S-phase progression stimulates both the mutagenic KU-independent pathway and mutagenic processing of KU-dependent intermediates, for nonhomologous end joining

Oncogene

Volumn 27, Issue 12, 2008, Pages 1726-1736

  Guirouilh Barbat, J ^a   Huck, S ^a   Lopez, B S ^a,b  

^a CNRS   (France)

^b INSTITUT DE RADIOPROTECTION ET DE SÛRETÉ NUCLÉAIRE   (France)

Author keywords

Cell cycle; Double strand break repair; Genetic instability; Mammalian cells; Nonhomologous end joining; S phase

Indexed keywords

DOUBLE STRANDED DNA;

ANIMAL CELL; ARTICLE; CELL CYCLE G1 PHASE; CELL CYCLE G2 PHASE; CELL CYCLE M PHASE; CELL CYCLE S PHASE; CELL PROLIFERATION; CELL STIMULATION; CHROMOSOME TRANSLOCATION; CONTROLLED STUDY; GENE DELETION; GENE FREQUENCY; GENE MUTATION; NONHUMAN; PRIORITY JOURNAL; SEQUENCE HOMOLOGY;

ANIMALS; ANTIGENS, NUCLEAR; ANTINEOPLASTIC AGENTS; BASE SEQUENCE; CHO CELLS; CRICETINAE; CRICETULUS; DNA BREAKS, DOUBLE-STRANDED; DNA REPAIR; DNA-BINDING PROTEINS; GENE DELETION; MIMOSINE; MOLECULAR SEQUENCE DATA; MUTAGENESIS; NOCODAZOLE; RECOMBINATION, GENETIC; S PHASE; SIGNAL TRANSDUCTION;

MAMMALIA;

EID: 40749132229     PISSN: 09509232     EISSN: 14765594     Source Type: Journal    
DOI: 10.1038/sj.onc.1210807     Document Type: Article

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