M
Matthias Bureik
Researcher at Tianjin University
Publications - 97
Citations - 1939
Matthias Bureik is an academic researcher from Tianjin University. The author has contributed to research in topics: Schizosaccharomyces pombe & Cytochrome P450. The author has an hindex of 24, co-authored 87 publications receiving 1674 citations. Previous affiliations of Matthias Bureik include Saarland University & Max Planck Society.
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Functional expression of human mitochondrial CYP11B2 in fission yeast and identification of a new internal electron transfer protein, etp1
TL;DR: It was found that overexpression of this gene significantly enhances steroid hydroxylase activity of CYP11B2 expressing fission yeast cells, and a gene was identified that codes for a protein with an amino terminal domain homologous to COX15 of Saccharomyces cerevisiae and a carboxy terminal ferredoxin domain to be named etp1 (electron-transfer protein 1).
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Development of a test system for inhibitors of human aldosterone synthase (CYP11B2): screening in fission yeast and evaluation of selectivity in V79 cells.
TL;DR: A potent and rather selective non-steroidal inhibitor of human CYP11B2 was detected with an IC(50) value of 59nM and a very potent inhibitor of both enzymes showing a stronger inhibitory activity against the cortisol producing CYP 11B1 was identified.
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The human steroid hydroxylases CYP1B1 and CYP11B2.
TL;DR: The pharmacological and toxicological importance of these steroid hydroxylases, the means for the identification of their potential inhibitors and possible biotechnological applications are discussed.
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Vitamin D3 Metabolism in Human Glioblastoma Multiforme: Functionality of CYP27B1 Splice Variants, Metabolism of Calcidiol, and Effect of Calcitriol
Britta Diesel,Jens Radermacher,Matthias Bureik,Rita Bernhardt,Markus Seifert,Jörg Reichrath,Ulrike Fischer,Eckart Meese +7 more
TL;DR: The findings show that glioblastoma multiforme cell lines metabolize calcidiol and the effect of vitamin D3 metabolites on proliferation, and various effects mediated by calcitriol are shown.
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Synthesis and evaluation of imidazolylmethylenetetrahydronaphthalenes and imidazolylmethyleneindanes: potent inhibitors of aldosterone synthase.
Sarah Ulmschneider,Ursula Müller-Vieira,Markus Mitrenga,Rolf W. Hartmann,Sandrine Oberwinkler-Marchais,Christian D. Klein,Matthias Bureik,Rita Bernhardt,Iris Antes,Thomas Lengauer +9 more
TL;DR: This study proposed aldosterone synthase (CYP11B2) as a novel target for the treatment of congestive heart failure and myocardial fibrosis and the synthesis and biological evaluation of substituted E- and Z-imidazolylmethylenetetrahydronaphthalenes and E-