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Self-Damage Caused by Dysregulation of the Complement Alternative Pathway: Relevance of the Factor H Protein Family

Frontiers in immunology, 2018-07, Vol.9, p.1607-1607

2018

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Advances in understanding the aetiology of atypical Haemolytic Uraemic Syndrome

British journal of haematology, 2010-09, Vol.150 (5), p.529-542

2010

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Xenoantibodies and Complement Activity Determinations by Flow Cytometry in Pig-to-Primate Xenotransplantation

Methods in molecular biology (Clifton, N.J.), 2020-01, Vol.2110, p.73

2020

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Combined Complement Gene Mutations in Atypical Hemolytic Uremic Syndrome Influence Clinical Phenotype

Journal of the American Society of Nephrology, 2013-03, Vol.24 (3), p.475-486

2013

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Characterization of complement factor H–related (CFHR) proteins in plasma reveals novel genetic variations of CFHR1 associated with atypical hemolytic uremic syndrome

Blood, 2009-11, Vol.114 (19), p.4261-4271

2009

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Complement as a diagnostic tool in immunopathology

Seminars in cell & developmental biology, 2019-01, Vol.85, p.86-97

2019

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Autoantibodies to complement components in C3 glomerulopathy and atypical hemolytic uremic syndrome

Immunology letters, 2014-08, Vol.160 (2), p.163-171

2014

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Nephritic Factors: An Overview of Classification, Diagnostic Tools and Clinical Associations

Frontiers in immunology, 2019-04, Vol.10, p.886-886

2019

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Gain-of-function mutations in complement factor B are associated with atypical hemolytic uremic syndrome

Proceedings of the National Academy of Sciences - PNAS, 2007-01, Vol.104 (1), p.240-245

2007

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C3 glomerulopathy-associated CFHR1 mutation alters FHR oligomerization and complement regulation

The Journal of clinical investigation, 2013-06, Vol.123 (6), p.2434-2446

2013

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An engineered construct combining complement regulatory and surface-recognition domains represents a minimal-size functional factor H

The Journal of immunology (1950), 2013-07, Vol.191 (2), p.912-921

2013

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Complement factor H variants I890 and L1007 while commonly associated with atypical hemolytic uremic syndrome are polymorphisms with no functional significance

Kidney international, 2012-01, Vol.81 (1), p.56-63

2012

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Eculizumab long-term therapy for pediatric renal transplant in aHUS with CFH/CFHR1 hybrid gene

Pediatric nephrology (Berlin, West), 2014, Vol.29 (1), p.149-153

2014

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Complement Genetic Variants and FH Desialylation in S. pneumoniae -Haemolytic Uraemic Syndrome

Frontiers in immunology, 2021-03, Vol.12, p.641656-641656

2021

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De novo gene conversion in the RCA gene cluster (1q32) causes mutations in complement factor H associated with atypical hemolytic uremic syndrome

Human mutation, 2006-03, Vol.27 (3), p.292-293

2006

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Factor H-related protein 1 neutralizes anti-factor H autoantibodies in autoimmune hemolytic uremic syndrome

Kidney international, 2011-08, Vol.80 (4), p.397-404

2011

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Atypical hemolytic uremic syndrome-associated variants and autoantibodies impair binding of factor h and factor h-related protein 1 to pentraxin 3

The Journal of immunology (1950), 2012-08, Vol.189 (4), p.1858-1867

2012

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Predisposition to atypical hemolytic uremic syndrome involves the concurrence of different susceptibility alleles in the regulators of complement activation gene cluster in 1q32

Human molecular genetics, 2005-03, Vol.14 (5), p.703-712

2005

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High Complement Factor H-Related (FHR)-3 Levels Are Associated With the Atypical Hemolytic-Uremic Syndrome-Risk Allele CFHR3B

Frontiers in immunology, 2018-04, Vol.9, p.848

2018

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Case Report: Combined Liver-Kidney Transplantation to Correct a Mutation in Complement Factor B in an Atypical Hemolytic Uremic Syndrome Patient

