Zobrazeno 1 - 10
of 111
pro vyhledávání: '"Guiquan Chen"'
Publikováno v:
IEEE Access, Vol 12, Pp 31334-31356 (2024)
As large-scale lithium-ion battery energy storage power facilities are built, the issues of safety operations become more complex. The existing difficulties revolve around effective battery health evaluation, cell-to-cell variation evaluation, circul
Externí odkaz:
https://doaj.org/article/c330853e645846bfba123076ac652155
Autor:
Xuehui Fan, Jianyang Cao, Mingxia Li, Dechou Zhang, Ibrahim El‐Battrawy, Guiquan Chen, Xiaobo Zhou, Guoqiang Yang, Ibrahim Akin
Publikováno v:
Advanced Science, Vol 11, Iss 14, Pp n/a-n/a (2024)
Abstract The emergence of acute ischemic stroke (AIS) induced cardiovascular dysfunctions as a bidirectional interaction has gained paramount importance in understanding the intricate relationship between the brain and heart. Post AIS, the ensuing ca
Externí odkaz:
https://doaj.org/article/34c5de8a029a4eec90f0a1c88bf74828
Autor:
Qi Cheng, Jing Wu, Yingqian Xia, Qing Cheng, Yinjuan Zhao, Peixiang Zhu, Wangling Zhang, Shihu Zhang, Lei Zhang, Yushan Yuan, Chaojun Li, Guiquan Chen, Bin Xue
Publikováno v:
Molecular Brain, Vol 16, Iss 1, Pp 1-17 (2023)
Abstract The prenylation of proteins is involved in a variety of biological functions. However, it remains unknown whether it plays an important role in the morphogenesis of the cerebellum. To address this question, we generated a mouse model, in whi
Externí odkaz:
https://doaj.org/article/7c0e40876e9345f9be9a35ff85aafd1e
Autor:
Duoli Zhang, Tao Zou, Qingsong Liu, Jie Chen, Mintao Xiao, Anfu Zheng, Zhuo Zhang, Fukuan Du, Yalan Dai, Shixin Xiang, Xu Wu, Mingxing Li, Yu Chen, Yueshui Zhao, Jing Shen, Guiquan Chen, Zhangang Xiao
Publikováno v:
PeerJ, Vol 11, p e15799 (2023)
METTL7A is a protein-coding gene expected to be associated with methylation, and its expression disorder is associated with a range of diseases. However, few research have been carried out to explore the relationship between METTL7A and tumor maligna
Externí odkaz:
https://doaj.org/article/ba1343e0078f4d86829dc5576cd8944f
Autor:
Chaoli Huang, Yuanyuan Wang, Zifeng Wu, Jiali Xu, Ling Zhou, Di Wang, Ling Yang, Bin Zhu, Guiquan Chen, Cunming Liu, Chun Yang
Publikováno v:
Translational Psychiatry, Vol 11, Iss 1, Pp 1-7 (2021)
Abstract Ketamine has been demonstrated to be a rapid-onset and long-lasting antidepressant, but its underlying molecular mechanisms remain unclear. Recent studies have emerged microRNAs as important modulators for depression treatment. In this study
Externí odkaz:
https://doaj.org/article/c07fa6cdaaed4221afdccceed37be024
Autor:
He Wang, Mengjia Liu, Gang Zou, Long Wang, Wenbin Duan, Xue He, Muhuo Ji, Xiaochuan Zou, Yimin Hu, Jianjun Yang, Guiquan Chen
Publikováno v:
Neurobiology of Disease, Vol 148, Iss , Pp 105212- (2021)
PDK1 (3-Phosphoinositide dependent protein kinase-1) is a member in the PI3K (phosphatidylinositol 3 kinase) pathway and is implicated in neurodevelopmental disease with microcephaly. Although the role of PDK1 in neurogenesis has been broadly studied
Externí odkaz:
https://doaj.org/article/75e8b54112864a5db7e4fb9a1b021f53
Autor:
Xiaolian Ye, Gang Zou, Jinxing Hou, Huiru Bi, Cuihua Zhou, Runmin Wang, Yun Xu, Chun Wang, Guiquan Chen, Zhenyu Yin, Jinping Zhang, Chaoli Huang
Publikováno v:
Biochemistry and Biophysics Reports, Vol 24, Iss , Pp 100817- (2020)
Prolonged neuroinflammation is a driving force for neurodegenerative disease, and agents against inflammatory responses are regarded as potential treatment strategies. Here we aimed to evaluate the prevention effects on gliosis by dexamethasone (DEX)
Externí odkaz:
https://doaj.org/article/da7d1925b5bc4257a974f6a48a4e5ad9
Publikováno v:
International Journal of Molecular Sciences, Vol 15, Iss 12, Pp 22604-22625 (2014)
The variable patterns of DNA methylation in mammals have been linked to a number of physiological processes, including normal embryonic development and disease pathogenesis. Active removal of DNA methylation, which potentially regulates neuronal gene
Externí odkaz:
https://doaj.org/article/26da1bed6d4a4fc6b8bb18e170d02b66
Autor:
Congyu Xu, Linjie Yu, Jinxing Hou, Rosemary J. Jackson, He Wang, Chaoli Huang, Tingting Liu, Qihui Wang, Xiaochuan Zou, Richard G. Morris, Tara L. Spires-Jones, Zhongzhou Yang, Zhenyu Yin, Yun Xu, Guiquan Chen
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 11 (2017)
Decreased expression but increased activity of PDK1 has been observed in neurodegenerative disease. To study in vivo function of PDK1 in neuron survival during cortical development, we generate forebrain-specific PDK1 conditional knockout (cKO) mice.
Externí odkaz:
https://doaj.org/article/fa20350283234f61ba26a2251002152c
Autor:
Yonglu Tian, Chaojuan Yang, Shujiang Shang, Yijun Cai, Xiaofei Deng, Jian Zhang, Feng Shao, Desheng Zhu, Yunbo Liu, Guiquan Chen, Jing Liang, Qiang Sun, Zilong Qiu, Chen Zhang
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 10 (2017)
Fragile X syndrome (FXS) is a neurodevelopmental disorder caused by mutations in the FMR1 gene that inactivate expression of the gene product, the fragile X mental retardation 1 protein (FMRP). In this study, we used clustered regularly interspaced s
Externí odkaz:
https://doaj.org/article/4fd00068c86a4200b4133bc8c691814a