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1

Human stem cell models of polyglutamine diseases: Sources for disease models and cell therapy

He, Lang, Chen, Zhao, Peng, Linliu, Tang, Beisha, Jiang, Hong

Journal:

Experimental Neurology

Year:

2021

File:

PDF, 11.53 MB

2021

2

Mutational analysis in early-onset familial Alzheimer's disease in Mainland China

Jiao, Bin, Tang, Beisha, Liu, Xiaoyan, Xu, Jun, Wang, Yanjiang, Zhou, Lin, Zhang, Fufeng, Yan, Xinxiang, Zhou, Yafang, Shen, Lu

Journal:

Neurobiology of Aging

Year:

2014

Language:

english

File:

PDF, 893 KB

english, 2014

3

PMP22 -Related neuropathies and other clinical manifestations in Chinese han patients with charcot-marie-tooth disease type 1

Zhan, Yajing, Zi, Xiaohong, Hu, Zhengmao, Peng, Ying, Wu, Lingqian, Li, Xiaobo, Jiang, Mingming, Liu, Lei, Xie, Yongzhi, Xia, Kun, Tang, Beisha, Zhang, Ruxu

Journal:

Year:

2015

Language:

english

File:

PDF, 1.46 MB

english, 2015

4

Differentiation of Primary Central Nervous System Lymphoma and High-Grade Glioma with Dynamic Susceptibility Contrast-Enhanced Perfusion Magnetic Resonance Imaging

Liao, Weihua, Liu, Yunhai, Wang, Xiaoyi, Jiang, Xinya, Tang, Beisha, Fang, Jiasheng, Chen, Changqing, Hu, Zhongliang

Journal:

Acta Radiologica

Year:

2009

Language:

english

File:

PDF, 587 KB

english, 2009

5

Primary erythromelalgia: a review

Tang, Zhaoli, Chen, Zhao, Tang, Beisha, Jiang, Hong

Journal:

Orphanet Journal of Rare Diseases

Year:

2015

Language:

english

File:

PDF, 990 KB

english, 2015

6

Effect of theCYP2D6andAPOEPolymorphisms on the Efficacy of Donepezil in Patients with Alzheimer’s Disease: A Systematic Review and Meta-Analysis

Tingting Xiao,Bin Jiao,Weiwei Zhang,Beisha Tang,Lu Shen

Journal:

Year:

2016

Language:

english

File:

PDF, 1.27 MB

english, 2016

7

Genotype–phenotype correlation and frequency of distribution in a cohort of Chinese Charcot–Marie–Tooth patients associated with GDAP1 mutations

Pakhrin, Pukar Singh, Xie, Yongzhi, Hu, Zhengmao, Li, Xiaobo, Liu, Lei, Huang, Shunxiang, Wang, Binghao, Yang, Zihan, Zhang, Jiejun, Liu, Xin, Xia, Kun, Tang, Beisha, Zhang, Ruxu

Journal:

Journal of Neurology

Year:

2018

Language:

english

File:

PDF, 1.08 MB

english, 2018

8

Genetic Analysis of LRRK2 R1628P in Parkinson’s Disease in Asian Populations

Zhang, Yuan, Sun, Qiying, Yi, Minhan, Zhou, Xun, Guo, Jifeng, Xu, Qian, Tang, Beisha, Yan, Xinxiang

Journal:

Parkinson's Disease

Year:

2017

Language:

english

File:

PDF, 1.43 MB

english, 2017

9

Contra-Directional Expression of Serum Homocysteine and Uric Acid as Important Biomarkers of Multiple System Atrophy Severity: A Cross-Sectional Study

Chen, Dan, Wei, Xiaobo, Zou, Jing, Wang, Rui, Liu, Xu, Xu, Xiaofeng, Lu, Jianjun, Wang, Zhanhang, Tang, Beisha, Wang, Brian, Jin, Kunlin, Wang, Qing

Journal:

Frontiers in Cellular Neuroscience

Year:

2015

Language:

english

File:

PDF, 2.78 MB

english, 2015

10

Clinical characteristics of PD patients with LRRK2 G2385R and R1628P variants

Liang, Dongxiao, Shu, Li, Pan, Hongxu, Xu, Qian, Guo, Jifeng, Yan, Xinxiang, Tang, Beisha, Sun, Qiying

Journal:

Neuroscience Letters

Year:

2018

Language:

english

File:

