BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

247 related articles for article (PubMed ID: 11354637)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. Mutations in the fibrinogen gene cluster accounting for congenital afibrinogenemia: an update and report of 10 novel mutations.
    Neerman-Arbez M; de Moerloose P
    Hum Mutat; 2007 Jun; 28(6):540-53. PubMed ID: 17295221
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. Congenital fibrinogen disorder caused by digenic mutations of the
    Wang X; Tang N; Shen N; Lu Y; Li D
    Hematology; 2020 Dec; 25(1):145-148. PubMed ID: 32228225
    [No Abstract]   [Full Text] [Related]  

  • 11. A novel nonsense mutation in the FGA gene in a Chinese family with congenital afibrinogenaemia.
    Wu S; Wang Z; Dong N; Bai X; Ruan C
    Blood Coagul Fibrinolysis; 2005 Apr; 16(3):221-6. PubMed ID: 15795544
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The molecular basis of inherited afibrinogenaemia.
    Neerman-Arbez M
    Thromb Haemost; 2001 Jul; 86(1):154-63. PubMed ID: 11487003
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. 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]  

  • 18. 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]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 13.