טוען...
Force-induced on-rate switching and modulation by mutations in gain-of-function von Willebrand diseases
Mutations in the ultralong vascular protein von Willebrand factor (VWF) cause the common human bleeding disorder, von Willebrand disease (VWD). The A1 domain in VWF binds to glycoprotein Ibα (GPIbα) on platelets, in a reaction triggered, in part, by alterations in flow during bleeding. Gain-of-funct...
שמור ב:
| הוצא לאור ב: | Proc Natl Acad Sci U S A |
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| Main Authors: | , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
National Academy of Sciences
2015
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4403213/ https://ncbi.nlm.nih.gov/pubmed/25810255 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1501689112 |
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