Tang Z - Search Results

1

Knockout of Nr2e3 prevents rod photoreceptor differentiation and leads to selective L-/M-cone photoreceptor degeneration in zebrafish.

Xie S, Han S, Qu Z, Liu F, Li J, Yu S, Reilly J, Tu J, Liu X, Lu Z, Hu X, Yimer TA, Qin Y, Huang Y, Lv Y, Jiang T, Shu X, Tang Z, Jia H, Wong F, Liu M. Xie S, et al. Among authors: tang z. Biochim Biophys Acta Mol Basis Dis. 2019 Jun 1;1865(6):1273-1283. doi: 10.1016/j.bbadis.2019.01.022. Epub 2019 Jan 23. Biochim Biophys Acta Mol Basis Dis. 2019. PMID: 30684641 Free article.

2

Two novel missense mutations of GATA4 gene in Chinese patients with sporadic congenital heart defects.

Tang ZH, Xia L, Chang W, Li H, Shen F, Liu JY, Wang Q, Liu MG. Tang ZH, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006 Apr;23(2):134-7. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006. PMID: 16604480

3

Novel HSF4 mutation causes congenital total white cataract in a Chinese family.

Ke T, Wang QK, Ji B, Wang X, Liu P, Zhang X, Tang Z, Ren X, Liu M. Ke T, et al. Among authors: tang z. Am J Ophthalmol. 2006 Aug;142(2):298-303. doi: 10.1016/j.ajo.2006.03.056. Am J Ophthalmol. 2006. PMID: 16876512

4

A novel de novo frameshift mutation of RPGR ORF15 is associated with X-linked retinitis pigmentosa in a Chinese family.

Chang W, Ding Q, Tang Z, Liu P, Jiang F, Ke T, Ren X, Wang Z, Liu J, Wang QK, Liu M. Chang W, et al. Among authors: tang z. Mol Vis. 2007 Aug 30;13:1548-54. Mol Vis. 2007. PMID: 17893654

5

[A novel COL4A5 splicing mutation causing Alport syndrome in a Chinese family].

Tang Z, Dai Y, Wan Z, Zhan T, Tan J, Ren X, Liu J, Wang Q, Liu M. Tang Z, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008 Dec;25(6):649-52. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008. PMID: 19065523 Chinese.

6

Novel USH2A compound heterozygous mutations cause RP/USH2 in a Chinese family.

Liu X, Tang Z, Li C, Yang K, Gan G, Zhang Z, Liu J, Jiang F, Wang Q, Liu M. Liu X, et al. Among authors: tang z. Mol Vis. 2010 Mar 17;16:454-61. doi: 10.1167/3.9.454. Mol Vis. 2010. PMID: 20309401 Free PMC article.

7

Identification of a novel homozygous nonsense mutation in EYS in a Chinese family with autosomal recessive retinitis pigmentosa.

Huang Y, Zhang J, Li C, Yang G, Liu M, Wang QK, Tang Z. Huang Y, et al. Among authors: tang z. BMC Med Genet. 2010 Aug 10;11:121. doi: 10.1186/1471-2350-11-121. BMC Med Genet. 2010. PMID: 20696082 Free PMC article.

8

Mucolipidosis in a Chinese family with compound heterozygous mutations at the GNPTAB gene.

Zhan T, Cui X, Xing X, Ren A, Gan G, Liu Y, Zhang J, Tang Z, Liu M. Zhan T, et al. Among authors: tang z. Clin Chim Acta. 2011 Jul 15;412(15-16):1469-71. doi: 10.1016/j.cca.2011.04.025. Epub 2011 Apr 28. Clin Chim Acta. 2011. PMID: 21549105

9

A novel SCN1A missense mutation causes generalized epilepsy with febrile seizures plus in a Chinese family.

Cui X, Zeng F, Liu Y, Zhang J, Archacki S, Zhan T, Du R, Tang Z, Liu J, Wang QK, Liu M. Cui X, et al. Among authors: tang z. Neurosci Lett. 2011 Sep 26;503(1):27-30. doi: 10.1016/j.neulet.2011.08.001. Epub 2011 Aug 6. Neurosci Lett. 2011. PMID: 21843600

10

Mutation p.Leu354Pro in EDA causes severe hypohidrotic ectodermal dysplasia in a Chinese family.

Liu Y, Yu X, Wang L, Li C, Archacki S, Huang C, Liu JY, Wang Q, Liu M, Tang Z. Liu Y, et al. Among authors: tang z. Gene. 2012 Jan 10;491(2):246-50. doi: 10.1016/j.gene.2011.10.009. Epub 2011 Oct 10. Gene. 2012. PMID: 22008666

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