From Chromosomal Aberrations to Transcriptome Analysis: Four Decades of Research in Bivalve Genotoxicity. [PDF]
Khatir Z, Leitão A.
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Safety evaluation of the food enzyme β-fructofuranosidase from the non-genetically modified <i>Aspergillus</i> sp. strain ATCC 20611. [PDF]
EFSA Food Enzymes Panel (FEZ) +18 more
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Safety evaluation of the food enzyme α-amylase from the non-genetically modified <i>Aspergillus</i> sp. strain AR-SHFA-109. [PDF]
EFSA Panel on Food Enzymes (FEZ) +15 more
europepmc +1 more source
Updated safety evaluation of the food enzyme phospholipase A<sub>2</sub> from the genetically modified <i>Trichoderma reesei</i> strain RF8793. [PDF]
EFSA Panel on Food Enzymes (FEZ) +14 more
europepmc +1 more source
Do the azo food colorings carmoisine and ponceau 4R have a genotoxic potential? [PDF]
Kara SG +3 more
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Lack of Genotoxic and Carcinogenic Potential for Nonsugar Sweeteners: A Review of Animal and Mechanistic Evidence. [PDF]
Marchitti SA +3 more
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Genotoxicity in Unconventional Mammalian Models of Wild, Urban, and Agricultural Ecosystems: A Systematic Review Under the One Health Approach. [PDF]
Gorla NBM, Nieves M, Ferré DM.
europepmc +1 more source
Safety evaluation of the food enzyme abstract aspergillopepsin I from the non-genetically modified <i>Aspergillus niger</i> strain CCTCC M 2023234. [PDF]
EFSA Panel on Food Enzymes (FEZ) +14 more
europepmc +1 more source
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Sampling times in micronucleus testing
Mutation Research Letters, 1992A series of micronucleus inducers were evaluated in the mouse bone marrow micronucleus test to determine if a 72-h sampling time enhances the sensitivity for detecting genotoxic agents. Male and female Swiss albino mice were dosed once with 7,12- dimethylbenz[a]anthracene, 6-mercaptopurine, benzo[a]pyrene, benzene, cyclophosphamide, 2 ...
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The micronucleus test methodological aspects
Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis, 1973Abstract Changes in the cellular compositiion of bone marrow were studied in relation to dose of Trenimon® and time after treatment. Strong mutagenic effects caused a partial depletion of the marrow cavities of nucleated blood cell precursors, with subsequent retention of newly formed erythrocytes and inundation with peripheral blood.
Von Ledebur, M, Schmid, Werner
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