Targeting truncated APE1 in mitochondria enhances cell survival after oxidative stress

Free Radical Biology and Medicine

Volumn 45, Issue 5, 2008, Pages 592-601

  Li, Meng Xia ^a   Wang, Dong ^a   Zhong, Zhao Yang ^a   Xiang, De Bing ^a   Li, Zeng Peng ^a   Xie, Jia Yin ^a   Yang, Zhen Zhou ^a   Jin, Feng ^a   Qing, Yi ^a  

^a THIRD MILITARY MEDICAL UNIVERSITY   (China)

Author keywords

APE1; Base excision repair; Mitochondria; Overexpression; Oxidative stress

Indexed keywords

DNA (APURINIC OR APYRIMIDINIC SITE) LYASE; HYDROGEN PEROXIDE; MITOCHONDRIAL DNA; RECOMBINANT PROTEIN;

ARTICLE; CELL FRACTIONATION; CELL SURVIVAL; CELL TYPE; CONFOCAL LASER MICROSCOPY; CONTROLLED STUDY; DNA DAMAGE; DNA REPAIR; ENDOTHELIUM CELL; EXCISION REPAIR; GENE OVEREXPRESSION; HUMAN; HUMAN CELL; IMMUNOFLUORESCENCE MICROSCOPY; MITOCHONDRION; NUCLEOTIDE SEQUENCE; OXIDATIVE STRESS; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; UMBILICAL VEIN; WESTERN BLOTTING;

CELL SURVIVAL; CELLS, CULTURED; DNA, MITOCHONDRIAL; DNA-(APURINIC OR APYRIMIDINIC SITE) LYASE; GENE EXPRESSION REGULATION; HUMANS; MITOCHONDRIA; OXIDATIVE STRESS; RECOMBINANT PROTEINS;

EID: 48649109679     PISSN: 08915849     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.freeradbiomed.2008.05.007     Document Type: Article

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