BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

152 related articles for article (PubMed ID: 34196169)

  • 1. A homozygous duplication of the FGG exon 8-intron 8 junction causes congenital afibrinogenemia. Lessons learned from the study of a large consanguineous Turkish family.
    Guipponi M; Masclaux F; Sloan-Béna F; Di Sanza C; Özbek N; Peyvandi F; Menegatti M; Casini A; Malbora B; Neerman-Arbez M
    Haematologica; 2022 May; 107(5):1064-1071. PubMed ID: 34196169
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular analysis of the fibrinogen gene cluster in 16 patients with congenital afibrinogenemia: novel truncating mutations in the FGA and FGG genes.
    Neerman-Arbez M; de Moerloose P; Honsberger A; Parlier G; Arnuti B; Biron C; Borg JY; Eber S; Meili E; Peter-Salonen K; Ripoll L; Vervel C; d'Oiron R; Staeger P; Antonarakis SE; Morris MA
    Hum Genet; 2001 Mar; 108(3):237-40. PubMed ID: 11354637
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Outcome of donor splice site mutations accounting for congenital afibrinogenemia reflects order of intron removal in the fibrinogen alpha gene (FGA).
    Attanasio C; David A; Neerman-Arbez M
    Blood; 2003 Mar; 101(5):1851-6. PubMed ID: 12406899
    [TBL] [Abstract][Full Text] [Related]  

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

  • 5. 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; 182():133-140. PubMed ID: 31479941
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutations in the fibrinogen aalpha gene account for the majority of cases of congenital afibrinogenemia.
    Neerman-Arbez M; de Moerloose P; Bridel C; Honsberger A; Schönbörner A; Rossier C; Peerlinck K; Claeyssens S; Di Michele D; d'Oiron R; Dreyfus M; Laubriat-Bianchin M; Dieval J; Antonarakis SE; Morris MA
    Blood; 2000 Jul; 96(1):149-52. PubMed ID: 10891444
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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; 100(13):4478-84. PubMed ID: 12393540
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Identification of a novel mutation in congenital afibrinogenemia in Iranian patients.
    Nojehdeh ST; Mojbafan M; Masoodifard M; Amini M; Zeinali S
    Blood Coagul Fibrinolysis; 2021 Jul; 32(5):323-327. PubMed ID: 33901106
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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; 102(13):4413-5. PubMed ID: 12893758
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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; 20(5):385-7. PubMed ID: 19417632
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Activation of multiple cryptic donor splice sites by the common congenital afibrinogenemia mutation, FGA IVS4 + 1 G-->T.
    Attanasio C; de Moerloose P; Antonarakis SE; Morris MA; Neerman-Arbez M
    Blood; 2001 Mar; 97(6):1879-81. PubMed ID: 11238133
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Expression and analysis of a split premature termination codon in FGG responsible for congenital afibrinogenemia: escape from RNA surveillance mechanisms in transfected cells.
    Neerman-Arbez M; Germanos-Haddad M; Tzanidakis K; Vu D; Deutsch S; David A; Morris MA; de Moerloose P
    Blood; 2004 Dec; 104(12):3618-23. PubMed ID: 15284111
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prenatal diagnosis for congenital afibrinogenemia caused by a novel nonsense mutation in the FGB gene in a Palestinian family.
    Neerman-Arbez M; Vu D; Abu-Libdeh B; Bouchardy I; Morris MA
    Blood; 2003 May; 101(9):3492-4. PubMed ID: 12511408
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Afibrinogenemia: first identification of a splicing mutation in the fibrinogen gamma chain gene leading to a major gamma chain truncation.
    Asselta R; Duga S; Simonic T; Malcovati M; Santagostino E; Giangrande PL; Mannucci PM; Tenchini ML
    Blood; 2000 Oct; 96(7):2496-500. PubMed ID: 11001902
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cortical atrophy and hypofibrinogenemia due to FGG and TBCD mutations in a single family: a case report.
    Stephen J; Nampoothiri S; Vinayan KP; Yesodharan D; Remesh P; Gahl WA; Malicdan MCV
    BMC Med Genet; 2018 May; 19(1):80. PubMed ID: 29769041
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [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]  

  • 19. [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; 34(9):751-6. PubMed ID: 24103871
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [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]  

    [Next]    [New Search]
    of 8.