Frontiers in immunology, 2021-10, Vol.12, p.751093

2021

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The interactive Factor H-atypical hemolytic uremic syndrome mutation database and website: update and integration of membrane cofactor protein and Factor I mutations with structural models

Human mutation, 2007-03, Vol.28 (3), p.222-234

2007

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Clustering of Missense Mutations in the C-Terminal Region of Factor H in Atypical Hemolytic Uremic Syndrome

American journal of human genetics, 2001-02, Vol.68 (2), p.478-484

2001

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Functional implications of the recognition of complement factor H-related protein 1 (CFHR1) by anti-factor H autoantibodies in autoimmune haemolytic uraemic syndrome

Molecular immunology, 2010-08, Vol.47 (13), p.2205-2206

2010

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Contribución de variantes funcionales y cuantitativas del Factor H y las proteínas FHRs (Factor H-Related proteins) del Complemento en patología renal

Nefrología, 2022-05, Vol.42 (3), p.280-289

2022

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Factor H-Related Protein 1 Drives Disease Susceptibility and Prognosis in C3 Glomerulopathy

Journal of the American Society of Nephrology, 2022-06, Vol.33 (6), p.1137-1153

2022

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Self-Damage Caused by Dysregulation of the Complement Alternative Pathway: Relevance of the Factor H Protein Family

Advances in understanding the aetiology of atypical Haemolytic Uraemic Syndrome

Xenoantibodies and Complement Activity Determinations by Flow Cytometry in Pig-to-Primate Xenotransplantation

Combined Complement Gene Mutations in Atypical Hemolytic Uremic Syndrome Influence Clinical Phenotype

Characterization of complement factor H–related (CFHR) proteins in plasma reveals novel genetic variations of CFHR1 associated with atypical hemolytic uremic syndrome

Complement as a diagnostic tool in immunopathology

Autoantibodies to complement components in C3 glomerulopathy and atypical hemolytic uremic syndrome

Nephritic Factors: An Overview of Classification, Diagnostic Tools and Clinical Associations

Gain-of-function mutations in complement factor B are associated with atypical hemolytic uremic syndrome

C3 glomerulopathy-associated CFHR1 mutation alters FHR oligomerization and complement regulation

An engineered construct combining complement regulatory and surface-recognition domains represents a minimal-size functional factor H

Complement factor H variants I890 and L1007 while commonly associated with atypical hemolytic uremic syndrome are polymorphisms with no functional significance

Eculizumab long-term therapy for pediatric renal transplant in aHUS with CFH/CFHR1 hybrid gene

Complement Genetic Variants and FH Desialylation in S. pneumoniae -Haemolytic Uraemic Syndrome

De novo gene conversion in the RCA gene cluster (1q32) causes mutations in complement factor H associated with atypical hemolytic uremic syndrome

Factor H-related protein 1 neutralizes anti-factor H autoantibodies in autoimmune hemolytic uremic syndrome

Atypical hemolytic uremic syndrome-associated variants and autoantibodies impair binding of factor h and factor h-related protein 1 to pentraxin 3

Predisposition to atypical hemolytic uremic syndrome involves the concurrence of different susceptibility alleles in the regulators of complement activation gene cluster in 1q32

High Complement Factor H-Related (FHR)-3 Levels Are Associated With the Atypical Hemolytic-Uremic Syndrome-Risk Allele CFHR3B

Case Report: Combined Liver-Kidney Transplantation to Correct a Mutation in Complement Factor B in an Atypical Hemolytic Uremic Syndrome Patient

The interactive Factor H-atypical hemolytic uremic syndrome mutation database and website: update and integration of membrane cofactor protein and Factor I mutations with structural models

Clustering of Missense Mutations in the C-Terminal Region of Factor H in Atypical Hemolytic Uremic Syndrome

Functional implications of the recognition of complement factor H-related protein 1 (CFHR1) by anti-factor H autoantibodies in autoimmune haemolytic uraemic syndrome

Contribución de variantes funcionales y cuantitativas del Factor H y las proteínas FHRs (Factor H-Related proteins) del Complemento en patología renal

Factor H-Related Protein 1 Drives Disease Susceptibility and Prognosis in C3 Glomerulopathy

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