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Journal Article
Journal Article
Blood, ISSN 0006-4971, 09/2007, Volume 110, Issue 5, pp. 1516 - 1518
Journal Article
Clinical journal of the American Society of Nephrology, ISSN 1555-905X, 2013, Volume 8, Issue 3, pp. 407 - 415
Journal Article
Kidney international, ISSN 0085-2538, 2017, Volume 92, Issue 4, pp. 942 - 952
.... A deletion polymorphism affecting the genes encoding the complement factor H-related protein (FHR... 
complement | IgA nephropathy | glomerular disease | ACTIVATION | C3 GLOMERULOPATHY | CFHR1 | PATHWAY | OXFORD CLASSIFICATION | SUSCEPTIBILITY | MUTATION | UROLOGY & NEPHROLOGY | Clinical Investigation
Journal Article
Nature (London), ISSN 1476-4687, 2011, Volume 478, Issue 7367, pp. 76 - 81
.... Here we identify complement factor H (CFH) as a major MDA-binding protein that can block both the uptake of MDA-modified proteins by macrophages and MDA-induced proinflammatory effects in vivo in mice... 
PHAGOCYTOSIS | MULTIDISCIPLINARY SCIENCES | APOPTOTIC CELLS | MACULAR DEGENERATION | RISK | PHOSPHOLIPIDS | PROTEINS | END-PRODUCTS | RETINAL-PIGMENT EPITHELIUM | INNATE IMMUNITY | AGE | Inflammation - pathology | Protein Binding - genetics | Retina - metabolism | Epitopes - metabolism | Oxidative Stress | Humans | Malondialdehyde - chemistry | Complement System Proteins - immunology | Male | Complement System Proteins - metabolism | Necrosis | Inflammation - metabolism | Female | Malondialdehyde - metabolism | Protein Structure, Tertiary | Complement Factor H - immunology | Complement Inactivator Proteins - metabolism | Enzyme-Linked Immunosorbent Assay | Mice, Inbred C57BL | Complement Inactivator Proteins - immunology | Inflammation - immunology | Binding Sites - genetics | Mutation - genetics | Macular Degeneration - metabolism | Animals | Complement Factor H - metabolism | Malondialdehyde - immunology | Epitopes - chemistry | Mice | Complement Factor H - genetics | Lipid Peroxidation | Macrophages, Peritoneal - metabolism | Malondialdehyde - antagonists & inhibitors | Apoptosis | Complement Inactivator Proteins - genetics | Macular Degeneration - pathology | Macular degeneration | Oxidative stress | Complement factor H | Care and treatment | Physiological aspects | Research | Health aspects | Risk factors | Proteins | Flow cytometry | Plasma | Pathogenesis | Low density lipoprotein | Mass spectrometry | Molecular weight | Binding sites
Journal Article
Proceedings of the National Academy of Sciences - PNAS, ISSN 1091-6490, 2011, Volume 108, Issue 7, pp. 2897 - 2902
.... It is unresolved how host and nonhost surfaces are distinguished at the molecular level, but key components are domains 19-20 of the complement regulator factor H (FH... 
Molecules | Glycosaminoglycans | Hemolytic uremic syndrome | Molecular structure | Lead | Heparin | Physiological regulation | Binding sites | Endothelial cells | Crystal structure | Hemolysis | X-ray crystallography | Kidney diseases | Human mutations | Structure and function | MULTIDISCIPLINARY SCIENCES | SIALIC-ACID | POLYANIONS | IDENTIFICATION | hemolysis | human mutations | REGULATORY DOMAINS | CONVERTASE | ALTERNATIVE PATHWAY | structure and function | kidney diseases | ENDOTHELIAL-CELLS | FRAGMENT | MUTATIONS | BINDING-SITES | Surface Plasmon Resonance | Complement C3d - genetics | Complement C3d - immunology | Escherichia coli | Humans | Crystallography, X-Ray | DNA Primers - genetics | Complement C3d - metabolism | Binding Sites | Glycosaminoglycans - genetics | Complement Factor H - immunology | Mutagenesis, Site-Directed | Glycosaminoglycans - metabolism | Crystallization | Glycosaminoglycans - immunology | Hemolytic-Uremic Syndrome - immunology | Reverse Transcriptase Polymerase Chain Reaction | Pichia | Immunity, Innate - immunology | Chromatography, Affinity | Complement Factor H - metabolism | Analysis of Variance | Complement Pathway, Alternative - immunology | Complement Factor H - genetics | Atypical Hemolytic Uremic Syndrome | Immunology | Research | Properties | Hemolytic-uremic syndrome | Biological Sciences
Journal Article
Journal Article