Zobrazeno 1 - 10
of 340
pro vyhledávání: '"Zhi‐Ying Wu"'
Autor:
Zhen Guo, Chen Tian, Yang Shi, Xue-Ru Song, Wei Yin, Qing-Qing Tao, Jie Liu, Guo-Ping Peng, Zhi-Ying Wu, Yan-Jiang Wang, Zhen-Xin Zhang, Jing Zhang
Publikováno v:
Acta Neuropathologica Communications, Vol 12, Iss 1, Pp 1-19 (2024)
Abstract Accurate differential diagnosis among various dementias is crucial for effective treatment of Alzheimer’s disease (AD). The study began with searching for novel blood-based neuronal extracellular vesicles (EVs) that are more enriched in th
Externí odkaz:
https://doaj.org/article/a7a95c4cbfa741f6bd4a0e024bcebc83
Autor:
Rong‐Rong Lin, Lu‐Lu Jin, Yan‐Yan Xue, Zhe‐Sheng Zhang, Hui‐Feng Huang, Dian‐Fu Chen, Qian Liu, Zheng‐Wei Mao, Zhi‐Ying Wu, Qing‐Qing Tao
Publikováno v:
Advanced Science, Vol 11, Iss 24, Pp n/a-n/a (2024)
Abstract The blood brain barrier (BBB) limits the application of most therapeutic drugs for neurological diseases (NDs). Hybrid cell membrane‐coated nanoparticles derived from different cell types can mimic the surface properties and functionalitie
Externí odkaz:
https://doaj.org/article/ee4f8ff681c04f27bd4f57306e42e74f
Autor:
Chengcheng Wang, Roumin Wang, Lingzhou Zhao, Shasha Wang, Yan Liu, Jinhua Zhao, Yi Dong, Lingyan Liu, Peng Wei, Zhi-Ying Wu, Tao Yi
Publikováno v:
Redox Biology, Vol 70, Iss , Pp 103076- (2024)
Wilson's disease (WD) is a genetic disorder that primarily leads to the pathological accumulation of copper (Cu) in the liver, causing an abnormal increase in reactive oxygen species (ROS). The prevailing clinical therapy for WD involves lifelong use
Externí odkaz:
https://doaj.org/article/91d84e0a63304ed78c80e20e7ecac38f
Autor:
Xiao-Yan Li, Juan-Juan Xie, Jin-Hong Wang, Yu-Feng Bao, Yi Dong, Bin Gao, Ting Shen, Pei-Yu Huang, Hao-Chao Ying, Han Xu, Anna Wang Roe, Hsin-Yi Lai, Zhi-Ying Wu
Publikováno v:
Translational Neurodegeneration, Vol 12, Iss 1, Pp 1-4 (2023)
Externí odkaz:
https://doaj.org/article/2115fe655eec4c4b840666b7568d7147
Publikováno v:
Chinese Medical Journal, Vol 136, Iss 2, Pp 176-183 (2023)
Abstract. Background:. Juvenile amyotrophic lateral sclerosis (JALS) is an uncommon form of amyotrophic lateral sclerosis whose age at onset (AAO) is defined as prior to 25 years. FUS mutations are the most common cause of JALS. SPTLC1 was recently i
Externí odkaz:
https://doaj.org/article/df4b9e0210364b3ba7808c949b64b8cd
Autor:
Guo-Min Yang, Lingyi Xu, Rou-Min Wang, Xin Tao, Zi-Wei Zheng, Shenghai Chang, Demin Ma, Cheng Zhao, Yi Dong, Shan Wu, Jiangtao Guo, Zhi-Ying Wu
Publikováno v:
Cell Reports, Vol 42, Iss 5, Pp 112417- (2023)
Summary: The P-type ATPase ATP7B exports cytosolic copper and plays an essential role in the regulation of cellular copper homeostasis. Mutants of ATP7B cause Wilson disease (WD), an autosomal recessive disorder of copper metabolism. Here, we present
Externí odkaz:
https://doaj.org/article/e29daa0be93d41c7b0b4f82ddf3eac23
Autor:
Yan-Yan Xue, Hao-Ling Cheng, Hai-Lin Dong, Hou-Min Yin, Yun Yuan, Ling-Chao Meng, Zhi-Ying Wu, Hao Yu
Publikováno v:
BMC Neurology, Vol 21, Iss 1, Pp 1-5 (2021)
Abstract Background Charcot-Marie-Tooth (CMT) disease is a group of inherited peripheral neuropathies, which are subdivided into demyelinating and axonal forms. Biallelic mutations in POLR3B are the well-established cause of hypomyelinating leukodyst
Externí odkaz:
https://doaj.org/article/4d3ac404a0f84e209fcda2b393229cf9
Publikováno v:
Translational Neurodegeneration, Vol 10, Iss 1, Pp 1-15 (2021)
Abstract Background Although many causative genes have been uncovered in recent years, genetic diagnosis is still missing for approximately 50% of autosomal recessive cerebellar ataxia (ARCA) patients. Few studies have been performed to determine the
Externí odkaz:
https://doaj.org/article/df429179095e44c8b13a668724c3a889
Autor:
Hong-Fu Li, Yu-Lan Chen, Ling Zhuang, Dian-Fu Chen, Hua-Zhen Ke, Wen-Jiao Luo, Gong-Lu Liu, Sheng-Nan Wu, Wen-Hao Zhou, Zhi-Qi Xiong, Zhi-Ying Wu
Publikováno v:
Cell Discovery, Vol 7, Iss 1, Pp 1-4 (2021)
Externí odkaz:
https://doaj.org/article/2ca3f68050574d9285259ab5681da437
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
ObjectiveWe reported the case of a patient with Wilson's disease (WD) with acute-onset visual impairment and summarized previously reported cases to make physicians aware of the complicated clinical expressions of WD and improve diagnosis efficiency.
Externí odkaz:
https://doaj.org/article/3e5e650d1edd48f08576c4e98b4824dc