170 related articles for article (PubMed ID: 15284111)
1. 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]
2. 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]
3. 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]
4. 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]
5. [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]
6. 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]
7. Molecular basis of fibrinogen deficiency.
Neerman-Arbez M
Pathophysiol Haemost Thromb; 2006; 35(1-2):187-98. PubMed ID: 16855369
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. Congenital afibrinogenemia: mutations leading to premature termination codons in fibrinogen A alpha-chain gene are not associated with the decay of the mutant mRNAs.
Asselta R; Duga S; Spena S; Santagostino E; Peyvandi F; Piseddu G; Targhetta R; Malcovati M; Mannucci PM; Tenchini ML
Blood; 2001 Dec; 98(13):3685-92. PubMed ID: 11739173
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. 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]
14. [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]
15. 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]
16. 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]
17. 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]
18. [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]
19. Analysis of Iranian patients allowed the identification of the first truncating mutation in the fibrinogen Bbeta-chain gene causing afibrinogenemia.
Asselta R; Spena S; Duga S; Peyvandi F; Malcovati M; Mannucci PM; Tenchini ML
Haematologica; 2002 Aug; 87(8):855-9. PubMed ID: 12161363
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
