检索结果 - Simon Stritt

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  1. 1
    Homeostatic maintenance of the lymphatic vasculature

    Homeostatic maintenance of the lymphatic vasculature 由 Simon Stritt, Katarzyna Koltowska, Taija Mäkinen

    出版 2021
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  2. 2
    Inherited platelet diseases with normal platelet count: phenotypes, genotypes and diagnostic strategy

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

    出版 2020
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  3. 3
    Rap1-GTP–interacting adaptor molecule (RIAM) is dispensable for platelet integrin activation and function in mice

    Rap1-GTP–interacting adaptor molecule (RIAM) is dispensable for platelet integrin activation and function in mice 由 Simon Stritt, Karen Wolf, Viola Lorenz, Timo Vögtle, Shuchi Gupta, Michael R. Bösl, Bernhard Nieswandt

    出版 2014
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    Artigo
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  4. 4
    EphrinB2-EphB4 signalling provides Rho-mediated homeostatic control of lymphatic endothelial cell junction integrity

    EphrinB2-EphB4 signalling provides Rho-mediated homeostatic control of lymphatic endothelial cell junction integrity 由 Maike Frye, Simon Stritt, Henrik Ortsäter, Magda Nohemí Hernández-Vásquez, Mika Kaakinen, Andres Vicente, John Wiseman, Lauri Eklund, Jorge L. Martı́nez-Torrecuadrada, Dietmar Vestweber, Taija Mäkinen

    出版 2020
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    Artigo
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  5. 5
    Immune-interacting lymphatic endothelial subtype at capillary terminals drives lymphatic malformation

    Immune-interacting lymphatic endothelial subtype at capillary terminals drives lymphatic malformation 由 Milena Petkova, Marle Kraft, Simon Stritt, Inés Martínez‐Corral, Henrik Ortsäter, Michael Vanlandewijck, Bojana Jakic, Eulàlia Baselga, Sandra D. Castillo, Mariona Graupera, Christer Betsholtz, Taija Mäkinen

    出版 2023
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    Artigo
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  6. 6
    Megakaryocyte-specific Profilin1-deficiency alters microtubule stability and causes a Wiskott-Aldrich syndrome-like platelet defect.

    Megakaryocyte-specific Profilin1-deficiency alters microtubule stability and causes a Wiskott-Aldrich syndrome-like platelet defect. 由 Markus Bender, Simon Stritt, Paquita Nurden, Judith M.M. van Eeuwijk, Barbara Zieger, Karim Kentouche, Harald Schulze, Henner Morbach, David Stegner, Katrin G. Heinze, Sebastian Dütting, Shuchi Gupta, Walter Witke, Hervé Falet, Alain Fischer, John H. Hartwig, Bernhard Nieswandt

    出版 2014
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  7. 7
    Megakaryocyte-specific Profilin1-deficiency alters microtubule stability and causes a Wiskott–Aldrich syndrome-like platelet defect

    Megakaryocyte-specific Profilin1-deficiency alters microtubule stability and causes a Wiskott–Aldrich syndrome-like platelet defect 由 Markus Bender, Simon Stritt, Paquita Nurden, Judith M.M. van Eeuwijk, Barbara Zieger, Karim Kentouche, Harald Schulze, Henner Morbach, David Stegner, Katrin G. Heinze, Sebastian Dütting, Shuchi Gupta, Walter Witke, Hervé Falet, Alain Fischer, John H. Hartwig, Bernhard Nieswandt

    出版 2014
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  8. 8
    Defects in TRPM7 channel function deregulate thrombopoiesis through altered cellular Mg2+ homeostasis and cytoskeletal architecture

    Defects in TRPM7 channel function deregulate thrombopoiesis through altered cellular Mg2+ homeostasis and cytoskeletal architecture 由 Simon Stritt, Paquita Nurden, Rémi Favier, Marie Favier, Silvia Ferioli, Sanjeev Kiran Gotru, Judith M.M. van Eeuwijk, Harald Schulze, Alan T. Nurden, Michele P. Lambert, Ernest Turro, Stephanie Burger‐Stritt, Masayuki Matsushita, Lorenz Mittermeier, Paola Ballerini, Susanna Zierler, Michael Laffan, Vladimir Chubanov, Thomas Gudermann, Bernhard Nieswandt, Attila Braun

