The Factor H Variant Associated with Age-related Macular Degeneration (His-384) and the Non-disease-associated Form Bind Differentially to C-reactive Protein, Fibromodulin, DNA, and Necrotic Cells

This publication has 45 references indexed in Scilit:

• Variation in factor B (BF) and complement component 2 (C2) genes is associated with age-related macular degeneration
  Nature Genetics, 2006
• An interactive web database of factor H-associated hemolytic uremic syndrome mutations: insights into the structural consequences of disease-associated mutations
  Human Mutation, 2005
• Analysis of Binding Sites in Human C-reactive Protein for FcγRI, FcγRIIA, and C1q by Site-directed Mutagenesis
  Journal of Biological Chemistry, 2005
• A common site within factor H SCR 7 responsible for binding heparin, C‐reactive protein and streptococcal M protein
  European Journal of Immunology, 2003
• CCP1–4 of the C4b-binding protein α-chain are required for factor I mediated cleavage of complement factor C3b
  Molecular Immunology, 2003
• Complement and apoptosis
  Molecular Immunology, 2001
• Structure and composition of drusen associated with glomerulonephritis: Implications for the role of complement activation in drusen biogenesis
  Eye, 2001
• Fibromodulin distribution and association with collagen
  Matrix Biology, 1994
• Regulation of Alternative Pathway Complement Activation by Glycosaminoglycans: Specificity of the Polyanion Binding Site on Factor H
  Biochemical and Biophysical Research Communications, 1994
• Identification of a major human serum DNA-binding protein as β1H of the alternative pathway of complement activation
  Biochemical and Biophysical Research Communications, 1980