Pages that link to "Q24684822"

The following pages link to Human complement C3b inactivator: isolation, characterization, and demonstration of an absolute requirement for the serum protein beta1H for cleavage of C3b and C4b in solution (Q24684822):

Displaying 349 items.

• Borrelia valaisiana resist complement-mediated killing independently of the recruitment of immune regulators and inactivation of complement components (Q21090813) (← links)
• Structural analysis of the C-terminal region (modules 18-20) of complement regulator factor H (FH) (Q21134757) (← links)
• Borrelia recurrentis employs a novel multifunctional surface protein with anti-complement, anti-opsonic and invasive potential to escape innate immunity (Q21143848) (← links)
• Structure-guided identification of C3d residues essential for its binding to complement receptor 2 (CD21) (Q24290411) (← links)
• Identification of distinct C3b and C4b recognition sites in the human C3b/C4b receptor (CR1, CD35) by deletion mutagenesis (Q24294595) (← links)
• Complement receptor is an inhibitor of the complement cascade (Q24302183) (← links)
• Bivalent and co-operative binding of complement factor H to heparan sulfate and heparin (Q24311571) (← links)
• Effect of interferon-gamma on complement gene expression in different cell types (Q24527334) (← links)
• Interactions between human complement components factor H, factor I and C3b (Q24530290) (← links)
• Structural basis for engagement by complement factor H of C3b on a self surface (Q24604385) (← links)
• Characterization of shark complement factor I gene(s): genomic analysis of a novel shark-specific sequence (Q24642533) (← links)
• Factor I is required for the development of membranoproliferative glomerulonephritis in factor H-deficient mice (Q24651118) (← links)
• Human pathogenic Borrelia spielmanii sp. nov. resists complement-mediated killing by direct binding of immune regulators factor H and factor H-like protein 1 (Q24672482) (← links)
• Interaction of beta1H globulin with cell-bound C3b: quantitative analysis of binding and influence of alternative pathway components on binding (Q24684253) (← links)
• West Nile virus nonstructural protein NS1 inhibits complement activation by binding the regulatory protein factor H (Q27477691) (← links)
• Structure shows that a glycosaminoglycan and protein recognition site in factor H is perturbed by age-related macular degeneration-linked single nucleotide polymorphism (Q27644071) (← links)
• The Crystal Structure of Cobra Venom Factor, a Cofactor for C3- and C5-Convertase CVFBb (Q27654785) (← links)
• ErpC, a member of the complement regulator-acquiring family of surface proteins fromBorrelia burgdorferi, possesses an architecture previously unseen in this protein family (Q27678414) (← links)
• Further structural insights into the binding of complement factor H by complement regulator-acquiring surface protein 1 (CspA) ofBorrelia burgdorferi (Q27678417) (← links)
• Structural characterization of CspZ, a complement regulator factor H and FHL-1 binding protein from Borrelia burgdorferi (Q27690007) (← links)
• Properdin: a tightly regulated critical inflammatory modulator (Q28069187) (← links)
• Host recognition and target differentiation by factor H, a regulator of the alternative pathway of complement (Q28141398) (← links)
• Functional properties of complement factor H-related proteins FHR-3 and FHR-4: binding to the C3d region of C3b and differential regulation by heparin (Q28141946) (← links)
• Complement factor I deficiency in a family with recurrent infections (Q28262796) (← links)
• Structures of complement component C3 provide insights into the function and evolution of immunity (Q28273530) (← links)
• Molecular basis of complement factor I (CFI) polymorphism: one of two polymorphic suballeles responsible for CFI A is Japanese-specific (Q28295563) (← links)
• Production of biologically active complement factor H in therapeutically useful quantities (Q28300280) (← links)
• Disease-associated sequence variations congregate in a polyanion recognition patch on human factor H revealed in three-dimensional structure (Q28301693) (← links)
• Genetic polymorphism of human factor I (C3b inactivator) (Q28306478) (← links)
• The meningococcal vaccine candidate neisserial surface protein A (NspA) binds to factor H and enhances meningococcal resistance to complement (Q28474974) (← links)
• Microdialysis Sampling from Wound Fluids Enables Quantitative Assessment of Cytokines, Proteins, and Metabolites Reveals Bone Defect-Specific Molecular Profiles (Q28552772) (← links)
• Distribution of immunoreactivity for the adrenomedullin binding protein, complement factor H, in the rat brain (Q28565796) (← links)
• Complement factor I is upregulated in rat hepatocytes by interleukin-6 but not by interferon-gamma, interleukin-1beta, or tumor necrosis factor-alpha (Q28569082) (← links)
• Oxidative stress and the regulation of complement activation in human glaucoma (Q28577665) (← links)
• H-2-linked murine factor B phenotypes (Q28594761) (← links)
• Initiation of the alternative pathway of complement: recognition of activators by bound C3b and assembly of the entire pathway from six isolated proteins (Q28610965) (← links)
• Regulation of the amplification C3 convertase of human complement by an inhibitory protein isolated from human erythrocyte membrane (Q28610966) (← links)
• Characterization of the interaction of human C4b-binding protein with physiological ligands (Q28610984) (← links)
• Formation of the initial C3 convertase of the alternative complement pathway. Acquisition of C3b-like activities by spontaneous hydrolysis of the putative thioester in native C3 (Q28610996) (← links)
• Human C4-binding protein. II. Role in proteolysis of C4b by C3b-inactivator (Q28610997) (← links)
• C5 inhibition prevents renal failure in a mouse model of lethal C3 glomerulopathy (Q30274884) (← links)
