BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

215 related articles for article (PubMed ID: 17111197)

  • 1. A comprehensive analysis of 12 thrombophilic mutations and related parameters in patients with inflammatory bowel disease: data from Turkey.
    Yilmaz S; Bayan K; Tüzün Y; Batun S; Altintaş A
    J Thromb Thrombolysis; 2006 Dec; 22(3):205-12. PubMed ID: 17111197
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Analysis of inherited thrombophilic mutations and natural anticoagulant deficiency in patients with idiopathic portal hypertension.
    Bayan K; Tüzün Y; Yilmaz S; Canoruc N; Dursun M
    J Thromb Thrombolysis; 2009 Jul; 28(1):57-62. PubMed ID: 18685811
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A prospective case-control study analyzes 12 thrombophilic gene mutations in Turkish couples with recurrent pregnancy loss.
    Yenicesu GI; Cetin M; Ozdemir O; Cetin A; Ozen F; Yenicesu C; Yildiz C; Kocak N
    Am J Reprod Immunol; 2010 Feb; 63(2):126-36. PubMed ID: 19906129
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Recurrent pregnancy loss and its relation to combined parental thrombophilic gene mutations.
    Ozdemir O; Yenicesu GI; Silan F; Köksal B; Atik S; Ozen F; Göl M; Cetin A
    Genet Test Mol Biomarkers; 2012 Apr; 16(4):279-86. PubMed ID: 22047507
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Thrombophilic Gene Mutations in Relation to Different Manifestations of Venous Thromboembolism: A Single Tertiary Center Study.
    Bezgin T; Kaymaz C; Akbal Ö; Yılmaz F; Tokgöz HC; Özdemir N
    Clin Appl Thromb Hemost; 2018 Jan; 24(1):100-106. PubMed ID: 27729560
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Comparison of thrombophilic gene mutations among patients experiencing recurrent miscarriage and deep vein thrombosis.
    Coulam CB; Wallis D; Weinstein J; DasGupta DS; Jeyendran RS
    Am J Reprod Immunol; 2008 Nov; 60(5):426-31. PubMed ID: 18803625
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The effects of genetic polymorphisms and diabetes mellitus on the development of peripheral artery disease.
    Yalım Z; Tutgun Onrat S; Alan S; Aldemir M; Avşar A; Doğan İ; Onrat E
    Turk Kardiyol Dern Ars; 2020 Jul; 48(5):484-493. PubMed ID: 32633259
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Analysis of thrombophilic genetic mutations in patients with Sheehan's syndrome: is thrombophilia responsible for the pathogenesis of Sheehan's syndrome?
    Gokalp D; Tuzcu A; Bahceci M; Ayyildiz O; Yurt M; Celik Y; Alpagat G
    Pituitary; 2011 Jun; 14(2):168-73. PubMed ID: 21107737
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic polymorphisms associated with thrombophilia and vascular disease in women with unexplained late intrauterine fetal death: a multicenter study.
    Hefler L; Jirecek S; Heim K; Grimm C; Antensteiner G; Zeillinger R; Husslein P; Tempfer C
    J Soc Gynecol Investig; 2004 Jan; 11(1):42-4. PubMed ID: 14706682
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Which thrombophilic gene mutations are risk factors for recurrent pregnancy loss?
    Goodman CS; Coulam CB; Jeyendran RS; Acosta VA; Roussev R
    Am J Reprod Immunol; 2006 Oct; 56(4):230-6. PubMed ID: 16938111
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetic factors associated with the predisposition to late onset Alzheimer's disease.
    Durmaz A; Kumral E; Durmaz B; Onay H; Aslan GI; Ozkinay F; Pehlivan S; Orman M; Cogulu O
    Gene; 2019 Jul; 707():212-215. PubMed ID: 31102717
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Factor V Leiden G1691A, prothrombin G20210A, and MTHFR C677T mutations in Turkish inflammatory bowel disease patients.
    Yasa MH; Bolaman Z; Yukselen V; Kadikoylu G; Karaoglul AO; Batun S
    Hepatogastroenterology; 2007; 54(77):1438-42. PubMed ID: 17708272
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Multiple thrombophilic gene mutations rather than specific gene mutations are risk factors for recurrent miscarriage.
    Coulam CB; Jeyendran RS; Fishel LA; Roussev R
    Am J Reprod Immunol; 2006 May; 55(5):360-8. PubMed ID: 16635210
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Correlation with Platelet Parameters and Genetic Markers of Thrombophilia Panel (Factor II g.20210G>A, Factor V Leiden, MTHFR (C677T, A1298C), PAI-1, β-Fibrinogen, Factor XIIIA (V34L), Glycoprotein IIIa (L33P)) in Ischemic Strokes.
    Tasdemir S; Erdem HB; Sahin I; Ozel L; Ozdemir G; Eroz R; Tatar A
    Neuromolecular Med; 2016 Jun; 18(2):170-6. PubMed ID: 26951304
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Association of deep venous thrombosis with prothrombotic gene polymorphism identified in lung cancer cases.
    Arslan S; Manduz S; Epöztürk K; Karahan O; Akkurt I
    Mol Biol Rep; 2011 Apr; 38(4):2395-400. PubMed ID: 21080081
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Evaluation of Factor V G1691A, prothrombin G20210A, Factor XIII V34L, MTHFR A1298C, MTHFR C677T and PAI-1 4G/5G genotype frequencies of patients subjected to cardiovascular disease (CVD) panel in south-east region of Turkey.
    Oztuzcu S; Ergun S; Ulaşlı M; Nacarkahya G; Iğci YZ; Iğci M; Bayraktar R; Tamer A; Çakmak EA; Arslan A
    Mol Biol Rep; 2014 Jun; 41(6):3671-6. PubMed ID: 24532105
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Impact of hemostatic gene single point mutations in patients with non-diabetic coronary artery disease.
    Var A; Utük O; Akçali S; Sanlidağ T; Uyanik BS; Dinç G
    Mol Biol Rep; 2009 Nov; 36(8):2235-43. PubMed ID: 19123042
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Association of Polymorphisms in Coagulation Factor Genes and Enzymes of Homocysteine Metabolism With Arterial Ischemic Stroke in Children.
    Coen Herak D; Lenicek Krleza J; Radic Antolic M; Horvat I; Djuranovic V; Zrinski Topic R; Zadro R
    Clin Appl Thromb Hemost; 2017 Nov; 23(8):1042-1051. PubMed ID: 28301901
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Combined germline variations of thrombophilic genes promote genesis of lung cancer.
    Ozen F; Polat F; Arslan S; Ozdemir O
    Asian Pac J Cancer Prev; 2013; 14(9):5449-54. PubMed ID: 24175756
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic polymorphisms associated with retinal vein occlusion: a Greek case-control study and meta-analysis.
    Yioti GG; Panagiotou OA; Vartholomatos GA; Kolaitis NI; Pappa CN; Evangelou E; Stefaniotou MI
    Ophthalmic Genet; 2013 Sep; 34(3):130-9. PubMed ID: 23289804
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.