The complete amino acid sequence of human complement factor H
about
Structural analysis of the C-terminal region (modules 18-20) of complement regulator factor H (FH)Complement factor H allotype 402H is associated with increased C3b opsonization and phagocytosis of Streptococcus pyogenesHuman factor H deficiency. Mutations in framework cysteine residues and block in H protein secretion and intracellular catabolismEffect of interferon-gamma on complement gene expression in different cell typesInteractions between human complement components factor H, factor I and C3bIdentification of human complement Factor H as a ligand for L-selectinLfhA, a novel factor H-binding protein of Leptospira interrogansThe central portion of factor H (modules 10-15) is compact and contains a structurally deviant CCP moduleHuman genes for complement components C1r and C1s in a close tail-to-tail arrangementStructure of the N-terminal region of complement factor H and conformational implications of disease-linked sequence variationsStructural basis for complement factor H linked age-related macular degenerationIdentification of an alternative polyadenylation site in the human C3b/C4b receptor (complement receptor type 1) transcriptional unit and prediction of a secreted form of complement receptor type 1Solution Structure of CCP Modules 10–12 Illuminates Functional Architecture of the Complement Regulator, Factor HIdentification, characterization, and physiological actions of factor H as an adrenomedullin binding protein present in human plasmaComplement Evasion Mediated by Enhancement of Captured Factor H: Implications for Protection of Self-Surfaces from ComplementProduction of biologically active recombinant human factor H in PhyscomitrellaThe 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 attackRat complement factor H: molecular cloning, sequencing and quantification with a newly established ELISAMolecular cloning and sequence analysis of the cDNA encoding human apolipoprotein H (beta 2-glycoprotein I).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.Factor H mutations in hemolytic uremic syndrome cluster in exons 18-20, a domain important for host cell recognitionStructural and functional characterization of factor H mutations associated with atypical hemolytic uremic syndromeHaemolytic uraemic syndrome and mutations of the factor H gene: a registry-based study of German speaking countriesTranslational mini-review series on complement factor H: genetics and disease associations of human complement factor H.Disease-associated N-terminal complement factor H mutations perturb cofactor and decay-accelerating activities.Tissue-specific host recognition by complement factor H is mediated by differential activities of its glycosaminoglycan-binding regions.Complement control protein factor H: the good, the bad, and the inadequate.Impaired binding of the age-related macular degeneration-associated complement factor H 402H allotype to Bruch's membrane in human retina.Factor H facilitates adherence of Neisseria gonorrhoeae to complement receptor 3 on eukaryotic cells.Meningococcal disease and the complement system.Fusion protein comprising factor H domains 6 and 7 and human IgG1 Fc as an antibacterial immunotherapeuticMolecular characterization of the interaction between sialylated Neisseria gonorrhoeae and factor H.Combination of adrenomedullin with its binding protein accelerates cutaneous wound healing.Hereditary porcine membranoproliferative glomerulonephritis type II is caused by factor H deficiencyLocalization by site-directed mutagenesis of the site in human complement factor H that binds to Streptococcus pyogenes M protein.The molecular basis for hereditary porcine membranoproliferative glomerulonephritis type II: point mutations in the factor H coding sequence block protein secretion.Interferon gamma induces synthesis of complement alternative pathway proteins by human endothelial cells in culture.A novel sialic acid binding site on factor H mediates serum resistance of sialylated Neisseria gonorrhoeae.
P2860
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P2860
The complete amino acid sequence of human complement factor H
description
1988 nî lūn-bûn
@nan
1988年の論文
@ja
1988年論文
@yue
1988年論文
@zh-hant
1988年論文
@zh-hk
1988年論文
@zh-mo
1988年論文
@zh-tw
1988年论文
@wuu
1988年论文
@zh
1988年论文
@zh-cn
name
The complete amino acid sequence of human complement factor H
@en
The complete amino acid sequence of human complement factor H
@nl
type
label
The complete amino acid sequence of human complement factor H
@en
The complete amino acid sequence of human complement factor H
@nl
prefLabel
The complete amino acid sequence of human complement factor H
@en
The complete amino acid sequence of human complement factor H
@nl
P2093
P2860
P356
P1433
P1476
The complete amino acid sequence of human complement factor H
@en
P2093
P2860
P304
P356
10.1042/BJ2490593
P407
P577
1988-01-01T00:00:00Z