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.
253 related articles for article (PubMed ID: 16470721)
1. A novel mutation in the GATA4 gene in patients with Tetralogy of Fallot. Nemer G; Fadlalah F; Usta J; Nemer M; Dbaibo G; Obeid M; Bitar F Hum Mutat; 2006 Mar; 27(3):293-4. PubMed ID: 16470721 [TBL] [Abstract][Full Text] [Related]
2. GATA4 loss-of-function mutations underlie familial tetralogy of fallot. Yang YQ; Gharibeh L; Li RG; Xin YF; Wang J; Liu ZM; Qiu XB; Xu YJ; Xu L; Qu XK; Liu X; Fang WY; Huang RT; Xue S; Nemer G Hum Mutat; 2013 Dec; 34(12):1662-71. PubMed ID: 24000169 [TBL] [Abstract][Full Text] [Related]
3. Mutations of ZFPM2/FOG2 gene in sporadic cases of tetralogy of Fallot. Pizzuti A; Sarkozy A; Newton AL; Conti E; Flex E; Digilio MC; Amati F; Gianni D; Tandoi C; Marino B; Crossley M; Dallapiccola B Hum Mutat; 2003 Nov; 22(5):372-7. PubMed ID: 14517948 [TBL] [Abstract][Full Text] [Related]
4. A novel GATA6 mutation in patients with tetralogy of Fallot or atrial septal defect. Lin X; Huo Z; Liu X; Zhang Y; Li L; Zhao H; Yan B; Liu Y; Yang Y; Chen YH J Hum Genet; 2010 Oct; 55(10):662-7. PubMed ID: 20631719 [TBL] [Abstract][Full Text] [Related]
5. New mutations in ZFPM2/FOG2 gene in tetralogy of Fallot and double outlet right ventricle. De Luca A; Sarkozy A; Ferese R; Consoli F; Lepri F; Dentici ML; Vergara P; De Zorzi A; Versacci P; Digilio MC; Marino B; Dallapiccola B Clin Genet; 2011 Aug; 80(2):184-90. PubMed ID: 20807224 [TBL] [Abstract][Full Text] [Related]
6. Genetic screening of 104 patients with congenitally malformed hearts revealed a fresh mutation of GATA4 in those with atrial septal defects. Hamanoue H; Rahayuningsih SE; Hirahara Y; Itoh J; Yokoyama U; Mizuguchi T; Saitsu H; Miyake N; Hirahara F; Matsumoto N Cardiol Young; 2009 Sep; 19(5):482-5. PubMed ID: 19678963 [TBL] [Abstract][Full Text] [Related]
7. The effect of human GATA4 gene mutations on the activity of target gonadal promoters. Bouchard MF; Taniguchi H; Viger RS J Mol Endocrinol; 2009 Feb; 42(2):149-60. PubMed ID: 19008335 [TBL] [Abstract][Full Text] [Related]
8. [Novel GATA4 mutations identified in patients with congenital heart disease]. Wang J; Hu DY; Li XM; Xin YF; Zhou H; Wang LJ; Wang LM; Xu WJ Zhonghua Yi Xue Za Zhi; 2010 Mar; 90(10):667-71. PubMed ID: 20450724 [TBL] [Abstract][Full Text] [Related]
9. Mutations in the cardiac transcription factor GATA4 in patients with lone atrial fibrillation. Posch MG; Boldt LH; Polotzki M; Richter S; Rolf S; Perrot A; Dietz R; Ozcelik C; Haverkamp W Eur J Med Genet; 2010; 53(4):201-3. PubMed ID: 20363377 [TBL] [Abstract][Full Text] [Related]
10. Involvement of a novel GATA4 mutation in atrial septal defects. Liu XY; Wang J; Zheng JH; Bai K; Liu ZM; Wang XZ; Liu X; Fang WY; Yang YQ Int J Mol Med; 2011 Jul; 28(1):17-23. PubMed ID: 21373748 [TBL] [Abstract][Full Text] [Related]
11. Somatic mutations in the GATA6 gene underlie sporadic tetralogy of Fallot. Huang RT; Xue S; Xu YJ; Yang YQ Int J Mol Med; 2013 Jan; 31(1):51-8. PubMed ID: 23175051 [TBL] [Abstract][Full Text] [Related]
12. TBX20 loss-of-function mutation responsible for familial tetralogy of Fallot or sporadic persistent truncus arteriosus. Huang RT; Wang J; Xue S; Qiu XB; Shi HY; Li RG; Qu XK; Yang XX; Liu H; Li N; Li YJ; Xu YJ; Yang YQ Int J Med Sci; 2017; 14(4):323-332. PubMed ID: 28553164 [TBL] [Abstract][Full Text] [Related]
13. GATA4 mutations in 486 Chinese patients with congenital heart disease. Zhang W; Li X; Shen A; Jiao W; Guan X; Li Z Eur J Med Genet; 2008; 51(6):527-35. PubMed ID: 18672102 [TBL] [Abstract][Full Text] [Related]
14. Functionally significant, novel GATA4 variants are frequently associated with Tetralogy of Fallot. Dixit R; Narasimhan C; Balekundri VI; Agrawal D; Kumar A; Mohapatra B Hum Mutat; 2018 Dec; 39(12):1957-1972. PubMed ID: 30152191 [TBL] [Abstract][Full Text] [Related]
15. Somatic mutations in NKX2–5, GATA4, and HAND1 are not a common cause of tetralogy of Fallot or hypoplastic left heart. Esposito G; Butler TL; Blue GM; Cole AD; Sholler GF; Kirk EP; Grossfeld P; Perryman BM; Harvey RP; Winlaw DS Am J Med Genet A; 2011 Oct; 155A(10):2416-21. PubMed ID: 22043484 [TBL] [Abstract][Full Text] [Related]
16. GATA4 zinc finger mutations as a molecular rationale for septation defects of the human heart. Reamon-Buettner SM; Borlak J J Med Genet; 2005 May; 42(5):e32. PubMed ID: 15863664 [No Abstract] [Full Text] [Related]
17. Investigation of somatic NKX2-5, GATA4 and HAND1 mutations in patients with tetralogy of Fallot. Wang J; Lu Y; Chen H; Yin M; Yu T; Fu Q Pathology; 2011 Jun; 43(4):322-6. PubMed ID: 21519287 [TBL] [Abstract][Full Text] [Related]
18. Mutations in the 3'-untranslated region of GATA4 as molecular hotspots for congenital heart disease (CHD). Reamon-Buettner SM; Cho SH; Borlak J BMC Med Genet; 2007 Jun; 8():38. PubMed ID: 17592645 [TBL] [Abstract][Full Text] [Related]
19. Genetic analysis of the promoter region of the GATA4 gene in patients with ventricular septal defects. Wu G; Shan J; Pang S; Wei X; Zhang H; Yan B Transl Res; 2012 May; 159(5):376-82. PubMed ID: 22500510 [TBL] [Abstract][Full Text] [Related]