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.
192 related articles for article (PubMed ID: 25200836)
1. Promoter methylation and expression of the VANGL2 gene in the myocardium of pediatric patients with tetralogy of fallot. Yuan Y; Gao Y; Wang H; Ma X; Ma D; Huang G Birth Defects Res A Clin Mol Teratol; 2014 Dec; 100(12):973-84. PubMed ID: 25200836 [TBL] [Abstract][Full Text] [Related]
2. Elevated methylation of the RXRA promoter region may be responsible for its downregulated expression in the myocardium of patients with TOF. Zhang J; Ma X; Wang H; Ma D; Huang G Pediatr Res; 2014 May; 75(5):588-94. PubMed ID: 24513686 [TBL] [Abstract][Full Text] [Related]
3. CpG site hypomethylation at ETS1‑binding region regulates DLK1 expression in Chinese patients with Tetralogy of Fallot. Tian G; He L; Gu R; Sun J; Chen W; Qian Y; Ma X; Yan W; Zhao Z; Xu Z; Suo M; Sheng W; Huang G Mol Med Rep; 2022 Mar; 25(3):. PubMed ID: 35059744 [TBL] [Abstract][Full Text] [Related]
4. Mutation analysis of the Vangl2 coding region revealed no common cause for Tetralogy of Fallot. Erdal E; Erdal C; Bulut G; Kunter I; Kir M; Atabey N; Açikel U J Int Med Res; 2007; 35(6):867-72. PubMed ID: 18034999 [TBL] [Abstract][Full Text] [Related]
5. Association between the promoter methylation of the TBX20 gene and tetralogy of fallot. Yang X; Kong Q; Li Z; Xu M; Cai Z; Zhao C Scand Cardiovasc J; 2018 Oct; 52(5):287-291. PubMed ID: 30084275 [TBL] [Abstract][Full Text] [Related]
6. DNA methylation status of NKX2-5, GATA4 and HAND1 in patients with tetralogy of fallot. Sheng W; Qian Y; Wang H; Ma X; Zhang P; Diao L; An Q; Chen L; Ma D; Huang G BMC Med Genomics; 2013 Nov; 6():46. PubMed ID: 24182332 [TBL] [Abstract][Full Text] [Related]
7. CpG island shore methylation of ZFPM2 is identified in tetralogy of fallot samples. Sheng W; Chen L; Wang H; Ma X; Ma D; Huang G Pediatr Res; 2016 Jul; 80(1):151-8. PubMed ID: 26959486 [TBL] [Abstract][Full Text] [Related]
8. Methylation status of CpG sites in the NOTCH4 promoter region regulates NOTCH4 expression in patients with tetralogy of Fallot. Zhu Y; Ye M; Xu H; Gu R; Ma X; Chen M; Li X; Sheng W; Huang G Mol Med Rep; 2020 Nov; 22(5):4412-4422. PubMed ID: 33000281 [TBL] [Abstract][Full Text] [Related]
9. Mitogen-activated protein kinase signal pathways play an important role in right ventricular hypertrophy of tetralogy of Fallot. Zhang HS; Wu QY; Xu M; Zhou YX; Shui CX Chin Med J (Engl); 2012 Jul; 125(13):2243-9. PubMed ID: 22882842 [TBL] [Abstract][Full Text] [Related]
10. Ju ZR; Wang HJ; Ma XJ; Ma D; Huang GY Chin Med J (Engl); 2016 Oct; 129(20):2403-2408. PubMed ID: 27748330 [TBL] [Abstract][Full Text] [Related]
11. High CpG island methylation of p16 gene and loss of p16 protein expression associate with the development and progression of tetralogy of Fallot. Gao SJ; Zhang GF; Zhang RP J Genet; 2016 Dec; 95(4):831-837. PubMed ID: 27994181 [TBL] [Abstract][Full Text] [Related]
12. DNA methylation at CpG island shore and RXRα regulate NR2F2 in heart tissues of tetralogy of Fallot patients. Xiaodi L; Ming Y; Hongfei X; Yanjie Z; Ruoyi G; Ma X; Wei S; Guoying H Biochem Biophys Res Commun; 2020 Sep; 529(4):1209-1215. PubMed ID: 32819587 [TBL] [Abstract][Full Text] [Related]
13. Association of promoter methylation statuses of congenital heart defect candidate genes with Tetralogy of Fallot. Sheng W; Qian Y; Zhang P; Wu Y; Wang H; Ma X; Chen L; Ma D; Huang G J Transl Med; 2014 Jan; 12():31. PubMed ID: 24479926 [TBL] [Abstract][Full Text] [Related]
14. Association between mRNA levels of DNMT1, DNMT3A, DNMT3B, MBD2 and LINE-1 methylation status in infants with tetralogy of Fallot. Sheng W; Qian Y; Wang H; Ma X; Zhang P; Chen L; Ma D; Huang G Int J Mol Med; 2013 Sep; 32(3):694-702. PubMed ID: 23820632 [TBL] [Abstract][Full Text] [Related]
15. MicroRNA deregulation in right ventricular outflow tract myocardium in nonsyndromic tetralogy of fallot. Zhang J; Chang JJ; Xu F; Ma XJ; Wu Y; Li WC; Wang HJ; Huang GY; Ma D Can J Cardiol; 2013 Dec; 29(12):1695-703. PubMed ID: 24140236 [TBL] [Abstract][Full Text] [Related]
16. Decreased expression of neurotrophic tyrosine receptor kinase 3 is associated with the outflow tract defect of human tetralogy of Fallot. Kong B; Liu YL; Lü XD Chin Med J (Engl); 2009 Jan; 122(2):153-7. PubMed ID: 19187638 [TBL] [Abstract][Full Text] [Related]
17. DNA microarray and quantitative analysis reveal enhanced myocardial VEGF expression with stunted angiogenesis in human tetralogy of Fallot. Peters TH; Sharma V; Yilmaz E; Mooi WJ; Bogers AJ; Sharma HS Cell Biochem Biophys; 2013 Nov; 67(2):305-16. PubMed ID: 23897578 [TBL] [Abstract][Full Text] [Related]
18. Mutational analysis of JAG1 gene in non-syndromic tetralogy of Fallot children. Kola S; Koneti NR; Golla JP; Akka J; Gundimeda SD; Mundluru HP Clin Chim Acta; 2011 Nov; 412(23-24):2232-6. PubMed ID: 21893051 [TBL] [Abstract][Full Text] [Related]
19. DNA methylation status of TBX20 in patients with tetralogy of Fallot. Gong J; Sheng W; Ma D; Huang G; Liu F BMC Med Genomics; 2019 May; 12(1):75. PubMed ID: 31138201 [TBL] [Abstract][Full Text] [Related]
20. Comparative DNA methylation and gene expression analysis identifies novel genes for structural congenital heart diseases. Grunert M; Dorn C; Cui H; Dunkel I; Schulz K; Schoenhals S; Sun W; Berger F; Chen W; Sperling SR Cardiovasc Res; 2016 Oct; 112(1):464-77. PubMed ID: 27496870 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]