F
Franz Oesch
Researcher at University of Mainz
Publications - 580
Citations - 22320
Franz Oesch is an academic researcher from University of Mainz. The author has contributed to research in topics: Epoxide hydrolase & Microsomal epoxide hydrolase. The author has an hindex of 76, co-authored 578 publications receiving 21684 citations. Previous affiliations of Franz Oesch include University of Basel & National Institutes of Health.
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TCDD induces c-jun expression via a novel Ah (dioxin) receptor-mediated p38-MAPK-dependent pathway.
Carsten Weiss,Carsten Weiss,Dagmar Faust,Heike Dürk,Siva Kumar Kolluri,Siva Kumar Kolluri,Anke Pelzer,Sandra M. Schneider,Cornelia Dietrich,Franz Oesch,Martin Göttlicher +10 more
TL;DR: Activating ‘cross-talk’ with MAPK signaling as a novel principle of AhR action is established, which is apparently independent of the AhR's function as a DNA-binding transcriptional activator.
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Dual role of epoxide hydratase in both activation and inactivation of benzo(a)pyrene.
TL;DR: The findings indicate that when microsomes from untreated and phenobarbital-treated mice were used the main contributors to the mutagenicity were simple epoxides (or compounds arising non-enzymically from them) and the activation of dihydrodiols must, however, contribute to a significant extent when microSomes from methylcholanthrene-treated dogs were used.
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Cloning and molecular characterization of a soluble epoxide hydrolase from Aspergillus niger that is related to mammalian microsomal epoxide hydrolase.
Michael Arand,Heike Hemmer,Heike Dürk,Jacques C. Baratti,Alain Archelas,Roland Furstoss,Franz Oesch +6 more
TL;DR: The isolation of the gene and cDNA for the A. niger EH by use of inverse PCR yielded a fully active EH with similar characteristics to the fungal enzyme and offers a versatile tool for the bio-organic chemist for the chiral synthesis of a variety of fine chemicals.
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Xenobiotic-metabolizing enzymes in the skin of rat, mouse, pig, guinea pig, man, and in human skin models
TL;DR: This review attempts to summarize the information available in the open scientific literature on XME in the skin of human, rat, mouse, guinea pig, and pig as well as human primary skin cells, human cell lines, and reconstructed human skin models to suggest some models may tentatively be considered to approximate reasonable closeness to human skin.
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Multiple activation pathways of benzene leading to products with varying genotoxic characteristics.
Hansruedi Glatt,Robert E. Padykula,Glenn A. Berchtold,Gabriele Ludewig,Karl L. Platt,Jochen Klein,Franz Oesch +6 more
TL;DR: Benzene and 13 potential metabolites were investigated for genotoxicity in Salmonella typhimurium and V79 Chinese hamster cells and only the trans-1,2-dihydrodiol proved mutagenic in this strain, while the anti-diol epoxide was more potent than the syn-diastereomer.