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Deletion of Lys224 in regulatory domain 4 of Factor H reveals a novel pathomechanism for dense deposit disease (MPGN II)

Kidney international, 2006-07, Vol.70 (1), p.42-50

2006

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The C‐terminus of complement regulator Factor H mediates target recognition: evidence for a compact conformation of the native protein

Clinical and experimental immunology, 2006-05, Vol.144 (2), p.342-352

2006

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Monomeric CRP contributes to complement control in fluid phase and on cellular surfaces and increases phagocytosis by recruiting factor H

Cell death and differentiation, 2009-12, Vol.16 (12), p.1630-1640

2009

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Variations in the complement regulatory genes factor H (CFH) and factor H related 5 (CFHR5) are associated with membranoproliferative glomerulonephritis type II (dense deposit disease)

Journal of medical genetics, 2006-07, Vol.43 (7), p.582-589

2006

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A further link between innate and adaptive immunity: C3 deposition on antigen-presenting cells enhances the proliferation of antigen-specific T cells

International immunology, 1998-12, Vol.10 (12), p.1923-1930

1998

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Adjuvant effect of γ-inulin is mediated by C3 fragments deposited on antigen-presenting cells

Journal of leukocyte biology, 2001-01, Vol.69 (1), p.69-74

2001

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Human complement regulators interact with leptospiral immunoglobulin-like proteins contributing to immune evasion

Molecular immunology, 2011-08, Vol.48 (14), p.1700-1701

2011

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Factor H family proteins and human diseases

Trends in immunology, 2008-08, Vol.29 (8), p.380-387

2008

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Factor H-related protein 4 can serve as a platform for the assembly of an active C3 convertase via its interaction with C3b

Molecular immunology, 2011-08, Vol.48 (14), p.1706-1706

2011

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Attachment of the soluble complement regulator factor H to cell and tissue surfaces: relevance for pathology

Histology and histopathology, 2004-01, Vol.19 (1), p.251

2004

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Secreted aspartic protease 2 of Candida albicans cleaves factor H and the macrophage factor H-receptors

Molecular immunology, 2013-12, Vol.56 (3), p.313-313

2013

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Mannan‐binding lectin and C1q bind to distinct structures and exert differential effects on macrophages

European journal of immunology, 2000-06, Vol.30 (6), p.1706-1713

2000

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Comprehensive functional characterization of an engineered factor H construct combining complement regulatory and surface recognition domains

Molecular immunology, 2013-12, Vol.56 (3), p.289-290

2013

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Impaired binding of factor H to pentraxin 3 due to factor H mutations and autoantibodies associated with atypical hemolytic uremic syndrome

Molecular immunology, 2011-08, Vol.48 (14), p.1722-1722

2011

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Complement and diseases: Defective alternative pathway control results in kidney and eye diseases

Molecular immunology, 2006, Vol.43 (1), p.97-106

2006

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Characterization of factor H-related cell membrane molecules expressed by human B lymphocytes and neutrophil granulocytes

Immunology letters, 2001-05, Vol.77 (1), p.55-62

2001

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Functional analyses indicate a pathogenic role of factor H autoantibodies in atypical haemolytic uraemic syndrome

Nephrology, dialysis, transplantation, 2010-01, Vol.25 (1), p.136-144

2010

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Monoclonal anti-factor H antibodies in dense deposit disease

Molecular immunology, 2011-08, Vol.48 (14), p.1726-1726

2011

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Complement Receptor Type 1 (CD35) Mediates Inhibitory Signals in Human B Lymphocytes

The Journal of immunology (1950), 2002-03, Vol.168 (6), p.2782-2788

2002

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Mutations in factor H reduce binding affinity to C3b and heparin and surface attachment to endothelial cells in hemolytic uremic syndrome

The Journal of clinical investigation, 2003-04, Vol.111 (8), p.1181-1190

2003

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Binding of Complement Factor H to Endothelial Cells Is Mediated by the Carboxy-Terminal Glycosaminoglycan Binding Site

The American journal of pathology, 2005-10, Vol.167 (4), p.1173-1181

2005

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Anti-factor H antibody affecting factor H cofactor activity in a patient with dense deposit disease

Clinical kidney journal, 2012-04, Vol.5 (2), p.133-136

2012

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FHR-4A: a new factor H-related protein is encoded by the human FHR-4 gene

European journal of human genetics : EJHG, 2005-03, Vol.13 (3), p.321-329

2005

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Screening for anti-factor B autoantibody in a patient with acute renal injury due to dense deposit disease

Clinical nephrology, 2012-01, Vol.77 (1), p.85

2012

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Comparison of binding and functional effects of MBL and C1q on lymphocytes and macrophages

Immunopharmacology, 2000-08, Vol.49 (1-2), p.84-84

2000

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Deletion of Lys224 in regulatory domain 4 of Factor H reveals a novel pathomechanism for dense deposit disease (MPGN II)

The C‐terminus of complement regulator Factor H mediates target recognition: evidence for a compact conformation of the native protein

Monomeric CRP contributes to complement control in fluid phase and on cellular surfaces and increases phagocytosis by recruiting factor H

Variations in the complement regulatory genes factor H (CFH) and factor H related 5 (CFHR5) are associated with membranoproliferative glomerulonephritis type II (dense deposit disease)

A further link between innate and adaptive immunity: C3 deposition on antigen-presenting cells enhances the proliferation of antigen-specific T cells

Adjuvant effect of γ-inulin is mediated by C3 fragments deposited on antigen-presenting cells

Human complement regulators interact with leptospiral immunoglobulin-like proteins contributing to immune evasion

Factor H family proteins and human diseases

Factor H-related protein 4 can serve as a platform for the assembly of an active C3 convertase via its interaction with C3b

Attachment of the soluble complement regulator factor H to cell and tissue surfaces: relevance for pathology

Secreted aspartic protease 2 of Candida albicans cleaves factor H and the macrophage factor H-receptors

Mannan‐binding lectin and C1q bind to distinct structures and exert differential effects on macrophages

Comprehensive functional characterization of an engineered factor H construct combining complement regulatory and surface recognition domains

Impaired binding of factor H to pentraxin 3 due to factor H mutations and autoantibodies associated with atypical hemolytic uremic syndrome

Complement and diseases: Defective alternative pathway control results in kidney and eye diseases

Characterization of factor H-related cell membrane molecules expressed by human B lymphocytes and neutrophil granulocytes

Functional analyses indicate a pathogenic role of factor H autoantibodies in atypical haemolytic uraemic syndrome

Monoclonal anti-factor H antibodies in dense deposit disease

Complement Receptor Type 1 (CD35) Mediates Inhibitory Signals in Human B Lymphocytes

Mutations in factor H reduce binding affinity to C3b and heparin and surface attachment to endothelial cells in hemolytic uremic syndrome

Binding of Complement Factor H to Endothelial Cells Is Mediated by the Carboxy-Terminal Glycosaminoglycan Binding Site

Anti-factor H antibody affecting factor H cofactor activity in a patient with dense deposit disease

FHR-4A: a new factor H-related protein is encoded by the human FHR-4 gene

Screening for anti-factor B autoantibody in a patient with acute renal injury due to dense deposit disease

Comparison of binding and functional effects of MBL and C1q on lymphocytes and macrophages

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