    出版 2016
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    Artigo
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  9. 9
    TRPM7 Kinase Controls Calcium Responses in Arterial Thrombosis and Stroke in Mice

    TRPM7 Kinase Controls Calcium Responses in Arterial Thrombosis and Stroke in Mice 由 Sanjeev Kiran Gotru, Wenchun Chen, Peter Kraft, Isabelle C. Becker, Karen Wolf, Simon Stritt, Susanna Zierler, Heike M. Hermanns, Deviyani M. Rao, Anne‐Laure Perraud, Carsten Schmitz, René P. Zahedi, Peter J. Noy, Michael G. Tomlinson, Thomas Dandekar, Masayuki Matsushita, Vladimir Chubanov, Thomas Gudermann, Guido Stoll, Bernhard Nieswandt, Attila Braun

    出版 2017
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    Artigo
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  10. 10
    Lymphangiogenesis requires Ang2/Tie/PI3K signaling for VEGFR3 cell-surface expression

    Lymphangiogenesis requires Ang2/Tie/PI3K signaling for VEGFR3 cell-surface expression 由 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

    出版 2022
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  11. 11
    A Cdc42/RhoA regulatory circuit downstream of glycoprotein Ib guides transendothelial platelet biogenesis

    A Cdc42/RhoA regulatory circuit downstream of glycoprotein Ib guides transendothelial platelet biogenesis 由 Sebastian Dütting, Frédérique Gaits‐Iacovoni, David Stegner, Michael P. Popp, Adrien Antkowiak, Judith M.M. van Eeuwijk, Paquita Nurden, Simon Stritt, Tobias Heib, Katja Aurbach, Oğuzhan Angay, Deya Cherpokova, Niels Heinz, Ayesha Baig, Maximilian G. Gorelashvili, Frank M. Gerner, Katrin G. Heinze, Jerry Ware, Georg Krohne, Zaverio M. Ruggeri, Alan T. Nurden, Harald Schulze, Ute Modlich, Irina Pleines, Cord Brakebusch, Bernhard Nieswandt

    出版 2017
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  12. 12
    The SARS-CoV-2 receptor ACE2 is expressed in mouse pericytes but not endothelial cells: Implications for COVID-19 vascular research

    The SARS-CoV-2 receptor ACE2 is expressed in mouse pericytes but not endothelial cells: Implications for COVID-19 vascular research 由 Lars Muhl, Liqun He, Ying Sun, Maarja Andaloussi Mäe, Riikka Pietilä, Jianping Liu, Guillem Genové, Lei Zhang, Yuan Xie, Stefanos Leptidis, Giuseppe Mocci, Simon Stritt, Ahmed Osman, Andrey Anisimov, Karthik Amudhala Hemanthakumar, Markus Räsänen, Emil M. Hansson, Johan Björkegren, Michael Vanlandewijck, Klas Blomgren, Taija Mäkinen, Xiaorong Peng, Yizhou Hu, Patrik Ernfors, Thomas D. Arnold, Kari Alitalo, Urban Lendahl, Christer Betsholtz

    出版 2022
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  13. 13
    A gain-of-function variant in DIAPH1 causes dominant macrothrombocytopenia and hearing loss

    A gain-of-function variant in DIAPH1 causes dominant macrothrombocytopenia and hearing loss 由 Simon Stritt, Paquita Nurden, Ernest Turro, Daniel Greene, Sjoert B.G. Jansen, Sarah K. Westbury, R. Petersen, William J. Astle, Sandrine Marlin, Tadbir K. Bariana, Myrto Kostadima, Claire Lentaigne, Stephanie Maiwald, Sofia Papadia, Anne M. Kelly, Jonathan Stephens, Christopher J. Penkett, Sofie Ashford, Salih Tuna, Steve Austin, Tamam Bakchoul, Peter Collins, Rémi Favier, Michele P. Lambert, Mary Mathias, Carolyn M. Millar, Rutendo Mapeta, David J. Perry, Sol Schulman, Ilenia Simeoni, Chantal Thys, Keith Gomez, Wendy N. Erber, Kathleen Stirrups, Augusto Rendon, John R. Bradley, Chris Van Geet, F. Lucy Raymond, Michael Laffan, Alan T. Nurden, Bernhard Nieswandt, Sylvia Richardson, Kathleen Freson, Willem H. Ouwehand, Andrew Mumford

    出版 2016
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