Mutations in complement factor I as found in atypical hemolytic uremic syndrome lead to either altered secretion or altered function of factor I
about
Atypical hemolytic uremic syndromeAnalysis of binding sites on complement factor I that are required for its activityComplement System Part II: Role in ImmunityHaemolytic uraemic syndrome.Genetics and complement in atypical HUS.aHUS caused by complement dysregulation: new therapies on the horizon.Common genetic variants in complement genes other than CFH, CD46 and the CFHRs are not associated with aHUS.Factor I autoantibodies in patients with atypical hemolytic uremic syndrome: disease-associated or an epiphenomenon?Complement therapy in atypical haemolytic uraemic syndrome (aHUS).Atypical hemolytic uremic syndrome post-kidney transplantation: two case reports and review of the literatureReview: Complement and its regulatory proteins in kidney diseases.Rare genetic variants in the CFI gene are associated with advanced age-related macular degeneration and commonly result in reduced serum factor I levelsComplement Dysregulation and Disease: Insights from Contemporary Genetics.Mutations of complement factor I and potential mechanisms of neuroinflammation in acute hemorrhagic leukoencephalitis.Update on hemolytic uremic syndrome: Diagnostic and therapeutic recommendations.Local expression of complement factor I in breast cancer cells correlates with poor survival and recurrence.Endothelial cells: source, barrier, and target of defensive mediators.The complement system in age-related macular degeneration: A review of rare genetic variants and implications for personalized treatment.Complementopathies.Analysis of binding sites on complement factor I using artificial N-linked glycosylationDiseases of complement dysregulation-an overview.Complete factor I deficiency due to dysfunctional factor I with recurrent aseptic meningo-encephalitis.Cutaneous Vasculitis and Recurrent Infection Caused by Deficiency in Complement Factor I.Atypical hemolytic uremic syndrome
P2860
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P2860
Mutations in complement factor I as found in atypical hemolytic uremic syndrome lead to either altered secretion or altered function of factor I
description
2010 nî lūn-bûn
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2010 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2010年の論文
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2010年学术文章
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2010年学术文章
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2010年学术文章
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2010年学术文章
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2010年学术文章
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2010年學術文章
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name
Mutations in complement factor ...... r altered function of factor I
@ast
Mutations in complement factor ...... r altered function of factor I
@en
Mutations in complement factor ...... r altered function of factor I
@nl
type
label
Mutations in complement factor ...... r altered function of factor I
@ast
Mutations in complement factor ...... r altered function of factor I
@en
Mutations in complement factor ...... r altered function of factor I
@nl
prefLabel
Mutations in complement factor ...... r altered function of factor I
@ast
Mutations in complement factor ...... r altered function of factor I
@en
Mutations in complement factor ...... r altered function of factor I
@nl
P2093
P2860
P356
P1476
Mutations in complement factor ...... r altered function of factor I
@en
P2093
Anna M Blom
Bruno O Villoutreix
Leendert A Trouw
Nikolina Kalchishkova
Sara C Nilsson
Veronique Fremeaux-Bacchi
P2860
P304
P356
10.1002/EJI.200939280
P407
P577
2010-01-01T00:00:00Z