• The binding of factor H to a complex of physiological polyanions and C3b on cells is impaired in atypical hemolytic uremic syndrome. (Q30377280) (← links)
• Circular dichroism studies of human factor H A regulatory component of the complement system (Q30412123) (← links)
• Rat complement factor I: molecular cloning, sequencing and expression in tissues and isolated cells (Q30821832) (← links)
• Pig complement regulator factor H: molecular cloning and functional characterization. (Q33193498) (← links)
• Human Complement Factor H: Molecular Cloning and cDNA Expression Reveals Variability in the Factor H-Related mRNA Species of 1.4 kb (Q33323288) (← links)
• Complement factor H gene mutation associated with autosomal recessive atypical hemolytic uremic syndrome (Q33330770) (← links)
• Clustering of missense mutations in the C-terminal region of factor H in atypical hemolytic uremic syndrome. (Q33335833) (← links)
• Complement factor H and hemolytic uremic syndrome (Q33337391) (← links)
• Structural and functional characterization of factor H mutations associated with atypical hemolytic uremic syndrome (Q33345226) (← links)
• Atypical haemolytic uraemic syndrome and mutations in complement regulator genes (Q33368691) (← links)
• Translational mini-review series on complement factor H: genetics and disease associations of human complement factor H. (Q33377799) (← links)
• Translational mini-review series on complement factor H: renal diseases associated with complement factor H: novel insights from humans and animals. (Q33378236) (← links)
• Complement factor H: using atomic resolution structure to illuminate disease mechanisms (Q33382097) (← links)
• Mutations of factor H impair regulation of surface-bound C3b by three mechanisms in atypical hemolytic uremic syndrome (Q33384039) (← links)
• Genetics and complement in atypical HUS. (Q33389945) (← links)
• aHUS caused by complement dysregulation: new therapies on the horizon (Q33390198) (← links)
• Disease-associated N-terminal complement factor H mutations perturb cofactor and decay-accelerating activities (Q33393852) (← links)
• Crystallographic determination of the disease-associated T1184R variant of complement regulator factor H. (Q33395894) (← links)
• Complement factor H variants I890 and L1007 while commonly associated with atypical hemolytic uremic syndrome are polymorphisms with no functional significance (Q33396948) (← links)
• Mouse macrophage beta subunit (CD11b) cDNA for the CR3 complement receptor/Mac-1 antigen (Q33495248) (← links)
• Identification and functional characterisation of Complement Regulator Acquiring Surface Protein-1 of serum resistant Borrelia garinii OspA serotype 4 (Q33530563) (← links)
• Functional characterization of Borrelia spielmanii outer surface proteins that interact with distinct members of the human factor H protein family and with plasminogen (Q33557779) (← links)
• Antiphagocytic activity of streptococcal M protein: selective binding of complement control protein factor H. (Q33558301) (← links)
• Factor H in porcine seminal plasma protects sperm against complement attack in genital tracts (Q33582067) (← links)
• Discrimination between activators and nonactivators of the alternative pathway of complement: regulation via a sialic acid/polyanion binding site on factor H (Q33596128) (← links)
• Human complement regulators C4b-binding protein and C1 esterase inhibitor interact with a novel outer surface protein of Borrelia recurrentis (Q33598636) (← links)
• Inhibition of the alternative pathway of nonhuman infant complement by porin B2 contributes to virulence of Neisseria meningitidis in the infant rat model (Q33602953) (← links)
• Pathogenic Rickettsia species acquire vitronectin from human serum to promote resistance to complement-mediated killing (Q33638843) (← links)
• Targeted inhibition of the complement alternative pathway with complement receptor 2 and factor H attenuates collagen antibody-induced arthritis in mice (Q33687307) (← links)
• The factor H protein family (Q33688567) (← links)
• M protein of the group A Streptococcus binds to the seventh short consensus repeat of human complement factor H (Q33752194) (← links)
• The contrasting mechanisms of serum resistance of Neisseria gonorrhoeae and group B Neisseria meningitidis. (Q33852676) (← links)
• Complement activation following oxidative stress (Q33852682) (← links)
• Studies on murine Ss protein: demonstration that S region encodes structural gene for fourth component of complement (Q33976098) (← links)
• Variola virus immune evasion design: expression of a highly efficient inhibitor of human complement (Q34066011) (← links)
• Complement control protein factor H: the good, the bad, and the inadequate. (Q34067107) (← links)
• Excretion of complement proteins and its activation marker C5b-9 in IgA nephropathy in relation to renal function (Q34082044) (← links)
• Time-dependent Gene Profiling Indicates the Presence of Different Phases for Ischemia/Reperfusion Injury in Retina (Q34109774) (← links)
• Enhanced factor H binding to sialylated Gonococci is restricted to the sialylated lacto-N-neotetraose lipooligosaccharide species: implications for serum resistance and evidence for a bifunctional lipooligosaccharide sialyltransferase in Gonococci (Q34111593) (← links)
• Borrelia burgdorferi regulates expression of complement regulator-acquiring surface protein 1 during the mammal-tick infection cycle. (Q34111768) (← links)
• Characterization of a unique glycosylated anchor endopeptidase that cleaves the LPXTG sequence motif of cell surface proteins of Gram-positive bacteria (Q34153505) (← links)
• Mechanism of complement resistance of pathogenic Borrelia burgdorferi isolates (Q34257482) (← links)
• Regulation of the activity of platelet-bound C3 convertase of the alternative pathway of complement by platelet factor H (Q34340063) (← links)
