Yang XY - Search Results

1

Functional variant in methionine synthase reductase intron-1 significantly increases the risk of congenital heart disease in the Han Chinese population.

Zhao JY, Yang XY, Gong XH, Gu ZY, Duan WY, Wang J, Ye ZZ, Shen HB, Shi KH, Hou J, Huang GY, Jin L, Qiao B, Wang HY. Zhao JY, et al. Among authors: yang xy. Circulation. 2012 Jan 24;125(3):482-90. doi: 10.1161/CIRCULATIONAHA.111.050245. Epub 2011 Dec 16. Circulation. 2012. PMID: 22179537

2

Genetic polymorphisms of the TYMS gene are not associated with congenital cardiac septal defects in a Han Chinese population.

Zhao JY, Sun JW, Gu ZY, Wang J, Wang EL, Yang XY, Qiao B, Duan WY, Huang GY, Wang HY. Zhao JY, et al. Among authors: yang xy. PLoS One. 2012;7(2):e31644. doi: 10.1371/journal.pone.0031644. Epub 2012 Feb 23. PLoS One. 2012. PMID: 22384047 Free PMC article.

3

Identification of novel rare mutations of DACT1 in human neural tube defects.

Shi Y, Ding Y, Lei YP, Yang XY, Xie GM, Wen J, Cai CQ, Li H, Chen Y, Zhang T, Wu BL, Jin L, Chen YG, Wang HY. Shi Y, et al. Among authors: yang xy. Hum Mutat. 2012 Oct;33(10):1450-5. doi: 10.1002/humu.22121. Epub 2012 Jun 19. Hum Mutat. 2012. PMID: 22610794

4

A functional variant in the cystathionine β-synthase gene promoter significantly reduces congenital heart disease susceptibility in a Han Chinese population.

Zhao JY, Yang XY, Shi KH, Sun SN, Hou J, Ye ZZ, Wang J, Duan WY, Qiao B, Chen YJ, Shen HB, Huang GY, Jin L, Wang HY. Zhao JY, et al. Among authors: yang xy. Cell Res. 2013 Feb;23(2):242-253. doi: 10.1038/cr.2012.135. Epub 2012 Sep 18. Cell Res. 2013. PMID: 22986502 Free PMC article.

5

Mutations in the COPII vesicle component gene SEC24B are associated with human neural tube defects.

Yang XY, Zhou XY, Wang QQ, Li H, Chen Y, Lei YP, Ma XH, Kong P, Shi Y, Jin L, Zhang T, Wang HY. Yang XY, et al. Hum Mutat. 2013 Aug;34(8):1094-101. doi: 10.1002/humu.22338. Epub 2013 May 13. Hum Mutat. 2013. PMID: 23592378

6

miR-10a and miR-10b target the 3'-untranslated region of TBX5 to repress its expression.

Wang F, Yang XY, Zhao JY, Yu LW, Zhang P, Duan WY, Chong M, Gui YH. Wang F, et al. Among authors: yang xy. Pediatr Cardiol. 2014 Aug;35(6):1072-9. doi: 10.1007/s00246-014-0901-y. Epub 2014 Apr 9. Pediatr Cardiol. 2014. PMID: 24714979

7

Mild decrease in TBX20 promoter activity is a potentially protective factor against congenital heart defects in the Han Chinese population.

Yu LW, Wang F, Yang XY, Sun SN, Zheng YF, Li BB, Gui YH, Wang HY. Yu LW, et al. Among authors: yang xy. Sci Rep. 2016 Apr 1;6:23662. doi: 10.1038/srep23662. Sci Rep. 2016. PMID: 27034249 Free PMC article.

8

Genetic analysis of rare coding mutations of CELSR1-3 in congenital heart and neural tube defects in Chinese people.

Qiao X, Liu Y, Li P, Chen Z, Li H, Yang X, Finnell RH, Yang Z, Zhang T, Qiao B, Zheng Y, Wang H. Qiao X, et al. Clin Sci (Lond). 2016 Dec 1;130(24):2329-2340. doi: 10.1042/CS20160686. Epub 2016 Oct 18. Clin Sci (Lond). 2016. PMID: 27756857

9

A TBX5 3'UTR variant increases the risk of congenital heart disease in the Han Chinese population.

Wang F, Liu D, Zhang RR, Yu LW, Zhao JY, Yang XY, Jiang SS, Ma D, Qiao B, Zhang F, Jin L, Gui YH, Wang HY. Wang F, et al. Among authors: yang xy. Cell Discov. 2017 Jul 25;3:17026. doi: 10.1038/celldisc.2017.26. eCollection 2017. Cell Discov. 2017. PMID: 28761722 Free PMC article.

10

Novel Mutation of LRP6 Identified in Chinese Han Population Links Canonical WNT Signaling to Neural Tube Defects.

Shi Z, Yang X, Li BB, Chen S, Yang L, Cheng L, Zhang T, Wang H, Zheng Y. Shi Z, et al. Birth Defects Res. 2018 Jan 15;110(1):63-71. doi: 10.1002/bdr2.1122. Epub 2017 Sep 29. Birth Defects Res. 2018. PMID: 28960852

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