Increased incidence of mitochondrial cytochrome c-oxidase gene mutations in patients with myelodysplastic syndromes

British Journal of Haematology

Volumn 116, Issue 3, 2002, Pages 564-575

  Reddy, Poluru L ^a   Shetty, Vilasini T ^a   Dutt, Diya ^a   York, Aaron ^a   Dar, Saleem ^a   Mundle, Suneel D ^a   Allampallam, Krishnan ^a   Alvi, Sairah ^a   Galili, Naomi ^a   Saberwal, Gurveen Sethi ^a   Anthwal, Shalini ^a   Shaikh, Malihi ^a   Suleman, Samia ^a   Kamal, Shaista Y ^a   Raza, Azra ^a  

^a RUSH CANCER INSTITUTE   (United States)

Author keywords

Apoptosis; Cytochrome c oxidase genes; Iron laden mitochondria; Mitochondrial DNA mutations; Myelodysplastic syndromes

Indexed keywords

CYTOCHROME C OXIDASE; DNA; IRON; MITOCHONDRIAL ENZYME; NUCLEOTIDE;

APOPTOSIS; ARTICLE; ASPIRATION; BLOOD SMEAR; BONE MARROW BIOPSY; CELL FRACTIONATION; CELL LINEAGE; CHEEK; CHROMOSOME SUBSTITUTION; CLINICAL ARTICLE; CONTROLLED STUDY; CYTOPENIA; DENSITY; ELECTRON MICROSCOPY; GENE AMPLIFICATION; GENE DELETION; GENE INSERTION; GENE MUTATION; HEMATOPOIETIC CELL; HUMAN; HUMAN CELL; MITOCHONDRION; MUTATION RATE; MYELODYSPLASTIC SYNDROME; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SMEAR;

ADULT; AGED; AGED, 80 AND OVER; APOPTOSIS; BONE MARROW CELLS; DNA, MITOCHONDRIAL; ELECTRON TRANSPORT COMPLEX IV; FEMALE; HUMANS; IN SITU NICK-END LABELING; MALE; MIDDLE AGED; MITOCHONDRIA; MUTATION; MYELODYSPLASTIC SYNDROMES;

EID: 0036180269     PISSN: 00071048     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.0007-1048.2001.03323.x     Document Type: Article

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