PDF, 671 KB

english, 2018

11

MicroRNA-26a/Death-associated protein kinase 1 signaling induces synucleinopathy and dopaminergic neuron degeneration in Parkinson’s disease

Su, Ying, Deng, Man-Fei, Xiong, Wan, Xie, Ao-Ji, Guo, Jifeng, Liang, Zhi-Hou, Hu, Bo, Chen, Jian-Guo, Zhu, Xiongwei, Man, Heng-Ye, Lu, Youming, Liu, Dan, Tang, Beisha, Zhu, Ling-Qiang

Journal:

Biological Psychiatry

Year:

2018

Language:

english

File:

PDF, 4.47 MB

english, 2018

12

Lee Silverman Voice Treatment for dysarthria in patients with Parkinsonâs Disease: a systematic review and a metaâanalysis

Yuan, Feilan, Guo, Xingfang, Wei, Xiaobo, Xie, Fen, Zheng, Jialing, Huang, Yanjun, Huang, Zifeng, Chang, Zihan, Li, Hualing, Guo, Yang, Chen, Jian, Guo, Jifeng, Tang, Beisha, Deng, Bin, Wang, Qing

Journal:

European Journal of Neurology

Year:

2020

File:

PDF, 15.05 MB

2020

13

A novel mutation of KCNQ3 gene in a Chinese family with benign familial neonatal convulsions

Haiyan Li, Nan Li, Lu Shen, Hong Jiang, Qian Yang, Yanmin Song, Jifeng Guo, Kun Xia, Qian Pan, Beisha Tang

Journal:

Epilepsy Research

Year:

2008

Language:

english

File:

PDF, 417 KB

english, 2008

14

Dispensable role ofDrosophilaortholog of LRRK2 kinase activity in survival of dopaminergic neurons

Danling Wang, Beisha Tang, Guohua Zhao, Qian Pan, Kun Xia, Rolf Bodmer, Zhuohua Zhang

Journal:

Molecular Neurodegeneration

Year:

2008

Language:

english

File:

PDF, 1.55 MB

english, 2008

15

Variant in the 3′ region of SNCA associated with Parkinson’s disease and serum α-synuclein levels

Yacen Hu, Beisha Tang, Jifeng Guo, Xintian Wu, Qiying Sun, Changhe Shi, Liang Hu, Chunyu Wang, Lei Wang, Liming Tan, Lu Shen, Xinxiang Yan, Hainan Zhang

Journal:

Journal of Neurology

Year:

2012

Language:

english

File:

PDF, 314 KB

english, 2012

16

Spinocerebellar ataxia type 11 in the Chinese Han population

Qian Xu, Xiaohui Li, Junling Wang, JiPing Yi, Lifang Lei, Lu Shen, Hong Jiang, Kun Xia, Qian Pan, Beisha Tang

Journal:

Neurological Sciences

Year:

2010

Language:

english

File:

PDF, 125 KB

english, 2010

17

Spinocerebellar ataxia type 6: Systematic patho-anatomical study reveals different phylogenetically defined regions of the cerebellum and neural pathways undergo different evolutions of the degenerative process

Xuejing Wang, Hui Wang, Yujun Xia, Hong Jiang, Lu Shen, Shoubiao Wang, Ruowu Shen, Qian Xu, Xuegang Luo, Beisha Tang

Journal:

Year:

2010

Language:

english

File:

PDF, 6.20 MB

english, 2010

18

Hypoxia regulation of ATP13A2 (PARK9) gene transcription

Qian Xu, Hongling Guo, Xiaojie Zhang, Beisha Tang, Fang Cai, Weihui Zhou, Weihong Song

Journal:

Journal of Neurochemistry

Year:

2012

Language:

english

File:

PDF, 396 KB

english, 2012

19

Loss-of-function mutations infilaggringene associate with psoriasis vulgaris in Chinese population

Hu, Zhengmao, Xiong, Zhimin, Xu, Xiaojuan, Li, Fangfang, Lu, Lina, Li, Wei, Su, Juan, Liu, Yalan, Liu, Deyuan, Xie, Zhiguo, Peng, Yu, Kuang, Yehong, Wu, Lisha, Zhang, Jianglin, Pan, Qian, Tang, Beisha

Journal:

Year:

2012

Language:

english

File:

PDF, 630 KB

english, 2012

20

A neuropathological study at autopsy of early onset spinocerebellar ataxia 6

Xuejing Wang, Hui Wang, Yujun Xia, Hong Jiang, Lu Shen, Shoubiao Wang, Ruowu Shen, Liang Huang, Junling Wang, Qian Xu, Xiaohui Li, Xuegang Luo, Beisha Tang

