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Journal Abstract Search

99 related items for PubMed ID: 20580674

  • 1. Expression of four mutant fibrinogen gammaC domains in Pichia pastoris confirms them as causes of hypofibrinogenaemia.
    Sheen CR, Dear A, Brennan SO.
    Protein Expr Purif; 2010 Oct; 73(2):184-8. PubMed ID: 20580674
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  • 4. 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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  • 5. Mutations in the fibrinogen gene cluster accounting for congenital afibrinogenemia: an update and report of 10 novel mutations.
    Neerman-Arbez M, de Moerloose P.
    Hum Mutat; 2007 Jun 01; 28(6):540-53. PubMed ID: 17295221
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  • 8. Fibrinogen Nottingham II: a novel Bbeta Arg264gly substitution causing hypofibrinogenaemia.
    Hill MB, Brennan SO, Dear A, Strong J, Nejim T, Dolan G.
    Thromb Haemost; 2006 Sep 01; 96(3):378-80. PubMed ID: 16953282
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  • 9. Novel fibrinogen gamma375 Arg-->Trp mutation (fibrinogen aguadilla) causes hepatic endoplasmic reticulum storage and hypofibrinogenemia.
    Brennan SO, Maghzal G, Shneider BL, Gordon R, Magid MS, George PM.
    Hepatology; 2002 Sep 01; 36(3):652-8. PubMed ID: 12198657
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  • 10. Hypofibrinogenaemia associated with common gamma82Ala-->Gly mutation is not mediated by altered mRNA splicing.
    Brennan SO, Homer VM, Davis RL, Meyer M, George PM.
    Thromb Haemost; 2006 Oct 01; 96(4):535-7. PubMed ID: 17003934
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  • 11. A novel fibrinogen Bbeta chain frameshift mutation in a patient with severe congenital hypofibrinogenaemia.
    Xu X, Wu J, Zhai Z, Zhou R, Wang X, Wang H, Ding K, Sun Z, Ni H.
    Thromb Haemost; 2006 Jun 01; 95(6):931-5. PubMed ID: 16732370
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  • 12. Mutant fibrinogen cleared from the endoplasmic reticulum via endoplasmic reticulum-associated protein degradation and autophagy: an explanation for liver disease.
    Kruse KB, Dear A, Kaltenbrun ER, Crum BE, George PM, Brennan SO, McCracken AA.
    Am J Pathol; 2006 Apr 01; 168(4):1299-308; quiz 1404-5. PubMed ID: 16565503
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  • 14. Manipulating the quality control pathway in transfected cells: low temperature allows rescue of secretion-defective fibrinogen mutants.
    Vu D, Di Sanza C, Neerman-Arbez M.
    Haematologica; 2008 Feb 01; 93(2):224-31. PubMed ID: 18223281
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  • 15. Fibrinogen Montreal: a novel missense mutation (Aa D496N) associated with hypofibrinogenaemia.
    Sheen CR, Brennan SO, Jabado N, George PM.
    Thromb Haemost; 2006 Aug 01; 96(2):231-2. PubMed ID: 16894470
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  • 16. Clinical and molecular characterisation of 21 patients affected by quantitative fibrinogen deficiency.
    Asselta R, Platè M, Robusto M, Borhany M, Guella I, Soldà G, Afrasiabi A, Menegatti M, Shamsi T, Peyvandi F, Duga S.
    Thromb Haemost; 2015 Mar 01; 113(3):567-76. PubMed ID: 25427968
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  • 18. Analysis of Iranian patients allowed the identification of the first truncating mutation in the fibrinogen Bbeta-chain gene causing afibrinogenemia.
    Asselta R, Spena S, Duga S, Peyvandi F, Malcovati M, Mannucci PM, Tenchini ML.
    Haematologica; 2002 Aug 01; 87(8):855-9. PubMed ID: 12161363
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  • 19. Sequence gamma 377-395(P2), but not gamma 190-202(P1), is the binding site for the alpha MI-domain of integrin alpha M beta 2 in the gamma C-domain of fibrinogen.
    Ugarova TP, Lishko VK, Podolnikova NP, Okumura N, Merkulov SM, Yakubenko VP, Yee VC, Lord ST, Haas TA.
    Biochemistry; 2003 Aug 12; 42(31):9365-73. PubMed ID: 12899623
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  • 20. Hypofibrinogenaemia associated with a novel heterozygous gamma289 Ala -->Val substitution (fibrinogen Dorfen).
    Dear A, Brennan SO, Dempfle CE, Kirschstein W, George PM.
    Thromb Haemost; 2004 Dec 12; 92(6):1291-5. PubMed ID: 15583736
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