Long Z - Search Results

1

Synaptic Loss in Spinocerebellar Ataxia Type 3 Revealed by SV2A Positron Emission Tomography.

Chen Z, Liao G, Wan N, He Z, Chen D, Tang Z, Long Z, Zou G, Peng L, Wan L, Wang C, Peng H, Shi Y, Tang Y, Li J, Li Y, Long T, Hou X, He L, Qiu R, Chen D, Wang J, Guo J, Shen L, Huang Y, Ashizawa T, Klockgether T, Tang B, Zhou M, Hu S, Jiang H. Chen Z, et al. Among authors: long t, long z. Mov Disord. 2023 Jun;38(6):978-989. doi: 10.1002/mds.29395. Epub 2023 Apr 6. Mov Disord. 2023. PMID: 37023261

2

[Localization of the gene for 4 hereditary multiple exostoses families].

Tang Y, Xia JH, Zhou JN, Li HJ, Wang DP, Dai HP, Long ZG, Tang BS, Huang L, Deng HX. Tang Y, et al. Among authors: long zg. Yi Chuan Xue Bao. 1998;25(1):1-7. Yi Chuan Xue Bao. 1998. PMID: 9648398 Chinese.

3

Mutation analysis of the TATA box-binding protein (TBP) gene in Chinese Han patients with spinocerebellar ataxia.

Xu Q, Li XH, Wang JL, Jiang H, Zhang S, Lei LF, Shen L, Xia K, Pan Q, Long ZG, Tang BS. Xu Q, et al. Among authors: long zg. J Clin Neurosci. 2009 Oct;16(10):1374-5. doi: 10.1016/j.jocn.2009.05.004. Epub 2009 Jul 5. J Clin Neurosci. 2009. PMID: 19581089

4

miR-25 alleviates polyQ-mediated cytotoxicity by silencing ATXN3.

Huang F, Zhang L, Long Z, Chen Z, Hou X, Wang C, Peng H, Wang J, Li J, Duan R, Xia K, Chuang DM, Tang B, Jiang H. Huang F, et al. Among authors: long z. FEBS Lett. 2014 Dec 20;588(24):4791-8. doi: 10.1016/j.febslet.2014.11.013. Epub 2014 Nov 20. FEBS Lett. 2014. PMID: 25451224 Free PMC article.

5

Two novel SNPs in ATXN3 3' UTR may decrease age at onset of SCA3/MJD in Chinese patients.

Long Z, Chen Z, Wang C, Huang F, Peng H, Hou X, Ding D, Ye W, Wang J, Pan Q, Li J, Xia K, Tang B, Ashizawa T, Jiang H. Long Z, et al. PLoS One. 2015 Feb 17;10(2):e0117488. doi: 10.1371/journal.pone.0117488. eCollection 2015. PLoS One. 2015. PMID: 25689313 Free PMC article.

6

Investigation of Gene Regulatory Networks Associated with Autism Spectrum Disorder Based on MiRNA Expression in China.

Huang F, Long Z, Chen Z, Li J, Hu Z, Qiu R, Zhuang W, Tang B, Xia K, Jiang H. Huang F, et al. Among authors: long z. PLoS One. 2015 Jun 10;10(6):e0129052. doi: 10.1371/journal.pone.0129052. eCollection 2015. PLoS One. 2015. PMID: 26061495 Free PMC article.

7

Alleviating neurodegeneration in Drosophila models of PolyQ diseases.

Long Z, Tang B, Jiang H. Long Z, et al. Cerebellum Ataxias. 2014 Jul 4;1:9. doi: 10.1186/2053-8871-1-9. eCollection 2014. Cerebellum Ataxias. 2014. PMID: 26331033 Free PMC article. Review.

8

Targeted Next-Generation Sequencing Revealed Novel Mutations in Chinese Ataxia Telangiectasia Patients: A Precision Medicine Perspective.

Chen Z, Ye W, Long Z, Ding D, Peng H, Hou X, Qiu R, Xia K, Tang B, Jiang H. Chen Z, et al. Among authors: long z. PLoS One. 2015 Oct 6;10(10):e0139738. doi: 10.1371/journal.pone.0139738. eCollection 2015. PLoS One. 2015. PMID: 26439923 Free PMC article.

9

miRNA profiling in autism spectrum disorder in China.

Huang F, Zhou T, Yao X, Yi J, Zhou F, Long Z, Hou X, Wang C, Chen Z, Jiang H. Huang F, et al. Among authors: long z. Genom Data. 2015 Aug 12;6:108-9. doi: 10.1016/j.gdata.2015.08.006. eCollection 2015 Dec. Genom Data. 2015. PMID: 26697346 Free PMC article.

10

Identification of a de novo DYNC1H1 mutation via WES according to published guidelines.

Ding D, Chen Z, Li K, Long Z, Ye W, Tang Z, Xia K, Qiu R, Tang B, Jiang H. Ding D, et al. Among authors: long z. Sci Rep. 2016 Feb 5;6:20423. doi: 10.1038/srep20423. Sci Rep. 2016. PMID: 26846447 Free PMC article.

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