Regulation by membrane sialic acid of beta1H-dependent decay-dissociation of amplification C3 convertase of the alternative complement pathway.
about
Cloning and characterization of gp36, a human mucin-type glycoprotein preferentially expressed in vascular endotheliumDual interaction of factor H with C3d and glycosaminoglycans in host-nonhost discrimination by complementStructural basis for complement factor H linked age-related macular degenerationThe complotype: dictating risk for inflammation and infectionStructural basis for sialic acid-mediated self-recognition by complement factor HThree SIBLINGs (small integrin-binding ligand, N-linked glycoproteins) enhance factor H's cofactor activity enabling MCP-like cellular evasion of complement-mediated attackCell- and Protein-Directed Glycosylation of Native Cleaved HIV-1 EnvelopeInitiation of the alternative pathway of complement: recognition of activators by bound C3b and assembly of the entire pathway from six isolated proteinsRegulation of the amplification C3 convertase of human complement by an inhibitory protein isolated from human erythrocyte membraneInhibition of complement activation on the surface of cells after incorporation of decay-accelerating factor (DAF) into their membranesMechanism of action of factor D of the alternative complement pathwayInfections of People with Complement Deficiencies and Patients Who Have Undergone SplenectomyThe binding of factor H to a complex of physiological polyanions and C3b on cells is impaired in atypical hemolytic uremic syndrome.Identification of complement regulatory domains in vaccinia virus complement control protein.Infectious diseases associated with complement deficiencies.Translational mini-review series on complement factor H: genetics and disease associations of human complement factor H.Translational mini-review series on complement factor H: renal diseases associated with complement factor H: novel insights from humans and animals.Recognition of malondialdehyde-modified proteins by the C terminus of complement factor H is mediated via the polyanion binding site and impaired by mutations found in atypical hemolytic uremic syndrome.Red blood cell Thomsen-Friedenreich antigen expression and galectin-3 plasma concentrations in Streptococcus pneumoniae-associated hemolytic uremic syndrome and hemolytic anemia.Antiphagocytic activity of streptococcal M protein: selective binding of complement control protein factor H.Anaerobic growth and cytidine 5'-monophospho-N-acetylneuraminic acid act synergistically to induce high-level serum resistance in Neisseria gonorrhoeae.Discrimination between activators and nonactivators of the alternative pathway of complement: regulation via a sialic acid/polyanion binding site on factor H.TnphoA-mediated disruption of K54 capsular polysaccharide genes in Escherichia coli confers serum sensitivity.A role for Bacteroides fragilis neuraminidase in bacterial growth in two model systemsStudies of group B streptococcal infection in mice deficient in complement component C3 or C4 demonstrate an essential role for complement in both innate and acquired immunity.Complementary recognition of alternative pathway activators by decay-accelerating factor and factor HM protein of the group A Streptococcus binds to the seventh short consensus repeat of human complement factor HAcquired resistance of Escherichia coli to complement lysis by binding of glycophosphoinositol-anchored protectin (CD59).Complement Evasion Strategies of Viruses: An Overview.Inhibition of the classical pathway of complement by meningococcal capsular polysaccharidesComplement control protein factor H: the good, the bad, and the inadequate.Novel Aeromonas hydrophila PPD134/91 genes involved in O-antigen and capsule biosynthesisMultifarious roles of sialic acids in immunity.Definition of a bacterial virulence factor: sialylation of the group B streptococcal capsule.Abnormality of glycophorin-alpha on paroxysmal nocturnal hemoglobinuria erythrocytes.Membrane-bound hemagglutinin mediates antibody and complement-dependent lysis of influenza virus-treated human platelets in autologous serumMeningococcal group W-135 and Y capsular polysaccharides paradoxically enhance activation of the alternative pathway of complement.A circulating inhibitor of fluid-phase amplification. C3 convertase formation in systemic lupus erythematosusCommon polymorphisms in C3, factor B, and factor H collaborate to determine systemic complement activity and disease riskHost-derived sialic acid is incorporated into Haemophilus influenzae lipopolysaccharide and is a major virulence factor in experimental otitis media
P2860
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P2860
Regulation by membrane sialic acid of beta1H-dependent decay-dissociation of amplification C3 convertase of the alternative complement pathway.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on April 1978
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Regulation by membrane sialic ...... lternative complement pathway.
@en
Regulation by membrane sialic ...... lternative complement pathway.
@nl
type
label
Regulation by membrane sialic ...... lternative complement pathway.
@en
Regulation by membrane sialic ...... lternative complement pathway.
@nl
prefLabel
Regulation by membrane sialic ...... lternative complement pathway.
@en
Regulation by membrane sialic ...... lternative complement pathway.
@nl
P2860
P356
P1476
Regulation by membrane sialic ...... lternative complement pathway.
@en
P2093
P2860
P304
P356
10.1073/PNAS.75.4.1971
P407
P577
1978-04-01T00:00:00Z