The endothelial cell receptor stabilin-2 regulates VWF-FVIII complex half-life and immunogenicity

Quantitative abnormalities of the von Willebrand factor–factor VIII (VWF-FVIII) complex associate with inherited bleeding or thrombotic disorders. Receptor-mediated interactions between plasma VWF-FVIII and phagocytic or immune cells can influence their hemostatic and immunogenic activities. Genetic...

Descrición completa

Gardado en:
Detalles Bibliográficos
Publicado en:J Clin Invest
Main Authors: Swystun, Laura L., Lai, Jesse D., Notley, Colleen, Georgescu, Ilinca, Paine, A. Simonne, Mewburn, Jeff, Nesbitt, Kate, Schledzewski, Kai, Géraud, Cyrill, Kzhyshkowska, Julia, Goerdt, Sergij, Hopman, Wilma, Montgomery, Robert R., James, Paula D., Lillicrap, David
Formato: Artigo
Idioma:Inglês
Publicado: American Society for Clinical Investigation 2018
Assuntos:
Research Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC6118640/
https://ncbi.nlm.nih.gov/pubmed/30124466
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI96400
Tags: Engadir etiqueta
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!

Títulos similares