Homeostatic regulation of base excision repair by a p53-induced phosphatase: Linking stress response pathways with DNA repair proteins

Cell Cycle

Volumn 3, Issue 11, 2004, Pages 1363-1366

  Lu, Xiongbin ^a   Nguyen, Thuy Ai ^a   Appella, Ettore ^b   Donehower, Lawrence A ^a  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

^b NATIONAL CANCER INSTITUTE   (United States)

Author keywords

Base excision repair; DNA repair; p53; PPM1D; UNG2; Uracil DNA glycolase; Wip1

Indexed keywords

ATM PROTEIN; ATR PROTEIN; CHECKPOINT KINASE 2; MITOGEN ACTIVATED PROTEIN KINASE P38; PHOSPHATASE; PROTEIN MDM2; PROTEIN P53; TUMOR SUPPRESSOR PROTEIN; URACIL DNA GLYCOSYLTRANSFERASE;

ACETYLATION; CELL CYCLE; CELL DEATH; CELL GROWTH; CELL PROLIFERATION; DNA DAMAGE; EXCISION REPAIR; GENE AMPLIFICATION; GENE OVEREXPRESSION; GENETIC TRANSCRIPTION; HOMEOSTASIS AND REGULATION; HUMAN; MEDIATOR; NONHUMAN; ONCOGENE; PROTEIN DEGRADATION; PROTEIN DEPHOSPHORYLATION; PROTEIN MODIFICATION; REVIEW; SIGNAL TRANSDUCTION; STRESS; TRANSCRIPTION INITIATION;

EID: 14644401653     PISSN: 15384101     EISSN: 15514005     Source Type: Journal    
DOI: 10.4161/cc.3.11.1241     Document Type: Review

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