Wang S - Search Results

1

A missense mutation of HOXA13 underlies hand-foot-genital syndrome in a Chinese family.

Cao L, Chen C, Leng Y, Yan L, Wang S, Zhang X, Luo Y. Cao L, et al. Among authors: wang s. J Genet. 2017 Sep;96(4):647-652. doi: 10.1007/s12041-017-0810-y. J Genet. 2017. PMID: 28947713

2

Novel point mutations in GDF5 associated with two distinct limb malformations in Chinese: brachydactyly type C and proximal symphalangism.

Yang W, Cao L, Liu W, Jiang L, Sun M, Zhang D, Wang S, Lo WHY, Luo Y, Zhang X. Yang W, et al. Among authors: wang s. J Hum Genet. 2008;53(4):368-374. doi: 10.1007/s10038-008-0253-7. Epub 2008 Feb 19. J Hum Genet. 2008. PMID: 18283415

3

A novel mutation in the EXT1 gene identified in a Han Chinese kindred with hereditary multiple exostosis.

Wen W, Zhang Y, Wang Y, Cao L, Wang S, Luo Y. Wen W, et al. Among authors: wang y, wang s. Genet Test Mol Biomarkers. 2010 Jun;14(3):371-6. doi: 10.1089/gtmb.2009.0165. Genet Test Mol Biomarkers. 2010. PMID: 20578942

4

Novel vitamin D 1α-hydroxylase gene mutations in a Chinese vitamin-D-dependent rickets type I patient.

Cao L, Liu F, Wang Y, Ma J, Wang S, Wang L, Zhang Y, Chen C, Luo Y, Ma H. Cao L, et al. Among authors: wang l, wang y, wang s. J Genet. 2011 Aug;90(2):339-42. doi: 10.1007/s12041-011-0070-1. J Genet. 2011. PMID: 21869486 No abstract available.

5

[The research of combining high resolution melting with multiplex ligation-dependent probe amplification technology in the mutation scanning for PAH gene].

Ji CY, Sun LL, Cao LH, Hu Y, Huang H, Wang SS, Luo Y. Ji CY, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Dec;28(6):649-53. doi: 10.3760/cma.j.issn.1003-9406.2011.06.011. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011. PMID: 22161097 Chinese.

6

Novel and recurrent mutations in the EXT1 and EXT2 genes in Chinese kindreds with multiple osteochondromas.

Wu Y, Xing X, Xu S, Ma H, Cao L, Wang S, Luo Y. Wu Y, et al. Among authors: wang s. J Orthop Res. 2013 Sep;31(9):1492-9. doi: 10.1002/jor.22378. Epub 2013 Apr 29. J Orthop Res. 2013. PMID: 23629877 Free article.

7

Overexpression of DOC-1R inhibits cell cycle G1/S transition by repressing CDK2 expression and activation.

Liu Q, Liu X, Gao J, Shi X, Hu X, Wang S, Luo Y. Liu Q, et al. Among authors: wang s. Int J Biol Sci. 2013 Jun 9;9(6):541-9. doi: 10.7150/ijbs.5763. Print 2013. Int J Biol Sci. 2013. PMID: 23781148 Free PMC article.

8

Cyclin G2 suppresses estrogen-mediated osteogenesis through inhibition of Wnt/β-catenin signaling.

Gao J, Liu Q, Liu X, Ji C, Qu S, Wang S, Luo Y. Gao J, et al. Among authors: wang s. PLoS One. 2014 Mar 3;9(3):e89884. doi: 10.1371/journal.pone.0089884. eCollection 2014. PLoS One. 2014. PMID: 24595300 Free PMC article.

9

Screening of Duchenne muscular dystrophy (DMD) mutations and investigating its mutational mechanism in Chinese patients.

Chen C, Ma H, Zhang F, Chen L, Xing X, Wang S, Zhang X, Luo Y. Chen C, et al. Among authors: wang s. PLoS One. 2014 Sep 22;9(9):e108038. doi: 10.1371/journal.pone.0108038. eCollection 2014. PLoS One. 2014. PMID: 25244321 Free PMC article.

10

Molecular Genetic Characterization of a Chinese Family with Severe Split Hand/Foot Malformation.

Cao L, Yang W, Wang S, Chen C, Zhang X, Luo Y. Cao L, et al. Among authors: wang s. Genet Test Mol Biomarkers. 2017 Jun;21(6):357-362. doi: 10.1089/gtmb.2016.0415. Epub 2017 Apr 19. Genet Test Mol Biomarkers. 2017. PMID: 28422522

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