The impact of homologous recombination repair deficiency on depleted uranium clastogenicity in Chinese hamster ovary cells: XRCC3 protects cells from chromosome aberrations, but increases chromosome fragmentation

Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis

Volumn 762, Issue 1, 2014, Pages 1-9

  Holmes, Amie L ^a   Joyce, Kellie ^a   Xie, Hong ^a   Falank, Carolyne ^a   Hinz, John M ^b   Wise, John Pierce ^a  

^a UNIVERSITY OF SOUTHERN MAINE   (United States)

^b WASHINGTON STATE UNIVERSITY   (United States)

Author keywords

Chromosome damage; Depleted uranium; Fragmentation; RAD51D; Uranium trioxide; XRCC3

Indexed keywords

DEPLETED URANIUM; RAD51 PROTEIN; UNCLASSIFIED DRUG; URANIUM; XRCC3 PROTEIN;

ARTICLE; CELL LEVEL; CELL PROTECTION; CHROMOSOME ABERRATION; CONTROLLED STUDY; CYTOTOXICITY; DNA FRAGMENTATION; FEMALE; GENE ACTIVITY; GENE FUSION; GENE LOSS; GENETIC COMPLEMENTATION; GENOTOXICITY; HUMAN; HUMAN CELL; PRIORITY JOURNAL; RECOMBINATION REPAIR; WILD TYPE; X CHROMOSOME;

CRICETULUS GRISEUS;

CHROMOSOME DAMAGE; DEPLETED URANIUM; FRAGMENTATION; RAD51D; URANIUM TRIOXIDE; XRCC3;

ANIMALS; CHO CELLS; CHROMOSOME ABERRATIONS; CHROMOSOMES, MAMMALIAN; CRICETULUS; DNA BREAKS, DOUBLE-STRANDED; DNA-BINDING PROTEINS; GENETIC COMPLEMENTATION TEST; MUTAGENS; RECOMBINATIONAL DNA REPAIR; URANIUM;

EID: 84897399238     PISSN: 00275107     EISSN: 09218262     Source Type: Journal    
DOI: 10.1016/j.mrfmmm.2014.02.001     Document Type: Article

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