von Willebrand factor: the old, the new and the unknown von LENTING, P. J., CASARI, C., CHRISTOPHE, O. D., DENIS, C. V.

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Clearance of von Willebrand factor von Casari, C., Lenting, P. J., Wohner, N., Christophe, O. D., Denis, C. V.

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The disappearing act of factor VIII von LENTING, P. J., CHRISTOPHE, O. D., GUÉGUEN, P.

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Increased metastatic potential of tumor cells in von Willebrand factor‐deficient mice von TERRAUBE, V., PENDU, R., BARUCH, D., GEBBINK, M. F. B. G., MEYER, D., LENTING, P. J., DENIS, C. V.

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Circulatory support devices: fundamental aspects and clinical management of bleeding and thrombosis von Susen, S., Rauch, A., Van Belle, E., Vincentelli, A., Lenting, P. J.

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Cysteine‐mutations in von Willebrand factor associated with increased clearance von SCHOOTEN, C. J., TJERNBERG, P., WESTEIN, E., TERRAUBE, V., CASTAMAN, G., MOURIK, J. A., HOLLESTELLE, M. J., VOS, H. L., BERTINA, R. M., BERG, H. M., EIKENBOOM, J. C. J., LENTING, P. J., DENIS, C. V.

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Factor VIII and von Willebrand factor are ligands for the carbohydrate-receptor Siglec-5 von Pegon, Julie N, Kurdi, Mohamad, Casari, Caterina, Odouard, Soline, Denis, Cécile V, Christophe, Olivier D, Lenting, Peter J

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Shear stress‐independent binding of von Willebrand factor‐type 2B mutants p.R1306Q & p.V1316M to LRP1 explains their increased clearance von Wohner, N., Legendre, P., Casari, C., Christophe, O. D., Lenting, P. J., Denis, C. V.

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Clearance mechanisms of von Willebrand factor and factor VIII von LENTING, P. J., VAN SCHOOTEN, C. J. M., DENIS, C. V.

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LRP/Amyloid β-Peptide Interaction Mediates Differential Brain Efflux of Aβ Isoforms von Deane, Rashid, Wu, Zhenhua, Sagare, Abhay, Davis, Judianne, Du Yan, Shi, Hamm, Katie, Xu, Feng, Parisi, Margaret, LaRue, Barbra, Hu, Hong Wei, Spijkers, Patricia, Guo, Huang, Song, Xiaomei, Lenting, Peter J., Van Nostrand, William E., Zlokovic, Berislav V.

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Circulatory support devices: fundamental aspects and clinical management of bleeding and thrombosis von Susen, S., Rauch, A., Van Belle, E., Vincentelli, A., Lenting, P.J.

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The von Willebrand factor self‐association is modulated by a multiple domain interaction von ULRICHTS, H., VANHOORELBEKE, K., GIRMA, J. P., LENTING, P. J., VAUTERIN, S., DECKMYN, H.

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Identification of a binding site for blood coagulation factor IXa on the light chain of human factor VIII von LENTING, P. J, DONATH, M.-J. S. H, VAN MOURIK, J. A, MERTENS, K

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Characterization of the interaction between von Willebrand factor and osteoprotegerin von SHAHBAZI, S., LENTING, P. J., FRIBOURG, C., TERRAUBE, V., DENIS, C. V., CHRISTOPHE, O. D.

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ADAMTS‐13: double trouble for von Willebrand factor von LENTING, P. J., RASTEGARLARI, G.

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The effect of exercise on von Willebrand factor and ADAMTS‐13 in individuals with type 1 and type 2B von Willebrand disease von STAKIW, J., BOWMAN, M., HEGADORN, C., PRUSS, C., NOTLEY, C., GROOT, E., LENTING, P. J., RAPSON, D., LILLICRAP, D., JAMES, P.

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von Willebrand factor propeptide and the occurrence of a first ischemic stroke von Van SCHIE, M. C., DE MAAT, M. P.M., DIPPEL, D. W.J., De GROOT, P. G., LENTING, P. J., LEEBEEK, F. W. G., HOLLESTELLE, M. J.

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von Willebrand factor A1 domain: stuck in the middle von LENTING, P. J., DENIS, C. V.

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The Light Chain of Factor VIII Comprises a Binding Site for Low Density Lipoprotein Receptor-related Protein von Lenting, Peter J., Neels, Jaap G., van den Berg, Birgit M.M., Clijsters, Patrick P.F.M., Meijerman, Daniel W.E., Pannekoek, Hans, van Mourik, Jan A., Mertens, Koen, van Zonneveld, Anton-Jan

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Regulation of von Willebrand factor-platelet interactions von Lenting, Peter J., Pegon, Julie N., Groot, Evelyn, de Groot, Philip G.

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