Identification of a new missense mutation in the mtDNA of hereditary hypertrophic, but not dilated cardiomyopathic hamsters

Molecular and Cellular Biochemistry

Volumn 252, Issue 1-2, 2003, Pages 73-81

  Minieri, Marilena ^a   Zingarelli, Mara ^a   Shubeita, Huda ^b   Vecchini, Alba ^c   Binaglia, Luciano ^c   Carotenuto, Felicia ^a   Fantini, Cristina ^a   Fiaccavento, Roberta ^a   Masuelli, Laura ^d   Coletti, Anna ^d   Simonelli, Lucilla ^d   Modesti, Andrea ^a   Di Nardo, Paolo ^a  

^a UNIVERSITY OF ROME TOR VERGATA   (Italy)

^b SAN DIEGO STATE UNIVERSITY   (United States)

^c UNIVERSITY OF PERUGIA   (Italy)

^d SAPIENZA UNIVERSITY OF ROME   (Italy)

Author keywords

Cytochrome c oxidase; Hamster cardiomyopathy; Missense mutation; Mitochondrial DNA

Indexed keywords

CYTOCHROME C OXIDASE; MITOCHONDRIAL DNA; SARCOGLYCAN;

AGE; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BRAIN REGION; CONTROLLED STUDY; DIFFERENTIAL DISPLAY; DISEASE SEVERITY; ENVIRONMENTAL FACTOR; ENZYME SUBUNIT; GENE DELETION; GENE IDENTIFICATION; GENE MUTATION; GENE SEQUENCE; HAMSTER; HEART; HEART DILATATION; HEART FUNCTION; HEREDITY; HETEROPLASMY; HYPERTROPHIC CARDIOMYOPATHY; MISSENSE MUTATION; MITOCHONDRION; NONHUMAN; NUCLEOTIDE SEQUENCE; PATHOGENESIS; PHENOTYPE; RESTRICTION MAPPING; SKELETAL MUSCLE; ULTRASTRUCTURE; UPREGULATION;

AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; BLOTTING, NORTHERN; CARDIOMEGALY; CLONING, MOLECULAR; CRICETINAE; DNA PRIMERS; DNA, COMPLEMENTARY; DNA, MITOCHONDRIAL; ELECTRON TRANSPORT COMPLEX IV; IN SITU HYBRIDIZATION; MITOCHONDRIA, HEART; MOLECULAR SEQUENCE DATA; MUTATION, MISSENSE; SEQUENCE HOMOLOGY, AMINO ACID; SEQUENCE HOMOLOGY, NUCLEIC ACID;

ANIMALIA; CRICETINAE;

EID: 12444318212     PISSN: 03008177     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1025542731335     Document Type: Article

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