Gu XJ - Search Results

1

The mutation spectrum of Parkinson-disease-related genes in early-onset Parkinson's disease in ethnic Chinese.

Chen YP, Yu SH, Zhang GH, Hou YB, Gu XJ, Ou RW, Shen Y, Song W, Chen XP, Zhao B, Cao B, Zhang LY, Sun MM, Liu FF, Wei QQ, Liu KC, Lin JY, Yang TM, Yang J, Wu Y, Jiang Z, Liu J, Cheng YF, Xiao Y, Su WM, Feng F, Cai YY, Li SR, Hu T, Yuan XQ, Zhou QQ, Shao N, Ma S, Shang HF. Chen YP, et al. Among authors: gu xj. Eur J Neurol. 2022 Nov;29(11):3218-3228. doi: 10.1111/ene.15509. Epub 2022 Aug 4. Eur J Neurol. 2022. PMID: 35861376

2

TMEM230 Mutations Are Rare in Han Chinese Patients with Autosomal Dominant Parkinson's Disease.

Wei Q, Ou R, Zhou Q, Chen Y, Cao B, Gu X, Zhao B, Wu Y, Song W, Shang HF. Wei Q, et al. Mol Neurobiol. 2018 Apr;55(4):2851-2855. doi: 10.1007/s12035-017-0542-2. Epub 2017 Apr 28. Mol Neurobiol. 2018. PMID: 28455698

3

An association study between SCFD1 rs10139154 variant and amyotrophic lateral sclerosis in a Chinese cohort.

Chen Y, Zhou Q, Gu X, Wei Q, Cao B, Liu H, Hou Y, Shang H. Chen Y, et al. Amyotroph Lateral Scler Frontotemporal Degener. 2018 Aug;19(5-6):413-418. doi: 10.1080/21678421.2017.1418006. Epub 2017 Dec 20. Amyotroph Lateral Scler Frontotemporal Degener. 2018. PMID: 29260601

4

Analysis of GWAS-linked variants in multiple system atrophy.

Gu X, Chen Y, Zhou Q, Lu YC, Cao B, Zhang L, Kuo MC, Wu YR, Wu RM, Tan EK, Shang HF; Asian Multiple System Atrophy Consortium (AMSAC). Gu X, et al. Neurobiol Aging. 2018 Jul;67:201.e1-201.e4. doi: 10.1016/j.neurobiolaging.2018.03.018. Epub 2018 Mar 23. Neurobiol Aging. 2018. PMID: 29661569

5

No association between 5 new GWAS-linked loci in Parkinson's disease and multiple system atrophy in a Chinese population.

Chen Y, Cao B, Gu X, Ou R, Wei Q, Liu H, Zhang L, Yuan X, Song W, Zhao B, Wu Y, Yuan L, Cheng J, Shang H. Chen Y, et al. Neurobiol Aging. 2018 Jul;67:202.e7-202.e8. doi: 10.1016/j.neurobiolaging.2018.03.027. Epub 2018 Apr 3. Neurobiol Aging. 2018. PMID: 29691093

6

Mutation screening of the TIA1 gene in Chinese patients with amyotrophic lateral sclerosis/frontotemporal dementia.

Gu X, Chen Y, Wei Q, Cao B, Ou R, Yuan X, Hou Y, Zhang L, Liu H, Chen X, Shang HF. Gu X, et al. Neurobiol Aging. 2018 Aug;68:161.e1-161.e3. doi: 10.1016/j.neurobiolaging.2018.04.010. Epub 2018 Apr 24. Neurobiol Aging. 2018. PMID: 29773329

7

Mutation screening of the KIF5A gene in Chinese patients with amyotrophic lateral sclerosis.

Gu X, Li C, Chen Y, Wei Q, Cao B, Ou R, Yuan X, Hou Y, Zhang L, Liu H, Wu Y, Song W, Zhao B, Chen X, Shang HF. Gu X, et al. J Neurol Neurosurg Psychiatry. 2019 Feb;90(2):245-246. doi: 10.1136/jnnp-2018-318395. Epub 2018 Jun 28. J Neurol Neurosurg Psychiatry. 2019. PMID: 29954873 No abstract available.

8

[Identification of compound heterozygous mutations of SACS gene in two patients from a pedigree with spastic ataxia of Charlevoix-Saguenay].

Li S, Chen Y, Yuan X, Wei Q, Ou R, Gu X, Shang H. Li S, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Aug 10;35(4):507-510. doi: 10.3760/cma.j.issn.1003-9406.2018.04.010. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 30098244 Chinese.

9

[Roles of exosomes in Parkinson's disease and amyotrophic lateral sclerosis].

Gu X, Chen Y, Shang H. Gu X, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Oct 10;35(5):757-761. doi: 10.3760/cma.j.issn.1003-9406.2018.05.032. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 30298513 Review. Chinese.

10

Decreased Glycogenolysis by miR-338-3p Promotes Regional Glycogen Accumulation Within the Spinal Cord of Amyotrophic Lateral Sclerosis Mice.

Li C, Wei Q, Gu X, Chen Y, Chen X, Cao B, Ou R, Shang H. Li C, et al. Front Mol Neurosci. 2019 May 7;12:114. doi: 10.3389/fnmol.2019.00114. eCollection 2019. Front Mol Neurosci. 2019. PMID: 31133799 Free PMC article.

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