Modeling how CD46 deficiency predisposes to atypical hemolytic uremic syndrome
- 5 October 2006
- journal article
- Published by Elsevier in Molecular Immunology
- Vol. 44 (7), 1559-1568
- https://doi.org/10.1016/j.molimm.2006.08.024
Abstract
No abstract availableKeywords
This publication has 48 references indexed in Scilit:
- Genetics of HUS: the impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcomeBlood, 2006
- Hemolytic Uremic Syndrome: An Example of Insufficient Complement Regulation on Self‐TissueAnnals of the New York Academy of Sciences, 2005
- The development of atypical haemolytic-uraemic syndrome is influenced by susceptibility factors in factor H and membrane cofactor protein: evidence from two independent cohortsJournal of Medical Genetics, 2005
- Complement Factor H Polymorphism in Age-Related Macular DegenerationScience, 2005
- Complement Factor H Polymorphism and Age-Related Macular DegenerationScience, 2005
- Mutations in CD46, a complement regulatory protein, predispose to atypical HUSTrends in Molecular Medicine, 2004
- Structure and composition of drusen associated with glomerulonephritis: Implications for the role of complement activation in drusen biogenesisEye, 2001
- Factor H Mutations in Hemolytic Uremic Syndrome Cluster in Exons 18–20, a Domain Important for Host Cell RecognitionAmerican Journal of Human Genetics, 2001
- Clustering of Missense Mutations in the C-Terminal Region of Factor H in Atypical Hemolytic Uremic SyndromeAmerican Journal of Human Genetics, 2001
- Control of C3b and C5b deposition by CD46 (membrane cofactor protein) after alternative but not classical complement activationEuropean Journal of Immunology, 1999