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Monday, November 9, 2020 | History

3 edition of Bioassay of p-cresidine for possible carcinogenicity found in the catalog.

Bioassay of p-cresidine for possible carcinogenicity

National Cancer Institute (U.S.). Division of Cancer Cause and Prevention.

Bioassay of p-cresidine for possible carcinogenicity

  • 197 Want to read
  • 36 Currently reading

Published by Dept. of Health, Education, and Welfare, Public Health Service, National Institutes of Health in Bethesda, Md .
Written in English

    Subjects:
  • Carcinogens.,
  • Azo dyes -- Toxicology.

  • Edition Notes

    StatementCarcinogenesis Testing Program, Division of Cancer Cause and Prevention, National Cancer Institute, National Institutes of Health.
    SeriesCarcinogenesis technical report series ; no. 142, DHEW publication ; no. (NIH) 78-1397, DHEW publication -- no. (NIH) 78-1397.
    The Physical Object
    Pagination117 p. in various pagings :
    Number of Pages117
    ID Numbers
    Open LibraryOL15231005M

    A bioassay of hexachlorophene for possible carcinogenicity was conducted by administering the test chemical in feed to Fischer rats. Groups of 24 rats of each sex were administered hexachlorophene at one of three doses, either 17, 50, or ppm, for weeks. Higher doses of ppm, used in 8-week subchronic. chemical being a carcinogen maybe obtained by comparing its structure and chemical and physi-cal characteristics with those of known carcino-gens and noncarcinogens. This first stage in an orderly determination of whether or not a chem-ical is a carcinogen requires the gathering of all available information about it. The information. Unfortunately, this book can't be printed from the OpenBook. If you need to print pages from this book, we recommend downloading it as a PDF. Visit arleenthalerphotography.com to get more information about this book, to buy it in print, or to download it as a free PDF. Below is the uncorrected machine-read text.


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Bioassay of p-cresidine for possible carcinogenicity by National Cancer Institute (U.S.). Division of Cancer Cause and Prevention. Download PDF EPUB FB2

Bioassay of p-cresidine for possible carcinogenicity. National Toxicology Program. A bioassay of p-cresidine for possible carcinogenicity was conducted using Fischer rats and B6C3F1 mice.

p-Cresidine was administered in the feed, at either of two concentrations, to groups of 50 male and 50 female animals of each species. Bioassay of p-cresidine for possible carcinogenicity (OCoLC) Material Type: Government publication, National government publication: Document Type: Book: All Authors / Contributors: National Cancer Institute (U.S.).

Division of Cancer Cause and Prevention.; Carcinogenesis Testing Program (U.S.); National Institutes of Health (U.S.) OCLC Number. A bioassay of p-cresidine for possible carcinogenicity was con­ ducted using Fischer rats and B6C3F1 mice.

p-Cresidine was ad­ ministered in the feed, at either of two concentrations, to groups of 50 male and 50 female animals of each species. The dietary con­ centrations used in the chronic bioassay for low and high dose rats.

Bioassay of p-cresidine 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.).

Division of Cancer Cause and Prevention. Note: Citations are based on reference standards. However, formatting rules can vary widely between applications and fields of interest or study.

The specific requirements or preferences of your reviewing publisher, classroom teacher, institution or organization should be applied. Bioassay of m-cresidine for possible carcinogenicity (OCoLC) Material Type: Government publication, National government publication: Document Type: Book: All Authors / Contributors: National Cancer Institute (U.S.).

Division of Cancer Cause and Prevention. OCLC Number: Notes: "CAS no. " Description. texts All Books All Texts latest This Just In Smithsonian Libraries FEDLINK Bioassay of lasiocarpine for possible carcinogenicity Item Preview Bioassay of lasiocarpine for possible carcinogenicity by National Cancer Institute (U.S.).

Division of Cancer Cause and Prevention. Publication date. A bioassay of p-cresidine for possible carcinogenicity was conducted using Fischer rats and B6C3F1 mice. p-Cresidine was administered in the feed, at either of two concentrations, to groups of 50 male and 50 female animals of each species.

