Localization of Disulfide Bonds in the Cystine Knot Domain of Human von Willebrand Factor von Katsumi, Akira, Tuley, Elodee A., Bodó, Imre, Sadler, J. Evan

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Structure of the gene for human von Willebrand factor von MANCUSO, D. J, TULEY, E. A, WESTFIELD, L. A, WORRALL, N. K, SHELTON-INLOES, B. B, SORACE, J. M, ALEVY, Y. G, SADLER, J. E

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Dominant type 1 von Willebrand disease caused by mutated cysteine residues in the D3 domain of von Willebrand factor von EIKENBHOOM, J. C. J, MATSUSHITA, T, REITSMA, P. H, TULEY, E. A, CASTAMAN, G, BRIËT, E, EVAN SADLER, J

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Disulfide bonds required to assemble functional von Willebrand factor multimers von ZHENGYU DONG, THOMA, R. S, CRIMMINS, D. L, MCCOURT, D. W, TULEY, E. A, SADLER, J. E

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Expression of von Willebrand Factor "Normandy": An Autosomal Mutation that Mimics Hemophilia A von Tuley, Elodee A., Gaucher, Christine, Jorieux, Sylvie, Worrall, Neil K., Sadler, J. Evan, Mazurier, Claudine

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Incomplete Embryonic Lethality and Fatal Neonatal Hemorrhage Caused by Prothrombin Deficiency in Mice von Xue, Jiachun, Wu, Qingyu, Westfield, Lisa A., Tuley, Elodee A., Lu, Deshun, Zhang, Qing, Shim, Kyuhwan, Zheng, Xinglong, Sadler, J. Evan

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Type IIB mutation His-505-->Asp implicates a new segment in the control of von Willebrand factor binding to platelet glycoprotein Ib von RABINOWITZ, I, RANDI, A. M, SHINDLER, K. S, TULEY, E. A, RUSTAGI, P. K, SADLER, J. E

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Human von Willebrand factor gene and pseudogene: structural analysis and differentiation by polymerase chain reaction von Mancuso, David J, Tuley, Elodee A, Westfield, Lisa A, Lester-Mancuso, Teresa L, Le Beau, Michelle M, Sorace, James M, Sadler, J. Evan

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The Mutation Arg (53) → Trp Causes von Willebrand Disease Normandy by Abolishing Binding to Factor VIII. Studies With Recombinant von Willebrand Factor von Jorieux, Sylvie, Tuley, Elodee A., Gaucher, Christine, Mazurier, Claudine, Sadler, J. Evan

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Protein Z, protein Z-dependent protease inhibitor (serpinA10), and the acute-phase response von Girard, T J, Lasky, N M, Tuley, E A, Broze, Jr, G J

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Severe Type III von Willebrand's Disease Caused by Deletion of Exon 42 of the von Willebrand Factor Gene: Family Studies That Identify Carriers of the Condition and a Compound Hete... von Peake, Ian R., Liddell, Malcolm B., Moodie, Patricia, Standen, Graham, Mancuso, David J., Tuley, Elodee A., Westfield, Lisa A., Sorace, James M., Sadler, J. Evan, Verweij, Cornelis L., Bloom, Arthur L.

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Protein Z, protein Z‐dependent protease inhibitor (serpinA10), and the acute‐phase response von GIRARD, T. J., LASKY, N. M., TULEY, E. A., BROZE, G. J.

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Recombinant von Willebrand factor Arg578-->Gln. A type IIB von Willebrand disease mutation affects binding to glycoprotein Ib but not to collagen or heparin von RANDI, A. M, JORIEUX, S, TULEY, E. A, MAZURIER, C, SADLER, J. E

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Von Willebrand Disease Type B: A Missense Mutation Selectively Abolishes Ristocetin-Induced von Willebrand Factor Binding to Platelet Glycoprotein Ib von Rabinowitz, Ian, Tuley, Elodee A., Mancuso, David J., Randi, Anna M., Firkin, Barry G., Howard, Margaret A., Sadler, J. Evan

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Cleavage of the ADAMTS13 Propeptide Is Not Required for Protease Activity von Majerus, Elaine M., Zheng, Xinglong, Tuley, Elodee A., Sadler, J. Evan

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Type 1 von Willebrand disease mutation Cys1149Arg causes intracellular retention and degradation of heterodimers: a possible general mechanism for dominant mutations of oligomeric... von Bodó, Imre, Katsumi, Akira, Tuley, Elodee A., Eikenboom, Jeroen C.J., Dong, Zhengyu, Sadler, J. Evan

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Recombinant von Willebrand factor Arg super(578) arrow right Gln: A type IIB von Willebrand disease mutation affects binding to glycoprotein Ib but not to collagen or heparin von Randi, A M, Jorieux, S, Tuley, E A, Mazurier, C, Sadler, JE

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Molecular Biology of von Willebrand Factor von SADLER, J. EVAN, MANCUSO, DAVID J., RANDI, ANNA M., TULEY, ELODEE A., WESTFIELD, LISA A.

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Type IIB mutation His-505 arrow right Asp implicates a new segment in the control of von Willebrand factor binding to platelet glycoprotein Ib von Rabinowitz, I, Randi, A M, Shindler, K S, Tuley, E A, Rustagi, P K, Sadler, JE

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Human von Willebrand gene and pseudogene: Structural analysis and differentiation by polymerase chain reaction von Mancuso, D J, Tuley, E A, Westfield, LA, Lester-Mancuso, T L, Le Beau, MM, Sorace, J M, Sadler, JE

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