BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

233 related articles for article (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
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 41(11):2072-6. PubMed ID: 12798584
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 14(12):1313-6. PubMed ID: 16896344
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 104(11):1567-73. PubMed ID: 10587520
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 20(1):75-6. PubMed ID: 12112663
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Familial atrial septal defect and atrioventricular conduction disturbance associated with a point mutation in the cardiac homeobox gene CSX/NKX2-5 in a Japanese patient.
    Hosoda T; Komuro I; Shiojima I; Hiroi Y; Harada M; Murakawa Y; Hirata Y; Yazaki Y
    Jpn Circ J; 1999 May; 63(5):425-6. PubMed ID: 10943630
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mutational spectrum in the cardiac transcription factor gene NKX2.5 (CSX) associated with congenital heart disease.
    Stallmeyer B; Fenge H; Nowak-Göttl U; Schulze-Bahr E
    Clin Genet; 2010 Dec; 78(6):533-40. PubMed ID: 20456451
    [TBL] [Abstract][Full Text] [Related]  

  • 8. NKX2.5 mutations in patients with congenital heart disease.
    McElhinney DB; Geiger E; Blinder J; Benson DW; Goldmuntz E
    J Am Coll Cardiol; 2003 Nov; 42(9):1650-5. PubMed ID: 14607454
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The cardiac homeobox gene Csx/Nkx2.5 lies genetically upstream of multiple genes essential for heart development.
    Tanaka M; Chen Z; Bartunkova S; Yamasaki N; Izumo S
    Development; 1999 Mar; 126(6):1269-80. PubMed ID: 10021345
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 108(2):189-201. PubMed ID: 11457872
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Complex modular cis-acting elements regulate expression of the cardiac specifying homeobox gene Csx/Nkx2.5.
    Tanaka M; Wechsler SB; Lee IW; Yamasaki N; Lawitts JA; Izumo S
    Development; 1999 Apr; 126(7):1439-50. PubMed ID: 10068637
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Loss of function and inhibitory effects of human CSX/NKX2.5 homeoprotein mutations associated with congenital heart disease.
    Kasahara H; Lee B; Schott JJ; Benson DW; Seidman JG; Seidman CE; Izumo S
    J Clin Invest; 2000 Jul; 106(2):299-308. PubMed ID: 10903346
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 236(9):2475-84. PubMed ID: 17685485
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Cardiac transcription factor Csx/Nkx2-5: Its role in cardiac development and diseases.
    Akazawa H; Komuro I
    Pharmacol Ther; 2005 Aug; 107(2):252-68. PubMed ID: 15925411
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Developmental paradigms in heart disease: insights from tinman.
    Prall OW; Elliott DA; Harvey RP
    Ann Med; 2002; 34(3):148-56. PubMed ID: 12173684
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Congenital heart disease caused by mutations in the transcription factor NKX2-5.
    Schott JJ; Benson DW; Basson CT; Pease W; Silberbach GM; Moak JP; Maron BJ; Seidman CE; Seidman JG
    Science; 1998 Jul; 281(5373):108-11. PubMed ID: 9651244
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 7(4):423-433. PubMed ID: 25028484
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 298(4):493-500. PubMed ID: 12408979
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 87(10):888-95. PubMed ID: 11073884
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.