These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

180 related articles for article (PubMed ID: 31267299)

  • 1. Next generation sequencing in bleeding disorders: two novel variants in the F5 gene (Valencia-1 and Valencia-2) associated with mild factor V deficiency.
    Moret A; Zúñiga Á; Ibáñez M; Cid AR; Haya S; Ferrando F; Blanquer A; Cervera J; Bonanad S
    J Thromb Thrombolysis; 2019 Nov; 48(4):674-678. PubMed ID: 31267299
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Design and application of a 23-gene panel by next-generation sequencing for inherited coagulation bleeding disorders.
    Bastida JM; Del Rey M; Lozano ML; Sarasquete ME; Benito R; Fontecha ME; Fisac R; García-Frade LJ; Aguilar C; Martínez MP; Pardal E; Aguilera C; Pérez B; Ramos R; Cardesa MR; Martin-Antorán JM; Silvestre LA; Cebeira MJ; Bermejo N; Riesco S; Mendoza MC; García-Sanz R; González-Díaz M; Hernández-Rivas JM; González-Porras JR
    Haemophilia; 2016 Jul; 22(4):590-7. PubMed ID: 26879396
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Functional characterization of a novel missense mutation identified in a Turkish patient affected by severe coagulation factor V deficiency.
    Paraboschi EM; Kayiran SM; Özbek N; Gürakan B; Peyvandi F; Guella I; Duga S; Asselta R
    Haemophilia; 2012 Mar; 18(2):205-10. PubMed ID: 21777354
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Homozygous F5 deep-intronic splicing mutation resulting in severe factor V deficiency and undetectable thrombin generation in platelet-rich plasma.
    Castoldi E; Duckers C; Radu C; Spiezia L; Rossetto V; Tagariello G; Rosing J; Simioni P
    J Thromb Haemost; 2011 May; 9(5):959-68. PubMed ID: 21320286
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Characterization of an apparently synonymous F5 mutation causing aberrant splicing and factor V deficiency.
    Nuzzo F; Bulato C; Nielsen BI; Lee K; Wielders SJ; Simioni P; Key NS; Castoldi E
    Haemophilia; 2015 Mar; 21(2):241-248. PubMed ID: 25470420
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Factor 5 mutation profile in German patients with homozygous and heterozygous factor V deficiency.
    Delev D; Pavlova A; Heinz S; Seifried E; Oldenburg J
    Haemophilia; 2009 Sep; 15(5):1143-53. PubMed ID: 19486170
    [TBL] [Abstract][Full Text] [Related]  

  • 7. In vitro and ex vivo rescue of a nonsense mutation responsible for severe coagulation factor V deficiency.
    Todaro AM; Radu CM; Ciccone M; Toffanin S; Serino ML; Campello E; Bulato C; Lunghi B; Gemmati D; Cuneo A; Hackeng TM; Simioni P; Bernardi F; Castoldi E
    J Thromb Haemost; 2024 Feb; 22(2):410-422. PubMed ID: 37866515
    [TBL] [Abstract][Full Text] [Related]  

  • 8. High Mutational Heterogeneity, and New Mutations in the Human Coagulation Factor V Gene. Future Perspectives for Factor V Deficiency Using Recombinant and Advanced Therapies.
    Bernal S; Pelaez I; Alias L; Baena M; De Pablo-Moreno JA; Serrano LJ; Camero MD; Tizzano EF; Berrueco R; Liras A
    Int J Mol Sci; 2021 Sep; 22(18):. PubMed ID: 34575869
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Novel splicing (c.6529-1G>T) and missense (c.1667G>A) mutations causing factor V deficiency.
    Maharaj S; Saenz Ayala S; Hu X; Chang S; Sharma V; Majerus J; Pruthi R
    Blood Coagul Fibrinolysis; 2021 Jul; 32(5):344-348. PubMed ID: 33769317
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular characterization of three novel splicing mutations causing factor V deficiency and analysis of the F5 gene splicing pattern.
    Dall'Osso C; Guella I; Duga S; Locatelli N; Paraboschi EM; Spreafico M; Afrasiabi A; Pechlaner C; Peyvandi F; Tenchini ML; Asselta R
    Haematologica; 2008 Oct; 93(10):1505-13. PubMed ID: 18728029
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Phenotypic and genetic analysis of a pedigree affected with hereditary FV deficiency due to a novel deletional variant of F5 gene].
    Ding H; Su K; Hu L; Zhang H; Zhu L; Yang L; Jin Y; Wang M
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Nov; 36(11):1100-1103. PubMed ID: 31703135
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Identification of four novel mutations in F5 associated with congenital factor V deficiency.
    Kanaji S; Kanaji T; Honda M; Nakazato S; Wakayama K; Tabata Y; Shibata S; Gondo H; Nakamura I; Node K; Miura M; Miyahara M; Okamura T; Nagumo F; Ohta S; Izuhara K
    Int J Hematol; 2009 Jan; 89(1):71-75. PubMed ID: 19052695
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Five novel mutations in the gene for human blood coagulation factor V associated with type I factor V deficiency.
    van Wijk R; Nieuwenhuis K; van den Berg M; Huizinga EG; van der Meijden BB; Kraaijenhagen RJ; van Solinge WW
    Blood; 2001 Jul; 98(2):358-67. PubMed ID: 11435304
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinical and molecular characterization of 6 patients affected by severe deficiency of coagulation factor V: Broadening of the mutational spectrum of factor V gene and in vitro analysis of the newly identified missense mutations.
    Montefusco MC; Duga S; Asselta R; Malcovati M; Peyvandi F; Santagostino E; Mannucci PM; Tenchini ML
    Blood; 2003 Nov; 102(9):3210-6. PubMed ID: 12816860
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A Comprehensive Overview of Coagulation Factor V and Congenital Factor V Deficiency.
    Tabibian S; Shiravand Y; Shams M; Safa M; Gholami MS; Heydari F; Ahmadi A; Rashidpanah J; Dorgalaleh A
    Semin Thromb Hemost; 2019 Jul; 45(5):523-543. PubMed ID: 31121608
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification of three F5 gene mutations associated with inherited coagulation factor V deficiency in two Chinese pedigrees.
    Fu QH; Zhou RF; Liu LG; Wang WB; Wu WM; Ding QL; Hu YQ; Wang XF; Wang ZY; Wang HL
    Haemophilia; 2004 May; 10(3):264-70. PubMed ID: 15086325
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Severe factor V deficiency: exon skipping in the factor V gene causing a partial deletion of the C1 domain.
    Asselta R; Montefusco MC; Duga S; Malcovati M; Peyvandi F; Mannucci PM; Tenchini ML
    J Thromb Haemost; 2003 Jun; 1(6):1237-44. PubMed ID: 12871325
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Parahemophilia: new insights into factor v deficiency.
    Thalji N; Camire RM
    Semin Thromb Hemost; 2013 Sep; 39(6):607-12. PubMed ID: 23893775
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Understanding the Impact of Aberrant Splicing in Coagulation Factor V Deficiency.
    Paraboschi EM; Menegatti M; Peyvandi F; Duga S; Asselta R
    Int J Mol Sci; 2019 Feb; 20(4):. PubMed ID: 30791524
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Coexistence of a novel homozygous nonsense mutation in exon 13 of the factor V gene with the homozygous Leiden mutation in two unrelated patients with severe factor V deficiency.
    van Wijk R; Montefusco MC; Duga S; Asselta R; van Solinge W; Malcovati M; Tenchini ML; Mannucci PM
    Br J Haematol; 2001 Sep; 114(4):871-4. PubMed ID: 11564077
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.