E2F1 regulates the base excision repair gene XRCC1 and promotes DNA repair

Journal of Biological Chemistry

Volumn 283, Issue 22, 2008, Pages 15381-15389

  Chen, Dexi ^a,b   Yu, Zhiyong ^a,c   Zhu, Zhiyi ^a   Lopez, Charles D ^a  

^a OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

^b CAPITAL MEDICAL UNIVERSITY   (China)

^c SHANDONG CANCER HOSPITAL AND INSTITUTE   (China)

Author keywords

[No Author keywords available]

Indexed keywords

BINDING ENERGY; BINDING SITES; BIOCHEMISTRY; CELL CULTURE; CELL DEATH; DNA; GENES; MAINTENANCE; NUCLEIC ACIDS; ORGANIC ACIDS; REPAIR; TRANSCRIPTION FACTORS;

APOPTOSIS; BASE EXCISION REPAIRS; CHINESE HAMSTERS; DNA DAMAGES; DNA REPAIRS; ECTOPIC EXPRESSIONS; EXCISION REPAIRS; GENOMIC STABILITIES; IN CELLS; INACTIVE MUTANTS; INDUCED APOPTOSIS; LUCIFERASE REPORTERS; METHYLMETHANE SULFONATES; MOUSE EMBRYO FIBROBLASTS; S-PHASE;

TRANSCRIPTION;

MESYLIC ACID METHYL ESTER; TRANSCRIPTION FACTOR E2F1; XRCC1 PROTEIN; DNA BINDING PROTEIN; E2F1 PROTEIN, MOUSE; MESYLIC ACID; MESYLIC ACID DERIVATIVE; X-RAY REPAIR CROSS COMPLEMENTING PROTEIN 1;

ANIMAL CELL; ARTICLE; CELL SURVIVAL; CONTROLLED STUDY; DNA DAMAGE; DNA REPAIR; EXCISION REPAIR; GENOMIC INSTABILITY; MOLECULAR CLONING; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; WILD TYPE; ANIMAL; APOPTOSIS; CELL CYCLE S PHASE; CELL LINE; CHO CELL; CRICETULUS; CYTOLOGY; DNA RESPONSIVE ELEMENT; DRUG EFFECT; EMBRYO (ANATOMY); FIBROBLAST; GENE DELETION; GENETICS; HAMSTER; METABOLISM; NUCLEOTIDE SEQUENCE; PHYSIOLOGY;

CRICETULUS GRISEUS;

ANIMALS; APOPTOSIS; BASE SEQUENCE; CELL LINE; CHO CELLS; CRICETINAE; CRICETULUS; DNA REPAIR; DNA-BINDING PROTEINS; E2F1 TRANSCRIPTION FACTOR; EMBRYO, MAMMALIAN; FIBROBLASTS; GENOMIC INSTABILITY; MESYLATES; MICE; RESPONSE ELEMENTS; S PHASE; SEQUENCE DELETION;

EID: 47249124194     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M710296200     Document Type: Article

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