Sara Nilsson (Former)
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- 2023
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Mark
Citrullination of C1-inhibitor as a mechanism of impaired complement regulation in rheumatoid arthritis
(
- Contribution to journal › Article
- 2022
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Mark
Functional Analysis of Variants in Complement Factor I Identified in Age-Related Macular Degeneration and Atypical Hemolytic Uremic Syndrome
(
- Contribution to journal › Article
- 2020
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Mark
Plasma C4d Correlates With C4d Deposition in Kidneys and With Treatment Response in Lupus Nephritis Patients
(
- Contribution to journal › Article
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Mark
Effect of rare coding variants in the CFI gene on Factor I expression levels
(
- Contribution to journal › Article
- 2019
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Mark
Measuring plasma C4D to monitor immune complexes in lupus nephritis
(
- Contribution to journal › Article
- 2018
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Mark
Functional analyses of rare genetic variants in complement component C9 identified in patients with age-related macular degeneration
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- Contribution to journal › Article
- 2017
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Mark
The functional effect of rare variants in complement genes on C3b degradation in patients with age-related macular degeneration
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- Contribution to journal › Article
- 2016
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Mark
C4b-binding protein protects β-cells from islet amyloid polypeptide-induced cytotoxicity
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- Contribution to journal › Article
- 2015
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Mark
Functional characterization of two novel non-synonymous alterations in CD46 and a Q950H change in factor H found in atypical hemolytic uremic syndrome patients.
(
- Contribution to journal › Article
- 2014
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Mark
Purification and functional characterization of factor I.
(
- Contribution to journal › Article
- 2013
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Mark
A functional variant in the CFI gene confers a high risk of age-related macular degeneration
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- Contribution to journal › Article
- 2012
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Mark
Analysis of binding sites on complement factor I using artificial N-linked glycosylation.
(
- Contribution to journal › Article
-
Mark
Factor H autoantibodies and deletion of Complement Factor H-Related protein-1 in rheumatic diseases in comparison to atypical hemolytic uremic syndrome
(
- Contribution to journal › Article
- 2011
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Mark
Molecular characterization of two novel cases of complete complement inhibitor Factor I deficiency.
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- Contribution to journal › Article
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Mark
Complement factor I in health and disease.
(
- Contribution to journal › Article
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Mark
Mutations in genes encoding complement inhibitors CD46 and CFH affect the age at nephritis onset in patients with systemic lupus erythematosus
(
- Contribution to journal › Article
- 2010
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Mark
Analysis of binding sites on complement Factor I that are required for its activity
(
- Contribution to journal › Published meeting abstract
-
Mark
Mutations in components of complement influence the outcome of Factor I-associated atypical hemolytic uremic syndrome
(
- Contribution to journal › Article
-
Mark
Mutations in complement factor I as found in atypical hemolytic uremic syndrome lead to either altered secretion or altered function of factor I
(
- Contribution to journal › Article
-
Mark
Analysis of binding sites on complement factor I that are required for its activity.
(
- Contribution to journal › Article
- 2009
-
Mark
Genetic, molecular and functional analyses of factor I - an inhibitor of the complement system
(
- Thesis › Doctoral thesis (compilation)
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Mark
Genetic, molecular and functional analyses of complement factor I deficiency.
(
- Contribution to journal › Article
- 2008
-
Mark
Molecular and functional analysis of complement factor I mutations in atypical haemolytic uraemic syndrome patients
(
- Contribution to journal › Published meeting abstract
- 2007
-
Mark
A mutation in factor I that is associated with atypical hemolytic uremic syndrome does not affect the function of factor I in complement regulation.
(
- Contribution to journal › Article
- 2006
-
Mark
Recessiveness and Dominance in Barley Mutants Deficient in Mg-Chelatase Subunit D, an AAA Protein Involved in Chlorophyll Biosynthesis.
(
- Contribution to journal › Article
- 2005
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Mark
C4b-binding protein binds to necrotic cells and DNA, limiting DNA release and inhibiting complement activation.
(
- Contribution to journal › Article