The lack of binding of methyl-n-amyl ketone (MAK) to rat liver DNA as demonstrated by direct binding measurements, and 32P-postlabeling techniques

Mutation Research - Genetic Toxicology and Environmental Mutagenesis

Volumn 442, Issue 2, 1999, Pages 133-147

  Barber, Eugene D ^a   Miller, Karen R ^b   Banton, Marcy I ^c   Vijayaraj Reddy, M ^d,e  

^a Bldg 320 Eastman Kodak Kodak Park   (United States)

^b EASTMAN CHEMICAL COMPANY   (United States)

^c Shell Chemical Company   (United States)

^d Department of Genetic and Molecular Toxicology   (United States)

^e Stonybrook Laboratories Inc   (United States)

Author keywords

2 Heptanone; DNA binding; In vitro; In vivo; Methyl amyl ketone

Indexed keywords

KETONE DERIVATIVE; PHOSPHORUS 32;

ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; DNA ADDUCT; DNA BINDING; FEMALE; GENOTOXICITY; IN VITRO STUDY; IN VIVO STUDY; INHALATION; ISOTOPE LABELING; LIVER; LIVER MICROSOME; NONHUMAN; PRIORITY JOURNAL; RAT; SCINTILLATION SPECTROMETRY;

ANIMALS; AUTORADIOGRAPHY; CHROMATOGRAPHY, THIN LAYER; DNA; DNA ADDUCTS; FEMALE; KETONES; LIVER; MICROSOMES, LIVER; PHOSPHORUS RADIOISOTOPES; RATS; RATS, INBRED F344;

EID: 0033009245     PISSN: 13835718     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1383-5718(99)00072-8     Document Type: Article

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