brosel, Sonja ^a   Acin Perez, Rebeca ^b   Slavkovich, Vesna ^a   Nishino, Ichizo ^a,c   Khan, Raffay ^a   Goldberg, Ira J ^a   Graziano, Joseph ^a   Manfredi, Giovanni ^b   Schon, Eric A ^a  

^a NewYork Presbyterian Hospital   (United States)

^b WEILL CORNELL MEDICAL COLLEGE   (United States)

^c NATIONAL INSTITUTE OF NEUROSCIENCE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CELL PROTEIN; COPPER; CYTOCHROME C OXIDASE; SYNTHESIS OF CYTOCHROME C OXIDASE 2; UNCLASSIFIED DRUG; SCO2 PROTEIN, MOUSE;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; CYTOCHROME C OXIDASE DEFICIENCY; EMBRYO DEATH; GENE MUTATION; HETEROZYGOTE; HISTOPATHOLOGY; HOMOZYGOTE; KNOCKOUT MOUSE; MITOCHONDRION; MOUSE; MUSCLE WEAKNESS; MUTATIONAL ANALYSIS; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN ASSEMBLY; RESPIRATORY CHAIN; ANIMAL; ANIMAL EMBRYO; ANTIBODY SPECIFICITY; DISEASE MODEL; ENZYME ASSAY; ENZYMOLOGY; GENETICS; IMMUNOHISTOCHEMISTRY; METABOLISM; MOUSE MUTANT; MUSCLE; MUTATION; PATHOLOGY; WESTERN BLOTTING;

MUS;

ANIMALS; BLOTTING, WESTERN; COPPER; CYTOCHROME-C OXIDASE DEFICIENCY; DISEASE MODELS, ANIMAL; ELECTRON TRANSPORT COMPLEX IV; EMBRYO, MAMMALIAN; ENZYME ASSAYS; IMMUNOHISTOCHEMISTRY; MICE; MICE, KNOCKOUT; MITOCHONDRIA; MUSCLES; MUTATION; ORGAN SPECIFICITY;

EID: 77649285631     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddp477     Document Type: Article

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