Metabolic labeling of human cells with tritiated nucleosides results in activation of the ATM-dependent p53 signaling pathway and acceleration of DNA repair

Oncogene

Volumn 22, Issue 36, 2003, Pages 5562-5571

  Mirzayans, Razmik ^a   Pollock, Scott ^a   Scott, April ^a   Gao, Cindy Q ^a   Murray, David ^a  

^a UNIVERSITY OF ALBERTA   (Canada)

Author keywords

CPDs; Growth arrest; Nucleotide excision repair; p21WAF1; p53; Radiolabeled nucleosides; UV

Indexed keywords

ATM PROTEIN; CARBON 14; NUCLEOSIDE; PROTEIN P21; PROTEIN P53; PYRIMIDINE DIMER; THYMIDINE; TRITIUM; URIDINE;

ARTICLE; BIOLOGICAL MONITORING; CELL ACTIVATION; CELL GROWTH; CELL LABELING; CELL PROLIFERATION; CONTROLLED STUDY; DNA DAMAGE; DNA REPAIR; EXCISION REPAIR; GENE INDUCTION; GENOTOXICITY; GROWTH INHIBITION; HUMAN; HUMAN CELL; IMMUNOFLUORESCENCE; ISOTOPE LABELING; NUCLEIC ACID SYNTHESIS; PRIORITY JOURNAL; PROTEIN ANALYSIS; ULTRAVIOLET RADIATION;

CELL CYCLE PROTEINS; CELL DIVISION; CYCLIN-DEPENDENT KINASE INHIBITOR P21; CYCLINS; DNA DAMAGE; DNA REPAIR; DNA-BINDING PROTEINS; FLUORESCENT ANTIBODY TECHNIQUE; HUMANS; NUCLEOSIDES; PROTEIN-SERINE-THREONINE KINASES; RNA, MESSENGER; SIGNAL TRANSDUCTION; TRITIUM; TUMOR SUPPRESSOR PROTEIN P53; TUMOR SUPPRESSOR PROTEINS;

TRITIUM;

EID: 0041836256     PISSN: 09509232     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.onc.1206514     Document Type: Article

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