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Frederick A. Beland

Researcher at National Center for Toxicological Research

Publications -  331
Citations -  14460

Frederick A. Beland is an academic researcher from National Center for Toxicological Research. The author has contributed to research in topics: Carcinogen & DNA adduct. The author has an hindex of 60, co-authored 324 publications receiving 13339 citations. Previous affiliations of Frederick A. Beland include Food and Drug Administration & University of Arkansas for Medical Sciences.

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An evaluation of the biological and toxicological properties of Aloe barbadensis (miller), Aloe vera.

TL;DR: A review of the botany, physical and chemical properties, and biological activities of the Aloe vera plant finds that it contains multiple constituents with potential biological and toxicological activities, yet the active components elude definition.
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Malachite Green: A Toxicological Review

TL;DR: Results from carcinogenicity bioassays with malachite green have been equivocal; however, it appears to act as a tumor promoter, perhaps because of its ability to induce the formation of reactive oxygen species.

Alcohol consumption and ethyl carbamate

Naomi E. Allen, +61 more
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A comparison of the tumors induced by coal tar and benzo[a]pyrene in a 2-year bioassay.

TL;DR: The tumorigenicity of two coal tar mixtures was compared and indicated that the benzo[a]pyrene in the coal tar diets could be responsible for the forestomach tumors, while the lung and liver tumors appeared to be due to other genotoxic components contained within thecoal tar mixture, whereas the small intestine tumors resulted from chemically-induced cell proliferation that occurred at high doses of coal tar.
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DNA adduct formation from acrylamide via conversion to glycidamide in adult and neonatal mice.

TL;DR: DNA adduct formation from AA treatment in adult mice showed a supralinear dose-response relationship, consistent with saturation of oxidative metabolism at higher doses, which increases the understanding of the mutagenic potential of GA and provides further evidence for a genotoxic mechanism in AA carcinogenesis.