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Journal Abstract Search

257 related items for PubMed ID: 24711018

  • 21. [Genetic Analysis of A Case of Congenital Dysfibrinogenemia Caused by Arg16His Mutation in Exon 2 of FGA].
    Zhang YL, Liu SY, Zhang ZL, Tao XY, Peng XX, Kong YY.
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2017 Oct; 25(5):1514-1517. PubMed ID: 29070135
    [Abstract] [Full Text] [Related]

  • 22. Congenital afibrinogenemia: Identification and characterization of two novel homozygous fibrinogen Aα and Bβ chain mutations in two Tunisian families.
    Amri Y, Toumi Nel H, Hadj Fredj S, de Moerloose P.
    Thromb Res; 2016 Jul; 143():11-6. PubMed ID: 27164460
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  • 23. [Fibrinogen beta chain gene mutation contributes to one congenital afibrinogenemia].
    Xu XC, Zhou RF, Wu JS, Fang Y, Wang XF, Zhai ZM, Wang HL.
    Zhonghua Xue Ye Xue Za Zhi; 2005 Mar; 26(3):137-9. PubMed ID: 15946523
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  • 24. Coexisting congenital dysfibrinogenemia with a novel mutation in fibrinogen γ chain (γ322 Phe→Ile, Fibrinogen Beijing) and haemophilia B in a family.
    Hua B, Li K, Lee A, Poon MC, Zhao Y.
    Haemophilia; 2015 Nov; 21(6):846-51. PubMed ID: 25982359
    [Abstract] [Full Text] [Related]

  • 25. [Functional study of abnormal fibrinogen caused by Arg275His mutation in fibrinogen γ chain].
    Zhou JY, Wang XF, Ding QL, Xu GQ, Zhang LW, Dai J, Lu YL, Xi XD, Wang HL.
    Zhonghua Xue Ye Xue Za Zhi; 2013 Mar; 34(3):190-4. PubMed ID: 23683413
    [Abstract] [Full Text] [Related]

  • 26. [Inherited afibrinogenemia caused by compound heterozygous mutations in the beta beta-chain of fibrinogen].
    Fang Y, Wang HL, Wang XF, Fu QH, Wang WB, Xie S, Zhou RF, Dai J, Wang ZY.
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2005 Dec; 13(6):1086-9. PubMed ID: 16403286
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  • 28. [Fibrinogen gamma-chain mutation, p.Ile171His, leads to hereditary hypofibrinogenemia].
    Liu JX, Wang CJ, Dai JH, Zhang MX, Lyu B, Jiang B.
    Zhonghua Nei Ke Za Zhi; 2022 Feb 01; 61(2):172-176. PubMed ID: 35090252
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  • 30. Molecular characterization of 7 patients affected by dys- or hypo-dysfibrinogenemia: Identification of a novel mutation in the fibrinogen Bbeta chain causing a gain of glycosylation.
    Asselta R, Robusto M, Platé M, Santoro C, Peyvandi F, Duga S.
    Thromb Res; 2015 Jul 01; 136(1):168-74. PubMed ID: 26006300
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  • 32. [Analysis of a family with congenital dysfibrinogenemia caused by an Arg275His mutation in the gamma chain of fibrinogen].
    Yan J, Deng D, Deng X, Luo M, Cheng P, Liao L, Lin F.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Apr 01; 33(2):160-3. PubMed ID: 27060305
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  • 37. 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 01; 131(4):342-8. PubMed ID: 23414568
    [Abstract] [Full Text] [Related]

  • 38. [Phenotypic and genetic analysis of two pedigrees affected with hereditary coagulation FXII deficiency].
    Li S, Shen C, Shu K, Liu J, Wang X, Li F, Yang X, Zhang Z, Chen B, Jiang M.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Dec 10; 35(6):800-803. PubMed ID: 30512149
    [Abstract] [Full Text] [Related]

  • 39. Fibrinogen as a Pleiotropic Protein Causing Human Diseases: The Mutational Burden of Aα, Bβ, and γ Chains.
    Paraboschi EM, Duga S, Asselta R.
    Int J Mol Sci; 2017 Dec 14; 18(12):. PubMed ID: 29240685
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  • 40. A novel fibrinogen gamma-chain mutation, p.Cys165Arg, causes disruption of the γ165Cys-Bβ227Cys disulfide bond and ultimately leads to hypofibrinogenemia.
    Zhou W, Luo M, Yan J, Xiang L, Wei A, Deng X, Liao L, Cheng P, Deng D, Lin F.
    Thromb Res; 2018 Dec 14; 172():128-134. PubMed ID: 30412834
    [Abstract] [Full Text] [Related]

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