Zobrazeno 1 - 10
of 92
pro vyhledávání: '"Yingshuang Zhang"'
Autor:
Chen Zhao, Xiaolu Liu, Jingchao Wang, Yan Zhang, Yingshuang Zhang, Yan Ma, Aping Sun, Hongsong Song, Liping Wang, Yuanjin Zhang, Xiaoxuan Liu, Wenqing Yuan, Shixian Gu, Dongsheng Fan, Shan Ye
Publikováno v:
Medical Education Online, Vol 29, Iss 1 (2024)
Undergraduate medical education in China has shifted from educator-centered learning to self-directed learning (SDL) over the past few decades. Careful design of public engagement activities can enable SDL and empower medical students to pioneer publ
Externí odkaz:
https://doaj.org/article/b77a6162a66e4fa4814671738ac7bb2c
Publikováno v:
Frontiers in Neurology, Vol 15 (2024)
BackgroundUpper motor neuron-dominant ALS (UMND ALS) is recognized to have early onset and good prognosis, but may have a rapid decline in motor function due to gait instability in the early stage. We investigated changes in lower extremity function
Externí odkaz:
https://doaj.org/article/13c67fa4e6d74ddbb1d95d05acbec671
Autor:
Pengyan Zhu, Xiaojing Shen, Xinting Wang, Xinlan Liu, Yingshuang Zhang, Ke Wang, Wenfen Gao, Xuanjun Wang, Wenjuan Yuan
Publikováno v:
Molecules, Vol 29, Iss 3, p 588 (2024)
In total, three related substances (RS) associated with sotalol hydrochloride (STHCl) were herein identified with a novel gradient high-performance liquid chromatography (HPLC) protocol. Further characterization of these substances was then performed
Externí odkaz:
https://doaj.org/article/d91b7c72ace94abfb5876c3580ee006b
Autor:
Xiangyi Liu, Yingshuang Zhang, Shuo Zhang, Aping Sun, Danfeng Zheng, Dongsheng Fan, Xiaoxuan Liu
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-7 (2022)
Abstract Background GNE myopathy is a rare distal myopathy caused by mutations of the GNE gene. A few cases of GNE myopathy accompanied by neurogenic features of electrophysiology mimicking hereditary motor neuropathy were reported recently. We confi
Externí odkaz:
https://doaj.org/article/3e196ff2e5994388b52ace658b2b69d1
Autor:
Weiyi Yu, Ji He, Xiangyi Liu, Jieying Wu, Xiying Cai, Yingshuang Zhang, Xiaoxuan Liu, Dongsheng Fan
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Background: Hereditary spastic paraplegia (HSP) constitutes a group of clinically and genetically rare neurodegenerative diseases characterized by progressive corticospinal tract degeneration. The phenotypes and genotypes of HSP are still expanding.
Externí odkaz:
https://doaj.org/article/898ef7808e44482e8544ce5f6ab853b0
Autor:
Jiayu Fu, Chen Zhao, Guanghao Hou, Xiaoxuan Liu, Mei Zheng, Yingshuang Zhang, Shuo Zhang, Danfeng Zheng, Yixuan Zhang, Xiao Huang, Shan Ye, Dongsheng Fan
Publikováno v:
Frontiers in Neurology, Vol 14 (2023)
BackgroundNeuronal intranuclear inclusion disease (NIID) is a slowly progressive neurodegenerative disease characterized by eosinophilic hyaline intranuclear inclusions and the GGC repeats in the 5'-untranslated region of NOTCH2NLC. The prevalent pre
Externí odkaz:
https://doaj.org/article/1d22e4b3e1604f4aab20d4842ffbcf15
Publikováno v:
Frontiers in Aging Neuroscience, Vol 14 (2022)
Parkinson's disease (PD) is one of the common neurodegenerative diseases that is characterized by selective degeneration of dopaminergic neurons in the substantia nigra, and misfolding of α-synuclein into aggregates is thought to contribute to its p
Externí odkaz:
https://doaj.org/article/be55302e1ed24eb89deff9a0997ace40
Autor:
Chongqing Wang, Dan Luo, Xue Zhang, Rong Huang, Yijun Cao, Gonggang Liu, Yingshuang Zhang, Hui Wang
Publikováno v:
Environmental Science and Ecotechnology, Vol 10, Iss , Pp 100167- (2022)
Increasing global population and decreasing arable land pose tremendous pressures to agricultural production. The application of conventional chemical fertilizers improves agricultural production, but causes serious environmental problems and signifi
Externí odkaz:
https://doaj.org/article/02639eaa64a24219b2b8c5dba0c54aac
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
Introduction: Charcot–Marie–Tooth disease type 2A (CMT2A) is a group of clinically and genetically heterogeneous disorders, which is mostly caused by mutations of the mitofusin2 (MFN2) gene. As the genotype–phenotype characteristics of CMT2A we
Externí odkaz:
https://doaj.org/article/8ece77e9a3ff4e26ba5716aa17e98d1e
Autor:
Wei Zhang, Bing Wen, Jun Lu, Yawen Zhao, Daojun Hong, Zhe Zhao, Cheng Zhang, Yuebei Luo, Xueliang Qi, Yingshuang Zhang, Xueqin Song, Yuying Zhao, Chongbo Zhao, Jing Hu, Huan Yang, Zhaoxia Wang, Chuanzhu Yan, Yun Yuan
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-12 (2019)
Abstract Background Neutral lipid storage disease with myopathy (NLSDM) is a rare clinical heterogeneous disorder caused by mutations in the patatin-like phospholipase domain-containing 2 (PNPLA2) gene. NLSDM usually presents skeletal myopathy, cardi
Externí odkaz:
https://doaj.org/article/33eba440eda848c2a7e7857afba47c25