Complement factor H deficiency and endocapillary glomerulonephritis due to paternal isodisomy and a novel factor H mutation
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Title
Complement factor H deficiency and endocapillary glomerulonephritis due to paternal isodisomy and a novel factor H mutation
Authors
Keywords
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Journal
GENES AND IMMUNITY
Volume 12, Issue 2, Pages 90-99
Publisher
Springer Nature
Online
2011-01-27
DOI
10.1038/gene.2010.63
References
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Related references
Note: Only part of the references are listed.- Translational Mini-Review Series on Complement Factor H: Renal diseases associated with complement factor H: novel insights from humans and animals
- (2010) M. C. Pickering et al. CLINICAL AND EXPERIMENTAL IMMUNOLOGY
- DEAP-HUS: Deficiency of CFHR plasma proteins and autoantibody-positive form of hemolytic uremic syndrome
- (2010) Peter F. Zipfel et al. PEDIATRIC NEPHROLOGY
- Hyperfunctional C3 convertase leads to complement deposition on endothelial cells and contributes to atypical hemolytic uremic syndrome
- (2009) L. T. Roumenina et al. BLOOD
- Factor H-related protein 1 (CFHR-1) inhibits complement C5 convertase activity and terminal complex formation
- (2009) S. Heinen et al. BLOOD
- Mutations in complement factor I as found in atypical hemolytic uremic syndrome lead to either altered secretion or altered function of factor I
- (2009) Sara C. Nilsson et al. EUROPEAN JOURNAL OF IMMUNOLOGY
- Characterization of an NF-κB-regulated, miRNA-146a-mediated down-regulation of complement factor H (CFH) in metal-sulfate-stressed human brain cells
- (2009) Aileen I. Pogue et al. JOURNAL OF INORGANIC BIOCHEMISTRY
- Mutations in components of complement influence the outcome of Factor I-associated atypical hemolytic uremic syndrome
- (2009) Frank Bienaime et al. KIDNEY INTERNATIONAL
- Structure of complement fragment C3b–factor H and implications for host protection by complement regulators
- (2009) Jin Wu et al. NATURE IMMUNOLOGY
- Thrombomodulin Mutations in Atypical Hemolytic–Uremic Syndrome
- (2009) Mieke Delvaeye et al. NEW ENGLAND JOURNAL OF MEDICINE
- Complement activation and inhibition: a delicate balance
- (2009) A.P. Sjöberg et al. TRENDS IN IMMUNOLOGY
- Mutations in complement C3 predispose to development of atypical hemolytic uremic syndrome
- (2008) V. Fremeaux-Bacchi et al. BLOOD
- Structure of the N-terminal Region of Complement Factor H and Conformational Implications of Disease-linked Sequence Variations
- (2008) Henry G. Hocking et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Genetic deficiency of complement factor H in a patient with age-related macular degeneration and membranoproliferative glomerulonephritis
- (2008) Tamara Montes et al. MOLECULAR IMMUNOLOGY
- Hemolytic uremic syndrome recurrence after renal transplantation
- (2008) Chantal Loirat et al. PEDIATRIC TRANSPLANTATION
- The Staphylococcus aureus Protein Sbi Acts as a Complement Inhibitor and Forms a Tripartite Complex with Host Complement Factor H and C3b
- (2008) Katrin Haupt et al. PLoS Pathogens
- Activator-specific requirement of properdin in the initiation and amplification of the alternative pathway complement
- (2007) Y. Kimura et al. BLOOD
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