Chargement en cours...
Sialyltransferase ST3Gal-IV operates as a dominant modifier of hemostasis by concealing asialoglycoprotein receptor ligands
A number of poorly characterized genetic modifiers contribute to the extensive variability of von Willebrand disease, the most prevalent bleeding disorder in humans. We find that a genetic lesion inactivating the murine ST3Gal-IV sialyltransferase causes a bleeding disorder associated with an autoso...
Enregistré dans:
| Auteurs principaux: | , , , , , , , |
|---|---|
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
The National Academy of Sciences
2002
|
| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC126621/ https://ncbi.nlm.nih.gov/pubmed/12097641 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.142005099 |
| Tags: |
Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!
|