• Prevention of C5 activation ameliorates spontaneous and experimental glomerulonephritis in factor H-deficient mice (Q34537391) (← links)
• Cigarette smoke can activate the alternative pathway of complement in vitro by modifying the third component of complement (Q34537546) (← links)
• Attempts to prepare suitable complement regulatory molecules for clinical xenotransplantation (Q34582615) (← links)
• A circulating inhibitor of fluid-phase amplification. C3 convertase formation in systemic lupus erythematosus (Q34629373) (← links)
• Alpha-2,3-sialyltransferase enhances Neisseria gonorrhoeae survival during experimental murine genital tract infection (Q34721170) (← links)
• A meningococcal factor H binding protein mutant that eliminates factor H binding enhances protective antibody responses to vaccination (Q34993283) (← links)
• Cell and molecular biology of the multifunctional peptide, adrenomedullin (Q35010860) (← links)
• Atypical hemolytic uremic syndrome and mutation analysis of factor H gene in two Tunisian families (Q35026701) (← links)
• Affinity purification of human factor H on polypeptides derived from streptococcal m protein: enrichment of the Y402 variant (Q35053992) (← links)
• Interaction of Leptospira elongation factor Tu with plasminogen and complement factor H: a metabolic leptospiral protein with moonlighting activities (Q35060728) (← links)
• Molecular characterization of the interaction between sialylated Neisseria gonorrhoeae and factor H. (Q35063071) (← links)
• Localization by site-directed mutagenesis of the site in human complement factor H that binds to Streptococcus pyogenes M protein. (Q35566789) (← links)
• Plasma complement factor H is associated with disease activity of patients with ANCA-associated vasculitis (Q35810445) (← links)
• Fine Mapping of the Interaction between C4b-Binding Protein and Outer Membrane Proteins LigA and LigB of Pathogenic Leptospira interrogans. (Q35827083) (← links)
• Alternative Pathway Inhibition by Exogenous Factor H Fails to Attenuate Inflammation and Vascular Leakage in Experimental Pneumococcal Sepsis in Mice (Q35922386) (← links)
• Quantitative Modeling of the Alternative Pathway of the Complement System (Q35975481) (← links)
• Factor H mediated cell surface protection from complement is critical for the survival of PNH erythrocytes. (Q35990700) (← links)
• Mutational analysis of Kaposica reveals that bridging of MG2 and CUB domains of target protein is crucial for the cofactor activity of RCA proteins (Q36179379) (← links)
• Design of meningococcal factor H binding protein mutant vaccines that do not bind human complement factor H. (Q36211092) (← links)
• The rickettsial OmpB β-peptide of Rickettsia conorii is sufficient to facilitate factor H-mediated serum resistance (Q36211176) (← links)
• Identification of a 145,000 Mr membrane protein as the C3d receptor (CR2) of human B lymphocytes (Q36254495) (← links)
• Complement activation and cardiac surgery: a novel target for improving outcomes (Q36269099) (← links)
• Third component of human complement: Localization of the internal thiolester bond (Q36281685) (← links)
• The immunohistochemical analysis of membrane-bound CD55, CD59 and fluid-phase FH and FH-like complement inhibitors in cancers of ovary and corpus uteri origin. (Q36305634) (← links)
• Release of soluble immune complexes from immune adherence receptors on human erythrocytes is mediated by C3b inactivator independently of β1H and is accompanied by generation of C3c (Q36308579) (← links)
• Complement Factor H Binds to Human Serum Apolipoprotein E and Mediates Complement Regulation on High Density Lipoprotein Particles. (Q36323504) (← links)
• Bactericidal activity of the alternative complement pathway generated from 11 isolated plasma proteins (Q36341359) (← links)
• Surface-associated heparin inhibits zymosan-induced activation of the human alternative complement pathway by augmenting the regulatory action of the control proteins on particle-bound C3b (Q36343010) (← links)
• Release of endogenous C3b inactivator from lymphocytes in response to triggering membrane receptors for beta 1H globulin (Q36344262) (← links)
• Identification of a C3bi-specific membrane complement receptor that is expressed on lymphocytes, monocytes, neutrophils, and erythrocytes. (Q36346014) (← links)
• Quantitation of in vitro opsonic activity of human antibody induced by a vaccine consisting of the type III-specific polysaccharide of group B streptococcus (Q36346039) (← links)
• Characterization of the lymphocyte membrane receptor for factor H (beta 1H-globulin) with an antibody to anti-factor H idiotype (Q36346502) (← links)
• Breakdown of C3 after complement activation. Identification of a new fragment C3g, using monoclonal antibodies (Q36346672) (← links)
• Unique role of the complement receptor CR1 in the degradation of C3b associated with immune complexes (Q36347257) (← links)
• Inhibition of neutrophil function by fluid phase C3b of complement. (Q36348157) (← links)
• Generation of three different fragments of bound C3 with purified factor I or serum. II. Location of binding sites in the C3 Fragments for Factors B and H, complement receptors , and bovine conglutinin (Q36348883) (← links)
• C3b covalently bound to IgG demonstrates a reduced rate of inactivation by factors H and I (Q36349666) (← links)
• Deposition of C3b and iC3b onto particulate activators of the human complement system. Quantitation with monoclonal antibodies to human C3 (Q36350126) (← links)
• Opsonization of bacteroides by the alternative complement pathway reconstructed from isolated plasma proteins (Q36352460) (← links)
• Antibody-independent activation of the alternative complement pathway by measles virus-infected cells (Q36353461) (← links)
