Pages that link to "Q28141398"

The following pages link to Host recognition and target differentiation by factor H, a regulator of the alternative pathway of complement (Q28141398):

Displaying 50 items.

• Structural analysis of the C-terminal region (modules 18-20) of complement regulator factor H (FH) (Q21134757) ‎ (← links)
• Initial sequence of the chimpanzee genome and comparison with the human genome (Q22122468) ‎ (← links)
• Bivalent and co-operative binding of complement factor H to heparan sulfate and heparin (Q24311571) ‎ (← links)
• Differential binding of host complement inhibitor factor H by Borrelia burgdorferi Erp surface proteins: a possible mechanism underlying the expansive host range of Lyme disease spirochetes (Q24537183) ‎ (← links)
• Structural basis for engagement by complement factor H of C3b on a self surface (Q24604385) ‎ (← links)
• The central portion of factor H (modules 10-15) is compact and contains a structurally deviant CCP module (Q24646284) ‎ (← links)
• Alternative Pathway Dysregulation and the Conundrum of Complement Activation by IgG4 Immune Complexes in Membranous Nephropathy (Q26747416) ‎ (← links)
• Role of factor H binding protein in Neisseria meningitidis virulence and its potential as a vaccine candidate to broadly protect against meningococcal disease (Q26995760) ‎ (← 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)
• Solution Structure of CCP Modules 10–12 Illuminates Functional Architecture of the Complement Regulator, Factor H (Q27673696) ‎ (← links)
• Diversity in the C3b Convertase Contact Residues and Tertiary Structures of the Staphylococcal Complement Inhibitor (SCIN) Protein Family (Q27675598) ‎ (← links)
• Identification, characterization, and physiological actions of factor H as an adrenomedullin binding protein present in human plasma (Q28211285) ‎ (← links)
• Production of biologically active complement factor H in therapeutically useful quantities (Q28300280) ‎ (← links)
• The interaction between factor H and Von Willebrand factor (Q31133820) ‎ (← links)
• Factor H binds to washed human platelets. (Q33364421) ‎ (← links)
• An interactive web database of factor H-associated hemolytic uremic syndrome mutations: insights into the structural consequences of disease-associated mutations (Q33369200) ‎ (← links)
• Phenotypic expression of factor H mutations in patients with atypical hemolytic uremic syndrome. (Q33370511) ‎ (← links)
• A classification of hemolytic uremic syndrome and thrombotic thrombocytopenic purpura and related disorders (Q33371578) ‎ (← links)
• Translational mini-review series on complement factor H: renal diseases associated with complement factor H: novel insights from humans and animals. (Q33378236) ‎ (← 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)
• Tissue-specific host recognition by complement factor H is mediated by differential activities of its glycosaminoglycan-binding regions (Q33405609) ‎ (← links)
• Review: Complement and its regulatory proteins in kidney diseases (Q33647738) ‎ (← links)
• Comparative proteomic analysis of serum from patients with systemic sclerosis and sclerodermatous GVHD. Evidence of defective function of factor H (Q33668640) ‎ (← links)
• The alternative pathway is required, but not alone sufficient, for retinal pathology in mouse laser-induced choroidal neovascularization (Q33800561) ‎ (← links)
• Acquisition of regulators of complement activation by Streptococcus pyogenes serotype M1 (Q34184576) ‎ (← links)
• Identification of acidic pH-dependent ligands of pentameric C-reactive protein (Q34285524) ‎ (← links)
• Factor h and properdin recognize different epitopes on renal tubular epithelial heparan sulfate. (Q34344501) ‎ (← links)
• Genome-wide association study for serum complement C3 and C4 levels in healthy Chinese subjects (Q34426540) ‎ (← links)
• C5a receptor-deficient dendritic cells promote induction of Treg and Th17 cells (Q34579613) ‎ (← links)
• Glycan-based interactions involving vertebrate sialic-acid-recognizing proteins (Q34623034) ‎ (← links)
• Zinc binding to the Tyr402 and His402 allotypes of complement factor H: possible implications for age-related macular degeneration. (Q34976109) ‎ (← links)
• Impact of the common genetic associations of age-related macular degeneration upon systemic complement component C3d levels (Q35133241) ‎ (← links)
• Complement-related proteins control the flavivirus infection of Aedes aegypti by inducing antimicrobial peptides (Q35145628) ‎ (← links)
• Research on complement: old issues revisited and a novel sphere of influence. (Q35155940) ‎ (← links)
• A neuron-specific antiviral mechanism prevents lethal flaviviral infection of mosquitoes (Q35542492) ‎ (← links)
• Age-Related Macular Degeneration: A Disease of Systemic or Local Complement Dysregulation? (Q35750545) ‎ (← links)
• Genetic factors for choroidal neovascularization associated with high myopia (Q36136294) ‎ (← links)
• Evaluation of 10 AMD Associated Polymorphisms as a Cause of Choroidal Neovascularization in Highly Myopic Eyes (Q36137281) ‎ (← links)
• Mapping the Complement Factor H-Related Protein 1 (CFHR1):C3b/C3d Interactions (Q36182912) ‎ (← 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)
• Complement is an essential component of the immune response to adeno-associated virus vectors (Q36484108) ‎ (← links)
• Identification of hot spots in the variola virus complement inhibitor (SPICE) for human complement regulation (Q36498115) ‎ (← links)
• The role of complement in danger sensing and transmission (Q36499763) ‎ (← 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)
• Heparan sulfate, including that in Bruch's membrane, inhibits the complement alternative pathway: implications for age-related macular degeneration. (Q36804333) ‎ (← links)
• Deficiency of decay-accelerating factor and complement receptor 1-related gene/protein y on murine platelets leads to complement-dependent clearance by the macrophage phagocytic receptor CRIg (Q36835163) ‎ (← links)
• The alternative complement pathway revisited (Q37141297) ‎ (← links)
• Polyanion-induced self-association of complement factor H. (Q37181643) ‎ (← links)
• The protective function of human C-reactive protein in mouse models of Streptococcus pneumoniae infection (Q37233964) ‎ (← links)