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Tuley, E. A., Gaucher, C., Jorieux, S., Worrall, N. K., Sadler, J. E., Mazurier, C. (1991) Expression of von Willebrand factor "Normandy": an autosomal mutation that mimics hemophilia A. Proceedings of the National Academy of Sciences, 88 (14) 6377-6381 doi:10.1073/pnas.88.14.6377

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Reference TypeJournal (article/letter/editorial)
TitleExpression of von Willebrand factor "Normandy": an autosomal mutation that mimics hemophilia A.
JournalProceedings of the National Academy of Sciences
AuthorsTuley, E. A.Author
Gaucher, C.Author
Jorieux, S.Author
Worrall, N. K.Author
Sadler, J. E.Author
Mazurier, C.Author
Year1991 (July 15)Volume88
Issue14
PublisherProceedings of the National Academy of Sciences
DOIdoi:10.1073/pnas.88.14.6377Search in ResearchGate
Generate Citation Formats
Mindat Ref. ID1498658Long-form Identifiermindat:1:5:1498658:9
GUID0
Full ReferenceTuley, E. A., Gaucher, C., Jorieux, S., Worrall, N. K., Sadler, J. E., Mazurier, C. (1991) Expression of von Willebrand factor "Normandy": an autosomal mutation that mimics hemophilia A. Proceedings of the National Academy of Sciences, 88 (14) 6377-6381 doi:10.1073/pnas.88.14.6377
Plain TextTuley, E. A., Gaucher, C., Jorieux, S., Worrall, N. K., Sadler, J. E., Mazurier, C. (1991) Expression of von Willebrand factor "Normandy": an autosomal mutation that mimics hemophilia A. Proceedings of the National Academy of Sciences, 88 (14) 6377-6381 doi:10.1073/pnas.88.14.6377
In(1991, July) Proceedings of the National Academy of Sciences Vol. 88 (14) Proceedings of the National Academy of Sciences

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Rabinowitz, I., Tuley, E. A., Mancuso, D. J., Randi, A. M., Firkin, B. G., Howard, M. A., Sadler, J. E. (1992) von Willebrand disease type B: a missense mutation selectively abolishes ristocetin-induced von Willebrand factor binding to platelet glycoprotein Ib. Proceedings of the National Academy of Sciences, 89 (20) 9846-9849 doi:10.1073/pnas.89.20.9846
Gao, W., Anderson, P. J., Majerus, E. M., Tuley, E. A., Sadler, J. E. (2006) Exosite interactions contribute to tension-induced cleavage of von Willebrand factor by the antithrombotic ADAMTS13 metalloprotease. Proceedings of the National Academy of Sciences, 103 (50) 19099-19104 doi:10.1073/pnas.0607264104
Nichols, W. C., Lyons, S. E., Harrison, J. S., Cody, R. L., Ginsburg, D. (1991) Severe von Willebrand disease due to a defect at the level of von Willebrand factor mRNA expression: detection by exonic PCR-restriction fragment length polymorphism analysis. Proceedings of the National Academy of Sciences, 88 (9) 3857-3861 doi:10.1073/pnas.88.9.3857
Cooney, K. A., Lyons, S. E., Ginsburg, D. (1992) Functional analysis of a type IIB von Willebrand disease missense mutation: increased binding of large von Willebrand factor multimers to platelets. Proceedings of the National Academy of Sciences, 89 (7) 2869-2872 doi:10.1073/pnas.89.7.2869
Yao, S. N., Wilson, J. M., Nabel, E. G., Kurachi, S., Hachiya, H. L., Kurachi, K. (1991) Expression of human factor IX in rat capillary endothelial cells: toward somatic gene therapy for hemophilia B. Proceedings of the National Academy of Sciences, 88 (18) 8101-8105 doi:10.1073/pnas.88.18.8101
Miller, J. L., Cunningham, D., Lyle, V. A., Finch, C. N. (1991) Mutation in the gene encoding the alpha chain of platelet glycoprotein Ib in platelet-type von Willebrand disease. Proceedings of the National Academy of Sciences, 88 (11) 4761-4765 doi:10.1073/pnas.88.11.4761
Brinkhous, K. M., Hedner, U., Garris, J. B., Diness, V., Read, M. S. (1989) Effect of recombinant factor VIIa on the hemostatic defect in dogs with hemophilia A, hemophilia B, and von Willebrand disease. Proceedings of the National Academy of Sciences, 86 (4) 1382-1386 doi:10.1073/pnas.86.4.1382
Emiliani, S., Van Lint, C., Fischle, W., Paras, P., Ott, M., Brady, J., Verdin, E. (1996) A point mutation in the HIV-1 Tat responsive element is associated with postintegration latency. Proceedings of the National Academy of Sciences, 93 (13) 6377-6381 doi:10.1073/pnas.93.13.6377
Sadler, J. E., Shelton-Inloes, B. B., Sorace, J. M., Harlan, J. M., Titani, K., Davie, E. W. (1985) Cloning and characterization of two cDNAs coding for human von Willebrand factor. Proceedings of the National Academy of Sciences, 82 (19) 6394-6398 doi:10.1073/pnas.82.19.6394
Eikenboom, J. C., Vink, T., Briet, E., Sixma, J. J., Reitsma, P. H. (1994) Multiple substitutions in the von Willebrand factor gene that mimic the pseudogene sequence. Proceedings of the National Academy of Sciences, 91 (6) 2221-2224 doi:10.1073/pnas.91.6.2221
Ware, J., Dent, J. A., Azuma, H., Sugimoto, M., Kyrle, P. A., Yoshioka, A., Ruggeri, Z. M. (1991) Identification of a point mutation in type IIB von Willebrand disease illustrating the regulation of von Willebrand factor affinity for the platelet membrane glycoprotein Ib-IX receptor. Proceedings of the National Academy of Sciences, 88 (7) 2946-2950 doi:10.1073/pnas.88.7.2946
 
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