Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Kun Cheng Liu"'
Autor:
Yang‐Fan Cheng, Kun‐Cheng Liu, Tian‐Mi Yang, Yi Xiao, Qi‐Rui Jiang, Jing‐Xuan Huang, Sirui Zhang, Qian‐Qian Wei, Ru‐Wei Ou, Chun‐Yu Li, Xiao‐Jing Gu, Jean‐Marc Burgunder, Hui‐Fang Shang
Publikováno v:
Brain and Behavior, Vol 13, Iss 11, Pp n/a-n/a (2023)
Abstract Background and aim Huntington's disease (HD) is an autosomal dominant inherited neurodegenerative disorder caused by CAG repeats expansion. Cognitive decline contributes to the loss of daily activity in manifest HD. We aimed to examine the c
Externí odkaz:
https://doaj.org/article/8b1ab19aa9d9438da3df0e48b49ceb15
Autor:
Jun-Yu Lin, Ling-Yu Zhang, Bei Cao, Qian-Qian Wei, Ru-Wei Ou, Yan-Bing Hou, Kun-Cheng Liu, Xin-Ran Xu, Zheng Jiang, Xiao-Jing Gu, Jiao Liu, Hui-Fang Shang, Li-Shao Guo
Publikováno v:
Chinese Medical Journal, Vol 134, Iss 6, Pp 690-698 (2021)
Abstract. Background:. Sleep disorders are common but under-researched symptoms in patients with multiple system atrophy (MSA). We investigated the frequency and factors associated with sleep-related symptoms in patients with MSA and the impact of sl
Externí odkaz:
https://doaj.org/article/a1205226cb6a4162b4651ea66ee05f1c
Autor:
Yong-Ping Chen, Ru-Wei Ou, Xiao-Jing Gu, Ling-Yu Zhang, Bei Cao, Yan-Bing Hou, Kun-Cheng Liu, Jun-Yu Lin, Qian-Qian Wei, Bi Zhao, Ying Wu, Hui-Fang Shang
Publikováno v:
Translational Neurodegeneration, Vol 10, Iss 1, Pp 1-3 (2021)
Externí odkaz:
https://doaj.org/article/4ba4889ced6b4dc2bbcac00f989600a1
Autor:
Chun Yu Li, Ru Wei Ou, Yong Ping Chen, Xiao Jing Gu, Qian Qian Wei, Yan Bing Hou, Bei Cao, Ling Yu Zhang, Jun Yu Lin, Kun Cheng Liu, Wei Song, Bi Zhao, Ying Wu, Hui Fang Shang
Publikováno v:
Journal of Internal Medicine. 291:698-701
Autor:
Yong‐Ping Chen, Shi‐Hui Yu, Guo‐Hui Zhang, Yan‐Bing Hou, Xiao‐Jing Gu, Ru‐Wei Ou, Ying Shen, Wei Song, Xue‐Ping Chen, Bi Zhao, Bei Cao, Ling‐Yu Zhang, Ming‐Ming Sun, Fei‐Fei Liu, Qian‐Qian Wei, Kun‐Cheng Liu, Jun‐Yu Lin, Tian‐Mi Yang, Jing Yang, Ying Wu, Zheng Jiang, Jiao Liu, Yang‐Fan Cheng, Yi Xiao, Wei‐Ming Su, Fei Feng, Ying‐Ying Cai, Shi‐Rong Li, Tao Hu, Xiao‐Qin Yuan, Qing‐Qing Zhou, Na Shao, Sha Ma, Hui‐Fang Shang
Publikováno v:
European journal of neurologyREFERENCES. 29(11)
Recent genetic progress has shown many causative/risk genes linked to Parkinson's disease (PD), mainly in patients of European ancestry. The study aimed to investigate the PD-related genes and determine the mutational spectrum of early-onset PD in et
Autor:
Jun-Yu Lin, Ling-Yu Zhang, Bei Cao, Qian-Qian Wei, Ru-Wei Ou, Yan-Bing Hou, Kun-Cheng Liu, Xin-Ran Xu, Zheng Jiang, Xiao-Jing Gu, Jiao Liu, Hui-Fang Shang, Li-Shao Guo
Publikováno v:
Chinese Medical Journal
Chinese Medical Journal, Vol 134, Iss 6, Pp 690-698 (2021)
Chinese Medical Journal, Vol 134, Iss 6, Pp 690-698 (2021)
Background:. Sleep disorders are common but under-researched symptoms in patients with multiple system atrophy (MSA). We investigated the frequency and factors associated with sleep-related symptoms in patients with MSA and the impact of sleep distur
Autor:
Yi Wei Liu, Yu-Ming Zhang, Li Chen, Yuan Guo, Hui Sheng Wang, Kun Cheng Liu, Jin Zhang, Li Zhang, Shu Xuan Lv, Wen Xie
Publikováno v:
Neurological Research. 41:791-801
Objectives: This study aimed to investigate the effect of serotonin6 (5-HT6) receptors in the dorsal hippocampus (dHip) on the regulation of Parkinson's disease (PD)-associated anxiety. Methods: We examined whether intra-dHip injection of both 5-HT6
Autor:
Yong-Ping Chen, Shi-Hui Yu, Qian-Qian Wei, Bei Cao, Xiao-Jing Gu, Xue-Ping Chen, Wei Song, Bi Zhao, Ying Wu, Ming-Ming Sun, Fei-Fei Liu, Yan-Bing Hou, Ru-Wei Ou, Ling-Yu Zhang, Kun-Cheng Liu, Jun-Yu Lin, Xin-Ran Xu, Chun-Yu Li, Jing Yang, Zheng Jiang
Publikováno v:
Journal of Medical Genetics; Sep2022, Vol. 59 Issue 9, p840-849, 10p
Autor:
Yongping Chen, Xiao Jing Gu, Huifang Shang, Xue Ping Chen, Wei Song, Ying Wu, Kun Cheng Liu, Bi Zhao, Chunyu Li, Yan Bing Hou, Yi Liu, L. Zhang, Qian Qian Wei, Bei Cao, Ru Wei Ou
Publikováno v:
Molecular neurobiology. 58(7)
Functional and genetic studies have identified association between several Zinc finger (ZNF) proteins and Parkinson's disease (PD). However, most of them were still awaiting further replications, especially in the Asian population. Here, we systemati
Autor:
Yong-Ping, Chen, Xiao-Jing, Gu, Ru-Wei, Ou, Ling-Yu, Zhang, Yan-Bing, Hou, Kun-Cheng, Liu, Bei, Cao, Qian-Qian, Wei, Wei, Song, Bi, Zhao, Ying, Wu, Jing-Qiu, Cheng, Hui-Fang, Shang
Publikováno v:
Molecular neurobiology. 58(4)
Recent genetic studies clearly indicate that variants in several lysosomal genes act as risk factors for idiopathic Parkinson's disease (PD). Variants in the co-activator of glucocerebrosidase gene (GBA) and the four active saposins (Sap A-D) which a