Søgeresultater - Simon Stritt

Inherited platelet diseases with normal platelet count: phenotypes, genotypes and diagnostic strategy af Paquita Nurden, Simon Stritt, Remi Favier, Alan T. Nurden

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APOLD1 loss causes endothelial dysfunction involving cell junctions, cytoskeletal architecture, and Weibel-Palade bodies, while disrupting hemostasis af Simon Stritt, Paquita Nurden, Alan T. Nurden, Jean-François Schved, Jean-Claude Bordet, Maguelonne Roux, Marie-Christine Alessi, David-Alexandre Trégouët, Taija Mäkinen, Muriel Giansily-Blaizot

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Coactosin-like 1 integrates signaling critical for shear-dependent thrombus formation in mouse platelets af Inga Scheller, Simon Stritt, Sarah Beck, Bing Peng, Irina Pleines, Katrin G. Heinze, Attila Braun, Oliver Otto, Robert Ahrends, Albert Sickmann, Markus Bender, Bernhard Nieswandt

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Profilin 1–mediated cytoskeletal rearrangements regulate integrin function in mouse platelets af Simon Stritt, Inga Birkholz, Sarah Beck, Simona Sorrentino, K. Tanuj Sapra, Julien Viaud, Johannes Heck, Frédérique Gaits-Iacovoni, Harald Schulze, Xiaoping Du, John H. Hartwig, Attila Braun, Markus Bender, Ohad Medalia, Bernhard Nieswandt

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Lymphangiogenesis requires Ang2/Tie/PI3K signaling for VEGFR3 cell-surface expression af Emilia A. Korhonen, Aino Murtomäki, Sawan Kumar Jha, Andrey Anisimov, Anne Pink, Yan Zhang, Simon Stritt, Inam Liaqat, Lukas Stanczuk, Laura Alderfer, Zhiliang Sun, Emmi Kapiainen, Abhishek Singh, Ibrahim Sultan, Anni Lantta, Veli-Matti Leppänen, Lauri Eklund, Yulong He, Hellmut G. Augustin, Kari Vaahtomeri, Pipsa Saharinen, Taija Mäkinen, Kari Alitalo

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