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 *

96 related articles for article (PubMed ID: 30793713)

  • 1. Identification of six novel factor viii gene variants using next generation sequencing and molecular dynamics simulation.
    Al-Allaf FA; Abduljaleel Z; Bogari NM; Owaidah TMA; Taher MM; Athar M; Elsendiony A; Abalkhail H; Abdellatif A; Elbjeirami W; Bouazzaoui A
    Acta Biochim Pol; 2019 Feb; 66(1):23-31. PubMed ID: 30793713
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mutational spectrum and deep intronic variants in the factor VIII gene of haemophilia A patients. Identification by next generation sequencing.
    Bach JE; Oldenburg J; Müller CR; Rost S
    Hamostaseologie; 2016 Nov; 36(Suppl. 2):S25-S28. PubMed ID: 27824209
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Identification of deep intronic variants in 15 haemophilia A patients by next generation sequencing of the whole factor VIII gene.
    Bach JE; Wolf B; Oldenburg J; Müller CR; Rost S
    Thromb Haemost; 2015 Oct; 114(4):757-67. PubMed ID: 25948085
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The spectrum of FVIII gene variants detected by next generation sequencing in 236 Chinese non-inversion hemophilia A pedigrees.
    Chen J; Li Q; Lin S; Li F; Huang L; Jin W; Yang X; Li Y; Li K; Xiong Y; Fan D; Zheng L; Luo D; Li L; Yang X
    Thromb Res; 2021 Jun; 202():8-13. PubMed ID: 33706050
    [TBL] [Abstract][Full Text] [Related]  

  • 5. High throughput mutation screening of the factor VIII gene (F8C) in hemophilia A: 37 novel mutations and genotype-phenotype correlation.
    Citron M; Godmilow L; Ganguly T; Ganguly A
    Hum Mutat; 2002 Oct; 20(4):267-74. PubMed ID: 12325022
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Identification of mutations in the F8 and F9 gene in families with haemophilia using targeted high-throughput sequencing.
    Lyu C; Xue F; Liu X; Liu W; Fu R; Sun T; Wu R; Zhang L; Li H; Zhang D; Yang R; Zhang L
    Haemophilia; 2016 Sep; 22(5):e427-34. PubMed ID: 27292088
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic analysis of bleeding disorders.
    Edison E; Konkle BA; Goodeve AC
    Haemophilia; 2016 Jul; 22 Suppl 5(Suppl 5):79-83. PubMed ID: 27405681
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molecular genotyping of hemophilia A in Saudi Arabia: report of 2 novel mutations.
    Owaidah TM; Alkhail HA; Zahrani HA; Musa AA; Saleh MA; Riash MA; Alodaib A; Abu Amero K
    Blood Coagul Fibrinolysis; 2009 Sep; 20(6):415-8. PubMed ID: 19448530
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Characterization of four novel molecular changes in the promoter region of the factor VIII gene.
    Nougier C; Roualdes O; Fretigny M; d'Oiron R; Costa C; Negrier C; Vinciguerra C
    Haemophilia; 2014 Mar; 20(2):e149-56. PubMed ID: 24372689
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The challenge of genetically unresolved haemophilia A patients: Interest of the combination of whole F8 gene sequencing and functional assays.
    Lassalle F; Jourdy Y; Jouan L; Swystun L; Gauthier J; Zawadzki C; Goudemand J; Susen S; Rivard GE; Lillicrap D
    Haemophilia; 2020 Nov; 26(6):1056-1063. PubMed ID: 33094873
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Application of a molecular diagnostic algorithm for haemophilia A and B using next-generation sequencing of entire F8, F9 and VWF genes.
    Bastida JM; González-Porras JR; Jiménez C; Benito R; Ordoñez GR; Álvarez-Román MT; Fontecha ME; Janusz K; Castillo D; Fisac RM; García-Frade LJ; Aguilar C; Martínez MP; Bermejo N; Herrero S; Balanzategui A; Martin-Antorán JM; Ramos R; Cebeiro MJ; Pardal E; Aguilera C; Pérez-Gutierrez B; Prieto M; Riesco S; Mendoza MC; Benito A; Hortal Benito-Sendin A; Jiménez-Yuste V; Hernández-Rivas JM; García-Sanz R; González-Díaz M; Sarasquete ME
    Thromb Haemost; 2017 Jan; 117(1):66-74. PubMed ID: 27734074
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Identification of deep intronic individual variants in patients with hemophilia A by next-generation sequencing of the whole factor VIII gene.
    Inaba H; Shinozawa K; Amano K; Fukutake K
    Res Pract Thromb Haemost; 2017 Oct; 1(2):264-274. PubMed ID: 30046696
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genotype Hemophilia Screening Program Identified 2 Novel Variants Including a Novel Variant (c.5816-2A > G) Causing a Pathogenic Variant of the Factor 8 Gene.
    Owaidah T; Bakr S; Al-Numair N; AbaAlkhail H; Alzahrani H; Saleh M; Khogeer H; Tarawah A; Akkad H; Al-Allaf F
    Clin Appl Thromb Hemost; 2023; 29():10760296231182410. PubMed ID: 37525882
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Molecular Analysis of Factor VIII and Factor IX Genes in Hemophilia Patients: Identification of Novel Mutations and Molecular Dynamics Studies.
    Al-Allaf FA; Taher MM; Abduljaleel Z; Bouazzaoui A; Athar M; Bogari NM; Abalkhail HA; Owaidah TM
    J Clin Med Res; 2017 Apr; 9(4):317-331. PubMed ID: 28270892
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Study of mutations in Jordanian patients with haemophilia A: identification of five novel mutations.
    Awidi A; Ramahi M; Alhattab D; Mefleh R; Dweiri M; Bsoul N; Magablah A; Arafat E; Barqawi M; Bishtawi M; Haddadeen E; Falah M; Tarawneh B; Swaidan S; Fauori S
    Haemophilia; 2010 Jan; 16(1):136-42. PubMed ID: 19817879
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Introns 1 and 22 inversions and F8 gene sequencing for molecular diagnosis of hemophilia A in Chile].
    Poggi H; Honorato J; Romeo E; Zúñiga P; Quiroga T; Lagos M
    Rev Med Chil; 2011 Feb; 139(2):189-96. PubMed ID: 21773656
    [TBL] [Abstract][Full Text] [Related]  