• Epstein-Barr virus regulates activation and processing of the third component of complement (Q36355255) (← links)
• Induction of immune cytolysis: tumor-cell killing by complement is initiated by covalent complex of monoclonal antibody and stable C3/C5 convertase (Q36384230) (← links)
• A novel sialic acid binding site on factor H mediates serum resistance of sialylated Neisseria gonorrhoeae (Q36400453) (← links)
• Binding of complement factor H to loop 5 of porin protein 1A: a molecular mechanism of serum resistance of nonsialylated Neisseria gonorrhoeae (Q36404057) (← links)
• Evidence for presence of an internal thiolester bond in third component of human complement. (Q36409419) (← links)
• Human complement factor H: isolation of cDNA clones and partial cDNA sequence of the 38-kDa tryptic fragment containing the binding site for C3b. (Q36419473) (← links)
• Prevalence of factor H-binding protein variants and NadA among meningococcal group B isolates from the United States: implications for the development of a multicomponent group B vaccine (Q36464572) (← links)
• The meningococcal vaccine candidate GNA1870 binds the complement regulatory protein factor H and enhances serum resistance (Q36470692) (← links)
• A Novel Factor H-Fc Chimeric Immunotherapeutic Molecule against Neisseria gonorrhoeae (Q36553903) (← links)
• Structure of murine complement component C3. II. Nucleotide sequence of cloned complementary DNA coding for the alpha chain (Q36587071) (← links)
• Essential role of surface-bound complement factor H in controlling immune complex-induced arthritis (Q36714001) (← links)
• Insights into the Effects of Complement Factor H on the Assembly and Decay of the Alternative Pathway C3 Proconvertase and C3 Convertase (Q36778860) (← links)
• Defining the Binding Region in Factor H to Develop a Therapeutic Factor H-Fc Fusion Protein against Non-Typeable Haemophilus influenzae (Q36792484) (← links)
• Detection of complement activation using monoclonal antibodies against C3d. (Q36793448) (← links)
• Streptococcus pyogenes Employs Strain-dependent Mechanisms of C3b Inactivation to Inhibit Phagocytosis and Killing of Bacteria (Q36884841) (← links)
• Translational mini-review series on complement factor H: structural and functional correlations for factor H. (Q37032788) (← links)
• C4b-Binding protein, a regulatory protein of complement (Q37097672) (← links)
• Analysis of a unique interaction between the complement regulatory protein factor H and the periodontal pathogen Treponema denticola. (Q37144937) (← links)
• Polyanion-induced self-association of complement factor H. (Q37181643) (← links)
• Complement-mediated opsonization of invasive group A Streptococcus pyogenes strain AP53 is regulated by the bacterial two-component cluster of virulence responder/sensor (CovRS) system (Q37189577) (← links)
• Functional comparison of the binding of factor H short consensus repeat 6 (SCR 6) to factor H binding protein from Neisseria meningitidis and the binding of factor H SCR 18 to 20 to Neisseria gonorrhoeae porin (Q37191341) (← links)
• The C-terminus of complement factor H is essential for host cell protection (Q37238656) (← links)
• The tick-over theory revisited: formation and regulation of the soluble alternative complement C3 convertase (C3(H2O)Bb) (Q37240329) (← links)
• CspA-mediated binding of human factor H inhibits complement deposition and confers serum resistance in Borrelia burgdorferi (Q37256498) (← links)
• Identification of three physically and functionally distinct binding sites for C3b in human complement factor H by deletion mutagenesis (Q37306486) (← links)
• Update on hemolytic uremic syndrome: Diagnostic and therapeutic recommendations (Q37322141) (← links)
• Affected erythrocytes of patients with paroxysmal nocturnal hemoglobinuria are deficient in the complement regulatory protein, decay accelerating factor (Q37346265) (← links)
• Deficiency of an erythrocyte membrane protein with complement regulatory activity in paroxysmal nocturnal hemoglobinuria (Q37348185) (← links)
• The molecular basis of hereditary complement factor I deficiency (Q37351993) (← links)
• Factor H and neisserial pathogenesis (Q37401428) (← links)
• The role of complement in gonococcal infection of cervical epithelia (Q37456620) (← links)
• Binding of complement regulatory proteins to group A Streptococcus (Q37456631) (← links)
• Developmentally regulated expression by Trypanosoma cruzi of molecules that accelerate the decay of complement C3 convertases (Q37480820) (← links)
• Generation of multiple fluid-phase C3b:plasma protein complexes during complement activation: possible implications in C3 glomerulopathies (Q37499843) (← links)
• Evidence for linkage between the loci coding for the binding protein for the fourth component of human complement (C4BP) and for the C3b/C4b receptor (Q37580578) (← links)
• Regulation by membrane sialic acid of β1H-dependent decay-dissociation of amplification C3 convertase of the alternative complement pathway (Q37584606) (← links)
• Complement C3 convertase: Cell surface restriction of β1H control and generation of restriction on neuraminidase-treated cells (Q37586846) (← links)
• Studies on the murine Ss protein: demonstration that the Ss protein is functionally the fourth component of complement (Q37586909) (← links)
• Factor h: a complement regulator in health and disease, and a mediator of cellular interactions. (Q38223669) (← links)
• An initiator element and a proximal cis-acting sequence are essential for transcriptional activation of the complement factor I (CFI) gene (Q38319366) (← links)
• Painting factor H onto mesenchymal stem cells protects the cells from complement- and neutrophil-mediated damage (Q38407079) (← links)
• Complement: an overview for the clinician (Q38515940) (← links)
