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Journal Abstract Search

145 related items for PubMed ID: 27748330

  • 21. 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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  • 22. 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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  • 23. Investigation of somatic NKX2-5, GATA4 and HAND1 mutations in patients with tetralogy of Fallot.
    Wang J, Lu Y, Chen H, Yin M, Yu T, Fu Q.
    Pathology; 2011 Jun 25; 43(4):322-6. PubMed ID: 21519287
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  • 24. New mutations in ZFPM2/FOG2 gene in tetralogy of Fallot and double outlet right ventricle.
    De Luca A, Sarkozy A, Ferese R, Consoli F, Lepri F, Dentici ML, Vergara P, De Zorzi A, Versacci P, Digilio MC, Marino B, Dallapiccola B.
    Clin Genet; 2011 Aug 25; 80(2):184-90. PubMed ID: 20807224
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  • 28. HIRA, a DiGeorge Syndrome Candidate Gene, Confers Proper Chromatin Accessibility on HSCs and Supports All Stages of Hematopoiesis.
    Chen C, Sun MA, Warzecha C, Bachu M, Dey A, Wu T, Adams PD, Macfarlan T, Love P, Ozato K.
    Cell Rep; 2020 Feb 18; 30(7):2136-2149.e4. PubMed ID: 32075733
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  • 29. Identification of Region-Specific Myocardial Gene Expression Patterns in a Chronic Swine Model of Repaired Tetralogy of Fallot.
    Charron S, Roubertie F, Benoist D, Dubes V, Gilbert SH, Constantin M, Vieillot D, Elbes D, Quesson B, Bordachar P, Haissaguerre M, Bernus O, Thambo JB, Rooryck C.
    PLoS One; 2015 Feb 18; 10(8):e0134146. PubMed ID: 26252659
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  • 31. Transcriptomic analysis of patients with tetralogy of Fallot reveals the effect of chronic hypoxia on myocardial gene expression.
    Ghorbel MT, Cherif M, Jenkins E, Mokhtari A, Kenny D, Angelini GD, Caputo M.
    J Thorac Cardiovasc Surg; 2010 Aug 18; 140(2):337-345.e26. PubMed ID: 20416888
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  • 33. Mutations of ZFPM2/FOG2 gene in sporadic cases of tetralogy of Fallot.
    Pizzuti A, Sarkozy A, Newton AL, Conti E, Flex E, Digilio MC, Amati F, Gianni D, Tandoi C, Marino B, Crossley M, Dallapiccola B.
    Hum Mutat; 2003 Nov 18; 22(5):372-7. PubMed ID: 14517948
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  • 37. Silencing mutations in JAG1 gene may play crucial roles in the pathogenesis of Tetralogy of Fallot.
    Safari-Arababadi A, Behjati-Ardakani M, Kalantar SM, Jaafarinia M.
    Cell Mol Biol (Noisy-le-grand); 2018 Mar 31; 64(4):103-107. PubMed ID: 29631691
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  • 39. Myocardial expression of heat shock protein 70i protects early postoperative right ventricular function in cyanotic tetralogy of Fallot.
    Peng EW, McCaig D, Pollock JC, MacArthur K, Lyall F, Danton MH.
    J Thorac Cardiovasc Surg; 2011 May 31; 141(5):1184-91. PubMed ID: 21397265
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  • 40. Human Genetics of Tetralogy of Fallot and Double-Outlet Right Ventricle.
    Dorn C, Perrot A, Grunert M, Rickert-Sperling S.
    Adv Exp Med Biol; 2024 May 31; 1441():629-644. PubMed ID: 38884738
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