Von Willebrand factor regulates complement on endothelial cells

Atypical hemolytic uremic syndrome and thrombotic thrombocytopenic purpura have traditionally been considered separate entities. Defects in the regulation of the complement alternative pathway occur in atypical hemolytic uremic syndrome, and defects in the cleavage of von Willebrand factor (VWF)-mul...

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Bibliografski detalji
Izdano u:Kidney Int
Glavni autori: Noone, Damien G., Riedl, Magdalena, Pluthero, Fred G., Bowman, Mackenzie L., Liszewski, M. Kathryn, Lu, Lily, Quan, Yi, Balgobin, Steve, Schneppenheim, Reinhard, Schneppenheim, Sonja, Budde, Ulrich, James, Paula, Atkinson, John P., Palaniyar, Nades, Kahr, Walter H.A., Licht, Christoph
Format: Artigo
Jezik:Inglês
Izdano: 2016
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Article
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6591736/
https://ncbi.nlm.nih.gov/pubmed/27236750
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.kint.2016.03.023
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