• Binding of complement factor H to endothelial cells is mediated by the carboxy-terminal glycosaminoglycan binding site (Q38596477) (← links)
• Immune evasion of leptospira species by acquisition of human complement regulator C4BP. (Q38892814) (← links)
• Protection of host cells by complement regulators. (Q38991019) (← links)
• The complement factor H-related proteins (Q38991052) (← links)
• Release of endogenous anti-inflammatory complement regulators FHL-1 and factor H protects synovial fibroblasts during rheumatoid arthritis (Q39012595) (← links)
• Different regulation of factor H and FHL-1/reconectin by inflammatory mediators and expression of the two proteins in rheumatoid arthritis (RA). (Q39012599) (← links)
• FHL-1/reconectin and factor H: two human complement regulators which are encoded by the same gene are differently expressed and regulated (Q39012605) (← links)
• Human complement factor H and factor H-like protein 1 are expressed in human retinal pigment epithelial cells (Q39053892) (← links)
• Complement Evasion by Pathogenic Leptospira. (Q39075995) (← links)
• Role of fibrinogen in complement inhibition by streptococcal M protein (Q39077444) (← links)
• Mapping of the domains required for decay acceleration activity of the human factor H-like protein 1 and factor H. (Q39154806) (← links)
• Interaction of human complement factor H variants Tyr⁴⁰² and His⁴⁰² with Leptospira spp. (Q39462743) (← links)
• CR1 and the cell membrane proteins that bind C3 and C4. A basic and clinical review (Q39483817) (← links)
• PspC, a pneumococcal surface protein, binds human factor H. (Q39520120) (← links)
• Demonstration of β1h globulin together with c3 in the dermal-epidermal junction of patients with systemic lupus erythematosus (Q39523058) (← links)
• Requirements for beta1H globulin and C3b inactivator in the control of the alternative complement pathway in human serum (Q39528374) (← links)
• Deposition of β1h globulin in kidneys of patients with immune renal disease (Q39536959) (← links)
• The Biology and Detection of Immune Complexes (Q39590911) (← links)
• Membrane complement receptors specific for bound fragments of C3. (Q39614176) (← links)
• Regulation of complement (Q39628216) (← links)
• The yeast Candida albicans binds complement regulators factor H and FHL-1. (Q39656217) (← links)
• Structure of Complement C3(H2O) Revealed By Quantitative Cross-Linking/Mass Spectrometry And Modeling (Q39718125) (← links)
• The complement system in pemphigus, bullous pemphigoid and herpes gestationis (Q39799267) (← links)
• Activation of the complement system by pathogenic fungi (Q39820650) (← links)
• Activation of the Complement System by Antibody-Antigen Complexes: The Classical Pathway (Q39856020) (← links)
• The disease-protective complement factor H allotypic variant Ile62 shows increased binding affinity for C3b and enhanced cofactor activity (Q39968584) (← links)
• Molecular Biology and Chemistry of the Alternative Pathway of Complement (Q40098618) (← links)
• Characterization of complement receptors (Q40113958) (← links)
• The quest for an intrinsic C3 activating factor in human glomerular disease. (Q40115835) (← links)
• The alternative pathway of complement (Q40118346) (← links)
• The Regulation of Complement Activity by Pharmacologic Agents (Q40123049) (← links)
• Cellular and subcellular mediators of acute inflammation. (Q40150223) (← links)
• Activation of the complement system (Q40162126) (← links)
• The Significance of Complement in Immunohematology (Q40177478) (← links)
• Accelerated decay of C3b to iC3b when C3b is bound to the Cryptococcus neoformans capsule (Q40269086) (← links)
• Molecular characterization of the interaction of Borrelia parkeri and Borrelia turicatae with human complement regulators (Q40331294) (← links)
• Membrane-associated proteins regulating the complement system: functions and deficiencies (Q40488634) (← links)
• Structure and function of recombinant cobra venom factor (Q40558288) (← links)
• Binding of a model regulator of complement activation (RCA) to a biomaterial surface: surface-bound factor H inhibits complement activation. (Q40690932) (← links)
• Development and application of an enzyme-linked immunosorbent assay for the quantitation of alternative complement pathway activation in human serum (Q40830914) (← links)
• Acquisition of negative complement regulators by the saprophyte Leptospira biflexa expressing LigA or LigB confers enhanced survival in human serum. (Q40853795) (← links)
• Identification of residues within the 727-767 segment of human complement component C3 important for its interaction with factor H and with complement receptor 1 (CR1, CD35). (Q40973594) (← links)
• Analysis of the promoter region of the murine complement factor H gene (Q41033520) (← links)
• The C-terminus of factor H: monoclonal antibodies inhibit heparin binding and identify epitopes common to factor H and factor H-related proteins (Q41044029) (← links)
• Borrelia burgdorferi complement regulator-acquiring surface protein 1 of the Lyme disease spirochetes is expressed in humans and induces antibody responses restricted to nondenatured structural determinants (Q41057832) (← links)
• Demonstration of the Complement Regulating Protein, β1H, in Skin Biopsies from Patients with Bullous Pemphigoid (Q41134840) (← links)
• Nonimmunoglobulin C3 activating factor in membranoproliferative glomerulonephritis (Q41135733) (← links)
• Deciphering the ligand-binding sites in the Borrelia burgdorferi complement regulator-acquiring surface protein 2 required for interactions with the human immune regulators factor H and factor H-like protein 1. (Q41177250) (← links)
• Glomerular deposition of complement-control proteins in acute and chronic glomerulonephritis (Q41194741) (← links)
• Regulation of C3 deposition on gp120 coated CD4 positive cells by decay accelerating factor and factor H. (Q41425849) (← links)
