Tan Z - Search Results

1

Chemical characterization of Auricularia auricula polysaccharides and its pharmacological effect on heart antioxidant enzyme activities and left ventricular function in aged mice.

Wu Q, Tan Z, Liu H, Gao L, Wu S, Luo J, Zhang W, Zhao T, Yu J, Xu X. Wu Q, et al. Among authors: tan z. Int J Biol Macromol. 2010 Apr 1;46(3):284-8. doi: 10.1016/j.ijbiomac.2010.01.016. Epub 2010 Jan 25. Int J Biol Macromol. 2010. PMID: 20105437

2

Mutations of the TGFBR2 gene in Chinese patients with Marfan-related syndrome.

Chen J, Li B, Yang Y, Hu J, Zhao T, Gong Y, Tan Z. Chen J, et al. Among authors: tan z. Clin Invest Med. 2010 Feb 1;33(1):E14-21. doi: 10.25011/cim.v33i1.11833. Clin Invest Med. 2010. PMID: 20144264

3

Microduplication of 3p25.2 encompassing RAF1 associated with congenital heart disease suggestive of Noonan syndrome.

Luo C, Yang YF, Yin BL, Chen JL, Huang C, Zhang WZ, Wang J, Zhang H, Yang JF, Tan ZP. Luo C, et al. Am J Med Genet A. 2012 Aug;158A(8):1918-23. doi: 10.1002/ajmg.a.35471. Epub 2012 Jul 11. Am J Med Genet A. 2012. PMID: 22786616

4

Duplication of 8q12 encompassing CHD7 is associated with a distinct phenotype but without duane anomaly.

Luo H, Xie L, Wang SZ, Chen JL, Huang C, Wang J, Yang JF, Zhang WZ, Yang YF, Tan ZP. Luo H, et al. Eur J Med Genet. 2012 Nov;55(11):646-9. doi: 10.1016/j.ejmg.2012.07.006. Epub 2012 Jul 31. Eur J Med Genet. 2012. PMID: 22902603

5

A 1.1Mb deletion in distal 13q deletion syndrome region with congenital heart defect and postaxial polydactyly: additional support for a CHD locus at distal 13q34 region.

Yang YF, Ai Q, Huang C, Chen JL, Wang J, Xie L, Zhang WZ, Yang JF, Tan ZP. Yang YF, et al. Gene. 2013 Oct 1;528(1):51-4. doi: 10.1016/j.gene.2013.03.145. Epub 2013 Apr 29. Gene. 2013. PMID: 23639964

6

Rare copy number variations containing genes involved in RASopathies: deletion of SHOC2 and duplication of PTPN11.

Chen JL, Zhu X, Zhao TL, Wang J, Yang YF, Tan ZP. Chen JL, et al. Mol Cytogenet. 2014 Apr 16;7:28. doi: 10.1186/1755-8166-7-28. eCollection 2014. Mol Cytogenet. 2014. PMID: 24739123 Free PMC article.

7

Rare de novo copy number variants in patients with congenital pulmonary atresia.

Xie L, Chen JL, Zhang WZ, Wang SZ, Zhao TL, Huang C, Wang J, Yang JF, Yang YF, Tan ZP. Xie L, et al. PLoS One. 2014 May 14;9(5):e96471. doi: 10.1371/journal.pone.0096471. eCollection 2014. PLoS One. 2014. PMID: 24826987 Free PMC article.

8

Whole-exome sequencing identifies Y1495X of SCN5A to be associated with familial conduction disease and sudden death.

Tan ZP, Xie L, Deng Y, Chen JL, Zhang WZ, Wang J, Yang JF, Yang YF. Tan ZP, et al. Sci Rep. 2014 Jul 10;4:5616. doi: 10.1038/srep05616. Sci Rep. 2014. PMID: 25010007 Free PMC article.

9

1q21.1 microduplication in a patient with mental impairment and congenital heart defect.

Sun G, Tan Z, Fan L, Wang J, Yang Y, Zhang W. Sun G, et al. Among authors: tan z. Mol Med Rep. 2015 Oct;12(4):5655-8. doi: 10.3892/mmr.2015.4166. Epub 2015 Jul 31. Mol Med Rep. 2015. PMID: 26238956 Free PMC article.

10

Duplication of 10q22.3-q23.3 encompassing BMPR1A and NGR3 associated with congenital heart disease, microcephaly, and mild intellectual disability.

Tang M, Yang YF, Xie L, Chen JL, Zhang WZ, Wang J, Zhao TL, Yang JF, Tan ZP. Tang M, et al. Am J Med Genet A. 2015 Dec;167A(12):3174-9. doi: 10.1002/ajmg.a.37347. Epub 2015 Sep 3. Am J Med Genet A. 2015. PMID: 26383923

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