Chen Y - Search Results

1

Spatial enrichment and genomic analyses reveal the link of NOMO1 with amyotrophic lateral sclerosis.

Guo J, You L, Zhou Y, Hu J, Li J, Yang W, Tang X, Sun Y, Gu Y, Dong Y, Chen X, Sato C, Zinman L, Rogaeva E, Wang J, Chen Y, Zhang M. Guo J, et al. Among authors: chen x, chen y. Brain. 2024 Aug 1;147(8):2826-2841. doi: 10.1093/brain/awae123. Brain. 2024. PMID: 38643019

2

Overexpression of lentivirus-mediated glial cell line-derived neurotrophic factor in bone marrow stromal cells and its neuroprotection for the PC12 cells damaged by lactacystin.

Su YR, Wang J, Wu JJ, Chen Y, Jiang YP. Su YR, et al. Among authors: chen y. Neurosci Bull. 2007 Mar;23(2):67-74. doi: 10.1007/s12264-007-0010-5. Neurosci Bull. 2007. PMID: 17592528 Free PMC article.

3

Association between novel TARDBP mutations and Chinese patients with amyotrophic lateral sclerosis.

Xiong HL, Wang JY, Sun YM, Wu JJ, Chen Y, Qiao K, Zheng QJ, Zhao GX, Wu ZY. Xiong HL, et al. Among authors: chen y. BMC Med Genet. 2010 Jan 19;11:8. doi: 10.1186/1471-2350-11-8. BMC Med Genet. 2010. PMID: 20082726 Free PMC article.

4

The synergistic effect between β-amyloid(1-42) and α-synuclein on the synapses dysfunction in hippocampal neurons.

Wang Y, Yu Z, Ren H, Wang J, Wu J, Chen Y, Ding Z. Wang Y, et al. Among authors: chen y. J Chem Neuroanat. 2015 Jan;63:1-5. doi: 10.1016/j.jchemneu.2014.11.001. Epub 2014 Nov 15. J Chem Neuroanat. 2015. Retraction in: J Chem Neuroanat. 2016 Jan;71:50. doi: 10.1016/j.jchemneu.2015.12.015 PMID: 25445382 Retracted.

5

Involvement of mortalin/GRP75/mthsp70 in the mitochondrial impairments induced by A53T mutant α-synuclein.

Liu FT, Chen Y, Yang YJ, Yang L, Yu M, Zhao J, Wu JJ, Huang F, Liu W, Ding ZT, Wang J. Liu FT, et al. Among authors: chen y. Brain Res. 2015 Apr 16;1604:52-61. doi: 10.1016/j.brainres.2015.01.050. Epub 2015 Feb 7. Brain Res. 2015. PMID: 25665531

6

Proteomic analysis of cerebrospinal fluid in amyotrophic lateral sclerosis.

Chen Y, Liu XH, Wu JJ, Ren HM, Wang J, Ding ZT, Jiang YP. Chen Y, et al. Exp Ther Med. 2016 Jun;11(6):2095-2106. doi: 10.3892/etm.2016.3210. Epub 2016 Mar 31. Exp Ther Med. 2016. PMID: 27284291 Free PMC article.

7

A novel mutation of VAPB in one Chinese familial amyotrophic lateral sclerosis pedigree and its clinical characteristics.

Sun YM, Dong Y, Wang J, Lu JH, Chen Y, Wu JJ. Sun YM, et al. Among authors: chen y. J Neurol. 2017 Dec;264(12):2387-2393. doi: 10.1007/s00415-017-8628-3. Epub 2017 Oct 9. J Neurol. 2017. PMID: 28993872

8

Autophagic Modulation by Trehalose Reduces Accumulation of TDP-43 in a Cell Model of Amyotrophic Lateral Sclerosis via TFEB Activation.

Wang Y, Liu FT, Wang YX, Guan RY, Chen C, Li DK, Bu LL, Song J, Yang YJ, Dong Y, Chen Y, Wang J. Wang Y, et al. Among authors: chen c, chen y. Neurotox Res. 2018 Jul;34(1):109-120. doi: 10.1007/s12640-018-9865-7. Epub 2018 Jan 30. Neurotox Res. 2018. PMID: 29383655

9

Association of the TBK1 mutation p.Ile334Thr with frontotemporal dementia and literature review.

Yu H, Yu W, Luo SS, Yang YJ, Liu FT, Zhang Y, Chen Y, Sun YM, Wu JJ. Yu H, et al. Among authors: chen y. Mol Genet Genomic Med. 2019 Mar;7(3):e547. doi: 10.1002/mgg3.547. Epub 2019 Jan 22. Mol Genet Genomic Med. 2019. PMID: 30672142 Free PMC article. Review.

10

Amyotrophic lateral sclerosis due to a SOD1 mutation and X-linked recessive bulbospinal neuronopathy in a single family.

Sun YM, Dong Y, Lu JH, Wu JJ, Chen Y. Sun YM, et al. Among authors: chen y. Acta Neurol Belg. 2019 Dec;119(4):641-643. doi: 10.1007/s13760-019-01124-4. Epub 2019 Mar 16. Acta Neurol Belg. 2019. PMID: 30879265 No abstract available.

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