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Journal Abstract Search

341 related items for PubMed ID: 21317894

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  • 2. Both domain 19 and domain 20 of factor H are involved in binding to complement C3b and C3d.
    Bhattacharjee A, Lehtinen MJ, Kajander T, Goldman A, Jokiranta TS.
    Mol Immunol; 2010 May; 47(9):1686-91. PubMed ID: 20378178
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  • 3. Mutations of factor H impair regulation of surface-bound C3b by three mechanisms in atypical hemolytic uremic syndrome.
    Lehtinen MJ, Rops AL, Isenman DE, van der Vlag J, Jokiranta TS.
    J Biol Chem; 2009 Jun 05; 284(23):15650-8. PubMed ID: 19351878
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  • 8. Regulator-dependent mechanisms of C3b processing by factor I allow differentiation of immune responses.
    Xue X, Wu J, Ricklin D, Forneris F, Di Crescenzio P, Schmidt CQ, Granneman J, Sharp TH, Lambris JD, Gros P.
    Nat Struct Mol Biol; 2017 Aug 05; 24(8):643-651. PubMed ID: 28671664
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  • 9. Dual interaction of factor H with C3d and glycosaminoglycans in host-nonhost discrimination by complement.
    Kajander T, Lehtinen MJ, Hyvärinen S, Bhattacharjee A, Leung E, Isenman DE, Meri S, Goldman A, Jokiranta TS.
    Proc Natl Acad Sci U S A; 2011 Feb 15; 108(7):2897-902. PubMed ID: 21285368
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  • 10. Complement C3b/C3d and cell surface polyanions are recognized by overlapping binding sites on the most carboxyl-terminal domain of complement factor H.
    Hellwage J, Jokiranta TS, Friese MA, Wolk TU, Kampen E, Zipfel PF, Meri S.
    J Immunol; 2002 Dec 15; 169(12):6935-44. PubMed ID: 12471127
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  • 12. Combining SPR with atomic-force microscopy enables single-molecule insights into activation and suppression of the complement cascade.
    Makou E, Bailey RG, Johnston H, Parkin JD, Hulme AN, Hähner G, Barlow PN.
    J Biol Chem; 2019 Dec 27; 294(52):20148-20163. PubMed ID: 31719147
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  • 13. Each of the three binding sites on complement factor H interacts with a distinct site on C3b.
    Jokiranta TS, Hellwage J, Koistinen V, Zipfel PF, Meri S.
    J Biol Chem; 2000 Sep 08; 275(36):27657-62. PubMed ID: 10837479
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  • 14. Disturbed sialic acid recognition on endothelial cells and platelets in complement attack causes atypical hemolytic uremic syndrome.
    Hyvärinen S, Meri S, Jokiranta TS.
    Blood; 2016 Jun 02; 127(22):2701-10. PubMed ID: 27006390
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  • 16. Solution structure of TT30, a novel complement therapeutic agent, provides insight into its joint binding to complement C3b and C3d.
    Li K, Gor J, Holers VM, Storek MJ, Perkins SJ.
    J Mol Biol; 2012 May 04; 418(3-4):248-63. PubMed ID: 22387467
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  • 17. Structure of the N-terminal region of complement factor H and conformational implications of disease-linked sequence variations.
    Hocking HG, Herbert AP, Kavanagh D, Soares DC, Ferreira VP, Pangburn MK, Uhrín D, Barlow PN.
    J Biol Chem; 2008 Apr 04; 283(14):9475-87. PubMed ID: 18252712
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