• Functional mapping of YadA- and Ail-mediated binding of human factor H to Yersinia enterocolitica serotype O:3. (Q41442178) (← links)
• Characterization of complement factor H binding to Yersinia enterocolitica serotype O:3. (Q41442818) (← links)
• Contribution of the infection-associated complement regulator-acquiring surface protein 4 (ErpC) to complement resistance of Borrelia burgdorferi (Q41570062) (← links)
• Pathogenic Leptospira species acquire factor H and vitronectin via the surface protein LcpA. (Q41585170) (← links)
• Neisseria cinerea expresses a functional factor H binding protein which is recognised by immune responses elicited by meningococcal vaccines. (Q41673949) (← links)
• Human complement factor H. Tissue specificity in the expression of three different mRNA species (Q41682097) (← links)
• The role of C4-binding protein and {beta }1H in proteolysis of C4b and C3b (Q41690090) (← links)
• Identification and functional characterization of complement regulator-acquiring surface protein 1 of the Lyme disease spirochetes Borrelia afzelii and Borrelia garinii (Q41818115) (← links)
• Comparison of the C-mediating killing activity and C-activating properties of mouse monoclonal and polyclonal antibodies against Trypanosoma cruzi. (Q41819279) (← links)
• Limited tryptic cleavage of complement factor H abrogates recognition of sialic acid-containing surfaces by the alternative pathway of complement (Q41821311) (← links)
• A mechanism of activation of the alternative complement pathway by the classical pathway: protection of C3b from inactivation by covalent attachment to C4b. (Q41840694) (← links)
• Human complement component C4. Structural studies on the fragments derived from C4b by cleavage with C3b inactivator (Q41854854) (← links)
• Characterization of primary amino acid sequence of human complement control protein factor I from an analysis of cDNA clones (Q41864928) (← links)
• The opportunistic human pathogenic fungus Aspergillus fumigatus evades the host complement system (Q41874883) (← links)
• Degradation of human complement component C4b in the presence of the C4b-binding protein-protein S complex (Q41889954) (← links)
• Inadequate binding of immune regulator factor H is associated with sensitivity of Borrelia lusitaniae to human complement (Q41891766) (← links)
• Biosynthesis of the complement components and the regulatory proteins of the alternative complement pathway by human peripheral blood monocytes (Q41894352) (← links)
• Prediction from sequence comparisons of residues of factor H involved in the interaction with complement component C3b. (Q41906560) (← links)
• Truncated forms of human complement factor H. (Q41913701) (← links)
• Purification of the human complement control protein C3b inactivator (Q41962972) (← links)
• Two populations of complement factor H differ in their ability to bind to cell surfaces (Q41963730) (← links)
• Lysis of measles virus-infected cells by the purified cytolytic alternative complement pathway and antibody (Q41981035) (← links)
• Complement factor H binds at two independent sites to C-reactive protein in acute phase concentrations (Q42021566) (← links)
• Isolation of two molecular populations of human complement factor H by hydrophobic affinity chromatography (Q42045212) (← links)
• Isolation and characterization of a human alternative complement pathway-inhibiting protein from larval hemolymph of the silkworm, Bombyx mori (Q42055261) (← links)
• Interaction of target cell-bound C3bi and C3d with human lymphocyte receptors. Enhancement of antibody-mediated cellular cytotoxicity (Q42056441) (← links)
• Biosynthesis of the third component of complement (C3) by the human monocytic-cell line U-937. Induction by phorbol myristate acetate (Q42109304) (← links)
• Assembly of the cytolytic alternative pathway of complement from 11 isolated plasma proteins (Q42112065) (← links)
• Purification of human C3b inactivator by monoclonal-antibody affinity chromatography (Q42113655) (← links)
• Paroxysmal nocturnal hemoglobinuria: deficiency in factor H-like functions of the abnormal erythrocytes (Q42118967) (← links)
• CNBr cleavage of the light chain of human complement factor I and alignment of the fragments (Q42133761) (← links)
• MHC Class III products: an electron microscopic study of the C3 convertases of human complement (Q42133973) (← links)
• Role of genetic polymorphisms in factor H and MBL genes in Tunisian patients with immunoglobulin A nephropathy (Q42176542) (← links)
• Relation of putative thioester bond in C3 to activation of the alternative pathway and the binding of C3b to biological targets of complement (Q42242306) (← links)
• In vitro biosynthesis of complement factor I by human endothelial cells (Q42459180) (← links)
• Transcriptional modulation of the human complement factor I gene in Hep G2 cells by protein kinase C activation (Q42482125) (← links)
• Neoantigens in complement component C3 as detected by monoclonal antibodies. Mapping of the recognized epitopes by synthetic peptides. (Q42794180) (← links)
• Molecular modelling of the domain structure of factor I of human complement by X-ray and neutron solution scattering (Q42814747) (← links)
• Specificity of the thioester-containing reactive site of human C3 and its significance to complement activation (Q42828955) (← links)
• Localization of the complement-component-C3b-binding site and the cofactor activity for factor I in the 38kDa tryptic fragment of factor H (Q42848520) (← links)
• Loss of complement receptor type 1 (CR1) on ageing of erythrocytes. Studies of proteolytic release of the receptor (Q42853453) (← links)
• Interferon-induced transcriptional and post-transcriptional modulation of factor H and C4 binding-protein synthesis in human monocytes (Q42859242) (← links)
