The pivotal role of the complement system in aging and age-related macular degeneration: hypothesis re-visited

DH Anderson, MJ Radeke, NB Gallo, EA Chapin… - Progress in retinal and …, 2010 - Elsevier
During the past ten years, dramatic advances have been made in unraveling the biological
bases of age-related macular degeneration (AMD), the most common cause of irreversible …

Molecular pathology of age-related macular degeneration

X Ding, M Patel, CC Chan - Progress in retinal and eye research, 2009 - Elsevier
Age-related macular degeneration (AMD) is a leading cause of irreversible blindness in the
world. Although the etiology and pathogenesis of AMD remain largely unclear, a complex …

[HTML][HTML] Atypical hemolytic uremic syndrome and C3 glomerulopathy: conclusions from a “Kidney Disease: Improving Global Outcomes”(KDIGO) Controversies …

THJ Goodship, HT Cook, F Fakhouri, FC Fervenza… - Kidney international, 2017 - Elsevier
In both atypical hemolytic uremic syndrome (aHUS) and C3 glomerulopathy (C3G)
complement plays a primary role in disease pathogenesis. Herein we report the outcome of …

Complement factor H in host defense and immune evasion

R Parente, SJ Clark, A Inforzato, AJ Day - Cellular and Molecular Life …, 2017 - Springer
Complement is the major humoral component of the innate immune system. It recognizes
pathogen-and damage-associated molecular patterns, and initiates the immune response in …

[HTML][HTML] CD55 deficiency, early-onset protein-losing enteropathy, and thrombosis

A Ozen, WA Comrie, RC Ardy… - … England Journal of …, 2017 - Mass Medical Soc
Background Studies of monogenic gastrointestinal diseases have revealed molecular
pathways critical to gut homeostasis and enabled the development of targeted therapies …

Functional characterization of 105 factor H variants associated with aHUS: lessons for variant classification

H Martín Merinero, Y Zhang, E Arjona… - Blood, The Journal …, 2021 - ashpublications.org
Atypical hemolytic uremic syndrome (aHUS) is a life-threatening thrombotic microangiopathy
that can progress, when untreated, to end-stage renal disease. Most frequently, aHUS is …

[HTML][HTML] Glomeruli of dense deposit disease contain components of the alternative and terminal complement pathway

S Sethi, JD Gamez, JA Vrana, JD Theis, HR Bergen III… - Kidney international, 2009 - Elsevier
Dense Deposit Disease (DDD), or membranoproliferative glomerulonephritis type II, is a rare
renal disease characterized by dense deposits in the mesangium and along the glomerular …

Clinical significance of complement deficiencies

HD Pettigrew, SS Teuber… - Annals of the New York …, 2009 - Wiley Online Library
The complement system is composed of more than 30 serum and membrane‐bound
proteins, all of which are needed for normal function of complement in innate and adaptive …

Alternative complement pathway assessment in patients with atypical HUS

LT Roumenina, C Loirat, MA Dragon-Durey… - Journal of …, 2011 - Elsevier
The atypical Hemolytic Uremic Syndrome (aHUS) is a rare thrombotic microangiopathy
leading to end stage renal disease in approximately 60% of patients. Over the last decade, a …

Factor h: a complement regulator in health and disease, and a mediator of cellular interactions

A Kopp, M Hebecker, E Svobodová, M Józsi - Biomolecules, 2012 - mdpi.com
Complement is an essential part of innate immunity as it participates in host defense against
infections, disposal of cellular debris and apoptotic cells, inflammatory processes and …