Huang GY - Search Results

1

[Advanced molecular technologies for the diagnosis of congenital malformation in neonates].

Yang L, Wang HJ, Huang GY, Zhou WH. Yang L, et al. Among authors: huang gy. Zhongguo Dang Dai Er Ke Za Zhi. 2013 Nov;15(11):960-4. Zhongguo Dang Dai Er Ke Za Zhi. 2013. PMID: 24229588 Free article. Review. Chinese.

2

[Effects of hypothermia on cardiac function in neonates with asphyxia].

Zhou WH, Shao XM, Zhang XD, Chen C, Huang GY. Zhou WH, et al. Among authors: huang gy. Zhonghua Er Ke Za Zhi. 2003 Jun;41(6):460-2. Zhonghua Er Ke Za Zhi. 2003. PMID: 14749008 Clinical Trial. Chinese.

3

DNA sequencing of TGFβ2 in sporadic patients with tetralogy of Fallot.

Gao Y, Ma XJ, Huang GY, Zhang J, Wang HJ, Ma D, Wu Y. Gao Y, et al. Among authors: huang gy. Exp Ther Med. 2012 May;3(5):878-880. doi: 10.3892/etm.2012.492. Epub 2012 Feb 21. Exp Ther Med. 2012. PMID: 22969986 Free PMC article.

4

Roles of miR-1-1 and miR-181c in ventricular septal defects.

Li J, Cao Y, Ma XJ, Wang HJ, Zhang J, Luo X, Chen W, Wu Y, Meng Y, Zhang J, Yuan Y, Ma D, Huang GY. Li J, et al. Among authors: huang gy. Int J Cardiol. 2013 Sep 30;168(2):1441-6. doi: 10.1016/j.ijcard.2012.12.048. Epub 2013 Jan 24. Int J Cardiol. 2013. PMID: 23352489

5

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. Pediatr Cardiol. 2013;34(8):1823-8. doi: 10.1007/s00246-013-0696-2. Epub 2013 May 28. Pediatr Cardiol. 2013. PMID: 23712828

6

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. 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

7

Neonatal pulse oximetry screening improves detecting of critical congenital heart disease.

Ma XJ, Huang GY. Ma XJ, et al. Among authors: huang gy. Chin Med J (Engl). 2013 Jul;126(14):2736-40. Chin Med J (Engl). 2013. PMID: 23876906 Review.

8

Psychiatric illness and intellectual disability in the Prader-Willi syndrome with different molecular defects--a meta analysis.

Yang L, Zhan GD, Ding JJ, Wang HJ, Ma D, Huang GY, Zhou WH. Yang L, et al. Among authors: huang gy. PLoS One. 2013 Aug 14;8(8):e72640. doi: 10.1371/journal.pone.0072640. eCollection 2013. PLoS One. 2013. PMID: 23967326 Free PMC article.

9

[Histone acetylation and expression of acetylation-related enzymes in children with tetralogy of Fallot].

Xu J, Lin YX, Gu RY, Wang HJ, Ma XJ, Ma D, Huang GY. Xu J, et al. Among authors: huang gy. Zhongguo Dang Dai Er Ke Za Zhi. 2013 Oct;15(10):817-21. Zhongguo Dang Dai Er Ke Za Zhi. 2013. PMID: 24131830 Free article. Chinese.

10

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. Zhang J, et al. Among authors: huang gy. Can J Cardiol. 2013 Dec;29(12):1695-703. doi: 10.1016/j.cjca.2013.07.002. Epub 2013 Oct 18. Can J Cardiol. 2013. PMID: 24140236

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