• Structural and functional analysis of the complement component factor H with the use of different enzymes and monoclonal antibodies to factor H. (Q42867238) (← links)
• Non-enzymic activation of the covalent binding reaction of the complement protein C3. (Q42869732) (← links)
• The covalent-binding reaction of complement component C3 (Q42876404) (← links)
• The separation of functionally distinct forms of the third component of human complement (C3). (Q42883126) (← links)
• Expression, purification, cocrystallization and preliminary crystallographic analysis of sucrose octasulfate/human complement regulator factor H SCRs 6-8. (Q43167342) (← links)
• Monomeric CRP contributes to complement control in fluid phase and on cellular surfaces and increases phagocytosis by recruiting factor H. (Q43292217) (← links)
• Human complement factor H: two factor H proteins are derived from alternatively spliced transcripts (Q43612179) (← links)
• The binding of human complement proteins C5, factor B, beta 1H and properdin to complement fragment C3b on zymosan (Q43830771) (← links)
• Genetic and environmental factors influencing the human factor H plasma levels (Q43958315) (← links)
• Activation of the alternative pathway of complement by calcium-loaded erythrocytes resulting from loss of membrane phospholipid asymmetry (Q44446123) (← links)
• Binding of human complement regulators FHL-1 and factor H to CRASP-1 orthologs of Borrelia burgdorferi (Q44782441) (← links)
• Restoration of complement function in vivo by plasma infusion in factor I (C3b inactivator) deficiency (Q45173467) (← links)
• Evidence for an active hydrophobic form of factor H that is able to induce secretion of interleukin 1-β or by human monocytes (Q46237179) (← links)
• Role of human factor I and C3b receptor in the cleavage of surface-bound C3bi molecules (Q46388632) (← links)
• Exploitation of complement regulatory proteins by Borrelia and Francisella (Q46737549) (← links)
• Differences in interaction between immune complexes and complement receptors in serum and cerebrospinal fluid. (Q46841084) (← links)
• Differentiation of C3b receptors on human lymphocytes, phagocytes, erythrocytes and renal glomerulus cells by monoclonal antibodies (Q46936901) (← links)
• Characterization of alternative pathway inhibition by a serum derived, low molecular weight complement inhibitor (Q47244601) (← links)
• Isolation and characterization of a low molecular weight complement inhibitor present in normal human serum. (Q47284526) (← links)
• Immunological characterization of the complement regulator factor H-binding CRASP and Erp proteins of Borrelia burgdorferi. (Q47595731) (← links)
• Complement Immune Evasion by Spirochetes. (Q47757958) (← links)
• Cloning and characterization of the promoter for the human complement factor I (C3b/C4b inactivator) gene (Q48039355) (← links)
• Complement Resistance of Borrelia burgdorferi Correlates with the Expression of BbCRASP-1, a Novel Linear Plasmid-encoded Surface Protein That Interacts with Human Factor H and FHL-1 and Is Unrelated to Erp Proteins (Q48220868) (← links)
• The properdin pathway: an "alternative activation pathway" or a "critical amplification loop" for C3 and C5 activation? (Q49721910) (← links)
• Functional Characterization of the Disease-Associated N-Terminal Complement Factor H Mutation W198R. (Q50100348) (← links)
• Factor H binds to C3b (Q50291897) (← links)
• Factor H binds to C3bBb (Q50291902) (← links)
• Complement factor I complex formation (Q50291905) (← links)
• Complement Factor H Inhibits Anti-Neutrophil Cytoplasmic Autoantibody-Induced Neutrophil Activation by Interacting With Neutrophils. (Q52608526) (← links)
• Regulation of immunoglobulin secretion by factor H of human complement. (Q53543396) (← links)
• Regulatory system of guinea-pig complement C3b: Tests for compatibility of guinea-pig factors H and I with human factors (Q53861587) (← links)
• Isolation of an iC3b forming enzyme from peritoneal polymorphonuclear leukocytes of guinea pigs (Q53917651) (← links)
• 23 Purification and quantitation of the components of the alternative complement pathway (Q53929195) (← links)
• Cleavage of membrane bound C3bi, an intermediate of the third component of complement, to C3c and C3d-like fragments by crude leucocyte lysosomal lysates and purified leucocyte elastase. (Q53944268) (← links)
• Role of beta 1H for the binding of C3b-coated particles to human lymphoid and phagocytic cells. (Q53944376) (← links)
• Involvement of membrane-associated sialic acid in the resistance of sheep erythrocytes to lysis by mouse complement (Q54529966) (← links)
• Complement Component 3 Negatively Regulates Antibody Response by Modulation of Red Blood Cell Antigen. (Q55252352) (← links)
• Uncontrolled C3 activation causes membranoproliferative glomerulonephritis in mice deficient in complement factor H (Q57089510) (← links)
• Leptospiral Immunoglobulin-like Proteins Interact With Human Complement Regulators Factor H, FHL-1, FHR-1, and C4BP (Q58274952) (← links)
• Importance of Factors H and I for the Adherence of C3b-Coated Erythrocytes to Cells (Q58525025) (← links)
• Two distinct conformations of factor H regulate discrete complement-binding functions in the fluid phase and at cell surfaces (Q58738012) (← links)
• H deficiency in two brothers with atypical dense intramembranous deposit disease (Q59619455) (← links)
• Complement Factor H and Apolipoprotein E Participate in Regulation of Inflammation in THP-1 Macrophages (Q59813473) (← links)
• Further Insights Into the Interaction of Human and Animal Complement Regulator Factor H With Viable Lyme Disease Spirochetes (Q61805205) (← links)
• C3 glomerulopathy - understanding a rare complement-driven renal disease (Q64041044) (← links)
• Solubilization of C3 fragments deposited on cross-linked dextran gel beads (Q66958077) (← links)
• A radiometric assay for the combined measurement of phagocytosis and intracellular killing of Candida albicans (Q67275113) (← links)
