195 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]