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Misfolding of vWF to Pathologically Disordered Conformations Impacts the Severity of von Willebrand Disease

The primary hemostatic von Willebrand factor (vWF) functions to sequester platelets from rheological blood flow and mediates their adhesion to damaged subendothelium at sites of vascular injury. We have surveyed the effect of 16 disease-causing mutations identified in patients diagnosed with the ble...

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Autors principals: Tischer, Alexander, Madde, Pranathi, Moon-Tasson, Laurie, Auton, Matthew
Format: Artigo
Idioma:Inglês
Publicat: The Biophysical Society 2014
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4156683/
https://ncbi.nlm.nih.gov/pubmed/25185554
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bpj.2014.07.026
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