Contribution of platelet vs. endothelial VWF to platelet adhesion and hemostasis von KANAJI, S., FAHS, S. A., SHI, Q., HABERICHTER, S. L., MONTGOMERY, R. R.

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An optimized fluorogenic ADAMTS13 assay with increased sensitivity for the investigation of patients with thrombotic thrombocytopenic purpura von Muia, J., Gao, W., Haberichter, S. L., Dolatshahi, L., Zhu, J., Westfield, L. A., Covill, S. C., Friedman, K. D., Sadler, J. E.

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Clinical and laboratory phenotype variability in type 2M von Willebrand disease von Doruelo, A. L., Haberichter, S. L., Christopherson, P. A., Boggio, L. N., Gupta, S., Lentz, S. R., Shapiro, A. D., Montgomery, R. R., Flood, V. H.

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Critical von Willebrand factor A1 domain residues influence type VI collagen binding von FLOOD, V. H., GILL, J. C., CHRISTOPHERSON, P. A., BELLISSIMO, D. B., FRIEDMAN, K. D., HABERICHTER, S. L., LENTZ, S. R., MONTGOMERY, R. R.

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Comparison of type I, type III and type VI collagen binding assays in diagnosis of von Willebrand disease von FLOOD, V. H., GILL, J. C., CHRISTOPHERSON, P. A., WREN, J. S., FRIEDMAN, K. D., HABERICHTER, S. L., HOFFMANN, R. G., MONTGOMERY, R. R.

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von Willebrand factor propeptide to antigen ratio identifies platelet activation and reduced von Willebrand factor survival phenotype in mice von Jacobi, P. M., Kanaji, S., Jakab, D., Gehrand, A. L., Johnsen, J. M., Haberichter, S. L.

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Use of a mouse model to elucidate the phenotypic effects of the von Willebrand factor cleavage mutants, Y1605A/M1606A and R1597W von PRUSS, C. M., GOLDER, M., BRYANT, A., HEGADORN, C., HABERICHTER, S., LILLICRAP, D.

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Genome‐wide studies of von Willebrand factor propeptide identify loci contributing to variation in propeptide levels and von Willebrand factor clearance von Ozel, A. B., McGee, B., Siemieniak, D., Jacobi, P. M., Haberichter, S. L., Brody, L. C., Mills, J. L., Molloy, A. M., Ginsburg, D., Li, J. Z., Desch, K. C.

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Variability in platelet- and collagen-binding defects in type 2M von Willebrand disease von Larsen, D. M., Haberichter, S. L., Gill, J. C., Shapiro, A. D., Flood, V. H.

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Regulated release of VWF and FVIII and the biologic implications von Haberichter, S.L., Shi, Q., Montgomery, R.R.

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Reduced von Willebrand factor secretion is associated with loss of Weibel–Palade body formation von CASTAMAN, G., GIACOMELLI, S. H., JACOBI, P. M., OBSER, T., BUDDE, U., RODEGHIERO, F., SCHNEPPENHEIM, R., HABERICHTER, S. L.

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Homozygous type 2N R854W von Willebrand factor is poorly secreted and causes a severe von Willebrand disease phenotype von CASTAMAN, G., GIACOMELLI, S. H., JACOBI, P., OBSER, T., BUDDE, U., RODEGHIERO, F., HABERICHTER, S. L., SCHNEPPENHEIM, R.

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Genetic alteration of the D2 domain abolishes von Willebrand factor multimerization and trafficking into storage von HABERICHTER, S. L., ALLMANN, A. M., JOZWIAK, M. A., MONTGOMERY, R. R., GILL, J. C.

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Standardization of von Willebrand factor propeptide: value assignment to the WHO 6th IS Factor VIII/von Willebrand factor, plasma (07/316) von HUBBARD, A. R., HAMILL, M., EIKENBOOM, H. C. J., MONTGOMERY, R. R., MERTENS, K., HABERICHTER, S.

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von Willebrand's disease diagnosis and laboratory issues von CASTAMAN, G., MONTGOMERY, R. R., MESCHENGIESER, S. S., HABERICHTER, S. L., WOODS, A. I., LAZZARI, M. A.

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Induction of megakaryocytes to synthesize and store a releasable pool of human factor VIII von Wilcox, D. A., Shi, Q., Nurden, P., Haberichter, S. L., Rosenberg, J. B., Johnson, B. D., Nurden, A. T., Ii, G. C. White, Montgomery, R. R.

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A GPI‐anchored co‐receptor for tissue factor pathway inhibitor controls its intracellular trafficking and cell surface expression von MARONEY, S. A., CUNNINGHAM, A. C., FERREL, J., HU, R., HABERICHTER, S., MANSBACH, C. M., BRODSKY, R. A., DIETZEN, D. J., MAST, A. E.

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Von Willebrand factor storage and multimerization: 2 independent intracellular processes von Haberichter, Sandra L., Fahs, Scot A., Montgomery, Robert R.

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OC 60.1 Delineating VonWillebrand Factor Genetic Variants in Patients with a Von Willebrand Disease Diagnosis von Christopherson, P., Flood, V., Haberichter, S., Sadler, B., Di Paola, J., Montgomery, R.

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PB0833 VWF Expression Mostly Confirms Genetic Prediction Algorithms in Type 1 VWD Variants von Christopherson, P., Flood, V., Sadler, B., Di Paola, J., Montgomery, R., Haberichter, S.

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