These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

147 related articles for article (PubMed ID: 16043659)

  • 1. Recent advances in cardiac development with therapeutic implications for adult cardiovascular disease.
    Epstein JA; Parmacek MS
    Circulation; 2005 Jul; 112(4):592-7. PubMed ID: 16043659
    [No Abstract]   [Full Text] [Related]  

  • 2. [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; 102(3):120-5. PubMed ID: 21572484
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mutations of transcription factors in human with heart disease for understanding the development and mechanisms of congenital cardiovascular heart disease.
    Matsuoka R
    Adv Exp Med Biol; 2005; 565():349-57; discussion 405-15. PubMed ID: 16106988
    [No Abstract]   [Full Text] [Related]  

  • 4. Spectrum of atrial septal defects associated with mutations of NKX2.5 and GATA4 transcription factors.
    Sarkozy A; Conti E; Neri C; D'Agostino R; Digilio MC; Esposito G; Toscano A; Marino B; Pizzuti A; Dallapiccola B
    J Med Genet; 2005 Feb; 42(2):e16. PubMed ID: 15689439
    [No Abstract]   [Full Text] [Related]  

  • 5. Fresh fields and pathways new: recent genetic insights into cardiac malformation.
    Leong FT; Freeman LJ; Keavney BD
    Heart; 2009 Mar; 95(6):442-7. PubMed ID: 19252006
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Transcriptional regulation of cardiac development: implications for congenital heart disease and DiGeorge syndrome.
    Epstein JA; Buck CA
    Pediatr Res; 2000 Dec; 48(6):717-24. PubMed ID: 11102536
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mutations in GATA4, NKX2.5, CRELD1, and BMP4 are infrequently found in patients with congenital cardiac septal defects.
    Posch MG; Perrot A; Schmitt K; Mittelhaus S; Esenwein EM; Stiller B; Geier C; Dietz R; Gessner R; Ozcelik C; Berger F
    Am J Med Genet A; 2008 Jan; 146A(2):251-3. PubMed ID: 18076106
    [No Abstract]   [Full Text] [Related]  

  • 8. 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; 76(7):1703-11. PubMed ID: 22498567
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Epigenetic mechanisms in cardiac development and disease.
    Vallaster M; Vallaster CD; Wu SM
    Acta Biochim Biophys Sin (Shanghai); 2012 Jan; 44(1):92-102. PubMed ID: 22194017
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Nkx genes establish second heart field cardiomyocyte progenitors at the arterial pole and pattern the venous pole through Isl1 repression.
    Colombo S; de Sena-Tomás C; George V; Werdich AA; Kapur S; MacRae CA; Targoff KL
    Development; 2018 Feb; 145(3):. PubMed ID: 29361575
    [No Abstract]   [Full Text] [Related]  

  • 11. Developmental cardiology comes of age.
    Epstein JA
    Circ Res; 2000 Nov; 87(10):833-4. PubMed ID: 11073875
    [No Abstract]   [Full Text] [Related]  

  • 12. 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; 14(6):797-802. PubMed ID: 20874241
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Neural crest migration and mouse models of congenital heart disease.
    Gitler AD; Brown CB; Kochilas L; Li J; Epstein JA
    Cold Spring Harb Symp Quant Biol; 2002; 67():57-62. PubMed ID: 12858524
    [No Abstract]   [Full Text] [Related]  

  • 14. 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]  

  • 15. Homeodomain factor Nkx2-5 in heart development and disease.
    Harvey RP; Lai D; Elliott D; Biben C; Solloway M; Prall O; Stennard F; Schindeler A; Groves N; Lavulo L; Hyun C; Yeoh T; Costa M; Furtado M; Kirk E
    Cold Spring Harb Symp Quant Biol; 2002; 67():107-14. PubMed ID: 12858530
    [No Abstract]   [Full Text] [Related]  

  • 16. Ablation of Nkx2-5 at mid-embryonic stage results in premature lethality and cardiac malformation.
    Terada R; Warren S; Lu JT; Chien KR; Wessels A; Kasahara H
    Cardiovasc Res; 2011 Jul; 91(2):289-99. PubMed ID: 21285290
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Insights into the genetic structure of congenital heart disease from human and murine studies on monogenic disorders.
    Prendiville T; Jay PY; Pu WT
    Cold Spring Harb Perspect Med; 2014 Oct; 4(10):. PubMed ID: 25274754
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Transcription factor cascades in congenital heart malformation.
    Hatcher CJ; Diman NY; McDermott DA; Basson CT
    Trends Mol Med; 2003 Dec; 9(12):512-5. PubMed ID: 14659463
    [No Abstract]   [Full Text] [Related]  

  • 19. A gene that scrambles your heart.
    Hagmann M
    Science; 1999 Feb; 283(5405):1091,1093. PubMed ID: 10075562
    [No Abstract]   [Full Text] [Related]  

  • 20. Molecular basis of AV block and cardiac malformations.
    Mittmann C
    Cardiovasc Res; 2004 Oct; 64(1):1-2. PubMed ID: 15364605
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.