Xu Q - Search Results

1

The Association Between Lysosomal Storage Disorder Genes and Parkinson's Disease: A Large Cohort Study in Chinese Mainland Population.

Zhao YW, Pan HX, Liu Z, Wang Y, Zeng Q, Fang ZH, Luo TF, Xu K, Wang Z, Zhou X, He R, Li B, Zhao G, Xu Q, Sun QY, Yan XX, Tan JQ, Li JC, Guo JF, Tang BS. Zhao YW, et al. Among authors: xu k, xu q. Front Aging Neurosci. 2021 Nov 15;13:749109. doi: 10.3389/fnagi.2021.749109. eCollection 2021. Front Aging Neurosci. 2021. PMID: 34867278 Free PMC article.

2

[Studies on the CTA/CTG trinucleotide repeats of ATXN8OS gene in Chinese Hans].

Wang J, Zhang S, Xu Q, Li X, Song X, Jiang H, Shen L, Yan X, Pan Q, Xia K, Tang B. Wang J, et al. Among authors: xu q. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008 Oct;25(5):511-4. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008. PMID: 18841561 Chinese.

3

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: xu q. J Genet. 2008 Dec;87(3):283-6. doi: 10.1007/s12041-008-0045-z. J Genet. 2008. PMID: 19147916 No abstract available.

4

Spinocerebellar ataxia type 11 in the Chinese Han population.

Xu Q, Li X, Wang J, Yi J, Lei L, Shen L, Jiang H, Xia K, Pan Q, Tang B. Xu Q, et al. Neurol Sci. 2010 Feb;31(1):107-9. doi: 10.1007/s10072-009-0129-4. Epub 2009 Sep 19. Neurol Sci. 2010. PMID: 19768375

5

A novel LRRK2 mutation in a mainland Chinese patient with familial Parkinson's disease.

Wang L, Guo JF, Nie LL, Xu Q, Zuo X, Sun QY, Yan XX, Tang BS. Wang L, et al. Among authors: xu q. Neurosci Lett. 2010 Jan 14;468(3):198-201. doi: 10.1016/j.neulet.2009.10.080. Epub 2009 Oct 29. Neurosci Lett. 2010. PMID: 19879329

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. Among authors: xu q. 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

[Detection of the CAG trinucleotide repeats of MJD1 gene by recombinant DNA technology].

Zhang S, Wang JL, Xu Q, Li XH, Lei LF, Jiang H, Shen L, Yan XX, Pan Q, Xia K, Tang BS. Zhang S, et al. Among authors: xu q. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Aug;26(4):406-9. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009. PMID: 20017304 Chinese.

8

Spinocerebellar ataxia type 6: Systematic patho-anatomical study reveals different phylogenetically defined regions of the cerebellum and neural pathways undergo different evolutions of the degenerative process.

Wang X, Wang H, Xia Y, Jiang H, Shen L, Wang S, Shen R, Xu Q, Luo X, Tang B. Wang X, et al. Among authors: xu q. Neuropathology. 2010 Oct;30(5):501-14. doi: 10.1111/j.1440-1789.2009.01094.x. Neuropathology. 2010. PMID: 20113406

9

Novel GIGYF2 gene variants in patients with Parkinson's disease in Chinese population.

Wang L, Guo JF, Zhang WW, Xu Q, Zuo X, Shi CH, Luo LZ, Liu J, Hu L, Hu YC, She L, Jiang H, Yan XX, Xia K, Pan Q, Tang BS. Wang L, et al. Among authors: xu q. Neurosci Lett. 2010 Apr 5;473(2):131-5. doi: 10.1016/j.neulet.2010.02.037. Epub 2010 Feb 21. Neurosci Lett. 2010. PMID: 20178831

10

A spinocerebellar ataxia family with expanded alleles in the TATA-binding protein gene and ataxin-3 gene.

Xu Q, Li Q, Wang J, Jiang H, Shen L, Li X, Tang B. Xu Q, et al. Int J Neurosci. 2010 Feb;120(2):159-61. doi: 10.3109/00207450903389149. Int J Neurosci. 2010. PMID: 20199210

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