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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

410 related items for PubMed ID: 26865696

  • 21. Haploinsufficiency of the basic helix-loop-helix transcription factor HAND2 causes congenital heart defects.
    Cohen ASA, Simotas C, Webb BD, Shi H, Khan WA, Edelmann L, Scott SA, Singh R.
    Am J Med Genet A; 2020 May; 182(5):1263-1267. PubMed ID: 32134193
    [Abstract] [Full Text] [Related]

  • 22. A novel stop mutation truncating critical regions of the cardiac transcription factor NKX2-5 in a large family with autosomal-dominant inherited congenital heart disease.
    Pabst S, Wollnik B, Rohmann E, Hintz Y, Glänzer K, Vetter H, Nickenig G, Grohé C.
    Clin Res Cardiol; 2008 Jan; 97(1):39-42. PubMed ID: 17891520
    [Abstract] [Full Text] [Related]

  • 23. A Novel Missense Mutation of GATA4 in a Chinese Family with Congenital Heart Disease.
    Zhang X, Wang J, Wang B, Chen S, Fu Q, Sun K.
    PLoS One; 2016 Jan; 11(7):e0158904. PubMed ID: 27391137
    [Abstract] [Full Text] [Related]

  • 24. Genetic analysis of an enhancer of the NKX2-5 gene in ventricular septal defects.
    Qin X, Xing Q, Ma L, Meng H, Liu Y, Pang S, Yan B.
    Gene; 2012 Oct 15; 508(1):106-9. PubMed ID: 22824467
    [Abstract] [Full Text] [Related]

  • 25. PITX2 Loss-of-Function Mutation Contributes to Congenital Endocardial Cushion Defect and Axenfeld-Rieger Syndrome.
    Zhao CM, Peng LY, Li L, Liu XY, Wang J, Zhang XL, Yuan F, Li RG, Qiu XB, Yang YQ.
    PLoS One; 2015 Oct 15; 10(4):e0124409. PubMed ID: 25893250
    [Abstract] [Full Text] [Related]

  • 26. Novel GATA4 mutations in patients with congenital ventricular septal defects.
    Yang YQ, Wang J, Liu XY, Chen XZ, Zhang W, Wang XZ, Liu X, Fang WY.
    Med Sci Monit; 2012 Jun 15; 18(6):CR344-50. PubMed ID: 22648249
    [Abstract] [Full Text] [Related]

  • 27. ISL1 loss-of-function mutation contributes to congenital heart defects.
    Ma L, Wang J, Li L, Qiao Q, Di RM, Li XM, Xu YJ, Zhang M, Li RG, Qiu XB, Li X, Yang YQ.
    Heart Vessels; 2019 Apr 15; 34(4):658-668. PubMed ID: 30390123
    [Abstract] [Full Text] [Related]

  • 28. Prevalence and Spectrum of NKX2-5 Mutations Associated With Sporadic Adult-Onset Dilated Cardiomyopathy.
    Xu JH, Gu JY, Guo YH, Zhang H, Qiu XB, Li RG, Shi HY, Liu H, Yang XX, Xu YJ, Qu XK, Yang YQ.
    Int Heart J; 2017 Aug 03; 58(4):521-529. PubMed ID: 28690296
    [Abstract] [Full Text] [Related]

  • 29. A novel mutation in GATA4 gene associated with dominant inherited familial atrial septal defect.
    Chen Y, Han ZQ, Yan WD, Tang CZ, Xie JY, Chen H, Hu DY.
    J Thorac Cardiovasc Surg; 2010 Sep 03; 140(3):684-7. PubMed ID: 20347099
    [Abstract] [Full Text] [Related]

  • 30. Two novel and functional DNA sequence variants within an upstream enhancer of the human NKX2-5 gene in ventricular septal defects.
    Huang W, Meng H, Qiao Y, Pang S, Chen D, Yan B.
    Gene; 2013 Jul 25; 524(2):152-5. PubMed ID: 23644027
    [Abstract] [Full Text] [Related]

