Functional evaluation of complement factor I variants by immunoassays and SDS-PAGE
Factor I (FI) is an essential regulator of the complement system. Together with co-factors, FI degrades C3b, which inhibits further complement activation. Genetic mutations in FI are associated with pathological conditions like age-related macular degeneration and atypical hemolytic uremic syndome....
Main Authors: | Alexandra Gerogianni, Laura M. Baas, Dick J. Sjöström, Nicole C. A. J. van de Kar, Marit Pullen, Siem J. van de Peppel, Per H. Nilsson, Lambertus P. van den Heuvel |
---|---|
Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2023-10-01
|
Series: | Frontiers in Immunology |
Subjects: | |
Online Access: | https://www.frontiersin.org/articles/10.3389/fimmu.2023.1279612/full |
Similar Items
-
Challenges in diagnostic testing of nephritic factors
by: Marloes A. H. M. Michels, et al.
Published: (2022-11-01) -
Overactivity of Alternative Pathway Convertases in Patients With Complement-Mediated Renal Diseases
by: Marloes A. H. M. Michels, et al.
Published: (2018-04-01) -
Novel Assays to Distinguish Between Properdin-Dependent and Properdin-Independent C3 Nephritic Factors Provide Insight Into Properdin-Inhibiting Therapy
by: Marloes A. H. M. Michels, et al.
Published: (2019-06-01) -
Modeling complement activation on human glomerular microvascular endothelial cells
by: Kes H. Stevens, et al.
Published: (2023-10-01) -
Different Aspects of Classical Pathway Overactivation in Patients With C3 Glomerulopathy and Immune Complex-Mediated Membranoproliferative Glomerulonephritis
by: Marloes A. H. M. Michels, et al.
Published: (2021-08-01)