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Friday, July 31, 2020 | History

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

Bioassay of p-cresidine for possible carcinogenicity

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

  • 225 Want to read
  • 12 Currently reading

Published 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

    Subjects:
  • Carcinogens,
  • Azo dyes,
  • Toxicology

  • Edition Notes

    SeriesNIH publication -- no. 79-1397., National Cancer Institute carcinogenesis technical report series -- no. 142.
    The Physical Object
    Pagination116 p. in various pagings :
    Number of Pages116
    ID Numbers
    Open LibraryOL25904025M

    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. A List of Characters and Authors and Their Books. Welcome to niarbylbaycafe.com name is Graeme, and I run "BSIO" as I call it. The goal of this website is simple dudes: to list the series of every book .

    Regulatory agencies currently rely on rodent carcinogenicity bioassay data to predict whether or not a given chemical poses a carcinogenic threat to humans. We argue that it is always more useful to know a chemical's carcinogenic potency (with confidence limits) than to be able to say only qualitatively that it has been found to be a niarbylbaycafe.com by: Bioassay of p-Cresidine for Possible Carcinogenicity. Technical Report Series No. Technical Report Series No. US Department of Health, Education, and Welfare, National Institutes of Cited by:

    Jul 17,  · niarbylbaycafe.com means it's official. Federal government websites often end niarbylbaycafe.com niarbylbaycafe.com Before sharing sensitive information, make sure you're on a federal government site. The Carcinogenesis Bioassay in Perspective: Application in Identifying Human Cancer Hazards The selection process for chemicals tested in the rodent carcinogenicity bioassay has been biased.


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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, Bioassay of p-cresidine for possible carcinogenicity book 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 niarbylbaycafe.com by: Aniline and its derivatives are widely used as the intermediate for dyestuffs and a variety of polyurethane products (IARC, ).

Bladder cancers in workers exposed to aniline in the dyestuff industry were reported to be an occupational disease at first (Rehn, ).Cited by: Bioassay of tetrachlorvinphos for possible carcinogenicity Bioassay of tetrachlorvinphos for possible carcinogenicity by United States.

National Cancer Institute. Carcinogen Bioassay and Program Resources Branch. Publication date Topics Carcinogens, Pesticides Publisher. Bioassay of chlorobenzilate for possible carcinogenicity Item Preview remove-circle Share or Embed This Item.

Bioassay of chlorobenzilate for possible carcinogenicity by National Cancer Institute (U.S.). Division of Cancer Cause and Prevention. Publication date TopicsPages: Search for books, ebooks, Bioassay of sulfisoxazole for possible carcinogenicity.

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: