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Antibody Mediated Rejection Associated With Complement Factor H–Related Protein 3/1 Deficiency Successfully Treated With Eculizumab

American journal of transplantation, 2012-09, Vol.12 (9), p.2546-2553

2012

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Haemolytic uraemic syndrome and mutations of the factor H gene: a registry-based study of German speaking countries

Journal of medical genetics, 2003-09, Vol.40 (9), p.676-681

2003

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Complement in age-related macular degeneration: a focus on function

Eye (London), 2011-06, Vol.25 (6), p.683-693

2011

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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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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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The Hyphal and Yeast Forms of Candida albicans Bind the Complement Regulator C4b-Binding Protein

Infection and Immunity, 2004-11, Vol.72 (11), p.6633-6641

2004

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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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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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Further Characterization of Complement Regulator-Acquiring Surface Proteins of Borrelia burgdorferi

Infection and Immunity, 2001-12, Vol.69 (12), p.7800-7809

2001

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Trimer Stability of YadA Is Critical for Virulence of Yersinia enterocolitica

Infection and Immunity, 2010-06, Vol.78 (6), p.2677-2690

2010

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Ral activation promotes melanomagenesis

Oncogene, 2010-08, Vol.29 (34), p.4859-4864

2010

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The Yeast Candida albicans Binds Complement Regulators Factor H and FHL-1

Infection and Immunity, 2002-09, Vol.70 (9), p.5185-5192

2002

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Complement Resistance of Borrelia burgdorferi Correlates with the Expression of BbCRASP-1, a Novel Linear Plasmid-encoded Surface Protein That Interacts with Human Factor H and FHL-1 and Is Unrelated to Erp Proteins

The Journal of biological chemistry, 2004-01, Vol.279 (4), p.2421-2429

2004

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Exceptional Resistance of Human H2 Glioblastoma Cells to Complement-Mediated Killing by Expression and Utilization of Factor H and Factor H-Like Protein 1

The Journal of immunology (1950), 2000-06, Vol.164 (11), p.6075-6081

2000

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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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Secretion of soluble complement inhibitors factor H and factor H-like protein (FHL-1) by ovarian tumour cells

British journal of cancer, 2002-11, Vol.87 (10), p.1119-1127

2002

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Immune evasion of Borrelia burgdorferi by acquisition of human complement regulators FHL‐1/reconectin and Factor H

European journal of immunology, 2001-06, Vol.31 (6), p.1674-1684

2001

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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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Immune evasion of Borrelia burgdorferi: mapping of a complement‐inhibitor factor H‐binding site of BbCRASP‐3, a novel member of the Erp protein family

European journal of immunology, 2003-03, Vol.33 (3), p.697-707

2003

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The molecular basis of Familial hemolytic uremic syndrome : Mutation analysis of factor H gene reveals a hot spot in short consensus repeat 20

Journal of the American Society of Nephrology, 2001-02, Vol.12 (2), p.297-307

2001

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Complement factor H deficiency and endocapillary glomerulonephritis due to paternal isodisomy and a novel factor H mutation

Genes and immunity, 2011-03, Vol.12 (2), p.90-99

2011

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Streptococcus pneumoniae Evades Complement Attack and Opsonophagocytosis by Expressing the pspC Locus-Encoded Hic Protein That Binds to Short Consensus Repeats 8-11 of Factor H

The Journal of immunology (1950), 2002-02, Vol.168 (4), p.1886-1894

2002

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Immune evasion by acquisition of complement inhibitors: The mould Aspergillus binds both factor H and C4b binding protein

Molecular immunology, 2008-03, Vol.45 (5), p.1485-1493

2008

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Role for the Abi/Wave Protein Complex in T Cell Receptor-Mediated Proliferation and Cytoskeletal Remodeling

Current biology, 2006-01, Vol.16 (1), p.35-46

2006

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Optimizing Melphalan Pharmacokinetics in Regional Melanoma Therapy: Does Correcting for Ideal Body Weight Alter Regional Response or Toxicity?

Annals of surgical oncology, 2009-04, Vol.16 (4), p.953-961

2009

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Antibody Mediated Rejection Associated With Complement Factor H–Related Protein 3/1 Deficiency Successfully Treated With Eculizumab

Haemolytic uraemic syndrome and mutations of the factor H gene: a registry-based study of German speaking countries

Complement in age-related macular degeneration: a focus on function

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

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

The Hyphal and Yeast Forms of Candida albicans Bind the Complement Regulator C4b-Binding Protein

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

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)

Further Characterization of Complement Regulator-Acquiring Surface Proteins of Borrelia burgdorferi

Trimer Stability of YadA Is Critical for Virulence of Yersinia enterocolitica

Ral activation promotes melanomagenesis

The Yeast Candida albicans Binds Complement Regulators Factor H and FHL-1

Complement Resistance of Borrelia burgdorferi Correlates with the Expression of BbCRASP-1, a Novel Linear Plasmid-encoded Surface Protein That Interacts with Human Factor H and FHL-1 and Is Unrelated to Erp Proteins

Exceptional Resistance of Human H2 Glioblastoma Cells to Complement-Mediated Killing by Expression and Utilization of Factor H and Factor H-Like Protein 1

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

Secretion of soluble complement inhibitors factor H and factor H-like protein (FHL-1) by ovarian tumour cells

Immune evasion of Borrelia burgdorferi by acquisition of human complement regulators FHL‐1/reconectin and Factor H

Factor H family proteins and human diseases

Immune evasion of Borrelia burgdorferi: mapping of a complement‐inhibitor factor H‐binding site of BbCRASP‐3, a novel member of the Erp protein family

The molecular basis of Familial hemolytic uremic syndrome : Mutation analysis of factor H gene reveals a hot spot in short consensus repeat 20

Complement factor H deficiency and endocapillary glomerulonephritis due to paternal isodisomy and a novel factor H mutation

Streptococcus pneumoniae Evades Complement Attack and Opsonophagocytosis by Expressing the pspC Locus-Encoded Hic Protein That Binds to Short Consensus Repeats 8-11 of Factor H

Immune evasion by acquisition of complement inhibitors: The mould Aspergillus binds both factor H and C4b binding protein

Role for the Abi/Wave Protein Complex in T Cell Receptor-Mediated Proliferation and Cytoskeletal Remodeling

Optimizing Melphalan Pharmacokinetics in Regional Melanoma Therapy: Does Correcting for Ideal Body Weight Alter Regional Response or Toxicity?

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