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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Vydáno v:Kidney Int
Hlavní autoři: 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
Médium: Artigo
Jazyk:Inglês
Vydáno: 2016
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Article
On-line přístup: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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