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Christoph Wotzlaw

Researcher at University of Duisburg-Essen

Publications -  25
Citations -  1632

Christoph Wotzlaw is an academic researcher from University of Duisburg-Essen. The author has contributed to research in topics: Förster resonance energy transfer & Gene expression. The author has an hindex of 16, co-authored 25 publications receiving 1543 citations. Previous affiliations of Christoph Wotzlaw include Max Planck Society.

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Intracellular localisation of human HIF-1 alpha hydroxylases: implications for oxygen sensing.

TL;DR: It is proposed that PHDs and FIH-1 form an oxygen sensor cascade of distinct subcellular localisation, which results in the decreased ability of HIF-1 to bind to the transcriptional coactivator p300/CBP.
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Two-photon fluorescence absorption and emission spectra of dyes relevant for cell imaging

TL;DR: The potential of non‐linear laser scanning fluorescence microscopy is demonstrated here by visualizing multiple intracellular structures in living cells and combined with 3D reconstruction techniques, this approach gives a deeper insight into the spatial relationships of subcellular organelles.
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A Fenton reaction at the endoplasmic reticulum is involved in the redox control of hypoxia-inducible gene expression

TL;DR: The localized Fenton reaction appears to impact the expression of hypoxia-regulated genes by means of HIF-1α stabilization and coactivator recruitment.

Original Contribution The expression of the NADPH oxidase subunit p22phox is regulated by a redox-sensitive pathway in endothelial cells

TL;DR: Findings suggest a positive feedback mechanism whereby ROS, possibly generated by the NADPH oxidase, lead to elevated levels of p22phox and, thus, sustained ROS generation as is observed in endothelial dysfunction.
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The expression of the NADPH oxidase subunit p22phox is regulated by a redox-sensitive pathway in endothelial cells.

TL;DR: In this paper, the role of thrombin in regulating NADPH oxidase-dependent ROS production and expression of its subunit p22phox in the endothelial cell line EaHy926 was investigated.