K
Kim S. C. Weber
Researcher at Ludwig Maximilian University of Munich
Publications - 29
Citations - 4596
Kim S. C. Weber is an academic researcher from Ludwig Maximilian University of Munich. The author has contributed to research in topics: Chemokine & Monocyte. The author has an hindex of 24, co-authored 29 publications receiving 4446 citations. Previous affiliations of Kim S. C. Weber include University of Virginia & Merck KGaA.
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Journal ArticleDOI
JAM-1 is a ligand of the beta(2) integrin LFA-1 involved in transendothelial migration of leukocytes.
Georg Ostermann,Kim S. C. Weber,Alma Zernecke,Andreas Schröder,Christian Weber,Christian Weber +5 more
TL;DR: JAM-1 is a counter-receptor for LFA-1 that is ideally situated to guide and control transmigration during leukocyte recruitment and is also a ligand of the β2 integrin lymphocyte function–associated antigen 1.
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RANTES Deposition by Platelets Triggers Monocyte Arrest on Inflamed and Atherosclerotic Endothelium
Philipp von Hundelshausen,Philipp von Hundelshausen,Philipp von Hundelshausen,Kim S. C. Weber,Kim S. C. Weber,Kim S. C. Weber,Yuqing Huo,Yuqing Huo,Yuqing Huo,Amanda E. I. Proudfoot,Amanda E. I. Proudfoot,Amanda E. I. Proudfoot,Peter J. Nelson,Peter J. Nelson,Peter J. Nelson,Klaus Ley,Klaus Ley,Klaus Ley,Christian Weber +18 more
TL;DR: The deposition of RANTES by platelets triggers shear-resistant monocyte arrest on inflamed or atherosclerotic endothelium and may epitomize a novel principle relevant to inflammatory or atherogenic monocyte recruitment from the circulation.
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HMG-CoA Reductase Inhibitors Decrease CD11b Expression and CD11b-Dependent Adhesion of Monocytes to Endothelium and Reduce Increased Adhesiveness of Monocytes Isolated From Patients With Hypercholesterolemia
TL;DR: The reduction ofCD11b expression and inhibition of CD11b-dependent monocyte adhesion to endothelium may crucially contribute to the clinical benefit of HMG-CoA reductase inhibitors in CHD, independent of cholesterol-lowering effects.
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Differential chemokine receptor expression and function in human monocyte subpopulations.
Christian Weber,Kai-Uwe Belge,P. von Hundelshausen,Georg Draude,B Steppich,Matthias Mack,Marion Frankenberger,Kim S. C. Weber,H. W. L. Ziegler-Heitbrock +8 more
TL;DR: Flow cytometric analysis of isolated human monocytes recovered after transendothelial chemotaxis assays revealed that the percentage of CD14+CD16+ cells was dramatically reduced in the fraction migrating toward MCP‐1 compared with the fraction that did not migrate or the input, showing that polarized CCR2 expression was accompanied by a differential chemotactic responsiveness.
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Expression of CCR2 by Endothelial Cells Implications for MCP-1 Mediated Wound Injury Repair and In Vivo Inflammatory Activation of Endothelium
TL;DR: This is the first demonstration of endothelial CCR2 expression ex vivo, inferring its involvement in inflammatory conditions and may have important implications for endothelial wound repair and inflammatory reactions.