BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

438 related articles for article (PubMed ID: 32610551)

  • 1. Genetic Variants in the
    Simurda T; Brunclikova M; Asselta R; Caccia S; Zolkova J; Kolkova Z; Loderer D; Skornova I; Hudecek J; Lasabova Z; Stasko J; Kubisz P
    Int J Mol Sci; 2020 Jun; 21(13):. PubMed ID: 32610551
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mutations Accounting for Congenital Fibrinogen Disorders: An Update.
    Richard M; Celeny D; Neerman-Arbez M
    Semin Thromb Hemost; 2022 Nov; 48(8):889-903. PubMed ID: 35073585
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Molecular genetics of quantitative fibrinogen disorders.
    Asselta R; Spena S; Duga S; Tenchini ML
    Cardiovasc Hematol Agents Med Chem; 2007 Apr; 5(2):163-73. PubMed ID: 17430139
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Fibrinogen as a Pleiotropic Protein Causing Human Diseases: The Mutational Burden of Aα, Bβ, and γ Chains.
    Paraboschi EM; Duga S; Asselta R
    Int J Mol Sci; 2017 Dec; 18(12):. PubMed ID: 29240685
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Identification of Two Novel Fibrinogen Bβ Chain Mutations in Two Slovak Families with Quantitative Fibrinogen Disorders.
    Simurda T; Zolkova J; Snahnicanova Z; Loderer D; Skornova I; Sokol J; Hudecek J; Stasko J; Lasabova Z; Kubisz P
    Int J Mol Sci; 2017 Dec; 19(1):. PubMed ID: 29286337
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The molecular basis of quantitative fibrinogen disorders.
    Asselta R; Duga S; Tenchini ML
    J Thromb Haemost; 2006 Oct; 4(10):2115-29. PubMed ID: 16999847
    [TBL] [Abstract][Full Text] [Related]  

  • 7. FGB mutations leading to congenital quantitative fibrinogen deficiencies: an update and report of four novel mutations.
    Casini A; Lukowski S; Quintard VL; Crutu A; Zak M; Regazzoni S; de Moerloose P; Neerman-Arbez M
    Thromb Res; 2014 May; 133(5):868-74. PubMed ID: 24560896
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Rare inherited disorders of fibrinogen.
    Acharya SS; Dimichele DM
    Haemophilia; 2008 Nov; 14(6):1151-8. PubMed ID: 19141154
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A novel fibrinogen mutation (γ Thr277Arg) causes hereditary hypofibrinogenemia in a Chinese family.
    Zhu L; Wang M; Xie H; Jin Y; Yang L; Xu P
    Blood Coagul Fibrinolysis; 2013 Sep; 24(6):642-4. PubMed ID: 23492915
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Hereditary Hypofibrinogenemia with Hepatic Storage.
    Asselta R; Paraboschi EM; Duga S
    Int J Mol Sci; 2020 Oct; 21(21):. PubMed ID: 33105716
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Laboratory and Genetic Investigation of Mutations Accounting for Congenital Fibrinogen Disorders.
    Neerman-Arbez M; de Moerloose P; Casini A
    Semin Thromb Hemost; 2016 Jun; 42(4):356-65. PubMed ID: 27019463
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genetic and clinical characterization of congenital fibrinogen disorders in Polish patients: Identification of three novel fibrinogen gamma chain mutations.
    Wypasek E; Klukowska A; Zdziarska J; Zawilska K; Treliński J; Iwaniec T; Mital A; Pietrys D; Sydor W; Neerman-Arbez M; Undas A
    Thromb Res; 2019 Oct; 182():133-140. PubMed ID: 31479941
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular characterization of 7 patients affected by dys- or hypo-dysfibrinogenemia: Identification of a novel mutation in the fibrinogen Bbeta chain causing a gain of glycosylation.
    Asselta R; Robusto M; Platé M; Santoro C; Peyvandi F; Duga S
    Thromb Res; 2015 Jul; 136(1):168-74. PubMed ID: 26006300
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Thrombosis-associated hypofibrinogenemia: novel abnormal fibrinogen variant FGG c.8G>A with oxidative posttranslational modifications.
    Ceznerová E; Kaufmanová J; Stikarová J; Pastva O; Loužil J; Chrastinová L; Suttnar J; Kotlín R; Dyr JE
    Blood Coagul Fibrinolysis; 2022 Jun; 33(4):228-237. PubMed ID: 35067535
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Epistatic and pleiotropic effects of polymorphisms in the fibrinogen and coagulation factor XIII genes on plasma fibrinogen concentration, fibrin gel structure and risk of myocardial infarction.
    Mannila MN; Eriksson P; Ericsson CG; Hamsten A; Silveira A
    Thromb Haemost; 2006 Mar; 95(3):420-7. PubMed ID: 16525568
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A rare heterozygous variant in FGB (Fibrinogen Merivale) causing hypofibrinogenemia in a Swedish family.
    Fager Ferrari M; Leinoe E; Rossing M; Norström E; Zetterberg E
    Blood Coagul Fibrinolysis; 2020 Oct; 31(7):481-484. PubMed ID: 32852326
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. Hepatic fibrinogen storage disease: identification of two novel mutations (p.Asp316Asn, fibrinogen Pisa and p.Gly366Ser, fibrinogen Beograd) impacting on the fibrinogen γ-module.
    Asselta R; Robusto M; Braidotti P; Peyvandi F; Nastasio S; D'Antiga L; Perisic VN; Maggiore G; Caccia S; Duga S
    J Thromb Haemost; 2015 Aug; 13(8):1459-67. PubMed ID: 26039544
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Congenital fibrinogen disorders: an update.
    de Moerloose P; Casini A; Neerman-Arbez M
    Semin Thromb Hemost; 2013 Sep; 39(6):585-95. PubMed ID: 23852822
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 22.