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141 related items for PubMed ID: 17565234

  • 1. Simulated point mutations in the Aalpha-chain of human fibrinogen support a role of the alphaC domain in the stabilization of fibrin gel.
    Colafranceschi M, Papi M, Giuliani A, Amiconi G, Colosimo A.
    Pathophysiol Haemost Thromb; 2006; 35(6):417-27. PubMed ID: 17565234
    [Abstract] [Full Text] [Related]

  • 2. Streptococcus gordonii FSS2 Challisin affects fibrin clot formation by digestion of the αC region and cleavage of the N -terminal region of the Bβ chains of fibrinogen.
    Harty DW, Farahani RM, Simonian MR, Hunter L, Hunter N.
    Thromb Haemost; 2012 Aug; 108(2):236-46. PubMed ID: 22552295
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  • 3. Residue gamma153Cys is essential for the formation of the complexes Aalphagamma and Bbetagamma, assembly intermediates for the AalphaBbetagamma complex and intact fibrinogen.
    Terasawa F, Fujita K, Okumura N.
    Clin Chim Acta; 2005 Mar; 353(1-2):157-64. PubMed ID: 15698603
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  • 4. Localization of an effective fibrin beta-chain polymerization site: implications for the polymerization mechanism.
    Hsieh Kh.
    Biochemistry; 1997 Aug 05; 36(31):9381-7. PubMed ID: 9235981
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  • 5. A frameshift mutation in the human fibrinogen Aalpha-chain gene (Aalpha(499)Ala frameshift stop) leading to dysfibrinogen San Giovanni Rotondo.
    Margaglione M, Vecchione G, Santacroce R, D'Angelo F, Casetta B, Papa ML, Grandone E, Di Minno G.
    Thromb Haemost; 2001 Dec 05; 86(6):1483-8. PubMed ID: 11776317
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  • 6. Analysis of A alpha 251 fibrinogen: the alpha C domain has a role in polymerization, albeit more subtle than anticipated from the analogous proteolytic fragment X.
    Gorkun OV, Henschen-Edman AH, Ping LF, Lord ST.
    Biochemistry; 1998 Nov 03; 37(44):15434-41. PubMed ID: 9799505
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  • 7. Factor XIIIa incorporates thymosin beta4 preferentially into the fibrin(ogen) alphaC-domains.
    Makogonenko E, Goldstein AL, Bishop PD, Medved L.
    Biochemistry; 2004 Aug 24; 43(33):10748-56. PubMed ID: 15311936
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  • 8. [Role of fibrinogen Bbeta-chain D-region 454-458 residues for assembly and secretion of intact fibrinogen].
    Terasawa F, Takezawa Y, Hirota-Kawadobora M, Okumura N.
    Rinsho Byori; 2011 Aug 24; 59(8):741-8. PubMed ID: 21942083
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  • 13. Direct evidence for specific interactions of the fibrinogen alphaC-domains with the central E region and with each other.
    Litvinov RI, Yakovlev S, Tsurupa G, Gorkun OV, Medved L, Weisel JW.
    Biochemistry; 2007 Aug 07; 46(31):9133-42. PubMed ID: 17630702
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  • 15. Identification of the Staphylococcus aureus MSCRAMM clumping factor B (ClfB) binding site in the alphaC-domain of human fibrinogen.
    Walsh EJ, Miajlovic H, Gorkun OV, Foster TJ.
    Microbiology (Reading); 2008 Feb 07; 154(Pt 2):550-558. PubMed ID: 18227259
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  • 16. Quality control of fibrinogen secretion in the molecular pathogenesis of congenital afibrinogenemia.
    Vu D, Di Sanza C, Caille D, de Moerloose P, Scheib H, Meda P, Neerman-Arbez M.
    Hum Mol Genet; 2005 Nov 01; 14(21):3271-80. PubMed ID: 16195396
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  • 17. Citrullinated fibrinogen shows defects in FPA and FPB release and fibrin polymerization catalyzed by thrombin.
    Okumura N, Haneishi A, Terasawa F.
    Clin Chim Acta; 2009 Mar 01; 401(1-2):119-23. PubMed ID: 19109936
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  • 18. Fibrinogen assembly and crosslinking on a fibrin fragment E template.
    Mosesson MW, Siebenlist KR, Hernandez I, Wall JS, Hainfeld JF.
    Thromb Haemost; 2002 Apr 01; 87(4):651-8. PubMed ID: 12008948
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  • 19. Structural insights into fibrinogen dynamics using amide hydrogen/deuterium exchange mass spectrometry.
    Marsh JJ, Guan HS, Li S, Chiles PG, Tran D, Morris TA.
    Biochemistry; 2013 Aug 13; 52(32):5491-502. PubMed ID: 23875785
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  • 20. Interaction of fibrinogen with n-alkylagaroses and its purification by critical hydrophobicity hydrophobic interaction chromatograpy.
    Jennissen HP, Demiroglou A.
    J Chromatogr A; 2006 Mar 24; 1109(2):197-213. PubMed ID: 16488424
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