Chromosome breakage is primarily responsible for the micronuclei induced by 1,4-dioxane in the bone marrow and liver of young CD-1 mice

Mutation Research - Genetic Toxicology and Environmental Mutagenesis

Volumn 586, Issue 1, 2005, Pages 28-37

  Roy, S K ^a,b   Thilagar, A K ^b   Eastmond, D A ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b SITEK Research Laboratories   (United States)

Author keywords

1,4 Dioxane; Bone marrow; Hepatocyte; Micronucleus; Mouse; Proliferation; Vinblastine sulfate

Indexed keywords

BROXURIDINE; DIOXANE;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; BONE MARROW; BONE MARROW CELL; CELL ASSAY; CELL LABELING; CELL PROLIFERATION; CENTROMERE; CHROMOSOME BREAKAGE; CONTROLLED STUDY; ERYTHROCYTE; FEEDING; FLUORESCENCE IN SITU HYBRIDIZATION; GENOTOXICITY; IMPLANTATION; LIVER; LIVER CELL; MALE; MEASUREMENT; MICRONUCLEUS; MOUSE; NONHUMAN; OSMOTIC PUMP; PRIORITY JOURNAL; SENSITIVITY ANALYSIS; STAINING; TISSUE;

ANIMALS; BONE MARROW; BROMODEOXYURIDINE; CARCINOGENICITY TESTS; CARCINOGENS; CELL PROLIFERATION; CHROMOSOMES; DIOXANES; ERYTHROCYTES; HEPATOCYTES; IN SITU HYBRIDIZATION, FLUORESCENCE; LIVER; MALE; MICE; MICE, MUTANT STRAINS; MICRONUCLEI, CHROMOSOME-DEFECTIVE;

ANIMALIA; RODENTIA;

EID: 23644444334     PISSN: 13835718     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.mrgentox.2005.05.007     Document Type: Article

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