检索结果 - Reinhard Schneppenheim

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  1. 1
    von Willebrand factor: the complex molecular genetics of a multidomain and multifunctional protein

    von Willebrand factor: the complex molecular genetics of a multidomain and multifunctional protein 由 Reinhard Schneppenheim, Ulrich Budde

    出版 2011
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  2. 2
    Update on von Willebrand factor multimers

    Update on von Willebrand factor multimers 由 Marcus Stockschlaeder, Reinhard Schneppenheim, Ulrich Budde

    出版 2014
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  3. 3
    von Willebrand factor mutation enhancing interaction with platelets in patients with normal multimeric structure.

    von Willebrand factor mutation enhancing interaction with platelets in patients with normal multimeric structure. 由 Lars Holmberg, Judith Dent, Reinhard Schneppenheim, Ulrich Budde, Jerry Ware, Z M Ruggeri

    出版 1993
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  4. 4
    Impact of mutations in the von Willebrand factor A2 domain on ADAMTS13-dependent proteolysis

    Impact of mutations in the von Willebrand factor A2 domain on ADAMTS13-dependent proteolysis 由 Wolf Hassenpflug, Ulrich Budde, Tobias Obser, Dorothea Angerhaus, E. Drewke, Sonja Schneppenheim, Reinhard Schneppenheim

    出版 2005
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  5. 5
    Platelet‐dependent von Willebrand factor activity. Nomenclature and methodology: communication from the SSC of the ISTH

    Platelet‐dependent von Willebrand factor activity. Nomenclature and methodology: communication from the SSC of the ISTH 由 Imre Bodó, Jeroen Eikenboom, Robert R. Montgomery, J. Patzke, Reinhard Schneppenheim, Jorge Di Paola

    出版 2015
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  6. 6
    Mutation spectrum in children with primary hemophagocytic lymphohistiocytosis: molecular and functional analyses ofPRF1, UNC13D, STX11, andRAB27A

    Mutation spectrum in children with primary hemophagocytic lymphohistiocytosis: molecular and functional analyses ofPRF1, UNC13D, STX11, andRAB27A 由 Udo zur Stadt, Karin Beutel, Susanne Kolberg, Reinhard Schneppenheim, H. Kabisch, Gritta Janka, Hans Christian Hennies

    出版 2005
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  7. 7
    Defective dimerization of von Willebrand factor subunits due to a Cys-> Arg mutation in type IID von Willebrand disease.

    Defective dimerization of von Willebrand factor subunits due to a Cys-> Arg mutation in type IID von Willebrand disease. 由 Reinhard Schneppenheim, Jacqueline Brassard, S. Krey, Ulrich Budde, T J Kunicki, Lars Holmberg, Jerry Ware, Zaverio M. Ruggeri

    出版 1996
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  8. 8
    A cluster of mutations in the D3 domain of von Willebrand factor correlates with a distinct subgroup of von Willebrand disease: type 2A/IIE

    A cluster of mutations in the D3 domain of von Willebrand factor correlates with a distinct subgroup of von Willebrand disease: type 2A/IIE 由 Reinhard Schneppenheim, Jan Michiels, Tobias Obser, Florian Oyen, Antje Pieconka, Sonja Schneppenheim, Kerstin Will, Barbara Zieger, Ulrich Budde

    出版 2010
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  9. 9
    Shear‐induced unfolding activates von Willebrand factor A2 domain for proteolysis

    Shear‐induced unfolding activates von Willebrand factor A2 domain for proteolysis 由 Carsten Baldauf, Reinhard Schneppenheim, Wolfram Stacklies, Tobias Obser, Antje Pieconka, Sonja Schneppenheim, Ulrich Budde, Jihan Zhou, Frauke Gräter

    出版 2009
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  10. 10
    Shear-Induced Unfolding and Enzymatic Cleavage of Full-Length VWF Multimers

    Shear-Induced Unfolding and Enzymatic Cleavage of Full-Length VWF Multimers 由 Svenja Lippok, Matthias Radtke, Tobias Obser, Lars Kleemeier, Reinhard Schneppenheim, Ulrich Budde, Roland R. Netz, Joachim O. Rädler

    出版 2016
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  11. 11
    Inflammation-associated ADAMTS13 deficiency promotes formation of ultra-large von Willebrand factor

    Inflammation-associated ADAMTS13 deficiency promotes formation of ultra-large von Willebrand factor 由 Clemens L. Bockmeyer, Ralf A. Claus, Ulrich Budde, Karim Kentouche, Reinhard Schneppenheim, Wolfgang Lösche, Konrad Reinhart, Frank M. Brunkhorst

    出版 2007
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  12. 12
    Germline variants in SMARCB1 and other members of the BAF chromatin-remodeling complex across human disease entities: a meta-analysis

    Germline variants in SMARCB1 and other members of the BAF chromatin-remodeling complex across human disease entities: a meta-analysis 由 Till Holsten, Susanne Bens, Florian Oyen, Karolina Nemes, Martin Hasselblatt, Uwe Kordes, Reiner Siebert, Michael C. Frühwald, Reinhard Schneppenheim, Ulrich Schüller

