Chen X - Search Results

1

Mutation Screening of TFG in α-Synucleinopathy and Amyotrophic Lateral Sclerosis.

Li C, Lin J, Gu X, Hou Y, Liu K, Jiang Q, Ou R, Wei Q, Chen X, Song W, Zhao B, Wu Y, Chen Y, Shang H. Li C, et al. Among authors: chen x, chen y. Mov Disord. 2022 Aug;37(8):1756-1761. doi: 10.1002/mds.29079. Epub 2022 May 31. Mov Disord. 2022. PMID: 35642252

2

High brain iron level in asymptomatic carriers of heterozygous ceruloplasmin gene mutations.

Chen Q, Chen XP, Zou L, Zhou D, Gong QY, Burgunder JM, Shang HF. Chen Q, et al. Mov Disord. 2008 Apr 30;23(6):916-7. doi: 10.1002/mds.21980. Mov Disord. 2008. PMID: 18311828 No abstract available.

3

Two novel mutations in the SPG11 gene causing hereditary spastic paraplegia associated with thin corpus callosum.

Zhang SS, Chen Q, Chen XP, Wang JG, Burgunder JM, Shang HF, Burgunder JM, Yang Y. Zhang SS, et al. Mov Disord. 2008 Apr 30;23(6):917-9. doi: 10.1002/mds.21942. Mov Disord. 2008. PMID: 18361476 No abstract available.

4

A novel mutation of the epsilon-sarcoglycan gene in a Chinese family with myoclonus-dystonia syndrome.

Chen XP, Zhang YW, Zhang SS, Chen Q, Burgunder JM, Wu SH, Yang Y, Luo ZM, Shang HF. Chen XP, et al. Mov Disord. 2008 Jul 30;23(10):1472-5. doi: 10.1002/mds.22008. Mov Disord. 2008. PMID: 18581468

5

RNA interference-mediated inhibition of wild-type Torsin A expression increases apoptosis caused by oxidative stress in cultured cells.

Chen XP, Hu XH, Wu SH, Zhang YW, Xiao B, Shang HF. Chen XP, et al. Neurochem Res. 2010 Aug;35(8):1214-23. doi: 10.1007/s11064-010-0177-4. Epub 2010 May 9. Neurochem Res. 2010. PMID: 20455020

6

Patterns of spontaneous brain activity in amyotrophic lateral sclerosis: a resting-state FMRI study.

Luo C, Chen Q, Huang R, Chen X, Chen K, Huang X, Tang H, Gong Q, Shang HF. Luo C, et al. Among authors: chen k, chen q, chen x. PLoS One. 2012;7(9):e45470. doi: 10.1371/journal.pone.0045470. Epub 2012 Sep 20. PLoS One. 2012. PMID: 23029031 Free PMC article.

7

S-nitrosylated protein disulfide isomerase contributes to mutant SOD1 aggregates in amyotrophic lateral sclerosis.

Chen X, Zhang X, Li C, Guan T, Shang H, Cui L, Li XM, Kong J. Chen X, et al. J Neurochem. 2013 Jan;124(1):45-58. doi: 10.1111/jnc.12046. Epub 2012 Nov 1. J Neurochem. 2013. PMID: 23043510 Free article.

8

Association of rs1182 polymorphism of the DYT1 gene with primary dystonia in Chinese population.

Chen Y, Chen K, Burgunder JM, Song W, Huang R, Zhao B, Cao B, Chen X, Jiang Y, Shang HF. Chen Y, et al. Among authors: chen k, chen x. J Neurol Sci. 2012 Dec 15;323(1-2):228-31. doi: 10.1016/j.jns.2012.09.025. Epub 2012 Oct 9. J Neurol Sci. 2012. PMID: 23058565

9

VPS35 Asp620Asn and EIF4G1 Arg1205His mutations are rare in Parkinson disease from southwest China.

Chen Y, Chen K, Song W, Chen X, Cao B, Huang R, Zhao B, Guo X, Burgunder J, Li J, Shang HF. Chen Y, et al. Among authors: chen k, chen x. Neurobiol Aging. 2013 Jun;34(6):1709.e7-8. doi: 10.1016/j.neurobiolaging.2012.11.003. Epub 2012 Dec 20. Neurobiol Aging. 2013. PMID: 23261770

10

PFN1 mutations are rare in Han Chinese populations with amyotrophic lateral sclerosis.

Chen Y, Zheng ZZ, Huang R, Chen K, Song W, Zhao B, Chen X, Yang Y, Yuan L, Shang HF. Chen Y, et al. Among authors: chen k, chen x. Neurobiol Aging. 2013 Jul;34(7):1922.e1-5. doi: 10.1016/j.neurobiolaging.2013.01.013. Epub 2013 Feb 19. Neurobiol Aging. 2013. PMID: 23428184

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