• Prevention of immune precipitation by purified components of the alternative pathway (Q67294456) (← links)
• Metabolism of factor B of serum complement in rheumatoid arthritis (Q67448290) (← links)
• Localization of the heparin-binding site on complement factor H (Q67902469) (← links)
• Polymorphism and deficiency of human factor H-related proteins p39 and p37 (Q68057356) (← links)
• Binding of C3 molecules to membranes via the SH-residue generated by the cleavage of a thioester bond can initiate complement activation (Q68283289) (← links)
• Demonstration of C3b receptor-like activity and of decay-accelerating factor-like activity on rabbit erythrocytes (Q68973741) (← links)
• Human complement factor H: expression of an additional truncated gene product of 43 kDa in human liver (Q69009980) (← links)
• Complement activation in IgA nephropathy (Q69031107) (← links)
• Effect of decay-accelerating factor on the assembly of the classical and alternative pathway C3 convertases in the presence of C4 or C3 nephritic factor (Q69124128) (← links)
• Generation of the bioactive kallikrein-derived fragment, C3d-k, by HANE-plasma (Q69825698) (← links)
• Combined homozygous factor H and heterozygous C2 deficiency in an Italian family (Q70053520) (← links)
• Location of the inter-chain disulfide bonds of the third component of human complement (Q70069344) (← links)
• The C3b inactivator of the human complement system: homology with serine proteases (Q70196420) (← links)
• Distribution of membrane cofactor protein of complement on human peripheral blood cells. An altered form is found on granulocytes (Q70210949) (← links)
• Biosynthesis and postsynthetic processing of human C3b/C4b inactivator (factor I) in three hepatoma cell lines (Q70213614) (← links)
• Regulation of Protease Activity (Q70336586) (← links)
• Detection of IgA class circulating immune complexes bound to anti-C3d antibody in patients with IgA nephropathy (Q70340076) (← links)
• Complement activation in chronic liver disease (Q70368083) (← links)
• Kinetics of interaction of immune complexes with complement receptors on human blood cells: modification of complexes during interaction with red cells (Q70449146) (← links)
• Pattern of degradation of human complement fragment, C3b (Q70558362) (← links)
• Correlation of C3d fixing circulating immune complexes with disease activity and clinical parameters in patients with systemic lupus erythematosus (Q71004353) (← links)
• 39 C3c-binding ELISA for the detection of immunoconglutinins and immunoglobulin aggregates (Q71049513) (← links)
• Characterization of a C3/C3b regulatory protein in normal human serum (Q71144763) (← links)
• C3-mediated release of prostaglandin from human monocytes. Behaviour in short-term culture (Q71251330) (← links)
• Immunological, structural and functional relationships between an anti-complementary protein from Crotalus atrox venom, cobra venom factor and human C3 (Q71504390) (← links)
• Analysis of the recognition mechanism of the alternative pathway of complement by monoclonal anti-factor H antibodies: evidence for multiple interactions between H and surface bound C3b (Q71548822) (← links)
• Preparation of an R3 reagent (serum depleted of the third component of human complement (C3)) by immunoadsorption. Application to the hemolytic assay of human C3 (Q72133305) (← links)
• Relationship of β1H globulin and cleavage fragments of the third component of complement in the skin of patients with bullous pemphigoid and dermatitis herpetiformis (Q72641029) (← links)
• Control of immune complex and zymosan-mediated anaphylatoxin generation by proteins B and H of the alternative complement pathway (Q72720373) (← links)
• The release of lysosomal enzymes from human polymorphonuclear leukocytes by human C3e (Q72722249) (← links)
• Regulation of C3 and factor H synthesis of human glomerular mesangial cells by IL-1 and interferon-gamma (Q72722691) (← links)
• Activation of human monocytes by both human beta 1H and C3b (Q72756219) (← links)
• Conformational changes accompanying proteolytic cleavage of human complement protein C3b by the regulatory enzyme factor I and its cofactor H. Spectroscopic and enzymological studies (Q72779623) (← links)
• Immune complex alterations occur on the human red blood cell membrane (Q72792337) (← links)
• Potentiation of factor H by heparin: A rate-limiting mechanism for inhibition of the alternative complement pathway (Q72802884) (← links)
• Identification of a major human serum DNA-binding protein as β1H of the alternative pathway of complement activation (Q72855035) (← links)
• Transcriptional and post-transcriptional regulation of complement factor I (CFI) gene expression in Hep G2 cells by interleukin-6 (Q77521381) (← links)
• Chylomicron accelerates C3 tick-over by regulating the role of factor H, leading to overproduction of acylation stimulating protein (Q79635737) (← links)
• Persistent Breeding-Induced Endometritis in Mares - a Multifaceted Challenge: From Clinical Aspects to Immunopathogenesis and Pathobiology (Q89861955) (← links)
• Regulation of the Complement System by Pentraxins (Q92712488) (← links)
• Membrane-associated complement factor H on lymphoblastoid cell lines Raji expresses a co-factor activity for the factor I-mediated cleavage of C3b (Q93517922) (← links)
• Human complement factor H: an additional gene product of 43 kDa isolated from human plasma shows cofactor activity for the cleavage of the third component of complement (Q93521635) (← links)
• Deficiency of Mouse FHR-1 Homolog, FHR-E, Accelerates Sepsis, and Acute Kidney Injury Through Enhancing the LPS-Induced Alternative Complement Pathway (Q97420785) (← links)
• Characterization of Binding Properties of Individual Functional Sites of Human Complement Factor H (Q98735561) (← links)