Sandbox Reserved 1447

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== Function ==
== Function ==
The von Willebrand Factor (VWF) plays an important role in stopping the flow of blood, haemostasis. The VWF interacts with functional domains, the vascular wall, coagulation factor VIII, and platelet receptors. When there is a location of vascular injury, the VWF binds to platelets and delivers the coagulation factor VIII to that location of the injury.
The von Willebrand Factor (VWF) plays an important role in stopping the flow of blood, haemostasis. The VWF interacts with functional domains, the vascular wall, coagulation factor VIII, and platelet receptors. When there is a location of vascular injury, the VWF binds to platelets and delivers the coagulation factor VIII to that location of the injury.
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== Disease ==
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== Structure ==
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== Relevance ==
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== Disease ==
== Structural highlights ==
== Structural highlights ==

Revision as of 17:49, 28 April 2018

This Sandbox is Reserved from Jan 22 through May 22, 2018 for use in the course Biochemistry II taught by Jason Telford at the Maryville University, St. Louis, Missouri, USA. This reservation includes Sandbox Reserved 1446 through Sandbox Reserved 1455.
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von Willebrand Factor

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References

  1. Hanson, R. M., Prilusky, J., Renjian, Z., Nakane, T. and Sussman, J. L. (2013), JSmol and the Next-Generation Web-Based Representation of 3D Molecular Structure as Applied to Proteopedia. Isr. J. Chem., 53:207-216. doi:http://dx.doi.org/10.1002/ijch.201300024
  2. Herraez A. Biomolecules in the computer: Jmol to the rescue. Biochem Mol Biol Educ. 2006 Jul;34(4):255-61. doi: 10.1002/bmb.2006.494034042644. PMID:21638687 doi:10.1002/bmb.2006.494034042644

1. Desch, K. C. (2018). Regulation of plasma von Willebrand factor. F1000Research, 7, 96. http://doi.org/10.12688/f1000research.13056.1

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