HtrA2/Omi deficiency causes damage and mutation of mitochondrial DNA

Biochimica et Biophysica Acta - Molecular Cell Research

Volumn 1833, Issue 8, 2013, Pages 1866-1875

  Goo, Hui Gwan ^a   Jung, Min Kyo ^a   Han, Sung Sic ^a   Rhim, Hyangshuk ^b   Kang, Seongman ^a  

^a Korea University   (South Korea)

^b The Catholic University of Korea   (South Korea)

Author keywords

HtrA2; Mitochondrial DNA; Mutation; Omi; ROS

Indexed keywords

APTX1 PROTEIN; FLUORESCENT DYE; MITOCHONDRIAL DNA; POLG2 PROTEIN; PROTEIN; REACTIVE OXYGEN METABOLITE; SERINE PROTEINASE; SERINE PROTEINASE OMI; TWINKLE PROTEIN; UNCLASSIFIED DRUG;

AGAR GEL ELECTROPHORESIS; ARTICLE; CELL AGING; CELL DEATH; CONTROLLED STUDY; DNA CONFORMATION; DNA DAMAGE; DNA REPAIR; ELECTRON MICROSCOPY; ENZYME ACTIVITY; GENE MUTATION; GENE OVEREXPRESSION; HUMAN; HUMAN CELL; INTERCALATION COMPLEX; MITOCHONDRIAL DNA DISORDER; MITOCHONDRION; MORPHOLOGY; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROTEIN DEPLETION; UPREGULATION;

ANIMALS; BRAIN; CELL LINE, TUMOR; DNA DAMAGE; DNA REPAIR; DNA, MITOCHONDRIAL; HELA CELLS; HUMANS; MICE; MITOCHONDRIAL PROTEINS; MUTATION; NUCLEIC ACID CONFORMATION; REACTIVE OXYGEN SPECIES; SERINE ENDOPEPTIDASES;

EID: 84877796195     PISSN: 01674889     EISSN: 18792596     Source Type: Journal    
DOI: 10.1016/j.bbamcr.2013.03.016     Document Type: Article

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