Xie S - Search Results

1

Linkage analysis and whole-exome sequencing exclude extra mutations responsible for the parkinsonian phenotype of spinocerebellar ataxia-2.

Wang C, Xu Y, Feng X, Ma J, Xie S, Zhang Y, Tang BS, Chan P. Wang C, et al. Among authors: xie s. Neurobiol Aging. 2015 Jan;36(1):545.e1-7. doi: 10.1016/j.neurobiolaging.2014.07.039. Epub 2014 Aug 2. Neurobiol Aging. 2015. PMID: 25189117

2

Parkin dosage mutations in patients with early-onset sporadic and familial Parkinson's disease in Chinese: an independent pathogenic role.

Wang C, Ma H, Feng X, Xie S, Chan P. Wang C, et al. Among authors: xie s. Brain Res. 2010 Oct 28;1358:30-8. doi: 10.1016/j.brainres.2010.08.060. Epub 2010 Aug 26. Brain Res. 2010. PMID: 20800584

3

Exonic sequencing revealed no causative mutation in the BST1 gene in patients with Parkinson's disease.

Wang C, Feng X, Xie S, Gu Z, Chan P. Wang C, et al. Among authors: xie s. Neurobiol Aging. 2013 Nov;34(11):2695.e9-2695.e10. doi: 10.1016/j.neurobiolaging.2013.05.024. Epub 2013 Jul 2. Neurobiol Aging. 2013. PMID: 23827523

4

Association of Catechol-O-Methyltransferase and monoamine oxidase B gene polymorphisms with motor complications in parkinson's disease in a Chinese population.

Hao H, Shao M, An J, Chen C, Feng X, Xie S, Gu Z, Chan P; Chinese Parkinson Study Group. Hao H, et al. Among authors: xie s. Parkinsonism Relat Disord. 2014 Oct;20(10):1041-5. doi: 10.1016/j.parkreldis.2014.06.021. Epub 2014 Jul 4. Parkinsonism Relat Disord. 2014. PMID: 25034874 Review.

5

[Polymorphisms of catechol-O-methyltransferase and monoamine oxidase B genes among Chinese patients with Parkinson's disease].

Hao H, Shao M, An J, Chen C, Feng X, Xie S, Gu Z, Chen B. Hao H, et al. Among authors: xie s. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015 Feb;32(1):1-5. doi: 10.3760/cma.j.issn.1003-9406.2015.01.001. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015. PMID: 25636089 Chinese.

6

Identification of TARDBP Gly298Ser as a founder mutation for amyotrophic lateral sclerosis in Southern China.

Xu F, Huang S, Li XY, Lin J, Feng X, Xie S, Wang Z, Li X, Zhu J, Lai H, Xu Y, Huang X, Yao X, Wang C. Xu F, et al. Among authors: xie s. BMC Med Genomics. 2022 Aug 5;15(1):173. doi: 10.1186/s12920-022-01327-4. BMC Med Genomics. 2022. PMID: 35932023 Free PMC article.

7

High-depth whole-genome sequencing identifies structure variants, copy number variants and short tandem repeats associated with Parkinson's disease.

Wang C, Liu H, Li XY, Ma J, Gu Z, Feng X, Xie S, Tang BS, Chen S, Wang W, Wang J, Zhang J, Chan P. Wang C, et al. Among authors: xie s. NPJ Parkinsons Dis. 2024 Jul 23;10(1):134. doi: 10.1038/s41531-024-00722-1. NPJ Parkinsons Dis. 2024. PMID: 39043730 Free PMC article.

8

[Construction of lentiviral vectors encoding GDNF and GDNF expression in human neural stem cells].

Wang S, Ren P, Xie S, Zhu W, Wang Y, Guan Y, Zhang Y. Wang S, et al. Among authors: xie s. Sheng Wu Gong Cheng Xue Bao. 2008 Dec;24(12):2061-7. Sheng Wu Gong Cheng Xue Bao. 2008. PMID: 19306576 Chinese.

9

[Expression profile of clock genes during the process of embryonic stem cells differentiation].

Xie S, Cai YN, Guan YQ, Wu WQ, Xu YL, Zhang Y, Chen B. Xie S, et al. Zhonghua Yi Xue Za Zhi. 2007 Dec 4;87(45):3203-7. Zhonghua Yi Xue Za Zhi. 2007. PMID: 18399115 Chinese.

10

[Comparison of two tracing method of transplanted mouse embryonic stem cell].

Guan YQ, Xie S, Sun JM, Zou CL, Chen L, Zhang Y. Guan YQ, et al. Among authors: xie s. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2010 Aug;32(4):445-8. doi: 10.3881/j.issn.1000-503X.2010.04.019. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2010. PMID: 20868608 Chinese.

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