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Mirjam G.A. oude Egbrink

Researcher at Maastricht University

Publications -  91
Citations -  5176

Mirjam G.A. oude Egbrink is an academic researcher from Maastricht University. The author has contributed to research in topics: Platelet & Cancer. The author has an hindex of 30, co-authored 84 publications receiving 4360 citations.

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The endothelial glycocalyx: composition, functions, and visualization

TL;DR: A review of state-of-the-art knowledge on the composition and functions of the endothelial glycocalyx can be found in this article, where the contribution of the glyocalyx to diabetes, ischemia/reperfusion, and atherosclerosis is also reviewed.
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Monocyte/macrophage infiltration in tumors : modulators of angiogenesis

TL;DR: A combination therapy in which angiostatic agents are used as well is put forward as a novel strategy to treat cancer.
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Tumor angiogenesis modulates leukocyte-vessel wall interactions in vivo by reducing endothelial adhesion molecule expression.

TL;DR: The regulation of leukocyte-vessel wall interactions by the presence of a tumor may have an impact on the effectiveness of clinical immunotherapeutic treatment protocols, because immune effector cells may not be able to enter tumor tissue.
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Anti-angiogenesis therapy can overcome endothelial cell anergy and promote leukocyte-endothelium interactions and infiltration in tumors

TL;DR: The new angiostatic designer peptide anginex was most potent at overcoming EC anergy; the enhanced leukocyte‐vessel interactions led to an increase in the numbers of tumor infiltrating leukocytes, and the current results suggest that immunotherapy strategies can be improved by combination with anti‐angiogenesis.
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Nebivolol: a third-generation beta-blocker that augments vascular nitric oxide release: endothelial beta(2)-adrenergic receptor-mediated nitric oxide production.

TL;DR: In vivo metabolized nebivolol increases vascular NO production, and this phenomenon involves endothelial beta(2)-adrenergic receptor ligation, with a subsequent rise in endothelial free [Ca(2+)](i) and endothelial NO synthase-dependent NO production.