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Journal Abstract Search

229 related items for PubMed ID: 12074273

  • 1. Novel point mutation in the cardiac transcription factor CSX/NKX2.5 associated with congenital heart disease.
    Ikeda Y, Hiroi Y, Hosoda T, Utsunomiya T, Matsuo S, Ito T, Inoue J, Sumiyoshi T, Takano H, Nagai R, Komuro I.
    Circ J; 2002 Jun; 66(6):561-3. PubMed ID: 12074273
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  • 2. Cardiac homeobox gene NKX2-5 mutations and congenital heart disease: associations with atrial septal defect and hypoplastic left heart syndrome.
    Elliott DA, Kirk EP, Yeoh T, Chandar S, McKenzie F, Taylor P, Grossfeld P, Fatkin D, Jones O, Hayes P, Feneley M, Harvey RP.
    J Am Coll Cardiol; 2003 Jun 04; 41(11):2072-6. PubMed ID: 12798584
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  • 3. A novel CSX/NKX2-5 mutation causes autosomal-dominant AV block: are atrial fibrillation and syncopes part of the phenotype?
    Gutierrez-Roelens I, De Roy L, Ovaert C, Sluysmans T, Devriendt K, Brunner HG, Vikkula M.
    Eur J Hum Genet; 2006 Dec 04; 14(12):1313-6. PubMed ID: 16896344
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  • 4. Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathways.
    Benson DW, Silberbach GM, Kavanaugh-McHugh A, Cottrill C, Zhang Y, Riggs S, Smalls O, Johnson MC, Watson MS, Seidman JG, Seidman CE, Plowden J, Kugler JD.
    J Clin Invest; 1999 Dec 04; 104(11):1567-73. PubMed ID: 10587520
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  • 5. Progressive AV-block and anomalous venous return among cardiac anomalies associated with two novel missense mutations in the CSX/NKX2-5 gene.
    Gutierrez-Roelens I, Sluysmans T, Gewillig M, Devriendt K, Vikkula M.
    Hum Mutat; 2002 Jul 04; 20(1):75-6. PubMed ID: 12112663
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  • 10. Progressive atrioventricular conduction defects and heart failure in mice expressing a mutant Csx/Nkx2.5 homeoprotein.
    Kasahara H, Wakimoto H, Liu M, Maguire CT, Converso KL, Shioi T, Huang WY, Manning WJ, Paul D, Lawitts J, Berul CI, Izumo S.
    J Clin Invest; 2001 Jul 04; 108(2):189-201. PubMed ID: 11457872
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  • 13. Transient early embryonic expression of Nkx2-5 mutations linked to congenital heart defects in human causes heart defects in Xenopus laevis.
    Bartlett HL, Sutherland L, Kolker SJ, Welp C, Tajchman U, Desmarais V, Weeks DL.
    Dev Dyn; 2007 Sep 04; 236(9):2475-84. PubMed ID: 17685485
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  • 16. Developmental paradigms in heart disease: insights from tinman.
    Prall OW, Elliott DA, Harvey RP.
    Ann Med; 2002 Sep 04; 34(3):148-56. PubMed ID: 12173684
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  • 18. A mouse model of human congenital heart disease: high incidence of diverse cardiac anomalies and ventricular noncompaction produced by heterozygous Nkx2-5 homeodomain missense mutation.
    Ashraf H, Pradhan L, Chang EI, Terada R, Ryan NJ, Briggs LE, Chowdhury R, Zárate MA, Sugi Y, Nam HJ, Benson DW, Anderson RH, Kasahara H.
    Circ Cardiovasc Genet; 2014 Aug 04; 7(4):423-433. PubMed ID: 25028484
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  • 19. Dual effects of the homeobox transcription factor Csx/Nkx2-5 on cardiomyocytes.
    Monzen K, Zhu W, Kasai H, Hiroi Y, Hosoda T, Akazawa H, Zou Y, Hayashi D, Yamazaki T, Nagai R, Komuro I.
    Biochem Biophys Res Commun; 2002 Nov 08; 298(4):493-500. PubMed ID: 12408979
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  • 20. Cardiac septal and valvular dysmorphogenesis in mice heterozygous for mutations in the homeobox gene Nkx2-5.
    Biben C, Weber R, Kesteven S, Stanley E, McDonald L, Elliott DA, Barnett L, Köentgen F, Robb L, Feneley M, Harvey RP.
    Circ Res; 2000 Nov 10; 87(10):888-95. PubMed ID: 11073884
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