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 *

110 related articles for article (PubMed ID: 21659551)

  • 1. A knockout for knockin.
    Mosnier LO
    Blood; 2011 Jun; 117(23):6058-60. PubMed ID: 21659551
    [No Abstract]   [Full Text] [Related]  

  • 2. The development of inflammatory joint disease is attenuated in mice expressing the anticoagulant prothrombin mutant W215A/E217A.
    Flick MJ; Chauhan AK; Frederick M; Talmage KE; Kombrinck KW; Miller W; Mullins ES; Palumbo JS; Zheng X; Esmon NL; Esmon CT; Thornton S; Becker A; Pelc LA; Di Cera E; Wagner DD; Degen JL
    Blood; 2011 Jun; 117(23):6326-37. PubMed ID: 21436072
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Prothrombin 20210G>A genotype and C-reactive protein level.
    Hoppe B; Burmester GR; Häupl T
    Blood; 2011 Oct; 118(16):4495-6. PubMed ID: 22021457
    [No Abstract]   [Full Text] [Related]  

  • 4. Prothrombin: Another Clotting Factor After FV That Is Involved Both in Bleeding and Thrombosis.
    Girolami A; Cosi E; Ferrari S; Girolami B
    Clin Appl Thromb Hemost; 2018 Sep; 24(6):845-849. PubMed ID: 29690772
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Thrombin generation and activated protein C resistance in patients with essential thrombocythemia and polycythemia vera.
    Marchetti M; Castoldi E; Spronk HM; van Oerle R; Balducci D; Barbui T; Rosing J; Ten Cate H; Falanga A
    Blood; 2008 Nov; 112(10):4061-8. PubMed ID: 18768782
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Paradoxical bleeding and thrombotic episodes of dysprothrombinaemia due to a homozygous Arg382His mutation.
    Ding Q; Yang L; Zhao X; Wu W; Wang X; Rezaie AR
    Thromb Haemost; 2017 Feb; 117(3):479-490. PubMed ID: 27975099
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Prothrombin Scranton: substitution of an amino acid residue involved in the binding of Na+ (LYS-556 to THR) leads to dysprothrombinemia.
    Sun WY; Smirnow D; Jenkins ML; Degen SJ
    Thromb Haemost; 2001 Apr; 85(4):651-4. PubMed ID: 11341500
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinical significance of prothrombin G20210A mutation in homozygous patients.
    Shemesh A; Hoffman R; Nadir Y; Keren-Politansky A; Monreal M; Brenner B; Tzoran I
    Am J Hematol; 2017 Oct; 92(10):E618-E620. PubMed ID: 28707429
    [No Abstract]   [Full Text] [Related]  

  • 9. Exacerbated venous thromboembolism in mice carrying a protein S K196E mutation.
    Banno F; Kita T; Fernández JA; Yanamoto H; Tashima Y; Kokame K; Griffin JH; Miyata T
    Blood; 2015 Nov; 126(19):2247-53. PubMed ID: 26251307
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Protein Z-dependent protease inhibitor (ZPI) is a physiologically significant inhibitor of prothrombinase function.
    Huang X; Swanson R; Kroh HK; Bock PE
    J Biol Chem; 2019 May; 294(19):7644-7657. PubMed ID: 30918026
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prothrombin Saint-Denis: a natural variant with a point mutation resulting in Asp to Glu substitution at position 552 in prothrombin.
    Rouy S; Vidaud D; Alessandri JL; Dautzenberg MD; Venisse L; Guillin MC; Bezeaud A
    Br J Haematol; 2006 Mar; 132(6):770-3. PubMed ID: 16487178
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prothrombin deficiency caused by compound heterozygosity for two novel mutations in the prothrombin gene associated with a bleeding tendency.
    Stanchev H; Philips M; Villoutreix BO; Aksglaede L; Lethagen S; Thorsen S
    Thromb Haemost; 2006 Jan; 95(1):195-8. PubMed ID: 16543981
    [No Abstract]   [Full Text] [Related]  

  • 13. Antithrombin-resistant prothrombin Yukuhashi mutation also causes thrombomodulin resistance in fibrinogen clotting but not in protein C activation.
    Takagi Y; Kato I; Ando Y; Nakamura Y; Murata M; Takagi A; Murate T; Kojima T
    Thromb Res; 2014 Oct; 134(4):914-7. PubMed ID: 25149909
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prothrombin Arg541Trp Mutation Leads to Defective PC (Protein C) Pathway Activation and Constitutes a Novel Genetic Risk Factor for Venous Thrombosis.
    Wu X; Dai J; Xu X; Li F; Li L; Lu Y; Xu Q; Ding Q; Wu W; Wang X
    Arterioscler Thromb Vasc Biol; 2020 Feb; 40(2):483-494. PubMed ID: 31875702
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The Dual Regulatory Role of Amino Acids Leu480 and Gln481 of Prothrombin.
    Wiencek JR; Hirbawi J; Yee VC; Kalafatis M
    J Biol Chem; 2016 Jan; 291(4):1565-1581. PubMed ID: 26601957
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Chronic myeloid leukaemia with extreme thrombocytosis at presentation: incidence, clinical findings and outcome.
    Sora F; Iurlo A; Sica S; Latagliata R; Annunziata M; Galimberti S; Castagnetti F; Pregno P; Sgherza N; Celesti F; Bocchia M; Gozzini A; Fava C; Cattaneo D; Crugnola M; Montefusco E; Mauro E; Capodanno I; Breccia M
    Br J Haematol; 2018 Apr; 181(2):267-270. PubMed ID: 28169426
    [No Abstract]   [Full Text] [Related]  

  • 17. Amino acid pairs susceptible to variants in human protein C precursor.
    Wu G; Yan S
    Protein Pept Lett; 2005 Jul; 12(5):491-4. PubMed ID: 16029164
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic elimination of prothrombin in adult mice is not compatible with survival and results in spontaneous hemorrhagic events in both heart and brain.
    Mullins ES; Kombrinck KW; Talmage KE; Shaw MA; Witte DP; Ullman JM; Degen SJ; Sun W; Flick MJ; Degen JL
    Blood; 2009 Jan; 113(3):696-704. PubMed ID: 18927430
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Gene symbol: F2. Disease: Hypoprothrombinemia.
    Wang H; Wang W; Fu Q; Zhou R; Wu W; Ding Q; Hu Y; Wang X; Wang Z
    Hum Genet; 2005 May; 116(6):543. PubMed ID: 15991329
    [No Abstract]   [Full Text] [Related]  

  • 20. Increased Activated Protein C Response Rates Reduce the Thrombotic Risk of Factor V Leiden Carriers But Not of Prothrombin 20210G>A Carriers.
    Rühl H; Berens C; Winterhagen FI; Reda S; Müller J; Oldenburg J; Pötzsch B
    Circ Res; 2019 Aug; 125(5):523-534. PubMed ID: 31314700
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.