  • 31. A New ISL1 Loss-of-Function Mutation Predisposes to Congenital Double Outlet Right Ventricle.
    Wang Z, Song HM, Wang F, Zhao CM, Huang RT, Xue S, Li RG, Qiu XB, Xu YJ, Liu XY, Yang YQ.
    Int Heart J; 2019 Sep 27; 60(5):1113-1122. PubMed ID: 31484864
    [Abstract] [Full Text] [Related]

  • 32. GATA4 mutations in 357 unrelated patients with congenital heart malformation.
    Butler TL, Esposito G, Blue GM, Cole AD, Costa MW, Waddell LB, Walizada G, Sholler GF, Kirk EP, Feneley M, Harvey RP, Winlaw DS.
    Genet Test Mol Biomarkers; 2010 Dec 27; 14(6):797-802. PubMed ID: 20874241
    [Abstract] [Full Text] [Related]

  • 33. 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 27; 43(4):322-6. PubMed ID: 21519287
    [Abstract] [Full Text] [Related]

  • 34. GATA4 loss-of-function mutation underlies familial dilated cardiomyopathy.
    Li RG, Li L, Qiu XB, Yuan F, Xu L, Li X, Xu YJ, Jiang WF, Jiang JQ, Liu X, Fang WY, Zhang M, Peng LY, Qu XK, Yang YQ.
    Biochem Biophys Res Commun; 2013 Oct 04; 439(4):591-6. PubMed ID: 24041700
    [Abstract] [Full Text] [Related]

  • 35. Novel PITX2c loss-of-function mutations associated with complex congenital heart disease.
    Wei D, Gong XH, Qiu G, Wang J, Yang YQ.
    Int J Mol Med; 2014 May 04; 33(5):1201-8. PubMed ID: 24604414
    [Abstract] [Full Text] [Related]

  • 36. Genetic and functional analysis of the NKX2-5 gene promoter in patients with ventricular septal defects.
    Pang S, Shan J, Qiao Y, Ma L, Qin X, Wanyan H, Xing Q, Wu G, Yan B.
    Pediatr Cardiol; 2012 Dec 04; 33(8):1355-61. PubMed ID: 22576768
    [Abstract] [Full Text] [Related]

  • 37. Congenital heart diseases and their association with the variant distribution features on susceptibility genes.
    Su W, Zhu P, Wang R, Wu Q, Wang M, Zhang X, Mei L, Tang J, Kumar M, Wang X, Su L, Dong N.
    Clin Genet; 2017 Mar 04; 91(3):349-354. PubMed ID: 27426723
    [Abstract] [Full Text] [Related]

  • 38. A novel NKX2.5 loss-of-function mutation responsible for familial atrial fibrillation.
    Huang RT, Xue S, Xu YJ, Zhou M, Yang YQ.
    Int J Mol Med; 2013 May 04; 31(5):1119-26. PubMed ID: 23525379
    [Abstract] [Full Text] [Related]

  • 39. TBX20 loss-of-function mutation associated with familial dilated cardiomyopathy.
    Zhao CM, Bing-Sun, Song HM, Wang J, Xu WJ, Jiang JF, Qiu XB, Yuan F, Xu JH, Yang YQ.
    Clin Chem Lab Med; 2016 Feb 04; 54(2):325-32. PubMed ID: 26118961
    [Abstract] [Full Text] [Related]

  • 40. TBX5 loss-of-function mutation contributes to atrial fibrillation and atypical Holt-Oram syndrome.
    Guo DF, Li RG, Yuan F, Shi HY, Hou XM, Qu XK, Xu YJ, Zhang M, Liu X, Jiang JQ, Yang YQ, Qiu XB.
    Mol Med Rep; 2016 May 04; 13(5):4349-56. PubMed ID: 27035640
    [Abstract] [Full Text] [Related]

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