131 related articles for article (PubMed ID: 33038747)
1. Generation of a human induced pluripotent stem cell line, YCMi002-A, from a Factor VII deficiency patient carrying F7 mutations.
Kim DH; Park CY; Cho SR; Kim DW
Stem Cell Res; 2020 Dec; 49():102026. PubMed ID: 33038747
[TBL] [Abstract][Full Text] [Related]
2. F7 gene variants modulate protein levels in a large cohort of patients with factor VII deficiency. Results from a genotype-phenotype study.
Quintavalle G; Riccardi F; Rivolta GF; Martorana D; Di Perna C; Percesepe A; Tagliaferri A;
Thromb Haemost; 2017 Aug; 117(8):1455-1464. PubMed ID: 28447100
[TBL] [Abstract][Full Text] [Related]
3. Novel factor VII gene mutations in six families with hereditary coagulation factor VII deficiency.
Zhang X; Wang S; Leng S; Feng Q; Zhang Y; Xu S; Zhang L; Zhang X; Fang Y; Peng J; Sheng Z
J Clin Lab Anal; 2021 Sep; 35(9):e23905. PubMed ID: 34342048
[TBL] [Abstract][Full Text] [Related]
4. Identification of two novel mutations in three children with congenital factor VII deficiency.
Liang K; Nikuze L; Zhang F; Lu Z; Wei M; Wei H
Blood Coagul Fibrinolysis; 2021 Jul; 32(5):340-343. PubMed ID: 33587484
[TBL] [Abstract][Full Text] [Related]
5. [Haplotype Analysis of Coagulation Factor VII Gene in a Patient with Congenital Coagulation Factor VII Deficiency with Heterozygous p.Arg337Cys Mutation and o.Aro413Gin Polymorphism..].
Suzuki K; Yoshioka T; Obara T; Suwabe A
Rinsho Byori; 2016 May; 64(4):380-386. PubMed ID: 29182802
[TBL] [Abstract][Full Text] [Related]
6. Differential functional readthrough over homozygous nonsense mutations contributes to the bleeding phenotype in coagulation factor VII deficiency.
Branchini A; Ferrarese M; Lombardi S; Mari R; Bernardi F; Pinotti M
J Thromb Haemost; 2016 Oct; 14(10):1994-2000. PubMed ID: 27513915
[TBL] [Abstract][Full Text] [Related]
7. Novel heterozygous F7 gene mutation (c. C1286T) associated with congenital factor VII deficiency: A case report and literature review.
Tang H; Luan X; Li J; Jiang G; Zhen H; Li H; Xiang W; Zhou J
J Clin Lab Anal; 2022 May; 36(5):e24349. PubMed ID: 35349734
[TBL] [Abstract][Full Text] [Related]
8. Compound Heterozygous Mutations in the F7 Gene in 2 Unrelated Families With Congenital Factor VII Deficiency.
Ma C; Wang Y; Gao H; Xue L; Wu S; Xu X; Zhang H; Li C
J Pediatr Hematol Oncol; 2021 Nov; 43(8):e1059-e1061. PubMed ID: 33480651
[TBL] [Abstract][Full Text] [Related]
9. Inherited factor VII deficiency: identification of two novel mutations (A191V and T239P) in the catalytic domain.
Borensztajn K; Chafa O; Le Bonniec B; Wajcman H; Reghis A; Fischer AM; Tapon-Bretaudière J
Thromb Res; 2005; 116(2):115-20. PubMed ID: 15907525
[TBL] [Abstract][Full Text] [Related]
10. Recurrent mutations and genotype-phenotype correlations in hereditary factor VII deficiency in Korea.
Kwon MJ; Yoo KY; Lee KO; Kim SH; Kim HJ
Blood Coagul Fibrinolysis; 2011 Mar; 22(2):102-5. PubMed ID: 21206266
[TBL] [Abstract][Full Text] [Related]
11. [Molecular genetics and clinical features of nine patients with inherited coagulation factor VII deficiency].
Jin YH; Wang MS; Zheng FX; Xie YS; Xie HX; Xu PF
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Aug; 29(4):404-7. PubMed ID: 22875495
[TBL] [Abstract][Full Text] [Related]
12. Factor VII Gene Defects: Review of Functional Studies and Their Clinical Implications.
Shahbazi S; Mahdian R
Iran Biomed J; 2019 May; 23(3):165-74. PubMed ID: 30797223
[TBL] [Abstract][Full Text] [Related]
13. Factor VII deficiency and the FVII mutation database.
McVey JH; Boswell E; Mumford AD; Kemball-Cook G; Tuddenham EG
Hum Mutat; 2001; 17(1):3-17. PubMed ID: 11139238
[TBL] [Abstract][Full Text] [Related]
14. Prevalence of factor VII deficiency and molecular characterization of the F7 gene in Brazilian patients.
Rodrigues DN; Siqueira LH; Galizoni AM; Arruda VR; Annichino-Bizzacchi JM
Blood Coagul Fibrinolysis; 2003 Apr; 14(3):289-92. PubMed ID: 12695753
[TBL] [Abstract][Full Text] [Related]
15. Molecular analysis in a patient with severe factor VII deficiency and an inhibitor: report of a novel mutation (S103G).
Pruthi RK; Rodriguez V; Allen C; Slaby JA; Schmidt KA; Plumhoff EA
Eur J Haematol; 2007 Oct; 79(4):354-9. PubMed ID: 17692102
[TBL] [Abstract][Full Text] [Related]
16. Genotype and phenotype relationships in 10 Pakistani unrelated patients with inherited factor VII deficiency.
Borhany M; Boijout H; Pellequer JL; Shamsi T; Moulis G; Aguilar-Martinez P; Schved JF; Giansily-Blaizot M
Haemophilia; 2013 Nov; 19(6):893-7. PubMed ID: 23731332
[TBL] [Abstract][Full Text] [Related]
17. Twenty two novel mutations of the factor VII gene in factor VII deficiency.
Wulff K; Herrmann FH
Hum Mutat; 2000; 15(6):489-96. PubMed ID: 10862079
[TBL] [Abstract][Full Text] [Related]
18. A novel compound heterozygous variant linked to hematuria in a family with hereditary factor VII deficiency.
Hu YN; Gan YM; Zhang YP; Ruan DD; Zhu YB; Lin XF; Fang ZT; Liao LS; Tang FQ; Luo JW
J Gene Med; 2022 Feb; 24(2):e3398. PubMed ID: 34786791
[TBL] [Abstract][Full Text] [Related]
19. Using a minigene approach to characterize a novel splice site mutation in human F7 gene causing inherited factor VII deficiency in a Chinese pedigree.
Yu T; Wang X; Ding Q; Fu Q; Dai J; Lu Y; Xi X; Wang H
Haemophilia; 2009 Nov; 15(6):1262-6. PubMed ID: 19601987
[TBL] [Abstract][Full Text] [Related]
20. Heterozygous congenital Factor VII deficiency with the 9729del4 mutation, associated with severe spontaneous intracranial bleeding in an adolescent male.
Cramer TJ; Anderson K; Navaz K; Brown JM; Mosnier LO; von Drygalski A
Blood Cells Mol Dis; 2016 Mar; 57():8-12. PubMed ID: 26852649
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
