Liu M - 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: liu x, liu m, liu f. 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: liu m, liu p. 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 mutation in GDF5 causes autosomal dominant symphalangism in two Chinese families.

Wang X, Xiao F, Yang Q, Liang B, Tang Z, Jiang L, Zhu Q, Chang W, Jiang J, Jiang C, Ren X, Liu JY, Wang QK, Liu M. Wang X, et al. Among authors: liu m, liu jy. Am J Med Genet A. 2006 Sep 1;140A(17):1846-53. doi: 10.1002/ajmg.a.31372. Am J Med Genet A. 2006. PMID: 16892395

5

Mutation p.Arg954Trp of KIF21A causes congenital fibrosis of the extraocular muscles in a Chinese family.

Zhang XQ, Peng JH, Tang ZH, Xu CQ, Zhou X, Gong SX, Liu JY, Wang Q, Liu MG. Zhang XQ, et al. Yi Chuan Xue Bao. 2006 Aug;33(8):685-91. doi: 10.1016/S0379-4172(06)60100-5. Yi Chuan Xue Bao. 2006. PMID: 16939002

6

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: liu j, liu m, liu p. Mol Vis. 2007 Aug 30;13:1548-54. Mol Vis. 2007. PMID: 17893654

7

Identification and functional characterization of a novel splicing mutation in RP gene PRPF31.

Liu JY, Dai X, Sheng J, Cui X, Wang X, Jiang X, Tu X, Tang Z, Bai Y, Liu M, Wang QK. Liu JY, et al. Among authors: liu m. Biochem Biophys Res Commun. 2008 Mar 7;367(2):420-6. doi: 10.1016/j.bbrc.2007.12.156. Epub 2008 Jan 3. Biochem Biophys Res Commun. 2008. PMID: 18177735 Free PMC article.

8

[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. Among authors: liu j, liu m. 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.

9

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: liu j, liu m. Mol Vis. 2010 Mar 17;16:454-61. doi: 10.1167/3.9.454. Mol Vis. 2010. PMID: 20309401 Free PMC article.

10

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: liu m. BMC Med Genet. 2010 Aug 10;11:121. doi: 10.1186/1471-2350-11-121. BMC Med Genet. 2010. PMID: 20696082 Free PMC article.

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