    出版 2018
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  13. 13
    Cribriform Neuroepithelial Tumor (CRINET): A Nonrhabdoid Ventricular Tumor With INI1 Loss and Relatively Favorable Prognosis

    Cribriform Neuroepithelial Tumor (CRINET): A Nonrhabdoid Ventricular Tumor With INI1 Loss and Relatively Favorable Prognosis 由 Martin Hasselblatt, Florian Oyen, Stefan Gesk, Uwe Kordes, Brigitte Wrede, Markus Bergmann, Hansjörg Schmid, Michael C. Frühwald, Reinhard Schneppenheim, Reiner Siebert, Werner Paulus

    出版 2009
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  14. 14
    Denosumab: a potential new and innovative treatment option for aneurysmal bone cysts

    Denosumab: a potential new and innovative treatment option for aneurysmal bone cysts 由 Tobias Lange, Christoph Stehling, Birgit Fröhlich, Mark Klingenhöfer, Philip Kunkel, Reinhard Schneppenheim, Gabriele Escherich, Georg Gosheger, Jendrik Hardes, Heribert Jürgens, Tobias L. Schulte

    出版 2013
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  15. 15
    von Willebrand Factor Directly Interacts With DNA From Neutrophil Extracellular Traps

    von Willebrand Factor Directly Interacts With DNA From Neutrophil Extracellular Traps 由 Sandra Grässle, Volker Huck, K.I. Pappelbaum, Christian Gorzelanny, Camilo Aponte‐Santamaría, Carsten Baldauf, Frauke Gräter, Reinhard Schneppenheim, Tobias Obser, Stefan W. Schneider

    出版 2014
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  16. 16
    Linkage of familial hemophagocytic lymphohistiocytosis (FHL) type-4 to chromosome 6q24 and identification of mutations in syntaxin 11

    Linkage of familial hemophagocytic lymphohistiocytosis (FHL) type-4 to chromosome 6q24 and identification of mutations in syntaxin 11 由 Udo zur Stadt, Susanne Schmidt, Brigitte Kasper, Karin Beutel, A. Sarper Diler, Jan‐Inge Henter, H. Kabisch, Reinhard Schneppenheim, Peter Nürnberg, Gritta Janka, Hans Christian Hennies

    出版 2005
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  17. 17
    VWF propeptide and ratios between VWF, VWF propeptide, and FVIII in the characterization of type 1 von Willebrand disease

    VWF propeptide and ratios between VWF, VWF propeptide, and FVIII in the characterization of type 1 von Willebrand disease 由 Jeroen Eikenboom, Augusto B. Federici, Richard Dirven, Giancarlo Castaman, Francesco Rodeghiero, Ulrich Budde, Reinhard Schneppenheim, Javier Batlle, Maria Teresa Canciani, Jenny Goudemand, I. R. Peake, Anne Goodeve

    出版 2013
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  18. 18
    Force-Sensitive Autoinhibition of the von Willebrand Factor Is Mediated by Interdomain Interactions

    Force-Sensitive Autoinhibition of the von Willebrand Factor Is Mediated by Interdomain Interactions 由 Camilo Aponte‐Santamaría, Volker Huck, Sandra Posch, Agnieszka K. Bronowska, Sandra Grässle, Maria A. Brehm, Tobias Obser, Reinhard Schneppenheim, Peter Hinterdorfer, Stefan W. Schneider, Carsten Baldauf, Frauke Gräter

    出版 2015
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  19. 19
    Germline Nonsense Mutation and Somatic Inactivation of SMARCA4/BRG1 in a Family with Rhabdoid Tumor Predisposition Syndrome

    Germline Nonsense Mutation and Somatic Inactivation of SMARCA4/BRG1 in a Family with Rhabdoid Tumor Predisposition Syndrome 由 Reinhard Schneppenheim, Michael C. Frühwald, Stefan Gesk, Martin Hasselblatt, Astrid Jeibmann, Uwe Kordes, Markus Kreuz, Ivo Leuschner, Jose Ignacio Martin Subero, Tobias Obser, Florian Oyen, Inga Vater, Reiner Siebert

    出版 2010
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  20. 20
    Ultralarge von Willebrand Factor Fibers Mediate Luminal <i>Staphylococcus aureus</i> Adhesion to an Intact Endothelial Cell Layer Under Shear Stress

    Ultralarge von Willebrand Factor Fibers Mediate Luminal <i>Staphylococcus aureus</i> Adhesion to an Intact Endothelial Cell Layer Under Shear Stress 由 K.I. Pappelbaum, Christian Gorzelanny, Sandra Grässle, Jan Suckau, Matthias W. Laschke, Markus Bischoff, Corinne Bauer, Marina Schorpp‐Kistner, Christopher Weidenmaier, Reinhard Schneppenheim, Tobias Obser, Bhanu Sinha, Stefan W. Schneider

    出版 2013
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