F
Franck A. Atienzar
Researcher at UCB
Publications - 34
Citations - 2616
Franck A. Atienzar is an academic researcher from UCB. The author has contributed to research in topics: RAPD & DNA damage. The author has an hindex of 22, co-authored 34 publications receiving 2425 citations. Previous affiliations of Franck A. Atienzar include University of Plymouth.
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Journal ArticleDOI
Characterization of primary human hepatocytes, HepG2 cells, and HepaRG cells at the mRNA level and CYP activity in response to inducers and their predictivity for the detection of human hepatotoxins.
Helga Gerets,K. Tilmant,Brigitte Gerin,H. Chanteux,B. O. Depelchin,Stephane Dhalluin,Franck A. Atienzar +6 more
TL;DR: None of the models under study gave desirable sensitivities and a high metabolic capacity and CYP inducibility in cell lines does not necessarily correlate with a high sensitivity for the detection of hepatotoxic drugs.
Journal ArticleDOI
The random amplified polymorphic DNA (RAPD) assay and related techniques applied to genotoxicity and carcinogenesis studies: a critical review.
TL;DR: After proper optimisation, the RAPD is a reliable, sensitive and reproducible assay, has the potential to detect a wide range of DNA damage as well as mutations and therefore can be applied to genotoxicity and carcinogenesis studies and is suggested that these assays would continue to complement the use of emerging technologies.
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Qualitative assessment of genotoxicity using random amplified polymorphic DNA: Comparison of genomic template stability with key fitness parameters in Daphnia magna exposed to benzo[a]pyrene
TL;DR: Not only was the RAPD profiling method shown to be a rapid and reproducible assay of toxicant—induced DNA effects, but the qualitative measure of genomic template stability compared favorably with the traditional indices of fitness.
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Evaluation of the random amplified polymorphic DNA (RAPD) assay for the detection of DNA damage and mutations
TL;DR: The random amplified polymorphic DNA (RAPD) assay and related techniques like the arbitrarily primed polymerase chain reaction (AP-PCR) have been shown to detect genotoxin-induced DNA damage and mutations but further research is required to better understand the potential and limitations of the RAPD assay.
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Comparison of ultraviolet-induced genotoxicity detected by random amplified polymorphic DNA with chlorophyll fluorescence and growth in a marine macroalgae, Palmaria palmata.
Franck A. Atienzar,B. Cordi,Maria E. Donkin,A. J. Evenden,Awadhesh N. Jha,Michael H. Depledge +5 more
TL;DR: The RAPD method, used to detect DNA damage in the sublittoral macroalgae Palmaria palmata (Rhodophyta) exposed to both ambient and elevated irradiances of UV-B, may prove to be a valuable tool for investigating the specific effects of genotoxic agents upon marine algal populations.