BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

352 related articles for article (PubMed ID: 16855369)

  • 21. A rare heterozygous variant in FGB (Fibrinogen Merivale) causing hypofibrinogenemia in a Swedish family.
    Fager Ferrari M; Leinoe E; Rossing M; Norström E; Zetterberg E
    Blood Coagul Fibrinolysis; 2020 Oct; 31(7):481-484. PubMed ID: 32852326
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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; 139(1):128-32. PubMed ID: 17854317
    [TBL] [Abstract][Full Text] [Related]  

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

  • 24. FGB mutations leading to congenital quantitative fibrinogen deficiencies: an update and report of four novel mutations.
    Casini A; Lukowski S; Quintard VL; Crutu A; Zak M; Regazzoni S; de Moerloose P; Neerman-Arbez M
    Thromb Res; 2014 May; 133(5):868-74. PubMed ID: 24560896
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [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
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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; 18(12):. PubMed ID: 29240685
    [TBL] [Abstract][Full Text] [Related]  

  • 27. The 11 kb FGA deletion responsible for congenital afibrinogenaemia is mediated by a short direct repeat in the fibrinogen gene cluster.
    Neerman-Arbez M; Antonarakis SE; Honsberger A; Morris MA
    Eur J Hum Genet; 1999 Dec; 7(8):897-902. PubMed ID: 10602365
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A novel frameshift mutation in FGA (c.1846 del A) leading to congenital afibrinogenemia in a consanguineous Syrian family.
    Levrat E; Aboukhamis I; de Moerloose P; Farho J; Chamaa S; Reber G; Fort A; Neerman-Arbez M
    Blood Coagul Fibrinolysis; 2011 Mar; 22(2):148-50. PubMed ID: 21245743
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Mutational Epidemiology of Congenital Fibrinogen Disorders.
    Casini A; Blondon M; Tintillier V; Goodyer M; Sezgin ME; Gunes AM; Hanss M; de Moerloose P; Neerman-Arbez M
    Thromb Haemost; 2018 Nov; 118(11):1867-1874. PubMed ID: 30332696
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Pathogenesis study of inherited dysfibrinogenemia].
    Liao Z; Xu S; Tang H; Xie Y; Duan X; Liu C; Cheng Y; Chen Y; Wang D; Luo M; Tao Z
    Zhonghua Yi Xue Za Zhi; 2014 Mar; 94(10):742-6. PubMed ID: 24844956
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Molecular basis of quantitative fibrinogen disorders in 27 patients from India.
    Sumitha E; Jayandharan GR; Arora N; Abraham A; David S; Devi GS; Shenbagapriya P; Nair SC; George B; Mathews V; Chandy M; Viswabandya A; Srivastava A
    Haemophilia; 2013 Jul; 19(4):611-8. PubMed ID: 23560673
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Mutational screening of six afibrinogenemic patients: identification and characterization of four novel molecular defects.
    Monaldini L; Asselta R; Duga S; Peyvandi F; Karimi M; Malcovati M; Tenchini ML
    Thromb Haemost; 2007 Apr; 97(4):546-51. PubMed ID: 17393016
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Identification of three FGA mutations in two Chinese families with congenital afibrinogenaemia.
    Fang Y; Dai BT; Wang XF; Fu QH; Dai J; Xie F; Cai XH; Wang HL; Wang ZY
    Haemophilia; 2006 Nov; 12(6):615-20. PubMed ID: 17083511
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A novel mutation in the FGG gene causes hypofibrinogenemia in a Chinese family.
    Xie X; Du J; Geng S; Yi B; Li Q; Zuo J
    Hereditas; 2024 Feb; 161(1):9. PubMed ID: 38374144
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [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
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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; 19(1):. PubMed ID: 29286337
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Hereditary Hypofibrinogenemia with Hepatic Storage.
    Asselta R; Paraboschi EM; Duga S
    Int J Mol Sci; 2020 Oct; 21(21):. PubMed ID: 33105716
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A novel fibrinogen B beta chain frameshift mutation causes congenital afibrinogenaemia.
    Zhang J; Zhao X; Wang Z; Yu Z; Cao L; Zhang W; Bai X; Ruan C
    Thromb Haemost; 2013 Jul; 110(1):76-82. PubMed ID: 23740095
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Whole-exome sequencing identified novel mutations in FGA and FGG genes in the patients with decreased fibrinogen.
    Cao Z; Dong Y; Zeng J; Zhu H; Xie X; Liu J; Zhai Y; Li L
    Thromb Res; 2019 May; 177():79-82. PubMed ID: 30856382
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 18.