Ma X - Search Results

1

Effectiveness of community-based folate-oriented tertiary interventions on incidence of fetus and birth defects: a protocol for a single-blind cluster randomized controlled trial.

Li M, Zhang Y, Chen X, Wang D, Ji M, Jiang Y, Dou Y, Ma X, Sheng W, Yan W, Huang G. Li M, et al. Among authors: ma x. BMC Pregnancy Childbirth. 2020 Aug 20;20(1):475. doi: 10.1186/s12884-020-03154-w. BMC Pregnancy Childbirth. 2020. PMID: 32819312 Free PMC article.

2

The genotype and expression of the TGFβ2 gene in children with congenital conotruncal defects.

Meng Y, Ma X, Zhang J, Wang H, Ma D, Huang G. Meng Y, et al. Among authors: ma d, ma x. Pediatr Cardiol. 2013;34(8):1823-8. doi: 10.1007/s00246-013-0696-2. Epub 2013 May 28. Pediatr Cardiol. 2013. PMID: 23712828

3

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. Sheng W, et al. Among authors: ma d, ma x. Int J Mol Med. 2013 Sep;32(3):694-702. doi: 10.3892/ijmm.2013.1427. Epub 2013 Jul 2. Int J Mol Med. 2013. PMID: 23820632

4

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. Sheng W, et al. Among authors: ma d, ma x. BMC Med Genomics. 2013 Nov 1;6:46. doi: 10.1186/1755-8794-6-46. BMC Med Genomics. 2013. PMID: 24182332 Free PMC article.

5

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. Sheng W, et al. Among authors: ma d, ma x. J Transl Med. 2014 Jan 31;12:31. doi: 10.1186/1479-5876-12-31. J Transl Med. 2014. PMID: 24479926 Free PMC article.

6

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. Zhang J, et al. Among authors: ma d, ma x. Pediatr Res. 2014 May;75(5):588-94. doi: 10.1038/pr.2014.17. Epub 2014 Feb 10. Pediatr Res. 2014. PMID: 24513686

7

[Sequence analyses of HIRA gene 3'UTR region and related microRNA].

Wang X, Zhang J, Cao Y, Diao L, Wang H, Ma X, Ma D, Huang G. Wang X, et al. Among authors: ma d, ma x. Zhonghua Yi Xue Za Zhi. 2014 Apr 29;94(16):1223-6. Zhonghua Yi Xue Za Zhi. 2014. PMID: 24924885 Chinese.

8

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. Yuan Y, et al. Among authors: ma d, ma x. Birth Defects Res A Clin Mol Teratol. 2014 Dec;100(12):973-84. doi: 10.1002/bdra.23291. Epub 2014 Sep 8. Birth Defects Res A Clin Mol Teratol. 2014. PMID: 25200836

9

The expression profile analysis of NKX2-5 knock-out embryonic mice to explore the pathogenesis of congenital heart disease.

Li J, Cao Y, Wu Y, Chen W, Yuan Y, Ma X, Huang G. Li J, et al. Among authors: ma x. J Cardiol. 2015 Dec;66(6):527-31. doi: 10.1016/j.jjcc.2014.12.022. Epub 2015 Mar 24. J Cardiol. 2015. PMID: 25818641 Free article.

10

Pedigree-based Analysis of Inherited and Noninherited Risk Factors of Congenital Heart Defects.

Yuan Y, Chen W, Ma X, Wang H, Yan W, Huang G. Yuan Y, et al. Among authors: ma x. Early Hum Dev. 2015 Dec;91(12):713-8. doi: 10.1016/j.earlhumdev.2015.08.001. Epub 2015 Aug 29. Early Hum Dev. 2015. PMID: 26324253

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