174 related articles for article (PubMed ID: 9916133)
21. Identification and functional characterization of a novel nonsense mutation in FGA accounting for congenital afibrinogenemia in six Egyptian patients.
Abdel Wahab M; de Moerloose P; Fish RJ; Neerman-Arbez M
Blood Coagul Fibrinolysis; 2010 Mar; 21(2):164-7. PubMed ID: 20051841
[TBL] [Abstract][Full Text] [Related]
22. [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]
23. 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]
24. 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]
25. In vitro rescue of FGA deletion by lentiviral transduction of an afibrinogenemic patient's hepatocytes.
Stroka D; Keogh A; Vu D; Fort A; Stoffel MH; Kühni-Boghenbor K; Furer C; Banz V; Demarmels Biasiutti F; Lämmle B; Candinas D; Neerman-Arbez M
J Thromb Haemost; 2014 Nov; 12(11):1874-9. PubMed ID: 25163824
[TBL] [Abstract][Full Text] [Related]
26. Missense mutations in the human beta fibrinogen gene cause congenital afibrinogenemia by impairing fibrinogen secretion.
Duga S; Asselta R; Santagostino E; Zeinali S; Simonic T; Malcovati M; Mannucci PM; Tenchini ML
Blood; 2000 Feb; 95(4):1336-41. PubMed ID: 10666208
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. Alport syndrome. Molecular genetic aspects.
Hertz JM
Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. A novel fibrinogen Bbeta chain frameshift mutation in a patient with severe congenital hypofibrinogenaemia.
Xu X; Wu J; Zhai Z; Zhou R; Wang X; Wang H; Ding K; Sun Z; Ni H
Thromb Haemost; 2006 Jun; 95(6):931-5. PubMed ID: 16732370
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. 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]
33. Inherited abnormalities of fibrinogen: 10-year clinical experience of an Italian group.
Santacroce R; Cappucci F; Pisanelli D; Perricone F; Papa ML; Santoro R; Grandone E; Margaglione M
Blood Coagul Fibrinolysis; 2006 Jun; 17(4):235-40. PubMed ID: 16651864
[TBL] [Abstract][Full Text] [Related]
34. A G-to-A mutation in IVS-3 of the human gamma fibrinogen gene causing afibrinogenemia due to abnormal RNA splicing.
Margaglione M; Santacroce R; Colaizzo D; Seripa D; Vecchione G; Lupone MR; De Lucia D; Fortina P; Grandone E; Perricone C; Di Minno G
Blood; 2000 Oct; 96(7):2501-5. PubMed ID: 11001903
[TBL] [Abstract][Full Text] [Related]
35. Congenital hypofibrinogenemia associated with novel homozygous fibrinogen Aα and heterozygous Bβ chain mutations.
Castaman G; Rimoldi V; Giacomelli SH; Duga S
Thromb Res; 2015 Jul; 136(1):144-7. PubMed ID: 25981141
[TBL] [Abstract][Full Text] [Related]
36. An
Mischke R; Metzger J; Distl O
Genes (Basel); 2021 Jul; 12(7):. PubMed ID: 34356081
[TBL] [Abstract][Full Text] [Related]
37. Homozygous truncation of the fibrinogen A alpha chain within the coiled coil causes congenital afibrinogenemia.
Fellowes AP; Brennan SO; Holme R; Stormorken H; Brosstad FR; George PM
Blood; 2000 Jul; 96(2):773-5. PubMed ID: 10887149
[TBL] [Abstract][Full Text] [Related]
38. [Genetic analysis of an inherited afibrinogenemia family caused by a novel frameshift mutation in FGA].
Xue F; Ge J; Gu DS; DU WT; Sui T; Zhao HF; Zhang L; Yang RC
Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2009 Aug; 17(4):1021-5. PubMed ID: 19698251
[TBL] [Abstract][Full Text] [Related]
39. [Genetic analysis of a Chinese family with inherited afibrinogenemia].
Fang Y; Wang XF; Wang HL; Fu QH; Wu WM; Ding QL; Dai J; Hu YQ; Wang ZY
Zhonghua Yi Xue Za Zhi; 2003 Dec; 83(23):2054-7. PubMed ID: 14703415
[TBL] [Abstract][Full Text] [Related]
40. Molecular analysis of afibrinogenemic mutations caused by a homozygous FGA1238 bp deletion, and a compound heterozygous FGA1238 bp deletion and novel FGA c.54+3A>C substitution.
Takezawa Y; Terasawa F; Matsuda K; Sugano M; Tanaka A; Fujiwara M; Kainuma K; Okumura N
Int J Hematol; 2012 Jul; 96(1):39-46. PubMed ID: 22639050
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]