Zobrazeno 1 - 7
of 7
pro vyhledávání: '"James L. Ivett"'
Autor:
Sheila M. Galloway, James L. Ivett, Marilyn J. Aardema, Takeshi Morita, Motoi Ishidate, David Kirkland, Pasquale Mosesso, Toshio Sofuni
Publikováno v:
Mutation Research/Environmental Mutagenesis and Related Subjects. 312:241-261
The following summary represents a consensus of the working group except where noted. The items discussed are listed in the order in which they appear in the OECD guideline (473) for easy reference. Metabolic activation. S9 from animals induced eithe
Publikováno v:
Mutation Research/Genetic Toxicology. 298:43-51
Concentrated organic residues extracted from 5 blended aliquots of commercial beers were evaluated for their ability to induce sister chromatid exchange (SCE), chromosomal aberrations and forward mutation in Chinese hamster ovary (CHO) cells. Each ex
Autor:
James L Ivett, B Jessen, Bhasker Shetty, C C Capen, T E Ryan, R Gasser, Gregory J. Stevens, J C Theiss, Leigh Ann Burns-Naas, R M McClain, G Furman, W Evering, Mark Zorbas, E Wu, J C Cook, Stephanie Webber, M Chen
Publikováno v:
Humanexperimental toxicology. 24(12)
The carcinogenic potential of nelfinavir mesylate (nelfinavir) was evaluated in a 2-year oral (gavage) study on Sprague-Dawley rats at dose levels of 0 (control), 0 (vehicle control), 100, 300 and 1000 mg/kg per day. At the end of the treatment, incr
Autor:
Leigh Ann Burns-Naas, J. Ann McCay, Mark Zorbas, Kimber L. White, James L Ivett, Stephanie Webber
Publikováno v:
Humanexperimental toxicology. 24(2)
The objective of these investigations was to determine whether exposure to the HIV-1 protease inhibitor nelfinavir compromises immune function in Sprague Dawley rats. Animals (20/sex per group) were exposed orally for 1 or 6 months to nelfinavir at d
Autor:
Helen C. Cunny, James L Ivett, Jeffrey M. Charles, B. Bhaskar Gollapudi, Ronald D. Wilson, Hema Murli, James S. Bus
Publikováno v:
Mutation research. 444(1)
The potential for 2,4-D and seven of its salts and esters to induce cytogenetic abnormalities in mammalian cells in vivo was investigated in the mouse bone marrow micronucleus test. All the test materials were administered to male and female mice by
Autor:
Robert W. Kapp, Lawrence W. Masten, T. H. Gardiner, Richard H. McKee, James L. Ivett, Robert R. Young, Dale J. Marino, T. R. Tyler
Publikováno v:
Environmental and molecular mutagenesis. 22(2)
To assess the mutagenic potential of isopropanol, an in vitro Chinese hamster ovary (CHO) cell/HGPRT gene mutation assay and a bone marrow micronucleus study in mice were conducted. In the CHO/HGPRT assay, concentration levels ranged from 0.5 to 5.0
Autor:
Hemalatha Murli, James L. Ivett, John J. Mulvihill, Sherri J. Bale, Dilys M. Parry, Allen E. Bale
Publikováno v:
Cancer Genetics and Cytogenetics. 42:273-279
Previous studies of chromosome stability in the nevoid basal cell carcinoma syndrome have yielded inconsistent results and suffered from small sample sizes and less than optimal controls. We investigated chromosome fragility and sister chromatid exch