Parkinson's Disease and Cognitive Impairment

Por Yang, Yang, Tang, Bei-sha, Guo, Ji-feng
Publicado no Parkinsons Dis (2016)

Research advances on neurite outgrowth inhibitor B receptor

Por Zhang, Rui, Tang, Bei‐sha, Guo, Ji‐feng
Publicado no J Cell Mol Med (2020)

The Progress of Induced Pluripotent Stem Cells as Models of Parkinson's Disease

Por Kang, Ji-feng, Tang, Bei-sha, Guo, Ji-feng
Publicado no Stem Cells Int (2016)

PLA2G6-Associated Neurodegeneration (PLAN): Review of Clinical Phenotypes and Genotypes

Por Guo, Yu-pei, Tang, Bei-sha, Guo, Ji-feng
Publicado no Front Neurol (2018)

Microglial Activation in the Pathogenesis of Huntington’s Disease

Por Yang, Hui-Ming, Yang, Su, Huang, Shan-Shan, Tang, Bei-Sha, Guo, Ji-Feng
Publicado no Front Aging Neurosci (2017)

Effect of GBA Mutations on Phenotype of Parkinson's Disease: A Study on Chinese Population and a Meta-Analysis

Por Zhang, Yuan, Sun, Qi-ying, Zhao, Yu-wen, Shu, Li, Guo, Ji-feng, Xu, Qian, Yan, Xin-xiang, Tang, Bei-sha
Publicado no Parkinsons Dis (2015)

Identification of Ser465 as a novel PINK1 autophosphorylation site

Por Guo, Ji-feng, Yao, Ling-yan, Sun, Qi-ying, Cui, Yi-ting, Yang, Yang, Xu, Qian, Yan, Xin-xiang, Tang, Bei-sha
Publicado no Transl Neurodegener (2017)

Novel Compound Heterozygous Mutations in the PANK2 Gene in a Chinese Patient With Atypical Pantothenate Kinase-Associated Neurodegeneration

Por Zhang, Yu-hu, Tang, Bei-sha, Zhao, Ai-ling, Xia, Kun, Long, Zhi-gao, Guo, Ji-feng, Westaway, Shawn K., Hayflick, Susan J.
Publicado em 2005

Altered Functional Brain Connectomes between Sporadic and Familial Parkinson's Patients

Por Tang, Yan, Xiao, Xue, Xie, Hua, Wan, Chang-min, Meng, Li, Liu, Zhen-hua, Liao, Wei-hua, Tang, Bei-sha, Guo, Ji-feng
Publicado no Front Neuroanat (2017)

Genetic Identification Is Critical for the Diagnosis of Parkinsonism: A Chinese Pedigree with Early Onset of Parkinsonism

Por Yang, Yang, Tang, Bei-sha, Weng, Ling, Li, Nan, Shen, Lu, Wang, Jian, Zuo, Chuan-tao, Yan, Xin-xiang, Xia, Kun, Guo, Ji-feng
Publicado no PLoS One (2015)

Association study between SMPD1 p.L302P and sporadic Parkinson’s disease in ethnic Chinese population

Por Li, Kai, Tang, Bei-Sha, Yang, Nan-Nan, Kang, Ji-Feng, Liu, Zhen-Hua, Liu, Rui-Qi, Yan, Xin-Xiang, Shen, Lu, Guo, Ji-Feng
Publicado no Int J Clin Exp Med (2015)

Involvement of Bcl-2-associated athanogene (BAG)-family proteins in the neuroprotection by rasagiline

Por Guo, Ji-Feng, He, Shuang, Kang, Ji-Feng, Xu, Qian, Hu, Ya-Cen, Zhang, Hai-Nan, Wang, Chun-Yu, Yan, Xin-Xiang, Tang, Bei-Sha
Publicado no Int J Clin Exp Med (2015)

Analysis of EIF4G1 in ethnic Chinese

Por Li, Kai, Tang, Bei-sha, Guo, Ji-feng, Lou, Ming-xing, Lv, Zhan-yun, Liu, Zhen-hua, Tian, Yun, Song, Cheng-yuan, Xia, Kun, Yan, Xin-xiang
Publicado em 2013

Association study between SNP rs150689919 in the DNA demethylation gene, TET1, and Parkinson’s disease in Chinese Han population

Por Liao, Xin-xin, Zhan, Zi-xiong, Luo, Ying-ying, Li, Kai, Wang, Jun-ling, Guo, Ji-feng, Yan, Xin-xiang, Xia, Kun, Tang, Bei-sha, Shen, Lu
Publicado em 2013

C9orf72 mutation is rare in Alzheimer's disease, Parkinson's disease, and essential tremor in China

Por Jiao, Bin, Guo, Ji-feng, Wang, Ya-qin, Yan, Xin-xiang, Zhou, Lin, Liu, Xiao-yan, Zhang, Fu-feng, Zhou, Ya-fang, Xia, Kun, Tang, Bei-sha, Shen, Lu
Publicado em 2013

RAB39B gene mutations are not linked to familial Parkinson’s disease in China

Por Kang, Ji-feng, Luo, Yang, Tang, Bei-sha, Wan, Chang-min, Yang, Yang, Li, Kai, Liu, Zhen-hua, Sun, Qi-ying, Xu, Qian, Yan, Xin-xiang, Guo, Ji-feng
Publicado no Sci Rep (2016)

Clinical Features and Correlates of Excessive Daytime Sleepiness in Parkinson's Disease

Por Xiang, Ya-qin, Xu, Qian, Sun, Qi-ying, Wang, Zhi-qin, Tian, Yun, Fang, Liang-juan, Yang, Yang, Tan, Jie-qiong, Yan, Xin-xiang, Tang, Bei-sha, Guo, Ji-feng
Publicado no Front Neurol (2019)

BAG5 Interacts with DJ-1 and Inhibits the Neuroprotective Effects of DJ-1 to Combat Mitochondrial Oxidative Damage

Por Qin, Li-xia, Tan, Jie-qiong, Zhang, Hai-nan, Rizwana, Kousar, Lu, Jia-hong, Tang, Jian-guang, Jiang, Bo, Shen, Xiang-min, Guo, Ji-feng, Tang, Bei-sha, Tan, Li-ming, Wang, Chun-yu
Publicado no Oxid Med Cell Longev (2017)

Genetic Diagnosis of Two Dopa-Responsive Dystonia Families by Exome Sequencing

Por Sun, Zhan-fang, Zhang, Yu-han, Guo, Ji-feng, Sun, Qi-ying, Mei, Jun-pu, Zhou, Han-lin, Guan, Li-ping, Tian, Jin-yong, Hu, Zheng-mao, Li, Jia-da, Xia, Kun, Yan, Xin-xiang, Tang, Bei-sha
Publicado em 2014

Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesias

Por Wang, Jun-Ling, Cao, Li, Li, Xun-Hua, Hu, Zheng-Mao, Li, Jia-Da, Zhang, Jian-Guo, Liang, Yu, San-A, Li, Nan, Chen, Su-Qin, Guo, Ji-Feng, Jiang, Hong, Shen, Lu, Zheng, Lan, Mao, Xiao, Yan, Wei-Qian, Zhou, Ying, Shi, Yu-Ting, Ai, San-Xi, Dai, Mei-Zhi, Zhang, Peng, Xia, Kun, Chen, Sheng-Di, Tang, Bei-Sha
Publicado em 2011