Polyphosphate Activates von Willebrand Factor Interaction with Glycoprotein Ib in the Absence of Factor VIII In Vitro
Polyphosphate (polyP), a phosphate polymer released by activated platelets, may modulate various stages of hemostasis by binding to blood proteins. In this context, we previously reported that polyP binds to the von Willebrand factor (VWF). One of the most significant functions of VWF is to bind to...
- Autores:
-
Montilla Rodríguez, Liliana Marcela
Atienza- Navarro, Isabel
García- Cozar, Francisco Jose
Castro, Carmen
Rodriguez- Martorell, Francisco Javier
Ruiz, Felix A
- Tipo de recurso:
- Article of investigation
- Fecha de publicación:
- 2022
- Institución:
- Universidad Cooperativa de Colombia
- Repositorio:
- Repositorio UCC
- Idioma:
- OAI Identifier:
- oai:repository.ucc.edu.co:20.500.12494/52561
- Palabra clave:
- Factor VIII
Hemophilia A
Polyphosphate
Von Willebrand disease
Von Willebrand factor
- Rights
- openAccess
- License
- Atribución