Journal:

Journal of Clinical Neuroscience

Year:

2010

Language:

english

File:

PDF, 486 KB

english, 2010

21

A novel presenilin 1 mutation (Ser169del) in a Chinese family with early-onset Alzheimer's disease

Jifeng Guo, Jiaohua Wei, Shusheng Liao, Lei Wang, Hong Jiang, Beisha Tang

Journal:

Neuroscience Letters

Year:

2010

Language:

english

File:

PDF, 628 KB

english, 2010

22

Spinocerebellar ataxia type 27 (SCA27) is an uncommon cause of dominant ataxia among Chinese Han population

Zhao Chen, Xiaohui Li, Beisha Tang, Junling Wang, Yuting Shi, Zhanfang Sun, Li Zhang, Qian Pan, Kun Xia, Hong Jiang

Journal:

Neuroscience Letters

Year:

2012

Language:

english

File:

PDF, 378 KB

english, 2012

23

Genetic screening for mutations in the Nrdp1 gene in Parkinson disease patients in a Chinese population

Xiaoyun Mo, Deyuan Liu, Wei Li, Zhengmao Hu, Yiqiao Hu, Jingzhi Li, Jifeng Guo, Beisha Tang, Zhuohua Zhang, Yi Bai, Kun Xia

Journal:

Parkinsonism & Related Disorders

Year:

2010

Language:

english

File:

PDF, 114 KB

english, 2010

24

Genetic analysis of Spinocerebellar ataxia type 17 in Parkinson’s disease in mainland China

Qian Xu, Dandan Jia, Junling Wang, Jifeng Guo, Hong Jiang, Lifang Lei, Lu Shen, Qian Pan, Kun Xia, Xinxiang Yan, Beisha Tang

Journal:

Parkinsonism & Related Disorders

Year:

2010

Language:

english

File:

PDF, 216 KB

english, 2010

25

Association between PLA2G6 gene polymorphisms and Parkinson's disease in the Chinese Han population

Zhanyun Lv, Jifeng Guo, Qiying Sun, Kai Li, Rili Yu, Jinyong Tian, Xinxiang Yan, Beisha Tang

Journal:

Parkinsonism & Related Disorders

Year:

2012

Language:

english

File:

PDF, 121 KB

english, 2012

26

Spinocerebellar Ataxia Type 28 (SCA28) is an Uncommon Cause of Dominant Ataxia Among Chinese Kindreds

Jia, Dandan, Tang, Beisha, Chen, Zhao, Shi, Yuting, Sun, Zhanfang, Zhang, Li, Wang, Junling, Xia, Kun, Jiang, Hong

Journal:

International Journal of Neuroscience

Year:

2012

Language:

english

File:

PDF, 126 KB

english, 2012

27

DNA Methylation as a Biomarker for Neuropsychiatric Diseases

Ai, Sanxi, Shen, Lu, Guo, Jifeng, Feng, Xiang, Tang, Beisha

Journal:

International Journal of Neuroscience

Year:

2012

Language:

english

File:

PDF, 335 KB

english, 2012

28

A novel mutation in KCNQ2 gene causes benign familial neonatal convulsions in a Chinese family

Beisha Tang, Haiyan Li, Kun Xia, Hong Jiang, Qian Pan, Lu Shen, Zhigao Long, Guohua Zhao, Fang Cai

Journal:

Journal of the Neurological Sciences

Year:

2004

Language:

english

File:

PDF, 167 KB

english, 2004

29

Spinocerebellar ataxia type 6 in Mainland China: Molecular and clinical features in four families

Hong Jiang, Beisha Tang, Kun Xia, Yongxin Zhou, Bo Xu, Guohua Zhao, Haiyan Li, Lu Shen, Qian Pan, Fang Cai

Journal:

Journal of the Neurological Sciences

Year:

2005

Language:

english

File:

PDF, 108 KB

english, 2005

30

Mutation analysis of the ATM gene in two Chinese patients with ataxia telangiectasia

Hong Jiang, Beisha Tang, Kun Xia, Zhengmao Hu, Lu Shen, Jianguang Tang, Guohua Zhao, Yuhu Zhang, Fang Cai, Qian Pan, Zhigao Long, Guo Wang, Heping Dai

Journal:

Journal of the Neurological Sciences

Year:

