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Journal Abstract Search

212 related items for PubMed ID: 31386585

  • 1. The Functional Polymorphism R129W in the BVES Gene Is Associated with Sporadic Tetralogy of Fallot in the Han Chinese Population.
    Shi Y, Li Y, Wang Y, Zhuang J, Wang H, Hu M, Mo X, Yue S, Chen Y, Fan X, Chen J, Cai W, Zhu X, Wan Y, Zhong Y, Ye X, Li F, Zhou Z, Dai G, Luo R, Ocorr K, Jiang Z, Li X, Zhu P, Wu X, Yuan W.
    Genet Test Mol Biomarkers; 2019 Sep; 23(9):601-609. PubMed ID: 31386585
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  • 2. BVES downregulation in non-syndromic tetralogy of fallot is associated with ventricular outflow tract stenosis.
    Shi Y, Li Y, Wang Y, Zhu P, Chen Y, Wang H, Yue S, Xia X, Chen J, Jiang Z, Zhou C, Cai W, Yuan H, Wu Y, Wan Y, Li X, Zhu X, Zhou Z, Dai G, Li F, Mo X, Ye X, Fan X, Zhuang J, Wu X, Yuan W.
    Sci Rep; 2020 Aug 25; 10(1):14167. PubMed ID: 32843646
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  • 4. Functional polymorphisms of the neuropilin 1 gene are associated with the risk of tetralogy of Fallot in a Chinese Han population.
    Fan SH, Shen ZY, Xiao YM.
    Gene; 2018 May 05; 653():72-79. PubMed ID: 29432830
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  • 5. Genetic variations of VEGF gene were associated with tetralogy of fallot risk in a Chinese Han population.
    Yan L, Ge Q, Xi C, Zhang X, Guo Y.
    Genet Test Mol Biomarkers; 2015 May 05; 19(5):264-71. PubMed ID: 25894981
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  • 8. DNA methylation status of NKX2-5, GATA4 and HAND1 in patients with tetralogy of fallot.
    Sheng W, Qian Y, Wang H, Ma X, Zhang P, Diao L, An Q, Chen L, Ma D, Huang G.
    BMC Med Genomics; 2013 Nov 01; 6():46. PubMed ID: 24182332
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  • 12. Somatic mutations in NKX2–5, GATA4, and HAND1 are not a common cause of tetralogy of Fallot or hypoplastic left heart.
    Esposito G, Butler TL, Blue GM, Cole AD, Sholler GF, Kirk EP, Grossfeld P, Perryman BM, Harvey RP, Winlaw DS.
    Am J Med Genet A; 2011 Oct 01; 155A(10):2416-21. PubMed ID: 22043484
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  • 13. Analyses of GATA4, NKX2.5, and TFAP2B genes in subjects from southern China with sporadic congenital heart disease.
    Xiong F, Li Q, Zhang C, Chen Y, Li P, Wei X, Li Q, Zhou W, Li L, Shang X, Xu X.
    Cardiovasc Pathol; 2013 Oct 01; 22(2):141-5. PubMed ID: 22959235
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  • 15. Single nucleotide polymorphism of NKX2-5 gene with sporadic congenital heart disease in Chinese Bai population.
    Cao Y, Lan W, Li Y, Wei C, Zou H, Jiang L.
    Int J Clin Exp Pathol; 2015 Oct 01; 8(11):14917-24. PubMed ID: 26823822
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  • 17. A common variant in the PTPN11 gene contributes to the risk of tetralogy of Fallot.
    Goodship JA, Hall D, Topf A, Mamasoula C, Griffin H, Rahman TJ, Glen E, Tan H, Palomino Doza J, Relton CL, Bentham J, Bhattacharya S, Cosgrove C, Brook D, Granados-Riveron J, Bu'Lock FA, O'Sullivan J, Stuart AG, Parsons J, Cordell HJ, Keavney B.
    Circ Cardiovasc Genet; 2012 Jun 01; 5(3):287-92. PubMed ID: 22503907
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  • 18. Functionally significant, rare transcription factor variants in tetralogy of Fallot.
    Töpf A, Griffin HR, Glen E, Soemedi R, Brown DL, Hall D, Rahman TJ, Eloranta JJ, Jüngst C, Stuart AG, O'Sullivan J, Keavney BD, Goodship JA.
    PLoS One; 2014 Jun 01; 9(8):e95453. PubMed ID: 25093829
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  • 19. VEGF Gene Polymorphisms are Associated with Risk of Tetralogy of Fallot.
    Li X, Liu CL, Li XX, Li QC, Ma LM, Liu GL.
    Med Sci Monit; 2015 Nov 12; 21():3474-82. PubMed ID: 26558525
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