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 *

86 related articles for article (PubMed ID: 23429214)

  • 1. Spontaneous bilateral vertebral artery dissection secondary to PAI-1, MTHFR C677T and ACE gene mutations in a young man.
    Hotait M; Sawaya R
    Cerebrovasc Dis; 2013; 35(2):182-3. PubMed ID: 23429214
    [No Abstract]   [Full Text] [Related]  

  • 2. MTHFR C677T, FII G20210A, FV Leiden G1691A, NOS3 intron 4 VNTR, and APOE epsilon4 gene polymorphisms are not associated with spontaneous cervical artery dissection.
    Jara-Prado A; Alonso ME; Martínez Ruano L; Guerrero Camacho J; Leyva A; López M; Gutierrez-Castrellon P; Arauz A
    Int J Stroke; 2010 Apr; 5(2):80-5. PubMed ID: 20446941
    [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. Multifactor dimensionality reduction analysis of MTHFR, PAI-1, ACE, PON1, and eNOS gene polymorphisms in patients with early onset coronary artery disease.
    Agirbasli M; Guney AI; Ozturhan HS; Agirbasli D; Ulucan K; Sevinc D; Kirac D; Ryckman KK; Williams SM
    Eur J Cardiovasc Prev Rehabil; 2011 Dec; 18(6):803-9. PubMed ID: 21450592
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. [Association of genetic polymorphisms in plasminogen activator inhibitor-1 gene and 5,10-methylenetetrahydrofolate reductase gene with recurrent early spontaneous abortion].
    Guan LX; Du XY; Wang JX; Gao L; Wang RL; Li HB; Wang SX
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Jun; 22(3):330-3. PubMed ID: 15952129
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The role of genetics in coronary artery bypass surgery patients under 30 years of age.
    Sarikaya S; Aydin E; Ozen Y; Ozer T; Kirali K; Rabus MB
    Cardiovasc J Afr; 2017 Mar/Apr 23; 28(2):77-80. PubMed ID: 27805237
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Angiotensin converting enzyme and methylenetetrahydrofolate reductase gene variations in fibromyalgia syndrome.
    Inanir A; Yigit S; Tekcan A; Pinarli FA; Inanir S; Karakus N
    Gene; 2015 Jun; 564(2):188-92. PubMed ID: 25824380
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Isolated renal vein thrombosis associated with MTHFR-1298 and PAI-1 4G gene mutations.
    Cinemre H; Bilir C; Akdemir N
    Clin Appl Thromb Hemost; 2010 Dec; 16(6):708-10. PubMed ID: 19825918
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Two cousins with neonatal stroke, PAI-1 4G variant and MTHFR A1298C mutation.
    Golomb MR; Heiny M; Garg BP
    J Child Neurol; 2007 Jun; 22(6):753-5. PubMed ID: 17641264
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Association of Plasminogen Activator Inhibitor-1 Gene Polymorphisms and Methylene Tetrahydrofolate Reductase Polymorphisms with Spontaneous Miscarriages.
    Bubalo P; Buterin I; Šalek Z; Ðogić V; Zupančić-Šalek S
    Acta Haematol; 2017; 138(2):111-115. PubMed ID: 28858863
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Plasminogen activator inhibitor 1 and methylenetetrahydrofolate reductase gene mutations in iranian women with polycystic ovary syndrome.
    Idali F; Zareii S; Mohammad-Zadeh A; Reihany-Sabet F; Akbarzadeh-Pasha Z; Khorram-Khorshid HR; Zarnani AH; Jeddi-Tehrani M
    Am J Reprod Immunol; 2012 Nov; 68(5):400-7. PubMed ID: 22882325
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Association of von Willebrand factor activity with ACE I/D and MTHFR C677T polymorphisms in migraine.
    Tietjen GE; Herial NA; Utley C; White L; Yerga-Woolwine S; Joe B
    Cephalalgia; 2009 Sep; 29(9):960-8. PubMed ID: 19298544
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Frequency of thrombophilic genetic polymorphisms among Saudi subjects compared with other populations.
    Settin AA; Alghasham A; Ali A; Dowaidar M; Ismail H
    Hematology; 2012 May; 17(3):176-82. PubMed ID: 22664118
    [TBL] [Abstract][Full Text] [Related]  

  • 16. MTHFR C677T, A1298C and ACE I/D polymorphisms as risk factors for diabetic nephropathy among type 2 diabetic patients.
    El-Baz R; Settin A; Ismaeel A; Khaleel AA; Abbas T; Tolba W; Abd Allah W; Sobh MA
    J Renin Angiotensin Aldosterone Syst; 2012 Dec; 13(4):472-7. PubMed ID: 22554825
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Role of the ACE ID and MTHFR C677T polymorphisms in genetic susceptibility of migraine in a north Indian population.
    Joshi G; Pradhan S; Mittal B
    J Neurol Sci; 2009 Feb; 277(1-2):133-7. PubMed ID: 19081115
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. The role of classic risk factors and prothrombotic factor gene mutations in ischemic stroke risk development in young and middle-aged individuals.
    Supanc V; Sonicki Z; Vukasovic I; Solter VV; Zavoreo I; Kes VB
    J Stroke Cerebrovasc Dis; 2014 Mar; 23(3):e171-6. PubMed ID: 24189452
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic combination of angiotensin-converting enzyme with methylene tetrahydrofolate reductase polymorphisms and the risk of type 2 diabetes mellitus in Bahrain.
    Al-Harbi EM; Farid EM; Gumaa KA; Darwish AH; Alenizi M; Singh J
    J Renin Angiotensin Aldosterone Syst; 2015 Mar; 16(1):172-7. PubMed ID: 23447104
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.