  • 17. An intronic mutation c.6430-3C>G in the F8 gene causes splicing efficiency and premature termination in hemophilia A.
    Xia Z; Lin J; Lu L; Kim C; Yu P; Qi M
    Blood Coagul Fibrinolysis; 2018 Jun; 29(4):381-386. PubMed ID: 29652675
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Screening of mutations of hemophilia A in 40 Italian patients: a novel G-to-A mutation in intron 10 of the F8 gene as a putative cause of mild hemophilia A in southern Italy.
    Santacroce R; Santoro R; Sessa F; Iannaccaro P; Sarno M; Longo V; Gallone A; Vecchione G; Muleo G; Margaglione M
    Blood Coagul Fibrinolysis; 2008 Apr; 19(3):197-202. PubMed ID: 18388498
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The prevalence of factor VIII and IX inhibitors among Saudi patients with hemophilia: Results from the Saudi national hemophilia screening program.
    Owaidah T; Momen AA; Alzahrani H; Almusa A; Alkasim F; Tarawah A; Nouno RA; Batniji FA; Alothman F; Alomari A; Abu-Herbish S; Abu-Riash M; Siddiqui K; Ahmed M; Mohamed SY; Saleh M
    Medicine (Baltimore); 2017 Jan; 96(2):e5456. PubMed ID: 28079788
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Methylation analysis of the promoter region and intron 1 of the factor VIII gene in haemophilia A patients.
    Zimmermann MA; Hansmann T; Haaf T; Oldenburg J; Müller CR; Rost S
    Hamostaseologie; 2013; 33 Suppl 1():S46-9. PubMed ID: 24170290
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.