Chen SY - Search Results

1

A Novel Missense Mutation in the Spectrin Beta Nonerythrocytic 2 Gene Likely Associated with Spinocerebellar Ataxia Type 5.

Liu LZ, Ren M, Li M, Ren YT, Sun B, Sun XS, Chen SY, Li SY, Huang XS. Liu LZ, et al. Among authors: chen sy. Chin Med J (Engl). 2016 Oct 20;129(20):2516-2517. doi: 10.4103/0366-6999.191834. Chin Med J (Engl). 2016. PMID: 27748352 Free PMC article. No abstract available.

2

A novel 10-base pair insertion mutation in exon 5 of the SOD1 gene in a Chinese family with amyotrophic lateral sclerosis.

Chen S, Li M, Zhu W, Mao F, Wang J, Sun Z, Huang X. Chen S, et al. Neurobiol Aging. 2016 Sep;45:212.e1-212.e4. doi: 10.1016/j.neurobiolaging.2016.04.021. Epub 2016 May 3. Neurobiol Aging. 2016. PMID: 27297615

3

Screening for possible oligogenic pathogenesis in Chinese sporadic ALS patients.

Zhang H, Cai W, Chen S, Liang J, Wang Z, Ren Y, Liu W, Zhang X, Sun Z, Huang X. Zhang H, et al. Amyotroph Lateral Scler Frontotemporal Degener. 2018 Aug;19(5-6):419-425. doi: 10.1080/21678421.2018.1432659. Epub 2018 Feb 7. Amyotroph Lateral Scler Frontotemporal Degener. 2018. PMID: 29411640

4

A novel D90_K91insN mutation in exon 4 of the SOD1 gene caused familial amyotrophic lateral sclerosis in a Chinese pedigree.

Li Y, Sun B, Chen S, Ren Y, Cui F, Yang F, Chen Z, Ling L, Huang X. Li Y, et al. Amyotroph Lateral Scler Frontotemporal Degener. 2018 Nov;19(7-8):516-521. doi: 10.1080/21678421.2018.1457057. Epub 2018 Apr 2. Amyotroph Lateral Scler Frontotemporal Degener. 2018. PMID: 29609497

5

Hereditary and idiopathic spastic paraparesis: preliminary findings of a single center experience.

Cui F, Sun L, Qiao J, Xiong J, Zhao Y, Li J, Li M, Chen S, Huang X. Cui F, et al. Neurol Res. 2018 Dec;40(12):1088-1093. doi: 10.1080/01616412.2018.1522412. Neurol Res. 2018. PMID: 30352018

6

Genetic mutation analysis of hereditary spastic paraplegia: A retrospective study.

Cui F, Sun L, Qiao J, Li J, Li M, Chen S, Sun B, Huang X. Cui F, et al. Medicine (Baltimore). 2020 Jun 5;99(23):e20193. doi: 10.1097/MD.0000000000020193. Medicine (Baltimore). 2020. PMID: 32501971 Free PMC article.

7

TDP-43 and Phosphorylated TDP-43 Levels in Paired Plasma and CSF Samples in Amyotrophic Lateral Sclerosis.

Ren Y, Li S, Chen S, Sun X, Yang F, Wang H, Li M, Cui F, Huang X. Ren Y, et al. Front Neurol. 2021 Jun 14;12:663637. doi: 10.3389/fneur.2021.663637. eCollection 2021. Front Neurol. 2021. PMID: 34194383 Free PMC article.

8

Clinical and molecular characteristics of myotonia congenita in China: Case series and a literature review.

Li Y, Li M, Wang Z, Yang F, Wang H, Bai X, Sun B, Chen S, Huang X. Li Y, et al. Channels (Austin). 2022 Dec;16(1):35-46. doi: 10.1080/19336950.2022.2041292. Channels (Austin). 2022. PMID: 35170402 Free PMC article. Review.

9

Transcriptional Regulation of the Warburg Effect in Cancer by SIX1.

Li L, Liang Y, Kang L, Liu Y, Gao S, Chen S, Li Y, You W, Dong Q, Hong T, Yan Z, Jin S, Wang T, Zhao W, Mai H, Huang J, Han X, Ji Q, Song Q, Yang C, Zhao S, Xu X, Ye Q. Li L, et al. Cancer Cell. 2018 Mar 12;33(3):368-385.e7. doi: 10.1016/j.ccell.2018.01.010. Epub 2018 Feb 15. Cancer Cell. 2018. PMID: 29455928 Free article.

10

Influence of Programmed Death Ligand-1-Gene Polymorphism rs822336 on the Prognosis and Safety of Postoperative Patients with NSCLC Who Received Platinum-Based Adjuvant Chemotherapy.

Zhao M, Zhang J, Chen S, Wang Y, Tian Q. Zhao M, et al. Cancer Manag Res. 2020 Aug 4;12:6755-6766. doi: 10.2147/CMAR.S255072. eCollection 2020. Cancer Manag Res. 2020. PMID: 32801904 Free PMC article.

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