Zobrazeno 1 - 10
of 36
pro vyhledávání: '"G.J. Horbach"'
Publikováno v:
Mutation Research/Genetic Toxicology and Environmental Mutagenesis. 724:7-21
In the present study an automated image analysis assisted in vitro micronucleus assay was developed with the rodent cell line CHO-k1 and the human hepatoma cell line HepG2, which are both commonly used in regulatory genotoxicity assays. The HepG2 cel
Autor:
Wolfgang A. Schmalix, D Lang, G.J. Horbach, R Bocker, P Beaune, C Belloc, Helmut Greim, E.M. de Groene, V Siruguri, A Schneider, B Kleingeist, Johannes Doehmer
Publikováno v:
Archives of Biochemistry and Biophysics. 332:295-304
V79 Chinese hamster cells were constructed for stable expression of human cytochrome P450 3A4 with and without coexpression of human NADPH-cytochrome P450 oxidoreductase. Expression of the cDNAs was shown by Northern and Western analyses. Activity wa
Transgenic cell lines and changes in gene function and expression: Useful tools in toxicity testing?
Autor:
G.J. Horbach, E.M. de Groene
Publikováno v:
Toxicology in vitro : an international journal published in association with BIBRA. 9(4)
Molecular biology provides the toxicologist with powerful tools that can be used in the development and use of in vitro techniques in toxicity testing. As an example, a number of cDNAs coding for human cytochrome P-450 enzymes have been cloned, incor
Publikováno v:
Mutation Research-Genetic Toxicology and Environmental Mutagenesis, 2, 466, 143-159
Three different in vitro mutation assays were used to investigate the involvement of cytochrome P450 enzymes in the activation of the nitro- polycyclic aromatic hydrocarbons (nitroPAHs) 1-nitropyrene and 2- nitrofluorene and their reduced metabolites
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https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f3ab33936154aa59027290310d11411
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Publikováno v:
Journal of veterinary pharmacology and therapeutics. 21(2)
Publikováno v:
Research in Veterinary Science, 1, 66, 51-55
In humans, clinically relevant drug-drug interactions occur with some macrolide antibiotics via the formation of stable metabolic intermediate (MI) complexes with enzymes of the cytochrome P4503A (CYP3A) subfamily. The formation of such complexes can
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::880f9a54aba39251fe03cd5f920ac561
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Publikováno v:
Xenobiotica; the fate of foreign compounds in biological systems. 27(8)
1. The aim of the present study was to investigate the potency of various sulfonamides to inhibit tolbutamide hydroxylation (a CYP2C activity) in hepatic microsomal fractions and hepatocytes of the dwarf goat. Also a number of suggested substrates fo
Publikováno v:
European journal of pharmacology. 293(1)
An NIH/3T3 cell line, stably expressing human cytochrome P450-3A4 (CYP3A4) cDNA has been developed. This cell line was used in combination with a shuttle vector, containing the bacterial lacZ' gene as reporter gene, to study mutagenicity. Ethylmethan
Akademický článek
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Autor:
A. S. J. P. A. M. van Miert, J. Batzias, G.J. Horbach, R.F.M. Maas, Renger F. Witkamp, W.M. Zweers-Zeilmaker
Publikováno v:
Scopus-Elsevier
Xenobiotica, 11, 26, 1131-1141
Xenobiotica, 11, 26, 1131-1141
1. Cytochrome P450 activities in vivo and in vitro and enzyme induction by phenobarbital, beta-naphthoflavone, isoniazid and triacetyloleandomycin were investigated in the female dwarf goat. In vivo kinetics of antipyrine, sulphadimidine and caffeine
Externí odkaz:
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