Liu M - Search Results

1

A Novel CDH1 Mutation Causing Reduced E-Cadherin Dimerization Is Associated with Nonsyndromic Cleft Lip With or Without Cleft Palate.

Du S, Yang Y, Yi P, Luo J, Liu T, Chen R, Liu CJ, Ma T, Li Y, Wang C, Weng J, Liu M, Zhang L, Yang B, Zeng X, Liu JY. Du S, et al. Among authors: liu m, liu cj, liu t, liu jy. Genet Test Mol Biomarkers. 2019 Nov;23(11):759-765. doi: 10.1089/gtmb.2019.0092. Epub 2019 Oct 22. Genet Test Mol Biomarkers. 2019. PMID: 31638429

2

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

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

Identification of a CRYAB mutation associated with autosomal dominant posterior polar cataract in a Chinese family.

Liu M, Ke T, Wang Z, Yang Q, Chang W, Jiang F, Tang Z, Li H, Ren X, Wang X, Wang T, Li Q, Yang J, Liu J, Wang QK. Liu M, et al. Among authors: liu j. Invest Ophthalmol Vis Sci. 2006 Aug;47(8):3461-6. doi: 10.1167/iovs.05-1438. Invest Ophthalmol Vis Sci. 2006. PMID: 16877416

5

A novel de novo frame-shift mutation of the EDA gene in a Chinese Han family with hypohidrotic ectodermal dysplasia.

Huang C, Yang Q, Ke T, Wang H, Wang X, Shen J, Tu X, Tian J, Liu JY, Wang QK, Liu M. Huang C, et al. Among authors: liu m, liu jy. J Hum Genet. 2006;51(12):1133-1137. doi: 10.1007/s10038-006-0071-8. Epub 2006 Oct 26. J Hum Genet. 2006. PMID: 17066260

6

Identification of a novel GPR143 mutation in a large Chinese family with congenital nystagmus as the most prominent and consistent manifestation.

Liu JY, Ren X, Yang X, Guo T, Yao Q, Li L, Dai X, Zhang M, Wang L, Liu M, Wang QK. Liu JY, et al. Among authors: liu m. J Hum Genet. 2007;52(6):565-570. doi: 10.1007/s10038-007-0152-3. Epub 2007 May 22. J Hum Genet. 2007. PMID: 17516023

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 of a genetic locus for ichthyosis vulgaris on chromosome 10q22.3-q24.2.

Liu P, Yang Q, Wang X, Feng A, Yang T, Yang R, Wang P, Yuang M, Liu M, Liu JY, Wang QK. Liu P, et al. Among authors: liu m, liu jy. J Invest Dermatol. 2008 Jun;128(6):1418-22. doi: 10.1038/sj.jid.5701191. Epub 2007 Dec 13. J Invest Dermatol. 2008. PMID: 18079749 Free article.

10

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.

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