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Claus Kerkhoff

Researcher at University of Münster

Publications -  40
Citations -  7217

Claus Kerkhoff is an academic researcher from University of Münster. The author has contributed to research in topics: HaCaT & Receptor. The author has an hindex of 27, co-authored 39 publications receiving 6116 citations. Previous affiliations of Claus Kerkhoff include University of Rostock.

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Guidelines for the use and interpretation of assays for monitoring autophagy

Daniel J. Klionsky, +1287 more
- 01 Apr 2012 - 
TL;DR: These guidelines are presented for the selection and interpretation of methods for use by investigators who aim to examine macroautophagy and related processes, as well as for reviewers who need to provide realistic and reasonable critiques of papers that are focused on these processes.
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S100A9/S100A8: Myeloid representatives of the S100 protein family as prominent players in innate immunity.

TL;DR: An ever‐increasing body of information suggests that S 100A9 plays a prominent role in leukocyte trafficking and arachidonic acid metabolism, and elevated levels of S100A9 and S100 a8 in body fluids of inflamed tissues strengthen the view that these molecules are important players in fighting inflammation.
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S100A8/A9 at low concentration promotes tumor cell growth via RAGE ligation and MAP kinase-dependent pathway

TL;DR: The data indicate that S100A8/A9‐promoted cell growth occurs through RAGE signaling and activation of NF‐κB, which is mediated via RAGE ligation.
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Novel insights into structure and function of MRP8 (S100A8) and MRP14 (S100A9)

TL;DR: It is hypothesized that MRP8 and MRP14 play an important role in leukocyte trafficking, but do not affect neutrophil effector functions.
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The arachidonic acid-binding protein S100A8/A9 promotes NADPH oxidase activation by interaction with p67phox and Rac-2

TL;DR: S100A8/A9 plays an important role in phagocyte NADPH oxidase activation as demonstrated by the impaired oxidase activity in neutrophil‐like NB4 cells, after specific blockage of S100A9 expression, and bone marrow polymorphonuclear neutrophils from S 100A9−/− mice.