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Murine systemic thrombophilia and hemolytic uremic syndrome from a factor H point mutation
Complement plays a key role in host defense, but its dysregulation can cause autologous tissue injury. Complement activation is normally controlled by regulatory proteins, including factor H (FH) in plasma and membrane cofactor protein (MCP) on the cell surface. Mutations in FH and MCP are linked to...
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| Veröffentlicht in: | Blood |
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| Hauptverfasser: | , , , , , , , , , , , , , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
American Society of Hematology
2017
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5374733/ https://ncbi.nlm.nih.gov/pubmed/28057640 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2016-07-728253 |
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