- Home
- Publications
- Publication Search
- Publication Details
Title
Complement Factor I Variants in Complement-Mediated Renal Diseases
Authors
Keywords
-
Journal
Frontiers in Immunology
Volume 13, Issue -, Pages -
Publisher
Frontiers Media SA
Online
2022-05-10
DOI
10.3389/fimmu.2022.866330
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Factor H Autoantibodies and Complement-Mediated Diseases
- (2021) Yuzhou Zhang et al. Frontiers in Immunology
- Functional characterization of 105 Factor H variants associated with atypical HUS: lessons for variant classification.
- (2021) Hector Martin Merinero et al. BLOOD
- The mutational constraint spectrum quantified from variation in 141,456 humans
- (2020) Konrad J. Karczewski et al. NATURE
- Effect of rare coding variants in the CFI gene on Factor I expression levels
- (2020) Sarah de Jong et al. HUMAN MOLECULAR GENETICS
- C3(H2O) prevents rescue of complement-mediated C3 glomerulopathy in Cfh–/– Cfd–/– mice
- (2020) Yuzhou Zhang et al. JCI Insight
- Plasma C3d levels as a diagnostic marker for complete complement factor I deficiency
- (2020) Leslie Naesens et al. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
- Functional Analysis of Rare Genetic Variants in Complement Factor I (CFI) using a Serum-Based Assay in Advanced Age-related Macular Degeneration
- (2020) Anuja Java et al. Translational Vision Science & Technology
- C3 glomerulopathy — understanding a rare complement-driven renal disease
- (2019) Richard J. H. Smith et al. Nature Reviews Nephrology
- Genotype-phenotype correlations of low-frequency variants in the complement system in renal disease and age-related macular degeneration
- (2018) M.J. Geerlings et al. CLINICAL GENETICS
- Statistical Validation of Rare Complement Variants Provides Insights into the Molecular Basis of Atypical Hemolytic Uremic Syndrome and C3 Glomerulopathy
- (2018) Amy J. Osborne et al. JOURNAL OF IMMUNOLOGY
- C3 glomerulonephritis secondary to mutations in factors H and I: rapid recurrence in deceased donor kidney transplant effectively treated with eculizumab
- (2018) Neetika Garg et al. NEPHROLOGY DIALYSIS TRANSPLANTATION
- Genetic analysis of the complement pathway in C3 glomerulopathy
- (2018) Weiwei Zhao et al. NEPHROLOGY DIALYSIS TRANSPLANTATION
- Genetic Analysis of 400 Patients Refines Understanding and Implicates a New Gene in Atypical Hemolytic Uremic Syndrome
- (2018) Fengxiao Bu et al. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
- Genetic analysis and functional characterization of novel mutations in a series of patients with atypical hemolytic uremic syndrome
- (2016) Nóra Szarvas et al. MOLECULAR IMMUNOLOGY
- Complement gene variants determine the risk of immunoglobulin-associated MPGN and C3 glomerulopathy and predict long-term renal outcome
- (2016) Paraskevas Iatropoulos et al. MOLECULAR IMMUNOLOGY
- Rare genetic variants in the CFI gene are associated with advanced age-related macular degeneration and commonly result in reduced serum factor I levels
- (2015) D. Kavanagh et al. HUMAN MOLECULAR GENETICS
- High-Throughput Genetic Testing for Thrombotic Microangiopathies and C3 Glomerulopathies
- (2015) F. Bu et al. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
- The molecular and structural bases for the association of complement C3 mutations with atypical hemolytic uremic syndrome
- (2015) Rubén Martínez-Barricarte et al. MOLECULAR IMMUNOLOGY
- A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants
- (2015) Lars G Fritsche et al. NATURE GENETICS
- Complement System Part I – Molecular Mechanisms of Activation and Regulation
- (2015) Nicolas S. Merle et al. Frontiers in Immunology
- Defining the Complement Biomarker Profile of C3 Glomerulopathy
- (2014) Y. Zhang et al. Clinical Journal of the American Society of Nephrology
- Genetics and Outcome of Atypical Hemolytic Uremic Syndrome: A Nationwide French Series Comparing Children and Adults
- (2013) V. Fremeaux-Bacchi et al. Clinical Journal of the American Society of Nephrology
- Complete Factor I Deficiency Due to Dysfunctional Factor I with Recurrent Aseptic Meningo-Encephalitis
- (2013) Filomeen Haerynck et al. JOURNAL OF CLINICAL IMMUNOLOGY
- Comprehensive Genetic Analysis of Complement and Coagulation Genes in Atypical Hemolytic Uremic Syndrome
- (2013) F. Bu et al. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
- Combined Complement Gene Mutations in Atypical Hemolytic Uremic Syndrome Influence Clinical Phenotype
- (2013) E. Bresin et al. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
- Toward a working definition of C3 glomerulopathy by immunofluorescence
- (2013) Jean Hou et al. KIDNEY INTERNATIONAL
- Rare variants in CFI, C3 and C9 are associated with high risk of advanced age-related macular degeneration
- (2013) Johanna M Seddon et al. NATURE GENETICS
- A prevalent C3 mutation in aHUS patients causes a direct C3 convertase gain of function
- (2012) L. T. Roumenina et al. BLOOD
- Causes of Alternative Pathway Dysregulation in Dense Deposit Disease
- (2012) Y. Zhang et al. Clinical Journal of the American Society of Nephrology
- Atypical hemolytic uremic syndrome and genetic aberrations in the complement factor H-related 5 gene
- (2012) Dineke Westra et al. JOURNAL OF HUMAN GENETICS
- Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathies
- (2012) Aude Servais et al. KIDNEY INTERNATIONAL
- Pathogenesis of the C3 glomerulopathies and reclassification of MPGN
- (2012) Andrew S. Bomback et al. Nature Reviews Nephrology
- Molecular characterization of two novel cases of complete complement inhibitor Factor I deficiency
- (2011) Izabela M. Nita et al. MOLECULAR IMMUNOLOGY
- Complement factor I in health and disease
- (2011) Sara C. Nilsson et al. MOLECULAR IMMUNOLOGY
- Structural basis for complement factor I control and its disease-associated sequence polymorphisms
- (2011) P. Roversi et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Mutations in alternative pathway complement proteins in American patients with atypical hemolytic uremic syndrome
- (2010) Tara K. Maga et al. HUMAN MUTATION
- Pregnancy-Associated Hemolytic Uremic Syndrome Revisited in the Era of Complement Gene Mutations
- (2010) F. Fakhouri et al. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
- Glomeruli of Dense Deposit Disease contain components of the alternative and terminal complement pathway
- (2009) Sanjeev Sethi et al. KIDNEY INTERNATIONAL
- Mutations in components of complement influence the outcome of Factor I-associated atypical hemolytic uremic syndrome
- (2009) Frank Bienaime et al. KIDNEY INTERNATIONAL
- Genetic, molecular and functional analyses of complement factor I deficiency
- (2008) Sara C. Nilsson et al. EUROPEAN JOURNAL OF IMMUNOLOGY
- Molecular characterization of complement Factor I deficiency in two Spanish families
- (2008) Isabel María Ponce-Castro et al. MOLECULAR IMMUNOLOGY
Add your recorded webinar
Do you already have a recorded webinar? Grow your audience and get more views by easily listing your recording on Peeref.
Upload NowBecome a Peeref-certified reviewer
The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.
Get Started