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Minor Role of Plasminogen in Complement Activation on Cell Surfaces

Atypical hemolytic uremic syndrome (aHUS) is a rare, but severe thrombotic microangiopathy. In roughly two thirds of the patients, mutations in complement genes lead to uncontrolled activation of the complement system against self cells. Recently, aHUS patients were described with deficiency of the...

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Detalles Bibliográficos
Autores principales: Hyvärinen, Satu, Jokiranta, T. Sakari
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4670116/
https://www.ncbi.nlm.nih.gov/pubmed/26637181
http://dx.doi.org/10.1371/journal.pone.0143707