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.
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]
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]