Zobrazeno 1 - 10
of 62
pro vyhledávání: '"Ya-Ping Yan"'
Autor:
Ya-ling Zhang, Yuan Qu, Huan-huan Song, Guo Cheng, Fen Lu, Ting-ting Cui, Ye Gong, Xiao-li Ding, Yang Yang, Qian Zhang, Lu-ting Yang, Ya-ping Yan
Publikováno v:
Biomedicine & Pharmacotherapy, Vol 178, Iss , Pp 117188- (2024)
Multiple sclerosis (MS) is an autoimmune-mediated chronic inflammatory demyelinating disease of the central nervous system (CNS) that poses significant treatment challenges. Currently, it is believed that inflammatory and neuroprotective reactive ast
Externí odkaz:
https://doaj.org/article/774ff8927f4d4e9686a7811b52e0dcbe
Autor:
Ting Shen, Jia-Li Pu, Ya-Si Jiang, Yu-Mei Yue, Ting-Ting He, Bo-Yi Qu, Shuai Zhao, Ya-Ping Yan, Hsin-Yi Lai, Bao-Rong Zhang
Publikováno v:
Neural Regeneration Research, Vol 18, Iss 5, Pp 1154-1160 (2023)
Multiple single nucleotide polymorphisms may contribute to cognitive decline in Parkinson’s disease. However, the mechanism by which these single nucleotide polymorphisms modify brain imaging phenotype remains unclear. The aim of this study was to
Externí odkaz:
https://doaj.org/article/00cddb63b0cd4e5cbd8388ce1b393c70
Autor:
Chong-Yao Jin, Ran Zheng, Zhi-Hao Lin, Nai-Jia Xue, Ying Chen, Ting Gao, Yi-Qun Yan, Yi Fang, Ya-Ping Yan, Xin-Zhen Yin, Jun Tian, Jia-Li Pu, Bao-Rong Zhang
Publikováno v:
BMC Neurology, Vol 21, Iss 1, Pp 1-7 (2021)
Abstract Background To date, the genetic contribution to Parkinson’s disease (PD) remains unclear. Mutations in the collagen type VI alpha 3 (COL6A3) gene were recently identified as a cause of isolated dystonia. Since PD and dystonia are closely r
Externí odkaz:
https://doaj.org/article/91c89c30e7af4b629c7fccd8877e61c6
Autor:
Ye Gong, Ya-ling Zhang, Zhen Wang, Huan-huan Song, Yuan-chu Liu, Ao-wei Lv, Li-li Tian, Wen-li Zhu, Ying Fu, Xiao-li Ding, Lang-jun Cui, Ya-ping Yan
Publikováno v:
Journal of Neuroinflammation, Vol 17, Iss 1, Pp 1-12 (2020)
Abstract Background Neuromyelitis optica spectrum disorder (NMOSD), an autoimmune astrocytopathic disease associated with the anti-aquaporin-4 (AQP4) antibody, is characterized by extensive necrotic lesions primarily located on the optic nerves and s
Externí odkaz:
https://doaj.org/article/6f0e30035885473f8c6e58f8b68e5623
Autor:
Bo Li, Ya-Ping Yan, Chen Liang, Yu-Ying He, Ying Wang, Meng-Yuan Li, Si-Ting Chen, Yue Li, Ai-Xia Liu, Gui-Jun Yan, Zeng-Ming Yang
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 24, p 15573 (2022)
Endometrial decidualization plays a pivotal role during early pregnancy. Compromised decidualization has been tightly associated with recurrent implantation failure (RIF). Primary cilium is an antenna-like sensory organelle and acts as a signaling ne
Externí odkaz:
https://doaj.org/article/97e418ceee174940bbc853d88d2a0f4b
Autor:
Jia-Li Pu, Ting Gao, Xiao-Li Si, Ran Zheng, Chong-Yao Jin, Yang Ruan, Yi Fang, Ying Chen, Zhe Song, Xin-Zhen Yin, Ya-Ping Yan, Jun Tian, Bao-Rong Zhang
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
IntroductionMutations in the teneurin transmembrane protein 4 (TENM4) gene, known to be involved in neuropsychiatric disorders, have been identified in three pedigree of essential tremor (ET) from Spain. ET has overlapping clinical manifestations and
Externí odkaz:
https://doaj.org/article/928b9c32e45845e989c833df6dd28318
Autor:
Xiao-li Si, Lu-yan Gu, Zhe Song, Cheng Zhou, Yi Fang, Chong-yao Jin, Jing-jing Wu, Ting Gao, Tao Guo, Xiao-jun Guan, Xiao-jun Xu, Xin-zhen Yin, Ya-ping Yan, Min-min Zhang, Jia-li Pu
Publikováno v:
Frontiers in Aging Neuroscience, Vol 12 (2020)
BackgroundExcessive aggregation of α-synuclein is the key pathophysiological feature of Parkinson’s disease (PD). Rapid eye movement sleep behavior disorder (RBD) is also associated with synucleinopathies and considered as a powerful predictor of
Externí odkaz:
https://doaj.org/article/58055be66ecf4b9da875495a1c22b82e
Autor:
Ran Zheng, Chong‐Yao Jin, Ying Chen, Yang Ruan, Ting Gao, Zhi‐Hao Lin, Jia‐Xian Dong, Ya‐Ping Yan, Jun Tian, Jia‐Li Pu, Bao‐Rong Zhang
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 10, Pp n/a-n/a (2020)
Abstract Background To date, several studies have suggested that genes involved in monogenic forms of Parkinson's disease (PD) contribute to unrelated sporadic cases, but there is limited evidence in the Chinese population. Methods We performed a sys
Externí odkaz:
https://doaj.org/article/b76fe851104f4230a488344c330ceaaa
Autor:
Ying Chen, Nai‐Jia Xue, Yi Fang, Chong‐Yao Jin, Yao‐Lin Li, Jun Tian, Ya‐Ping Yan, Xin‐Zhen Yin, Bao‐Rong Zhang, Jia‐Li Pu
Publikováno v:
Movement Disorders Clinical Practice. 9:909-919
Parkinson's disease (PD), with either rapid eye movement sleep behavior disorder (RBD) or olfactory dysfunction (OD), has been associated with disease progression. However, there is currently heterogeneity in predicting prognosis.To identify whether