Su D - Search Results

1

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

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

A novel T→G splice site mutation of CRYBA1/A3 associated with autosomal dominant nuclear cataracts in a Chinese family.

Yang Z, Su D, Li Q, Yang F, Ma Z, Zhu S, Ma X. Yang Z, et al. Among authors: su d. Mol Vis. 2012;18:1283-8. Epub 2012 May 15. Mol Vis. 2012. PMID: 22665976 Free PMC article.

4

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

5

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.

6

The DNA methylation profile of PLA2G4C gene promoter in schizophrenia.

Xu H, Wang B, Su D, Yu Q, Li Q, Kou C, Shi J, Yu Y, Ma X. Xu H, et al. Among authors: su d. Psychiatry Res. 2012 Dec 30;200(2-3):1079-81. doi: 10.1016/j.psychres.2012.07.003. Epub 2012 Aug 9. Psychiatry Res. 2012. PMID: 22878031 No abstract available.

7

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.

8

Identification and functional analysis of GJA8 mutation in a Chinese family with autosomal dominant perinuclear cataracts.

Su D, Yang Z, Li Q, Guan L, Zhang H, E D, Zhang L, Zhu S, Ma X. Su D, et al. PLoS One. 2013;8(3):e59926. doi: 10.1371/journal.pone.0059926. Epub 2013 Mar 29. PLoS One. 2013. PMID: 23555834 Free PMC article.

9

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

10

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.

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