Wang YL - Search Results

1

TGM6 gene mutations in undiagnosed cerebellar ataxia patients.

Yang ZH, Shi MM, Liu YT, Wang YL, Luo HY, Wang ZL, Shi CH, Xu YM. Yang ZH, et al. Among authors: wang zl, wang yl. Parkinsonism Relat Disord. 2018 Jan;46:84-86. doi: 10.1016/j.parkreldis.2017.07.001. Epub 2017 Jul 4. Parkinsonism Relat Disord. 2018. PMID: 28927799 No abstract available.

2

Establishment of induced pluripotent stem cell line (ZZUi010-A) from an Alzheimer's disease patient carrying an APP gene mutation.

Wang Z, Zhang P, Wang Y, Shi C, Jing N, Sun H, Yang J, Liu Y, Wen X, Zhang J, Zhang S, Xu Y. Wang Z, et al. Stem Cell Res. 2017 Dec;25:213-216. doi: 10.1016/j.scr.2017.10.025. Epub 2017 Nov 3. Stem Cell Res. 2017. PMID: 29156377 Free article.

3

Association of variants in microRNA with Parkinson's disease in Chinese Han population.

Li F, Liu H, Cheng Y, Yang J, Liu Y, Wang Y, Yang Z, Shi C, Xu Y. Li F, et al. Neurol Sci. 2018 Feb;39(2):353-357. doi: 10.1007/s10072-017-3210-4. Epub 2017 Dec 5. Neurol Sci. 2018. PMID: 29209904

4

Analysis of variant rs3794087 in SLC1A2 and Parkinson's disease in a Chinese Han population: A case-control study and meta-analysis.

Cheng Y, Mao CY, Liu YT, Li F, Yang J, Liu H, Zhang C, Wang YL, Wu J, Shi CH, Xu YM. Cheng Y, et al. Among authors: wang yl. Neurosci Lett. 2018 Feb 14;666:165-168. doi: 10.1016/j.neulet.2017.12.045. Epub 2017 Dec 21. Neurosci Lett. 2018. PMID: 29275184

5

Establishment of induced pluripotent stem cell line (ZZUi009-A) from an Alzheimer's disease patient carrying a PSEN1 gene mutation.

Wang Y, Jing N, Su L, Shi C, Zhang P, Wang Z, Sun H, Yang J, Liu Y, Wen X, Zhang J, Zhang S, Xu Y. Wang Y, et al. Stem Cell Res. 2018 Mar;27:30-33. doi: 10.1016/j.scr.2017.12.005. Epub 2017 Dec 12. Stem Cell Res. 2018. PMID: 29304399 Free article.

6

Generation of induced pluripotent stem cell line (ZZUi004-A) from urine sample of a patient with spinocerebellar ataxia type 3.

Wang Y, Shi C, Wang Z, Sun H, Yang Z, Zhang F, Liu Y, Liu H, Jiang C, Zhang S, Xu Y, Wen X. Wang Y, et al. Stem Cell Res. 2018 Apr;28:71-74. doi: 10.1016/j.scr.2018.01.027. Epub 2018 Jan 31. Stem Cell Res. 2018. PMID: 29444500 Free article.

7

DNAJC12 mutation is rare in Chinese Han population with Parkinson's disease.

Fan Y, Yang ZH, Li F, Hu XC, Yue YW, Yang J, Liu YT, Liu H, Wang YL, Shi CH, Xu YM. Fan Y, et al. Among authors: wang yl. Neurobiol Aging. 2018 Aug;68:159.e1-159.e2. doi: 10.1016/j.neurobiolaging.2018.04.012. Epub 2018 May 2. Neurobiol Aging. 2018. PMID: 29801756

8

Novel compound heterozygous GFPT1 mutations in a family with limb-girdle myasthenia with tubular aggregates.

Luo HY, Zhao L, Mao CY, Yang ZH, Yang J, Wang YL, Niu HX, Liu YT, Shi CH, Xu YM. Luo HY, et al. Among authors: wang yl. Neuromuscul Disord. 2019 Jul;29(7):549-553. doi: 10.1016/j.nmd.2019.05.008. Epub 2019 May 28. Neuromuscul Disord. 2019. PMID: 31255525

9

Carboxyl Terminus of Hsp70-Interacting Protein Is Increased in Serum and Cerebrospinal Fluid of Patients With Spinocerebellar Ataxia Type 3.

Hu ZW, Yang ZH, Zhang S, Liu YT, Yang J, Wang YL, Mao CY, Zhang QM, Shi CH, Xu YM. Hu ZW, et al. Among authors: wang yl. Front Neurol. 2019 Oct 15;10:1094. doi: 10.3389/fneur.2019.01094. eCollection 2019. Front Neurol. 2019. PMID: 31749756 Free PMC article.

10

No biallelic intronic AAGGG repeat expansion in RFC1 was found in patients with late-onset ataxia and MSA.

Fan Y, Zhang S, Yang J, Mao CY, Yang ZH, Hu ZW, Wang YL, Liu YT, Liu H, Yuan YP, Shi CH, Xu YM. Fan Y, et al. Among authors: wang yl. Parkinsonism Relat Disord. 2020 Apr;73:1-2. doi: 10.1016/j.parkreldis.2020.02.017. Epub 2020 Feb 26. Parkinsonism Relat Disord. 2020. PMID: 32151945

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