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Journal Abstract Search

295 related items for PubMed ID: 8470043

  • 41. Altered mRNA expression due to insertion or substitution of thymine at position +3 of two splice-donor sites in the androgen receptor gene.
    Trifiro MA, Lumbroso R, Beitel LK, Vasiliou DM, Bouchard J, Deal C, Van Vliet G, Pinsky L.
    Eur J Hum Genet; 1997; 5(1):50-8. PubMed ID: 9156321
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  • 45. Fibrinogen Saint-Germain II: hypofibrinogenemia due to heterozygous gamma N345S mutation.
    de Raucourt E, de Mazancourt P, Maghzal GJ, Brennan SO, Mosesson MW.
    Thromb Haemost; 2005 Nov; 94(5):965-8. PubMed ID: 16363237
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  • 50. [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; 26(3):133-6. PubMed ID: 15946522
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  • 53. Two novel mutations in the fibrinogen γ nodule.
    Kotlín R, Pastva O, Stikarová J, Hlaváčková A, Suttnar J, Chrastinová L, Riedel T, Salaj P, Dyr JE.
    Thromb Res; 2014 Oct; 134(4):901-8. PubMed ID: 25074738
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  • 54. [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
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  • 58. Congenital afibrinogenemia: first identification of splicing mutations in the fibrinogen Bbeta-chain gene causing activation of cryptic splice sites.
    Spena S, Duga S, Asselta R, Malcovati M, Peyvandi F, Tenchini ML.
    Blood; 2002 Dec 15; 100(13):4478-84. PubMed ID: 12393540
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  • 59. Fibrinogen Mumbai: intracellular retention due to a novel G434D mutation in the Bbeta-chain gene.
    Monaldini L, Asselta R, Duga S, Peyvandi F, Ghosh K, Malcovati M, Tenchini ML.
    Haematologica; 2006 May 15; 91(5):628-33. PubMed ID: 16670068
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  • 60. Fibrinogen New Britain: characterization of an A alpha Arg 16-->His variant human fibrinogen.
    Webb CD, Hantgan RR, Byeff PD, Owen J.
    Blood Coagul Fibrinolysis; 1994 Apr 15; 5(2):233-8. PubMed ID: 8054455
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