2006

Language:

english

File:

PDF, 590 KB

english, 2006

31

Optogenetic Investigation of Neuropsychiatric Diseases

Huang, Fengzhen, Tang, Beisha, Jiang, Hong

Journal:

International Journal of Neuroscience

Year:

2013

Language:

english

File:

PDF, 367 KB

english, 2013

32

Association Study Between Vitamin D Receptor Gene Polymorphisms and Patients With Parkinson Disease in Chinese Han Population

Lv, Zhanyun, Tang, Beisha, Sun, Qiying, Yan, Xinxiang, Guo, Jifeng

Journal:

International Journal of Neuroscience

Year:

2013

Language:

english

File:

PDF, 143 KB

english, 2013

33

MicroRNA profiling in the serums of SCA3/MJD patients

Shi, Yuting, Huang, Fengzhen, Tang, Beisha, Li, Jiada, Wang, Junling, Shen, Lu, Xia, Kun, Jiang, Hong

Journal:

International Journal of Neuroscience

Year:

2014

Language:

english

File:

PDF, 757 KB

english, 2014

34

A diagnostic gene chip for hereditary spastic paraplegias

Luo, Yingying, Du, Juan, Zhan, Zixiong, Chen, Chong, Wang, Junling, Hu, Yiqiao, Hu, Zhengmao, Xia, Kun, Tang, Beisha, Shen, Lu

Journal:

Brain Research Bulletin

Year:

2013

Language:

english

File:

PDF, 1.40 MB

english, 2013

35

The BAG2 protein stabilises PINK1 by decreasing its ubiquitination

Che, Xiangqian, Tang, Beisha, Wang, Xuejing, Chen, Dong, Yan, Xinxiang, Jiang, Hong, Shen, Lu, Xu, Qian, Wang, Guanghui, Guo, Jifeng

Journal:

Biochemical and Biophysical Research Communications

Year:

2013

Language:

english

File:

PDF, 850 KB

english, 2013

36

Editorial Board

Jiao, Bin, Tang, Beisha, Liu, Xiaoyan, Xu, Jun, Wang, Yanjiang, Zhou, Lin, Zhang, Fufeng, Yan, Xinxiang, Zhou, Yafang, Shen, Lu

Journal:

Journal of Dairy Science

Year:

1975

Language:

english

File:

PDF, 95 KB

english, 1975

37

Investigation of TREM2, PLD3, and UNC5C variants in patients with Alzheimer's disease from mainland China

Jiao, Bin, Liu, Xiaoyan, Tang, Beisha, Hou, Lihua, Zhou, Lin, Zhang, Fufeng, Zhou, Yafang, Guo, Jifeng, Yan, Xinxiang, Shen, Lu

Journal:

Neurobiology of Aging

Year:

2014

Language:

english

File:

PDF, 114 KB

english, 2014

38

The APOE ε2 allele may decrease the age at onset in patients with spinocerebellar ataxia type 3 or Machado-Joseph disease from the Chinese Han population

Peng, Huirong, Wang, Chunrong, Chen, Zhao, Sun, Zhanfang, Jiao, Bin, Li, Kai, Huang, Fengzhen, Hou, Xuan, Wang, Junling, Shen, Lu, Xia, Kun, Tang, Beisha, Jiang, Hong

Journal:

Neurobiology of Aging

Year:

2014

Language:

english

File:

PDF, 381 KB

english, 2014

39

A deletion mutation of the VHL gene associated with a patient with sporadic von Hippel-Lindau disease

Jia, Dandan, Tang, Beisha, Shi, Yuting, Wang, Junling, Sun, Zhanfang, Chen, Zhao, Zhang, Li, Xia, Kun, Jiang, Hong

Journal:

Journal of Clinical Neuroscience

Year:

2013

Language:

english

File:

PDF, 1.43 MB

english, 2013

40

Identification of C9orf72 repeat expansions in patients with amyotrophic lateral sclerosis and frontotemporal dementia in mainland China

Jiao, Bin, Tang, Beisha, Liu, Xiaoyan, Yan, Xinxiang, Zhou, Lin, Yang, Yi, Wang, Junling, Xia, Kun, Shen, Lu

Journal:

Neurobiology of Aging

Year:

2014

Language:

english

File:

PDF, 357 KB

english, 2014

41

A Spinocerebellar Ataxia Family with Expanded Alleles in the Tata-Binding Protein Gene and Ataxin-3 Gene

