3 edition of Bioassay of 1-phenyl-3-methyl-5-pyrazolone for possible carcinogenicity. found in the catalog.
Bioassay of 1-phenyl-3-methyl-5-pyrazolone for possible carcinogenicity.
National Cancer Institute (U.S.). Division of Cancer Cause and Prevention.
by Dept. of Health, Education, and Welfare, Public Health Service, National Institutes of Health, National Cancer Institute, Division of Cancer Cause and Prevention, Carcinogenesis Testing Program in Bethesda, Md
Written in English
|Series||Carcinogenesis technical report series ; no. 141, DHEW publication ; no. (NIH) 78-1396, DHEW publication -- no. (NIH) 78-1396.|
|The Physical Object|
|Pagination||97 p. in various pagings :|
|Number of Pages||97|
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Get this from a library. Bioassay of 1-phenylmethylpyrazolone for possible carcinogenicity. [National Cancer Institute (U.S.).
Division of Cancer Cause and Prevention.]. Bioassay of 1-phenylmethylpyrazolone for possible carcinogenicity (OCoLC) Material Type: Document, Government publication, National government publication, Internet resource: Document Type: Internet Resource, Computer File: All Authors / Contributors: National Cancer Institute (U.S.).
A bioassay of 1-phenylmethylpyrazolone for possible carcinogenicity was conducted using Fischer rats and B6C3Fl mice.
l-Phenylmethylpyrazolone was admin in the feed, at either of two concn, to groups of 49 or 50 male and 50 female animals of each species. Author(s): Litton-Bionetics, inc.; National Institutes of Health (U.S.); Carcinogenesis Testing Program (U.S.) Title(s): Bioassay of 1-phenylmethylpyrazolone for possible carcinogenicity.
Toxicology/Poisons: Schlapp, Max MD and Edward Smith. NEW CRIMINOLOGY A CONSIDERATION OF THE CHEMICAL CAUSATION OF ABNORMAL BEHAVIOR NY 1st Boni and Liveright. QSARS of mutagens and carcinogens: Two case studies illustrating problems in the construction of models for two species rodent carcinogenicity bioassay results for carcinogens and noncarcinogens.
1 -Phenylmethylpyrazolone 0 - N-Phenyl-p-phenylenediamine 2 - l-Phenylthiourea 9 - Phthalamide Cited by: Mutation Research, () Elsevier MTR The genetic toxicology of Gene-Tox non-carcinogens Michael D.
Waters, Hinda B. Bergman and Stephen Nesnow Genetic Toxicology Division, Health Effects Research Laboratory, U.S. Environmental Protection Agency, Research Triangle Park, NC (U.S.A.) (Received 31 March ) (Accepted 3 April ) Keywords: Gene-Tox non Cited by: Micronuclei, hemoglobin adducts and respiratory tract irritation in mice after inhalation of toluene diisocyanate (TDI) and 4,4 '-methylenediphenyl diisocyanate (MDI).
Twenty-seven chemicals were tested for their mutagenic potential in the LY tk+/tk− mouse lymphoma cell forward mutation assay using procedures based upon those described by.
Strong carcinogenicity and contamination prevalence of aflatoxin B1, B2, G1, G2 and M1 in food necessitates the monitoring of these compounds. These aflatoxins have native fluorescence (ex nm, em nm), but the fluorescence intensity of B1 and G1 is weaker than that of B2 and G/5(1).
The obtained reducing glycans can be routinely derivatized with 2-aminobenzoic acid (2-AA), 1-phenylmethylpyrazolone (PMP), and potentially some other fluorescent reagents for comprehensive analysis. Alternatively, the core Î±-1,3-fucosylated N-glycans are released in mild alkaline medium and derivatized with PMP in situ, and their.
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The Dictionary of Substances and their Effects Second Edition The Dictionary of Substances and their Effects Second Edition EDITOR S Gangolli, Consultant, MRC Toxicology Unit, UK EDITORIAL ADVISORY BOARD Dr D Anderson, B I B R A InternationaZ, UK Dr J Chadwick, Health and Safety Executive, UK Professor L Ebdon, University of Plymouth, UK Dr D Cammon, CuIzfornia €PA, U S A .