BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

533 related articles for article (PubMed ID: 19135706)

  • 1. Characterization of a homozygous Gly11Val mutation in the Gla domain of coagulation factor X.
    Chafa O; Tagzirt M; Tapon-Bretaudière J; Reghis A; Fischer AM; LeBonniec BF
    Thromb Res; 2009 May; 124(1):144-8. PubMed ID: 19135706
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Reduced activation of the Gla19Ala FX variant via the extrinsic coagulation pathway results in symptomatic CRMred FX deficiency.
    Pinotti M; Marchetti G; Baroni M; Cinotti F; Morfini M; Bernardi F
    Thromb Haemost; 2002 Aug; 88(2):236-41. PubMed ID: 12195695
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The impact of Glu102Lys on the factor X function in a patient with a doubly homozygous factor X deficiency (Gla14Lys and Glu102Lys).
    Forberg E; Huhmann I; Jimenez-Boj E; Watzke HH
    Thromb Haemost; 2000 Feb; 83(2):234-8. PubMed ID: 10739379
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Factor X Shanghai and disruption of translocation to the endoplasmic reticulum.
    Wang WB; Fu QH; Yin J; Wu WM; Ding QL; Zhou RF; Hu YQ; Wang XF; Wang ZY; Wang HL
    Haematologica; 2005 Dec; 90(12):1659-64. PubMed ID: 16330440
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Analysis of the novel factor X gene mutation Glu51Lys in two families with factor X-Riyadh anomaly.
    Al-Hilali A; Wulff K; Abdel-Razeq H; Saud KA; Al-Gaili F; Herrmann FH
    Thromb Haemost; 2007 Apr; 97(4):542-5. PubMed ID: 17393015
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Homozygous missense mutation p.Val298Met of F10 gene causing hereditary coagulation factor X deficiency in a Chinese pedigree].
    Jin Y; Hao X; Cheng X; Yang L; Chen Y; Xie H; Wang Y; Wang M
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Jun; 33(3):296-9. PubMed ID: 27264807
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Characterization of mild coagulation factor VII deficiency: activity and clearance of the Arg315Trp and Arg315Lys variants in the Cys310-Cys329 loop (c170s).
    Furlan Freguia C; Toso R; Pollak ES; Arruda VR; Pinotti M; Bernardi F
    Haematologica; 2004 Dec; 89(12):1504-9. PubMed ID: 15590402
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Severe factor X deficiency in three unrelated Palestinian patients is caused by homozygosity for the mutation c302delG-correlation with thrombin generation and thromboelastometry.
    Livnat T; Shenkman B; Kenet G; Tamarin I; Gillis S; Varon D; Iijima K; Zivelin A; Salomon O
    Blood Coagul Fibrinolysis; 2011 Dec; 22(8):673-9. PubMed ID: 22008904
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Structure/function analyses of recombinant variants of human factor Xa: factor Xa incorporation into prothrombinase on the thrombin-activated platelet surface is not mimicked by synthetic phospholipid vesicles.
    Larson PJ; Camire RM; Wong D; Fasano NC; Monroe DM; Tracy PB; High KA
    Biochemistry; 1998 Apr; 37(14):5029-38. PubMed ID: 9538022
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Inherited coagulation factor X deficiency caused by two novel mutations in factor X gene].
    Wang WB; Wang HL; Wang XF; Fu QH; Zhou RF; Xie S; Hu YQ; Wang ZY
    Zhonghua Xue Ye Xue Za Zhi; 2004 Sep; 25(9):519-22. PubMed ID: 15569527
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Factor XDebrecen: Gly204Arg mutation in factor X causes the synthesis of a non-secretable protein and severe factor X deficiency.
    Bereczky Z; Bárdos H; Komáromi I; Kiss C; Haramura G; Ajzner E; Adány R; Muszbek L
    Haematologica; 2008 Feb; 93(2):299-302. PubMed ID: 18245654
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Characterization of porcine factor VII, X and comparison with human factor VII, X.
    Chen Y; Qiao J; Tan W; Lu Y; Qin S; Zhang J; Li S; Bu H; Cheng J
    Blood Cells Mol Dis; 2009; 43(1):111-8. PubMed ID: 19286401
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The tissue factor/factor VIIa/factor Xa complex: a model built by docking and site-directed mutagenesis.
    Norledge BV; Petrovan RJ; Ruf W; Olson AJ
    Proteins; 2003 Nov; 53(3):640-8. PubMed ID: 14579355
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Protein disulfide isomerase has no stimulatory chaperone effect on factor X activation by factor VIIa-soluble tissue factor.
    Persson E
    Thromb Res; 2008; 123(1):171-6. PubMed ID: 18550154
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Factor X Frankfurt I: molecular and functional characterization of a hereditary factor X deficiency (Gla+25 to Lys).
    Nöbauer-Huhmann IM; Höller W; Krinninger B; Turecek PL; Richter G; Scharrer I; Forberg E; Watzke HH
    Blood Coagul Fibrinolysis; 1998 Mar; 9(2):143-52. PubMed ID: 9622212
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Molecular characterization of two novel mutations causing factor X deficiency in a Chinese pedigree.
    Wang WB; Fu QH; Zhou RF; Wu WM; Ding QL; Hu YQ; Wang XF; Wang HL; Wang ZY
    Haemophilia; 2005 Jan; 11(1):31-7. PubMed ID: 15660986
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Impaired prothrombinase activity of factor X Gly381Asp results in severe familial CRM+ FX deficiency.
    Pinotti M; Camire RM; Baroni M; Rajab A; Marchetti G; Bernardi F
    Thromb Haemost; 2003 Feb; 89(2):243-8. PubMed ID: 12574802
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The clinical and laboratory significance of cases of congenital FX deficiency due to defects in the Gla-domain.
    Girolami A; Allemand E; Scandellari R; Lombardi AM; Girolami B
    Hematology; 2009 Jun; 14(3):177-81. PubMed ID: 19490765
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Role of the Gla and first epidermal growth factor-like domains of factor X in the prothrombinase and tissue factor-factor VIIa complexes.
    Thiec F; Cherel G; Christophe OD
    J Biol Chem; 2003 Mar; 278(12):10393-9. PubMed ID: 12529356
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Antibody-induced acute factor X deficiency: clinical manifestations and properties of the antibody.
    Rao LV; Zivelin A; Iturbe I; Rapaport SI
    Thromb Haemost; 1994 Sep; 72(3):363-71. PubMed ID: 7855785
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 27.