Results 21 to 30 of about 1,408,273 (290)

Factor H-related protein 1 in systemic lupus erythematosus [PDF]

open access: yesFrontiers in Immunology
BackgroundFactor H (FH) is a major soluble inhibitor of the complement system and part of a family comprising five related proteins (FHRs 1–5). Deficiency of FHR1 was described to be linked to an elevated risk of systemic lupus erythematosus (SLE).
Jessica S. Kleer   +9 more
doaj   +3 more sources

Human factor H-related protein 2 (CFHR2) regulates complement activation. [PDF]

open access: yesPLoS ONE, 2013
Mutations and deletions within the human CFHR gene cluster on chromosome 1 are associated with diseases, such as dense deposit disease, CFHR nephropathy or age-related macular degeneration. Resulting mutant CFHR proteins can affect complement regulation.
Hannes U Eberhardt   +10 more
doaj   +4 more sources

Role of factor H-related protein 3 in Pseudomonas aeruginosa bloodstream infections

open access: yesFrontiers in Immunology
Pseudomonas aeruginosa is a leading cause of nosocomial bloodstream infections. The outcome of these infections depends on the virulence of the microorganism as well as host-related conditions and factors.
Alex González-Alsina   +7 more
doaj   +5 more sources

Factor H-related protein 1 promotes complement-mediated opsonization of Pseudomonas aeruginosa

open access: yesFrontiers in Cellular and Infection Microbiology
Pseudomonas aeruginosa is an important human opportunistic pathogen responsible for a wide range of infections. The complement system is the main early host defense mechanism to control these infections. P.
Alex González-Alsina   +7 more
doaj   +4 more sources

Defining the Glycosaminoglycan Interactions of Complement Factor H–Related Protein 5 [PDF]

open access: yesThe Journal of Immunology, 2021
Abstract Complement activation is an important mediator of kidney injury in glomerulonephritis. Complement factor H (FH) and FH-related protein 5 (FHR-5) influence complement activation in C3 glomerulopathy and IgA nephropathy by differentially regulating glomerular complement.
Frederick Gyapon-Quast   +8 more
openaire   +4 more sources

Deregulation of Factor H by Factor H-Related Protein 1 Depends on Sialylation of Host Surfaces [PDF]

open access: yesFrontiers in Immunology, 2021
To discriminate between self and non-self surfaces and facilitate immune surveillance, the complement system relies on the interplay between surface-directed activators and regulators. The dimeric modulator FHR-1 is hypothesized to competitively remove the complement regulator FH from surfaces that strongly fix opsonic C3b molecules—a process known as “
Arthur Dopler   +10 more
openaire   +3 more sources

Complement Factor H and Related Proteins as Markers of Cardiovascular Risk in Pediatric Chronic Kidney Disease

open access: yesBiomedicines, 2022
Cardiovascular disease (CVD) is the main cause of mortality among chronic kidney disease (CKD) patients, both in adults and in children. Hypertension is one of the risk factors of CVD.
Wei-Ting Liao   +3 more
doaj   +1 more source

CFH and CFHR structural variants in atypical Hemolytic Uremic Syndrome: Prevalence, genomic characterization and impact on outcome

open access: yesFrontiers in Immunology, 2023
IntroductionAtypical hemolytic uremic syndrome (aHUS) is a rare disease that manifests with microangiopathic hemolytic anemia, thrombocytopenia, and acute renal failure, and is associated with dysregulation of the alternative complement pathway.
Rossella Piras   +11 more
doaj   +1 more source

Hypoglycemia-induced changes in complement pathways in type 2 diabetes

open access: yesAtherosclerosis Plus, 2021
Background and aims: An association between hypoglycaemia and adverse cardiovascular events has been suggested from longitudinal and retrospective cohort studies. The complement pathway proteins in hypoglycemia are not well studied. Here, we hypothesized
Abu Saleh Md Moin   +6 more
doaj   +1 more source

Case report: Novel FHR2 variants in atypical Hemolytic Uremic Syndrome: A case study of a translational medicine approach in renal transplantation

open access: yesFrontiers in Immunology, 2022
Atypical hemolytic–uremic syndrome (aHUS) is a severe thrombotic microangiopathy in which kidney involvement is common. aHUS can be due to either genetic or acquired abnormalities, with most abnormalities affecting the alternative complement pathway ...
Emma Diletta Stea   +11 more
doaj   +1 more source

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