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National Toxicology Program. A bioassay of beta-2'-deoxythioguanosine monohydrate (b-TGdR) for possible carcinogenicity was conducted by administering the test chemical by intraperitoneal injection to Sprague-Dawley rats and B6C3F1 mice.

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Search for books, ebooks, and physical Bioassay of malaoxon for possible carcinogenicity Published: () Bioassays of DDT, TDE, and p, p'-DDE for possible carcinogenicity Published: () Bioassay of dixathion for possible carcinogenicity Published: ( Replication of the p-cresidine (2-methoxymethylaniline) 24 week subchronic bioassays in male pdeficient mice.

Left, transitional cell or squamous cell carcinomas of the urinary blad- der or (right) hepatocellular carcinomas appearing between 16 and 24 weeks of exposure to 0, % or % p-cresidine in the arleenthalerphotography.com by: Aniline and its derivatives are widely used as the intermediate for dyestuffs and a variety of polyurethane products (IARC, ).

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Bibliographic Details; Corporate Authors: National Cancer Institute (U.S.). a Bioassay of sulfisoxazole for possible carcinogenicity |h [electronic resource] /. p‑Cresidine is reasonably anticipated to be a human carcinogen based on sufficient evidence of carcinogenicity from studies in experimen‑ tal animals.

Cancer Studies in Experimental Animals. Oral exposure to p‑cresidine caused tumors at several different tissue sites in mice and rats. A bioassay of p-cresidine for possible carcinogenicity was conducted using Fischer rats and B6C3F 1 mice. p-Cresidine was administered in the feed, at either of two concentrations, to groups of 50 male and 50 female animals of each species.

The dietary concentrations used in the chronic bioassay for low and high dose rats were and percent, respectively. Bioassay of estradiol mustard for possible carcinogenicity Published: () Bioassay of 2-aminonitrothiazole for possible carcinogenicity Published: () Bioassay of tris (2,3-dibromopropyl) phosphate for possible carcinogenicity Published: ().

Washington, DC. 9 National Cancer Institute Carcinogenesis Technical Report Series No. () Bioassay of p-cresidine for possible carcinogenicity. DHEW Publication No (NIH)Washington, DC.

10 National Cancer Institute Carcinogenesis Technical Report Series No. () Bioassay of o-toluidine hydrochloride for possible Cited by: The result of present study shows that p -cresidine is genotoxic in mouse bladder, the target organ for this carcinogen.

Among the 8 organs examined, o -anisidine induced DNA damage only in two of them, i.e. bladder and colon. However, o -anisidine has not yet been reported to produce cancer in the colon [10].Cited by: Jun 27,  · p-Cresidine: Target Organs and Levels of Evidence for TR Bioassay of p-Cresidine for Possible Carcinogenicity (CASRN ).

NCI,Bioassay of P-Cresidine for Possible Carcinogenicity, National Cancer Institute Carcinogenesis Technical Report Series No. Google Scholar Peto, R.,Carcinogenic effects of chronic-exposure to very low levels of toxic substances, Environmental Health Perspectives, Author: Kenny S.

Crump. Read chapter p-Cresidine: Aromatic Amines: An Assessment of the Biological and Environmental Effects Login Register Cart please consider the following text as a useful but insufficient proxy for the authoritative book pages.

Chapter 10 p-CRESIDINE NH2 ~ OCH3 ~ 1 CH3~ E=Cresidine (2-methoxymethylanaline) is a white crystalline solid.

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Toxicity and Carcinogenicity Studies of Chlorpromazine Hydrochloride and p -Cresidine in the p53 Heterozygous Mouse Model Article (PDF Available) in Toxicologic Pathology 30(6) ·.

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Author(s): Mason Research Institute.; National Institutes of Health (U.S.); Carcinogenesis Testing Program (U.S.) Title(s): Bioassay of p-cresidine for possible. taken to replace, where possible, the 2-year rodent bioassay with alternatives that more accurately predict carcinogenicity in humans.

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