Zhou YF - Search Results

1

SUMO-1 modification on K166 of polyQ-expanded ataxin-3 strengthens its stability and increases its cytotoxicity.

Zhou YF, Liao SS, Luo YY, Tang JG, Wang JL, Lei LF, Chi JW, Du J, Jiang H, Xia K, Tang BS, Shen L. Zhou YF, et al. PLoS One. 2013;8(1):e54214. doi: 10.1371/journal.pone.0054214. Epub 2013 Jan 31. PLoS One. 2013. PMID: 23382880 Free PMC article.

2

[The advances in research on phosphorylation of polyglutamine disease].

Zhou YF, Jiang H, Tang JG, Tang BS. Zhou YF, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008 Aug;25(4):414-7. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008. PMID: 18683139 Review. Chinese.

3

Novel mutations of the SPG11 gene in hereditary spastic paraplegia with thin corpus callosum.

Liao SS, Shen L, Du J, Zhao GH, Wang XY, Yang Y, Xiao ZQ, Yuan Y, Jiang H, Li N, Sun HD, Wang JL, Wang CY, Zhou YF, Mo XY, Xia K, Tang BS. Liao SS, et al. Among authors: zhou yf. J Neurol Sci. 2008 Dec 15;275(1-2):92-9. doi: 10.1016/j.jns.2008.07.038. Epub 2008 Oct 2. J Neurol Sci. 2008. PMID: 18835492

4

[Study on the single-nucleotide substitution (c.-16C to T) of the PURATROPHIN-1 gene in Chinese patients with spinocerebellar ataxia].

Zhou Y, Song X, Yi J, Jiang H, Wang J, Liao S, Tang B. Zhou Y, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008 Dec;25(6):646-8. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008. PMID: 19065522 Chinese.

5

Lack of variation of ATTCT pentanucleotide repeats at ATXN10 gene between clinically diagnosed ataxia patients and normal individuals originated from Chinese Han.

Wang JL, Jiang H, Zhang S, Xu Q, Zhou YF, Liao SS, Shen L, Yan XX, Zhu HX, Pan Q, Xia K, Tang BS. Wang JL, et al. Among authors: zhou yf. J Genet. 2008 Dec;87(3):283-6. doi: 10.1007/s12041-008-0045-z. J Genet. 2008. PMID: 19147916 No abstract available.

6

[Studies on the CAG repeat expansion in patients with hereditary spinocerebellar ataxia from Chinese Han].

Wang J, Xu Q, Lei L, Shen L, Jiang H, Li X, Zhou Y, Yi J, Zhou J, Yan X, Pan Q, Xia K, Tang B. Wang J, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Dec;26(6):620-5. doi: 10.3760/cma.j.issn.1003-9406.2009.06.004. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009. PMID: 19953482 Chinese.

7

[Polynucleotide repeat expansion of nine spinocerebellar ataxia subtypes and dentatorubral-pallidoluysian atrophy in healthy Chinese Han population].

Wang JL, Wu YQ, Lei LF, Shen L, Jiang H, Zhou YF, Yi JP, Zhou J, Yan XX, Pan Q, Xia K, Tang BS. Wang JL, et al. Among authors: zhou j, zhou yf. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010 Oct;27(5):501-5. doi: 10.3760/cma.j.issn.1003-9406.2010.05.006. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010. PMID: 20931525 Chinese.

8

TGM6 identified as a novel causative gene of spinocerebellar ataxias using exome sequencing.

Wang JL, Yang X, Xia K, Hu ZM, Weng L, Jin X, Jiang H, Zhang P, Shen L, Guo JF, Li N, Li YR, Lei LF, Zhou J, Du J, Zhou YF, Pan Q, Wang J, Wang J, Li RQ, Tang BS. Wang JL, et al. Among authors: zhou j, zhou yf. Brain. 2010 Dec;133(Pt 12):3510-8. doi: 10.1093/brain/awq323. Epub 2010 Nov 23. Brain. 2010. PMID: 21106500

9

[Roles of axonal transport affected by K141N mutant HSP22 in the pathogenesis of CMT2L].

Zhang FF, Lu XQ, Zhou YF, Shen L, Jiang H, Yan XX, Tang BS. Zhang FF, et al. Among authors: zhou yf. Zhonghua Yi Xue Za Zhi. 2012 Feb 21;92(7):496-8. doi: 10.3760/cma.j.issn.00376-2491-2012.07.017. Zhonghua Yi Xue Za Zhi. 2012. PMID: 22490975 Chinese.

10

Sodium valproate alleviates neurodegeneration in SCA3/MJD via suppressing apoptosis and rescuing the hypoacetylation levels of histone H3 and H4.

Yi J, Zhang L, Tang B, Han W, Zhou Y, Chen Z, Jia D, Jiang H. Yi J, et al. PLoS One. 2013;8(1):e54792. doi: 10.1371/journal.pone.0054792. Epub 2013 Jan 28. PLoS One. 2013. PMID: 23382971 Free PMC article.

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