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Journal Abstract Search

984 related items for PubMed ID: 12845333

  • 1. GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5.
    Garg V, Kathiriya IS, Barnes R, Schluterman MK, King IN, Butler CA, Rothrock CR, Eapen RS, Hirayama-Yamada K, Joo K, Matsuoka R, Cohen JC, Srivastava D.
    Nature; 2003 Jul 24; 424(6947):443-7. PubMed ID: 12845333
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  • 3. Genetic analysis of essential cardiac transcription factors in 256 patients with non-syndromic congenital heart defects.
    Kodo K, Nishizawa T, Furutani M, Arai S, Ishihara K, Oda M, Makino S, Fukuda K, Takahashi T, Matsuoka R, Nakanishi T, Yamagishi H.
    Circ J; 2012 Jul 24; 76(7):1703-11. PubMed ID: 22498567
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  • 6. Combined mutation screening of NKX2-5, GATA4, and TBX5 in congenital heart disease: multiple heterozygosity and novel mutations.
    Granados-Riveron JT, Pope M, Bu'lock FA, Thornborough C, Eason J, Setchfield K, Ketley A, Kirk EP, Fatkin D, Feneley MP, Harvey RP, Brook JD.
    Congenit Heart Dis; 2012 Jul 24; 7(2):151-9. PubMed ID: 22011241
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  • 7. Interaction of Gata4 and Gata6 with Tbx5 is critical for normal cardiac development.
    Maitra M, Schluterman MK, Nichols HA, Richardson JA, Lo CW, Srivastava D, Garg V.
    Dev Biol; 2009 Feb 15; 326(2):368-77. PubMed ID: 19084512
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  • 9. [Genetic screening of Gata4 and Nkx2.5 mutations in hereditary congenital heart defects: 5 familial cases].
    Pulignani S, Foffa I, Cresci M, Vittorini S, Ait-Ali L, Andreassi MG.
    Recenti Prog Med; 2011 Mar 15; 102(3):120-5. PubMed ID: 21572484
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  • 10. Biochemical analyses of eight NKX2.5 homeodomain missense mutations causing atrioventricular block and cardiac anomalies.
    Kasahara H, Benson DW.
    Cardiovasc Res; 2004 Oct 01; 64(1):40-51. PubMed ID: 15364612
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  • 13. TBX5 loss-of-function mutation contributes to familial dilated cardiomyopathy.
    Zhang XL, Qiu XB, Yuan F, Wang J, Zhao CM, Li RG, Xu L, Xu YJ, Shi HY, Hou XM, Qu XK, Xu YW, Yang YQ.
    Biochem Biophys Res Commun; 2015 Mar 27; 459(1):166-71. PubMed ID: 25725155
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  • 14. Disease Model of GATA4 Mutation Reveals Transcription Factor Cooperativity in Human Cardiogenesis.
    Ang YS, Rivas RN, Ribeiro AJS, Srivas R, Rivera J, Stone NR, Pratt K, Mohamed TMA, Fu JD, Spencer CI, Tippens ND, Li M, Narasimha A, Radzinsky E, Moon-Grady AJ, Yu H, Pruitt BL, Snyder MP, Srivastava D.
    Cell; 2016 Dec 15; 167(7):1734-1749.e22. PubMed ID: 27984724
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  • 15. Search of somatic GATA4 and NKX2.5 gene mutations in sporadic septal heart defects.
    Salazar M, Consoli F, Villegas V, Caicedo V, Maddaloni V, Daniele P, Caianiello G, Pachón S, Nuñez F, Limongelli G, Pacileo G, Marino B, Bernal JE, De Luca A, Dallapiccola B.
    Eur J Med Genet; 2011 Dec 15; 54(3):306-9. PubMed ID: 21276881
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  • 16. 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 15; 14(6):797-802. PubMed ID: 20874241
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  • 17. Functional analysis of novel TBX5 T-box mutations associated with Holt-Oram syndrome.
    Boogerd CJ, Dooijes D, Ilgun A, Mathijssen IB, Hordijk R, van de Laar IM, Rump P, Veenstra-Knol HE, Moorman AF, Barnett P, Postma AV.
    Cardiovasc Res; 2010 Oct 01; 88(1):130-9. PubMed ID: 20519243
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  • 20. Congenital heart disease-causing Gata4 mutation displays functional deficits in vivo.
    Misra C, Sachan N, McNally CR, Koenig SN, Nichols HA, Guggilam A, Lucchesi PA, Pu WT, Srivastava D, Garg V.
    PLoS Genet; 2012 Oct 01; 8(5):e1002690. PubMed ID: 22589735
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