Xu, Qian, Li, Qinghua, Wang, Junling, Jiang, Hong, Shen, Lu, Li, Xiaohui, Tang, Beisha

Journal:

International Journal of Neuroscience

Year:

2010

Language:

english

File:

PDF, 174 KB

english, 2010

42

Mutation and Clinical Characteristics of Autosomal-Dominant Hereditary Spastic Paraplegias in China

Luo, Yingying, Chen, Chong, Zhan, Zixiong, Wang, Yinguang, Du, Juan, Hu, Zhaoting, Liao, Xinxin, Zhao, Guohua, Wang, Junling, Yan, Xinxiang, Jiang, Hong, Pan, Qian, Xia, Kun, Tang, Beisha, Shen, Lu

Journal:

Neurodegenerative Diseases

Year:

2014

Language:

english

File:

PDF, 111 KB

english, 2014

43

C9orf72 hexanucleotide repeat expansion analysis in Chinese spastic paraplegia patients

Luo, Yingying, Jiao, Bin, Wang, Junling, Du, Juan, Yan, Xinxiang, Xia, Kun, Tang, Beisha, Shen, Lu

Journal:

Journal of the Neurological Sciences

Year:

2014

Language:

english

File:

PDF, 233 KB

english, 2014

44

Two novel MPZ mutations in Chinese CMT patients

Liu, Lei, Li, Xiaobo, Zi, Xiaohong, Huang, Shunxiang, Zhan, Yajing, Jiang, Mingming, Guo, Jifeng, Xia, Kun, Tang, Beisha, Zhang, Ruxu

Journal:

Journal of the Peripheral Nervous System

Year:

2013

Language:

english

File:

PDF, 604 KB

english, 2013

45

SNP rs11931074 of the SNCA gene may not be associated with multiple system atrophy in Chinese population

Sun, ZhanFang, Xiang, XiaoShuang, Tang, BeiSha, Chen, Zhao, Peng, HuiRong, Xia, Kun, Jiang, Hong

Journal:

International Journal of Neuroscience

Year:

2015

Language:

english

File:

PDF, 406 KB

english, 2015

46

miR-25 alleviates polyQ-mediated cytotoxicity by silencing ATXN3

Huang, Fengzhen, Zhang, Li, Long, Zhe, Chen, Zhao, Hou, Xuan, Wang, Chunrong, Peng, Huirong, Wang, Junling, Li, Jiada, Duan, Ranhui, Xia, Kun, Chuang, De-Maw, Tang, Beisha, Jiang, Hong

Journal:

Year:

2014

Language:

english

File:

PDF, 2.01 MB

english, 2014

47

Chinese homozygous Machado–Joseph disease (MJD)/SCA3: a case report

Zeng, Sheng, Zeng, Junsheng, He, Miao, Zeng, Xianfeng, Zhou, Yao, Liu, Zhen, Jiang, Hong, Tang, Beisha, Wang, Junling

Journal:

Journal of Human Genetics

Year:

2015

Language:

english

File:

PDF, 684 KB

english, 2015

48

Mutations of P4HA2 encoding prolyl 4-hydroxylase 2 are associated with nonsyndromic high myopia

Guo, Hui, Tong, Ping, Liu, Yanling, Xia, Lu, Wang, Tianyun, Tian, Qi, Li, Ying, Hu, Yiqiao, Zheng, Yu, Jin, Xuemin, Li, Yunping, Xiong, Wei, Tang, Beisha, Feng, Yong, Li, Jiada, Pan, Qian, Hu, Zhengma

Journal:

Genetics in Medicine

Year:

2015

Language:

english

File:

PDF, 4.51 MB

english, 2015

49

Effect of simvastatin onl-DOPA-induced abnormal involuntary movements of hemiparkinsonian rats

Wang, Tan, Cao, Xuebin, Zhang, Tian, Shi, Qingqing, Chen, Zhibin, Tang, Beisha

Journal:

Neurological Sciences

Year:

2015

Language:

english

File:

PDF, 1.43 MB

english, 2015

50

High Serum GFAP Levels in SCA3/MJD May Not Correlate with Disease Progression

Shi, Yuting, Wang, Chunrong, Huang, Fengzhen, Chen, Zhao, Sun, Zhanfang, Wang, Junling, Tang, Beisha, Ashizawa, Tetsuo, Klockgether, Thomas, Jiang, Hong

Journal:

Year:

2015

Language:

english

File:

PDF, 220 KB

english, 2015