Results 31 to 40 of about 28,482,475 (369)

C3 Glomerulonephritis associated with Anti-complement Factor H Autoantibodies in an Adolescent Male: A Case Report [PDF]

open access: yesChildhood Kidney Diseases, 2021
C3 glomerulonephritis (C3GN), a rare condition associated with dysregulation of the alternative pathway of the complement system, is histopathologically characterized by isolated or dominant C3 deposition in the renal glomeruli.
HyeSun Hyun   +4 more
doaj   +1 more source

Sweeteners for factor H [PDF]

open access: yesBlood, 2016
In this issue of Blood , [Hyvarinen et al][1][1][2] show that mutant forms of complement factor H, which are commonly associated with atypical hemolytic uremic syndrome (aHUS), have impairments in binding to sialic acid on C3b-coated erythrocytes, platelets, and endothelial cells.
openaire   +3 more sources

Anti-factor H antibody and its role in atypical hemolytic uremic syndrome

open access: yesFrontiers in Immunology, 2022
Atypical hemolytic uremic syndrome (aHUS) an important form of a thrombotic microangiopathy (TMA) that can frequently lead to acute kidney injury (AKI). An important subset of aHUS is the anti-factor H associated aHUS.
Rupesh Raina   +8 more
doaj   +1 more source

The effect of human factor H on immunogenicity of meningococcal native outer membrane vesicle vaccines with over-expressed factor H binding protein. [PDF]

open access: yesPLoS Pathogens, 2012
The binding of human complement inhibitors to vaccine antigens in vivo could diminish their immunogenicity. A meningococcal ligand for the complement down-regulator, factor H (fH), is fH-binding protein (fHbp), which is specific for human fH.
Peter T Beernink   +5 more
doaj   +1 more source

Association of genetic variants in complement factor H and factor H-related genes with systemic lupus erythematosus susceptibility. [PDF]

open access: yesPLoS Genetics, 2011
Systemic lupus erythematosus (SLE), a complex polygenic autoimmune disease, is associated with increased complement activation. Variants of genes encoding complement regulator factor H (CFH) and five CFH-related proteins (CFHR1-CFHR5) within the ...
Jian Zhao   +56 more
doaj   +1 more source

Complement factor H in host defense and immune evasion

open access: yesCellular and Molecular Life Sciences, 2016
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 coordination with innate and adaptive immunity.
Raffaella Parente   +3 more
semanticscholar   +1 more source

Complement Factor H-Related Protein 4A Is the Dominant Circulating Splice Variant of CFHR4

open access: yesFrontiers in Immunology, 2018
Recent research has elucidated circulating levels of almost all factor H-related (FHR) proteins. Some of these proteins are hypothesized to act as antagonists of the important complement regulator factor H (FH), fine-tuning complement regulation on human
Richard B. Pouw   +8 more
doaj   +1 more source

Murine Factor H Co-Produced in Yeast With Protein Disulfide Isomerase Ameliorated C3 Dysregulation in Factor H-Deficient Mice

open access: yesFrontiers in Immunology, 2021
Recombinant human factor H (hFH) has potential for treating diseases linked to aberrant complement regulation including C3 glomerulopathy (C3G) and dry age-related macular degeneration.
Heather Kerr   +18 more
doaj   +1 more source

Rainbow $H$-factors [PDF]

open access: yesThe Electronic Journal of Combinatorics, 2006
An $H$-factor of a graph $G$ is a spanning subgraph of $G$ whose connected components are isomorphic to $H$. Given a properly edge-colored graph $G$, a rainbow $H$-subgraph of $G$ is an $H$-subgraph of $G$ whose edges have distinct colors. A rainbow $H$-factor is an $H$-factor whose components are rainbow $H$-subgraphs.
openaire   +2 more sources

Complement factors (H) into thrombosis [PDF]

open access: yesBlood, 2017
In this issue of Blood, Ueda et al demonstrate that a mutation in factor H (FH) disrupts host cell interactions, leading to dysregulation of complement, systemic thrombotic angiopathy, and hemolytic uremic syndrome ...
openaire   +3 more sources

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