M
Marilyn J. Aardema
Researcher at Procter & Gamble
Publications - 96
Citations - 6123
Marilyn J. Aardema is an academic researcher from Procter & Gamble. The author has contributed to research in topics: Genotoxicity & Micronucleus test. The author has an hindex of 40, co-authored 95 publications receiving 5802 citations. Previous affiliations of Marilyn J. Aardema include University of Tennessee & Eli Lilly and Company.
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Evaluation of the ability of a battery of three in vitro genotoxicity tests to discriminate rodent carcinogens and non-carcinogens: I. Sensitivity, specificity and relative predictivity
TL;DR: It was possible to establish that positive results in all three tests indicate the chemical is greater than three times more likely to be a rodent carcinogen than a non-carcinogen, and a relative predictivity (RP) measure is a useful tool to assess the carcinogenic risk from a positive genotoxicity signal.
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Report from the in vitro micronucleus assay working group
Micheline Kirsch-Volders,Toshio Sofuni,Marilyn J. Aardema,Silvio Albertini,David A. Eastmond,Michael Fenech,Motoi Ishidate,Stephan Kirchner,Elisabeth Lorge,Takeshi Morita,Hannu Norppa,Jordi Surrallés,Annelies Vanhauwaert,Akihiro Wakata +13 more
TL;DR: The consensus agreement on the protocol for performing the in vitro micronucleus assay is presented in this paper, where the major recommendations concern: 1. Demonstration of cell proliferation: both cell lines and lymphocytes can be used, but demonstration of the cell proliferation in both control and treated cells is compulsory for the acceptance of the test.
Journal ArticleDOI
Report from the in vitro micronucleus assay working group
Micheline Kirsch-Volders,Toshio Sofuni,Marilyn J. Aardema,Silvio Albertini,David A. Eastmond,Michael Fenech,Motoi Ishidate,Elisabeth Lorge,Hannu Norppa,Jordi Surrallés,W. Von Der Hude,Akihiro Wakata +11 more
TL;DR: The guidelines for the conduct of specific aspects of the protocol were developed at the Washington International Workshop on Genotoxicity Test Procedures (March 25-26, 1999), the current methodologies and data for the in vitro micronucleus test were reviewed as mentioned in this paper.
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How to reduce false positive results when undertaking in vitro genotoxicity testing and thus avoid unnecessary follow-up animal tests: Report of an ECVAM Workshop.
David Kirkland,Stefan Pfuhler,David Tweats,Marilyn J. Aardema,Raffaella Corvi,Firouz Darroudi,Azeddine Elhajouji,Hansruedi Glatt,Paul W. Hastwell,M. Hayashi,Peter Kasper,Stephan Kirchner,Anthony M. Lynch,Daniel Marzin,Daniela Maurici,Jean-Roc Meunier,Lutz Müller,Gerhard J. Nohynek,James M. Parry,Elizabeth M. Parry,Véronique Thybaud,Ray Tice,Jan van Benthem,Philippe Vanparys,Paul D. White +24 more
TL;DR: It was concluded that better guidance on the likely mechanisms resulting in positive results that are not biologically relevant for human health, and how to obtain evidence for those mechanisms, is needed both for practitioners and regulatory reviewers.
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Toxicology and genetic toxicology in the new era of "toxicogenomics": impact of "-omics" technologies.
TL;DR: Toxicogenomics is defined as “the study of the relationship between the structure and activity of the genome (the cellular complement of genes) and the adverse biological effects of exogenous agents”, and there are powerful new methods for protein analysis and for analysis of cellular small molecules.