BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

98 related articles for article (PubMed ID: 15257949)

  • 1. Homozygosity of the T allele of the 46 C-->T polymorphism in the F12 gene is a risk factor for acute coronary artery disease in the Spanish population.
    Santamaría A; Martínez-Rubio A; Mateo J; Tirado I; Soria JM; Fontcuberta J
    Haematologica; 2004 Jul; 89(7):878-9. PubMed ID: 15257949
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Factor XII 46C --> T gene polymorphism in Chilean subjects with coronary artery disease and controls.
    Caamaño J; Jaramillo PC; Lanas C; Lanas F; Salazar LA
    Med Princ Pract; 2009; 18(2):137-42. PubMed ID: 19204433
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Association of C1019T polymorphism in the connexin 37 gene and coronary artery disease in Chinese Han population].
    Han YL; Xi SY; Zhang XL; Yan CH; Yang Y; Kang J
    Zhonghua Yi Xue Za Zhi; 2007 Jan; 87(2):100-4. PubMed ID: 17418016
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Association after linkage analysis indicates that homozygosity for the 46C-->T polymorphism in the F12 gene is a genetic risk factor for venous thrombosis.
    Tirado I; Soria JM; Mateo J; Oliver A; Souto JC; Santamaria A; Felices R; Borrell M; Fontcuberta J
    Thromb Haemost; 2004 May; 91(5):899-904. PubMed ID: 15116249
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Role of the CD14 C(-260)T promoter polymorphism in determining the first clinical manifestation of coronary artery disease.
    Rizzello V; Liuzzo G; Trabetti E; Di Giannuario G; Brugaletta S; Santamaria M; Piro M; Boccanelli A; Pignatti PF; Biasucci LM; Crea F
    J Cardiovasc Med (Hagerstown); 2010 Jan; 11(1):20-5. PubMed ID: 19829130
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Age and hypertension related changes in genotypes of MTHFR 677C>T, 1298A>C and PON1 -108C>T SNPs in men with coronary artery disease (CAD).
    Strauss E; Głuszek J; Pawlak AL
    J Physiol Pharmacol; 2005 Mar; 56 Suppl 2():65-75. PubMed ID: 16077191
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Influence of endothelial nitric oxide synthase gene polymorphisms (-786T>C, 4a4b, 894G>T) in Korean patients with coronary artery disease.
    Kim IJ; Bae J; Lim SW; Cha DH; Cho HJ; Kim S; Yang DH; Hwang SG; Oh D; Kim NK
    Thromb Res; 2007; 119(5):579-85. PubMed ID: 16842840
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The presence of apolipoprotein epsilon4 and epsilon2 alleles augments the risk of coronary artery disease in type 2 diabetic patients.
    Vaisi-Raygani A; Rahimi Z; Nomani H; Tavilani H; Pourmotabbed T
    Clin Biochem; 2007 Oct; 40(15):1150-6. PubMed ID: 17689519
    [TBL] [Abstract][Full Text] [Related]  

  • 9. eNOS gene intron 4 a/b VNTR polymorphism is a risk factor for coronary artery disease in Southern Turkey.
    Matyar S; Attila G; Acartürk E; Akpinar O; Inal T
    Clin Chim Acta; 2005 Apr; 354(1-2):153-8. PubMed ID: 15748612
    [TBL] [Abstract][Full Text] [Related]  

  • 10. High plasma homocysteine is associated with the risk of coronary artery disease independent of methylenetetrahydrofolate reductase 677C-->T genotypes.
    Lin PT; Huang MC; Lee BJ; Cheng CH; Tsai TP; Huang YC
    Asia Pac J Clin Nutr; 2008; 17(2):330-8. PubMed ID: 18586656
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The 3'-UTR C>T polymorphism of the oxidized LDL-receptor 1 (OLR1) gene does not associate with coronary artery disease in Italian CAD patients or with the severity of coronary disease.
    Sentinelli F; Filippi E; Fallarino M; Romeo S; Fanelli M; Buzzetti R; Berni A; Baroni MG
    Nutr Metab Cardiovasc Dis; 2006 Jul; 16(5):345-52. PubMed ID: 16829343
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Association of cholesteryl ester transfer protein -629C > A polymorphism with high-density lipoprotein cholesterol levels in coronary artery disease patients.
    Tanrikulu S; Ademoglu E; Gurdol F; Mutlu-Turkoglu U; Bilge AK; Nisanci Y
    Cell Biochem Funct; 2009 Oct; 27(7):452-7. PubMed ID: 19784962
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The functional promoter polymorphism of the coagulation factor XII gene is not associated with peripheral arterial disease.
    Yazdani-Biuki B; Krippl P; Brickmann K; Fuerst F; Langsenlehner U; Paulweber B; Pilger E; Wascher TC; Brezinschek HP; Renner W
    Angiology; 2010 Feb; 61(2):211-5. PubMed ID: 19625260
    [TBL] [Abstract][Full Text] [Related]  

  • 14. FXII (46C-->T) polymorphism and in vivo generation of FXII activity--gene frequencies and relationship in patients with coronary artery disease.
    Kohler HP; Futers TS; Grant PJ
    Thromb Haemost; 1999 May; 81(5):745-7. PubMed ID: 10365748
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Homozygosity of the T allele of the 46 C->T polymorphism in the F12 gene is a risk factor for ischemic stroke in the Spanish population.
    Santamaría A; Mateo J; Tirado I; Oliver A; Belvís R; Martí-Fábregas J; Felices R; Soria JM; Souto JC; Fontcuberta J
    Stroke; 2004 Aug; 35(8):1795-9. PubMed ID: 15232129
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Coronary artery disease and a functional polymorphism of hTERT.
    Matsubara Y; Murata M; Watanabe K; Saito I; Miyaki K; Omae K; Ishikawa M; Matsushita K; Iwanaga S; Ogawa S; Ikeda Y
    Biochem Biophys Res Commun; 2006 Sep; 348(2):669-72. PubMed ID: 16890917
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The differential effects of age on the association of KLOTHO gene polymorphisms with coronary artery disease.
    Rhee EJ; Oh KW; Lee WY; Kim SY; Jung CH; Kim BJ; Sung KC; Kim BS; Kang JH; Lee MH; Kim SW; Park JR
    Metabolism; 2006 Oct; 55(10):1344-51. PubMed ID: 16979405
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Relationship between the -374T/A RAGE gene polymorphism and angiographic coronary artery disease.
    Falcone C; Campo I; Emanuele E; Buzzi MP; Zorzetto M; Sbarsi I; Cuccia M
    Int J Mol Med; 2004 Dec; 14(6):1061-4. PubMed ID: 15547674
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Relationship between paraoxonase 1 55 Met/Leu, paraoxonase 2 148 Ala/Gly genetic polymorphisms and coronary artery disease].
    Chi DS; Ling WH; Ma J; Xia M; Hou MJ; Wang Q; Zhu HL; Tang ZH; Yu XP
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Jun; 23(3):289-93. PubMed ID: 16767666
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Lack of association between Glu(298) asp polymorphism of endothelial nitric oxide synthase (eNOS) gene and coronary artery disease in Tamilian population.
    Mathew J; Narayanan P; Sundaram R; Jayaraman B; Dutta TK; Raman SK; Chandrasekaran A
    Indian Heart J; 2008; 60(3):223-7. PubMed ID: 19240311
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.