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Journal Abstract Search

223 related items for PubMed ID: 23560673

  • 21. Molecular and clinical profile of congenital fibrinogen disorders in Iran, identification of two novel mutations.
    Tavasoli B, Safa M, Dorgalaleh A, Ghasemi JB, Rezaei Makhouri F, Rezvani MR, Ahmadi A, Tabibian S, Jazebi M, Baghaipour MR, Zaker F.
    Int J Lab Hematol; 2020 Oct; 42(5):619-627. PubMed ID: 32639687
    [Abstract] [Full Text] [Related]

  • 22. siRNA down-regulation of FGA mRNA in HepG2 cells demonstrated that heterozygous abnormality of the Aα-chain gene does not affect the plasma fibrinogen level.
    Takezawa Y, Matsuda K, Terasawa F, Sugano M, Honda T, Okumura N.
    Thromb Res; 2013 Apr; 131(4):342-8. PubMed ID: 23414568
    [Abstract] [Full Text] [Related]

  • 23. 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
    [Abstract] [Full Text] [Related]

  • 24. Identification of Two Novel Fibrinogen Bβ Chain Mutations in Two Slovak Families with Quantitative Fibrinogen Disorders.
    Simurda T, Zolkova J, Snahnicanova Z, Loderer D, Skornova I, Sokol J, Hudecek J, Stasko J, Lasabova Z, Kubisz P.
    Int J Mol Sci; 2017 Dec 29; 19(1):. PubMed ID: 29286337
    [Abstract] [Full Text] [Related]

  • 25. A novel fibrinogen mutation (γ Thr277Arg) causes hereditary hypofibrinogenemia in a Chinese family.
    Zhu L, Wang M, Xie H, Jin Y, Yang L, Xu P.
    Blood Coagul Fibrinolysis; 2013 Sep 29; 24(6):642-4. PubMed ID: 23492915
    [Abstract] [Full Text] [Related]

  • 26. Genetic and clinical characterization of congenital fibrinogen disorders in Polish patients: Identification of three novel fibrinogen gamma chain mutations.
    Wypasek E, Klukowska A, Zdziarska J, Zawilska K, Treliński J, Iwaniec T, Mital A, Pietrys D, Sydor W, Neerman-Arbez M, Undas A.
    Thromb Res; 2019 Oct 29; 182():133-140. PubMed ID: 31479941
    [Abstract] [Full Text] [Related]

  • 27. 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 29; 95(6):931-5. PubMed ID: 16732370
    [Abstract] [Full Text] [Related]

  • 28. A novel frameshift mutation in FGA accounting for congenital afibrinogenemia predicted to encode an aberrant peptide terminating 158 amino acids downstream.
    Robert-Ebadi H, de Moerloose P, El Khorassani M, El Khattab M, Neerman-Arbez M.
    Blood Coagul Fibrinolysis; 2009 Jul 29; 20(5):385-7. PubMed ID: 19417632
    [Abstract] [Full Text] [Related]

  • 29. Fibrinogen gene mutations accounting for congenital afibrinogenemia.
    Neerman-Arbez M.
    Ann N Y Acad Sci; 2001 Jul 29; 936():496-508. PubMed ID: 11460507
    [Abstract] [Full Text] [Related]

  • 30. [Congenital afibrinogenemia associated with a novel nonsense mutation in the FGA gene].
    Wu SY, Wang ZY, Dong NZ, Bai X, Ruan CG.
    Zhonghua Xue Ye Xue Za Zhi; 2005 Mar 29; 26(3):133-6. PubMed ID: 15946522
    [Abstract] [Full Text] [Related]

  • 31. Molecular characterization of the first missense mutation in the fibrinogen Aalpha-chain gene identified in a compound heterozygous afibrinogenemic patient.
    Platé M, Asselta R, Peyvandi F, Tenchini ML, Duga S.
    Biochim Biophys Acta; 2007 Jul 29; 1772(7):781-7. PubMed ID: 17531448
    [Abstract] [Full Text] [Related]

  • 32. Pseudo-exon activation caused by a deep-intronic mutation in the fibrinogen gamma-chain gene as a novel mechanism for congenital afibrinogenaemia.
    Spena S, Asselta R, Platé M, Castaman G, Duga S, Tenchini ML.
    Br J Haematol; 2007 Oct 29; 139(1):128-32. PubMed ID: 17854317
    [Abstract] [Full Text] [Related]

  • 33. [Congenital afibrinogenemia caused by a novel insertion mutation in the FGB gene].
    Zhang J, Zhao XJ, Wang ZY, Yu ZQ, Cao LJ, Ma ZN, Zhang J, Zhang W, Bai X, Ruan CG.
    Zhonghua Xue Ye Xue Za Zhi; 2013 Sep 29; 34(9):751-6. PubMed ID: 24103871
    [Abstract] [Full Text] [Related]

  • 34. Congenital afibrinogenemia: identification and expression of a missense mutation in FGB impairing fibrinogen secretion.
    Vu D, Bolton-Maggs PH, Parr JR, Morris MA, de Moerloose P, Neerman-Arbez M.
    Blood; 2003 Dec 15; 102(13):4413-5. PubMed ID: 12893758
    [Abstract] [Full Text] [Related]

  • 35. Molecular basis of fibrinogen deficiency.
    Neerman-Arbez M.
    Pathophysiol Haemost Thromb; 2006 Dec 15; 35(1-2):187-98. PubMed ID: 16855369
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  • 36. Congenital fibrinogen disorders: an update.
    de Moerloose P, Casini A, Neerman-Arbez M.
    Semin Thromb Hemost; 2013 Sep 15; 39(6):585-95. PubMed ID: 23852822
    [Abstract] [Full Text] [Related]

  • 37. Genetic Variants in the FGB and FGG Genes Mapping in the Beta and Gamma Nodules of the Fibrinogen Molecule in Congenital Quantitative Fibrinogen Disorders Associated with a Thrombotic Phenotype.
    Simurda T, Brunclikova M, Asselta R, Caccia S, Zolkova J, Kolkova Z, Loderer D, Skornova I, Hudecek J, Lasabova Z, Stasko J, Kubisz P.
    Int J Mol Sci; 2020 Jun 29; 21(13):. PubMed ID: 32610551
    [Abstract] [Full Text] [Related]

  • 38. Rare inherited disorders of fibrinogen.
    Acharya SS, Dimichele DM.
    Haemophilia; 2008 Nov 29; 14(6):1151-8. PubMed ID: 19141154
    [Abstract] [Full Text] [Related]

  • 39. Protein modelling to understand FGB mutations leading to congenital hypofibrinogenaemia.
    Casini A, Vilar R, Beauverd Y, Aslan D, Devreese K, Mondelaers V, Alberio L, Gubert C, de Moerloose P, Neerman-Arbez M.
    Haemophilia; 2017 Jul 29; 23(4):583-589. PubMed ID: 28306188
    [Abstract] [Full Text] [Related]

  • 40. Novel fibrinogen mutation γ314Thr→Pro (fibrinogen AI duPont) associated with hepatic fibrinogen storage disease and hypofibrinogenaemia.
    Brennan SO, Davis RL, Conard K, Savo A, Furuya KN.
    Liver Int; 2010 Nov 29; 30(10):1541-7. PubMed ID: 20666993
    [Abstract] [Full Text] [Related]

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