Su D - Search Results

1

No association of pri-miR-143 rs41291957 polymorphism with the risk of congenital heart disease in a Chinese population.

Yang L, Gao X, Luo H, Huang Q, Wei Y, Zhang G, Huang G, Su D, Chen L, Lu C, Yang J, Ma X. Yang L, et al. Among authors: su d. Pediatr Cardiol. 2014 Aug;35(6):1057-61. doi: 10.1007/s00246-014-0898-2. Epub 2014 Apr 22. Pediatr Cardiol. 2014. PMID: 24752771

2

Two novel mutations of the IRX4 gene in patients with congenital heart disease.

Cheng Z, Wang J, Su D, Pan H, Huang G, Li X, Li Z, Shen A, Xie X, Wang B, Ma X. Cheng Z, et al. Among authors: su d. Hum Genet. 2011 Nov;130(5):657-62. doi: 10.1007/s00439-011-0996-7. Epub 2011 May 5. Hum Genet. 2011. PMID: 21544582

3

CITED2 mutation links congenital heart defects to dysregulation of the cardiac gene VEGF and PITX2C expression.

Li Q, Pan H, Guan L, Su D, Ma X. Li Q, et al. Among authors: su d. Biochem Biophys Res Commun. 2012 Jul 13;423(4):895-9. doi: 10.1016/j.bbrc.2012.06.099. Epub 2012 Jun 23. Biochem Biophys Res Commun. 2012. PMID: 22735262

4

A nonsense mutation of CRYGC associated with autosomal dominant congenital nuclear cataracts and microcornea in a Chinese pedigree.

Guo Y, Su D, Li Q, Yang Z, Ma Z, Ma X, Zhu S. Guo Y, et al. Among authors: su d. Mol Vis. 2012;18:1874-80. Epub 2012 Jul 11. Mol Vis. 2012. PMID: 22876111 Free PMC article.

5

A novel mutation in CRYAA is associated with autosomal dominant suture cataracts in a Chinese family.

Su D, Guo Y, Li Q, Guan L, Zhu S, Ma X. Su D, et al. Mol Vis. 2012;18:3057-63. Epub 2012 Dec 26. Mol Vis. 2012. PMID: 23288997 Free PMC article.

6

No association of functional variant in pri-miR-218 and risk of congenital heart disease in a Chinese population.

Gao X, Yang L, Ma Y, Yang J, Zhang G, Huang G, Huang Q, Chen L, Fu F, Chen Y, Su D, Dong Y, Ma X, Lu C, Peng X. Gao X, et al. Among authors: su d. Gene. 2013 Jul 10;523(2):173-7. doi: 10.1016/j.gene.2013.03.119. Epub 2013 Apr 6. Gene. 2013. PMID: 23566829

7

Down-regulation of EBAF in the heart with ventricular septal defects and its regulation by histone acetyltransferase p300 and transcription factors smad2 and cited2.

Su D, Li Q, Guan L, Gao X, Zhang H, Dandan E, Zhang L, Ma X. Su D, et al. Biochim Biophys Acta. 2013 Dec;1832(12):2145-52. doi: 10.1016/j.bbadis.2013.07.013. Epub 2013 Jul 27. Biochim Biophys Acta. 2013. PMID: 23899608 Free article.

8

Cited2 participates in cardiomyocyte apoptosis and maternal diabetes-induced congenital heart abnormality.

Su D, Song JX, Gao Q, Guan L, Li Q, Shi C, Ma X. Su D, et al. Biochem Biophys Res Commun. 2016 Oct 28;479(4):887-892. doi: 10.1016/j.bbrc.2016.09.101. Epub 2016 Sep 25. Biochem Biophys Res Commun. 2016. PMID: 27680315

9

ROCK1/p53/NOXA signaling mediates cardiomyocyte apoptosis in response to high glucose in vitro and vivo.

Su D, Guan L, Gao Q, Li Q, Shi C, Liu Y, Sun L, Lu C, Ma X, Zhao J. Su D, et al. Biochim Biophys Acta Mol Basis Dis. 2017 Apr;1863(4):936-946. doi: 10.1016/j.bbadis.2017.01.021. Epub 2017 Jan 26. Biochim Biophys Acta Mol Basis Dis. 2017. PMID: 28131915 Free article.

10

TCF21 rs12190287 Polymorphisms Are Associated with Ventricular Septal Defects in a Chinese Population.

Yang L, Gao X, Luo H, Huang Q, Su D, Tan X, Lu C. Yang L, et al. Among authors: su d. Genet Test Mol Biomarkers. 2017 May;21(5):312-315. doi: 10.1089/gtmb.2016.0324. Epub 2017 Mar 27. Genet Test Mol Biomarkers. 2017. PMID: 28346832 Free PMC article.

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