about
Borrelia valaisiana resist complement-mediated killing independently of the recruitment of immune regulators and inactivation of complement componentsComplement in age-related macular degeneration: a focus on functionAnnexin-II, DNA, and histones serve as factor H ligands on the surface of apoptotic cellsAlternative Pathway Dysregulation and the Conundrum of Complement Activation by IgG4 Immune Complexes in Membranous NephropathyNonencapsulated Streptococcus pneumoniae: Emergence and PathogenesisComplement regulation: physiology and disease relevanceThe role of complement in the pathogenesis of renal ischemia-reperfusion injury and fibrosisThe complotype: dictating risk for inflammation and infectionMolecular basis of host specificity in human pathogenic bacteriaNeisseria meningitidis recruits factor H using protein mimicry of host carbohydratesBorrelia burgdorferi BBK32 Inhibits the Classical Pathway by Blocking Activation of the C1 Complement ComplexCollagen-like proteins of pathogenic streptococciCombination of factor H mutation and properdin deficiency causes severe C3 glomerulonephritisBinding of the human complement regulators CFHR1 and factor H by streptococcal collagen-like protein 1 (Scl1) via their conserved C termini allows control of the complement cascade at multiple levels.Novel developments in thrombotic microangiopathies: is there a common link between hemolytic uremic syndrome and thrombotic thrombocytic purpura?Deletion of Crry and DAF on murine platelets stimulates thrombopoiesis and increases factor H-dependent resistance of peripheral platelets to complement attack.A novel hybrid CFHR1/CFH gene causes atypical hemolytic uremic syndromeA novel atypical hemolytic uremic syndrome-associated hybrid CFHR1/CFH gene encoding a fusion protein that antagonizes factor H-dependent complement regulation.Factor H Family Proteins in Complement Evasion of Microorganisms.Complement factor H-related proteins CFHR2 and CFHR5 represent novel ligands for the infection-associated CRASP proteins of Borrelia burgdorferi.Protection of nonself surfaces from complement attack by factor H-binding peptides: implications for therapeutic medicine.A haplotype in CFH family genes confers high risk of rare glomerular nephropathies.Association of genetic variants in complement factor H and factor H-related genes with systemic lupus erythematosus susceptibility.Secreted Aspergillus fumigatus protease Alp1 degrades human complement proteins C3, C4, and C5.A 32 kb critical region excluding Y402H in CFH mediates risk for age-related macular degenerationFactor H facilitates adherence of Neisseria gonorrhoeae to complement receptor 3 on eukaryotic cells.Genome-wide association study for serum complement C3 and C4 levels in healthy Chinese subjects.Disruption of the alternative pathway convertase occurs at the staphylococcal surface via the acquisition of factor H by Staphylococcus aureus.Current concepts in C3 glomerulopathy.Identification of the primary mechanism of complement evasion by the periodontal pathogen, Treponema denticola.Determining the population frequency of the CFHR3/CFHR1 deletion at 1q32.Affinity purification of human factor H on polypeptides derived from streptococcal m protein: enrichment of the Y402 variantLocalization of complement factor H gene expression and protein distribution in the mouse outer retina.The role of complement in tumor growthEarly cytokine release in response to live Borrelia burgdorferi Sensu Lato Spirochetes is largely complement independent.Complement, age-related macular degeneration and a vision of the futureProgress and perspectives on the role of RPE cell inflammatory responses in the development of age-related macular degeneration.A rare penetrant mutation in CFH confers high risk of age-related macular degeneration.How does the macula protect itself from oxidative stress?Plasma levels of complement proteins from the alternative pathway in patients with age-related macular degeneration are independent of Complement Factor H Tyr⁴⁰²His polymorphism.
P2860
Q21090813-D04BC477-9722-477C-A9FB-E6557A800FD6Q24635874-4294AAAC-324A-45C1-B2F3-C34956521A1BQ24646683-C2C067E0-3F5E-41BE-91B7-6B5B72D14B82Q26747416-2B78C922-9C1D-4BE2-95B4-B1D69C707B17Q26752517-1936A9FA-D3B3-4A64-B9E7-B8444F065DFBQ26795441-D1760025-03B2-49C5-ABB8-5F8B8A4A1234Q26853263-D599FA89-EFF8-4700-82E1-809584D3A2C2Q26862665-5FC1324A-9AE2-4C96-8D6B-5813FCA39677Q26864388-927FDDCE-2041-4B8A-B191-F62B76059C6FQ27653843-BD37965C-1B64-4C5E-8287-B1144F6A8440Q28552790-7C7440B9-314C-4E0A-ABCE-FC5528E08822Q29248479-D73ACF97-EAC8-4E1F-B861-E18D34E98087Q30415634-9E63727A-274F-4137-8435-39787379C5F1Q33391952-86B4164A-1F17-49EB-978F-FE49E861AA1EQ33395774-36230EAB-C633-462B-AA1C-F60C7255FEFCQ33405750-8321408F-FD15-4974-A731-D93DD9CB7CAEQ33409307-4883C327-54AC-435C-A3EC-0ADC249626D9Q33415753-244C769F-EC4C-4966-8C85-6AC6F3C19733Q33700779-0D6FABD8-8DD2-49D6-967B-F1A0246DDF93Q33728030-CB9C6AC8-03E8-476E-8958-8C3113F508A4Q33825957-2F8369C6-58C3-423A-9727-28963F94B6C7Q33920982-06465FD0-9BB3-484D-9043-D8699A9DD27DQ33921170-15BBA342-24F1-4DC1-9C3A-1345FF8B3708Q34045118-E3F7700B-17F1-4CA9-B7DE-D51430C21CF2Q34055667-CAD2A17B-DC92-4CB4-B779-FCAD6E533E40Q34148222-B8452FEA-D451-4B66-89F8-B4B3F7C5F250Q34426540-43B2A7BA-FFAC-4306-A944-AD5C0CC3977DQ34463131-A36EDF23-F119-4B8C-AEE2-C2BA1D6CB04AQ34574482-9DB92BC3-4352-4EC1-B671-B6FB50898D1FQ34645012-88B40D5E-EB9F-4F4D-AF00-9C9C9073FC46Q34683659-6570D885-2884-48A6-84CF-2C174605E672Q35053992-D29B70CD-4702-41EB-9458-EB7A153A2D6FQ35070241-A05C083D-F125-471D-B83E-A1CF6083147FQ35231345-B402480B-13D4-43A0-80A2-2F7F484DDE38Q35284275-96279E37-2EBC-4F73-86E9-1424293D26D3Q35509833-6CD0D478-FE21-44CD-8A97-CD85D42519A5Q35557353-9F7A3059-DB02-47A2-8BAC-578DE6EA938DQ35577472-36B72C7A-7DB8-403C-8255-90BC4395E66CQ36083959-B7F8022C-BC90-440D-9DFD-2CEDAC5243FDQ36218190-91BC26EB-3318-423C-8DCA-531C2C90CF87
P2860
description
2008 nî lūn-bûn
@nan
2008 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Factor H family proteins and human diseases.
@ast
Factor H family proteins and human diseases.
@en
type
label
Factor H family proteins and human diseases.
@ast
Factor H family proteins and human diseases.
@en
prefLabel
Factor H family proteins and human diseases.
@ast
Factor H family proteins and human diseases.
@en
P356
P1433
P1476
Factor H family proteins and human diseases.
@en
P304
P356
10.1016/J.IT.2008.04.008
P577
2008-07-02T00:00:00Z