Liu M - Search Results

1

Rod genesis driven by mafba in an nrl knockout zebrafish model with altered photoreceptor composition and progressive retinal degeneration.

Liu F, Qin Y, Huang Y, Gao P, Li J, Yu S, Jia D, Chen X, Lv Y, Tu J, Sun K, Han Y, Reilly J, Shu X, Lu Q, Tang Z, Xu C, Luo D, Liu M. Liu F, et al. Among authors: liu m. PLoS Genet. 2022 Mar 4;18(3):e1009841. doi: 10.1371/journal.pgen.1009841. eCollection 2022 Mar. PLoS Genet. 2022. PMID: 35245286 Free PMC 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

A novel heterozygous mutation in the Indian hedgehog gene (IHH) is associated with brachydactyly type A1 in a Chinese family.

Liu M, Wang X, Cai Z, Tang Z, Cao K, Liang B, Ren X, Liu JY, Wang QK. Liu M, et al. Among authors: liu jy. J Hum Genet. 2006;51(8):727-731. doi: 10.1007/s10038-006-0012-6. Epub 2006 Jul 27. J Hum Genet. 2006. PMID: 16871364

4

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

5

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

6

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

7

A novel DSPP mutation is associated with type II dentinogenesis imperfecta in a Chinese family.

Zhang X, Chen L, Liu J, Zhao Z, Qu E, Wang X, Chang W, Xu C, Wang QK, Liu M. Zhang X, et al. Among authors: liu j, liu m. BMC Med Genet. 2007 Aug 8;8:52. doi: 10.1186/1471-2350-8-52. BMC Med Genet. 2007. PMID: 17686168 Free PMC article.

8

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

9

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.

10

[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.

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