A mutation in a mitochondrial ABC transporter results in mitochondrial dysfunction through oxidative damage of mitochondrial DNA

Molecular and General Genetics

Volumn 262, Issue 3, 1999, Pages 426-436

  Senbongi, H ^a,b   Ling, F ^a   Shibata, T ^a,b,c  

^a RIKEN   (Japan)

^b SAITAMA UNIVERSITY   (Japan)

^c JAPAN SCIENCE AND TECHNOLOGY AGENCY   (Japan)

Author keywords

ATM1; MHR1; Mitochondrial iron; Recombinational DNA repair; Saccharomyces cerevisiae

Indexed keywords

ABC TRANSPORTER; GLUCOSE; IRON; MALONIC ACID; MESYLIC ACID METHYL ESTER; MITOCHONDRIAL DNA; MUTANT PROTEIN;

AMINO ACID SUBSTITUTION; ARTICLE; CELL CULTURE; CONTROLLED STUDY; DNA DAMAGE; DNA REPAIR; DNA STRAND BREAKAGE; IRON ABSORPTION; MITOCHONDRIAL MEMBRANE; MITOCHONDRIAL RESPIRATION; NONHUMAN; OXIDATIVE STRESS; POINT MUTATION; PRIORITY JOURNAL; SACCHAROMYCES CEREVISIAE; ULTRAVIOLET RADIATION;

AMINO ACID SEQUENCE; ATP-BINDING CASSETTE TRANSPORTERS; CLONING, MOLECULAR; CROSSES, GENETIC; DNA DAMAGE; DNA REPAIR; DNA, MITOCHONDRIAL; FUNGAL PROTEINS; GENETIC COMPLEMENTATION TEST; IRON; METHYL METHANESULFONATE; MITOCHONDRIA; MOLECULAR SEQUENCE DATA; MUTAGENS; MUTATION; OXIDATIVE STRESS; OXYGEN CONSUMPTION; SACCHAROMYCES CEREVISIAE; SACCHAROMYCES CEREVISIAE PROTEINS; SEQUENCE HOMOLOGY, AMINO ACID; ULTRAVIOLET RAYS;

EID: 0032740768     PISSN: 00268925     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004380051102     Document Type: Article

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