Control of the amplification convertase of complement by the plasma protein beta1H
about
Structural analysis of the C-terminal region (modules 18-20) of complement regulator factor H (FH)Complement receptor is an inhibitor of the complement cascadeBivalent and co-operative binding of complement factor H to heparan sulfate and heparinInteractions between human complement components factor H, factor I and C3bRelapsing fever spirochetes Borrelia recurrentis and B. duttonii acquire complement regulators C4b-binding protein and factor HStructural basis for engagement by complement factor H of C3b on a self surfaceAnalysis of binding sites on complement factor I that are required for its activityThe central portion of factor H (modules 10-15) is compact and contains a structurally deviant CCP moduleFactor I is required for the development of membranoproliferative glomerulonephritis in factor H-deficient miceStructural basis for complement factor H linked age-related macular degenerationInteraction of beta1H globulin with cell-bound C3b: quantitative analysis of binding and influence of alternative pathway components on bindingHuman complement C3b inactivator: isolation, characterization, and demonstration of an absolute requirement for the serum protein beta1H for cleavage of C3b and C4b in solutionComplement and its role in protection and pathogenesis of flavivirus infectionsInsights into complement convertase formation based on the structure of the factor B-cobra venom factor complexSolution Structure of CCP Modules 10–12 Illuminates Functional Architecture of the Complement Regulator, Factor HProperdin: a tightly regulated critical inflammatory modulatorFunctional properties of complement factor H-related proteins FHR-3 and FHR-4: binding to the C3d region of C3b and differential regulation by heparinProduction of biologically active complement factor H in therapeutically useful quantitiesDisease-associated sequence variations congregate in a polyanion recognition patch on human factor H revealed in three-dimensional structureGenetic, molecular and functional analyses of complement factor I deficiencyThe meningococcal vaccine candidate neisserial surface protein A (NspA) binds to factor H and enhances meningococcal resistance to complementIsolation and characterization of a novel rat factor H-related protein that is up-regulated in glomeruli under complement attackOxidative stress and the regulation of complement activation in human glaucomaRat complement factor H: molecular cloning, sequencing and quantification with a newly established ELISARegulation of the amplification C3 convertase of human complement by an inhibitory protein isolated from human erythrocyte membraneModulation of the classical pathway C3 convertase by plasma proteins C4 binding protein and C3b inactivatorAnalysis of the interactions between properdin, the third component of complement (C3), and its physiological activation productsHuman C4-binding protein. II. Role in proteolysis of C4b by C3b-inactivatorStreptococcal M protein: molecular design and biological behavior.Complement factor H gene mutation associated with autosomal recessive atypical hemolytic uremic syndrome.Clustering of missense mutations in the C-terminal region of factor H in atypical hemolytic uremic syndrome.Structural and functional characterization of factor H mutations associated with atypical hemolytic uremic syndromeComplement in glomerular injury.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.Mutations of factor H impair regulation of surface-bound C3b by three mechanisms in atypical hemolytic uremic syndrome.aHUS caused by complement dysregulation: new therapies on the horizon.Crystallographic determination of the disease-associated T1184R variant of complement regulator factor H.Moss-Produced, Glycosylation-Optimized Human Factor H for Therapeutic Application in Complement Disorders.Antiphagocytic activity of streptococcal M protein: selective binding of complement control protein factor H.
P2860
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P2860
Control of the amplification convertase of complement by the plasma protein beta1H
description
1976 nî lūn-bûn
@nan
1976 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1976 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
1976年の論文
@ja
1976年論文
@yue
1976年論文
@zh-hant
1976年論文
@zh-hk
1976年論文
@zh-mo
1976年論文
@zh-tw
1976年论文
@wuu
name
Control of the amplification convertase of complement by the plasma protein beta1H
@ast
Control of the amplification convertase of complement by the plasma protein beta1H
@en
Control of the amplification convertase of complement by the plasma protein beta1H
@nl
type
label
Control of the amplification convertase of complement by the plasma protein beta1H
@ast
Control of the amplification convertase of complement by the plasma protein beta1H
@en
Control of the amplification convertase of complement by the plasma protein beta1H
@nl
prefLabel
Control of the amplification convertase of complement by the plasma protein beta1H
@ast
Control of the amplification convertase of complement by the plasma protein beta1H
@en
Control of the amplification convertase of complement by the plasma protein beta1H
@nl
P2093
P2860
P3181
P356
P1476
Control of the amplification convertase of complement by the plasma protein beta1H
@en
P2093
P2860
P304
P3181
P356
10.1073/PNAS.73.9.3268
P407
P577
1976-09-01T00:00:00Z