Differential proteolytic activation of factor VIII-von Willebrand factor complex by thrombin.
Blood coagulation factor VIII (fVIII) is a plasma protein that is decreased or absent in hemophilia A. It is isolated as a mixture of heterodimers that contain a variably sized heavy chain and a common light chain. Thrombin catalyzes the activation of fVIII in a reaction that is associated with clea...
שמור ב:
| הוצא לאור ב: | Proc Natl Acad Sci U S A |
|---|---|
| Principais autores: | , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
National Academy of Sciences
1989
|
| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC297873/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2505252/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.86.17.6508 |
| תגים: |
אין תגיות, היה/י הראשונ/ה לתייג את הרשומה!
|