Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Zi-Long Qiu"'
Autor:
Xingyu Pan, Jingrong Zhao, Zhiying Zhou, Jijun Chen, Zhenxing Yang, Yuxuan Wu, Meizhu Bai, Yang Jiao, Yun Yang, Xuye Hu, Tianling Cheng, Qianyun Lu, Bin Wang, Chang-Lin Li, Ying-Jin Lu, Lei Diao, Yan-Qing Zhong, Jing Pan, Jianmin Zhu, Hua-Sheng Xiao, Zi-Long Qiu, Jinsong Li, Zefeng Wang, Jingyi Hui, Lan Bao, Xu Zhang
Publikováno v:
eLife, Vol 10 (2021)
The congenital intellectual disability (ID)-causing gene mutations remain largely unclear, although many genetic variations might relate to ID. We screened gene mutations in Chinese Han children suffering from severe ID and found a single-nucleotide
Externí odkaz:
https://doaj.org/article/421c9d4b8f844bb7ba651e3f10b6f7d3
Autor:
Xing-Hua Yao, Min Wang, Xiang-Nan He, Fei He, Shu-Qing Zhang, Wenlian Lu, Zi-Long Qiu, Yong-Chun Yu
Publikováno v:
Nature Communications, Vol 7, Iss 1, Pp 1-15 (2016)
Electrical and chemical synapses coexist in neocortex interneurons. Here, Yao et al. show that during development, electrical and GABAergic chemical synapses form at the same time, and that this coupling synchronizes firing between layer 1 interneuro
Externí odkaz:
https://doaj.org/article/2586ec1a0aae4be2bf2c7e56ef5a3d0a
Autor:
Long-Xia Chen, Si-Min Ma, Peng Zhang, Zi-Chuan Fan, Man Xiong, Guo-Qiang Cheng, Yi Yang, Zi-Long Qiu, Wen-Hao Zhou, Jin Li
Publikováno v:
PLoS ONE, Vol 10, Iss 3, p e0115997 (2015)
Periventricular leukomalacia (PVL) is a common ischemic brain injury in premature infants for which there is no effective treatment. The objective of this study was to determine whether transplanted mouse oligodendrocyte progenitor cells (OPCs) have
Externí odkaz:
https://doaj.org/article/934bfd9db570407e9a803d63efd60082
Autor:
Si-Min Ma, Long-Xia Chen, Yi-Feng Lin, Hu Yan, Jing-Wen Lv, Man Xiong, Jin Li, Guo-Qiang Cheng, Yi Yang, Zi-Long Qiu, Wen-Hao Zhou
Publikováno v:
PLoS ONE, Vol 10, Iss 4, p e0123585 (2015)
Neural stem cell (NSC) proliferation and differentiation are required to replace neurons damaged or lost after hypoxic-ischemic events and recover brain function. Periostin (POSTN), a novel matricellular protein, plays pivotal roles in the survival,
Externí odkaz:
https://doaj.org/article/3cb8151d4e0f4299bb382b7ea3444ab8
Autor:
Shi-Hao Wu, Xiao Li, Dong-Dong Qin, Lin-Heng Zhang, Tian-Lin Cheng, Zhi-Fang Chen, Bin-Bin Nie, Xiao-Feng Ren, Jing Wu, Wen-Chao Wang, Ying-Zhou Hu, Yi-lin Gu, Long-Bao Lv, Yong Yin, Xin-Tian Hu, Zi-Long Qiu
Publikováno v:
Science Bulletin. 68:537
Autism spectrum disorder (ASD) is a class of severe neurodevelopmental disorders with a high incidence in young children, and its pathogenesis remains elusive. There is no effective treatment, and ASD children usually have a hard time in integrating
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b579dc71f10db0eaaf55578781f4782
https://doi.org/10.1101/2022.03.17.484827
https://doi.org/10.1101/2022.03.17.484827
Publikováno v:
Cancer Medicine
Circular RNAs (circRNAs) have been demonstrated to be involved in various biological processes. Nevertheless, the function of circRNAs in medulloblastoma (MB) is still unknown. The present study aimed to investigate the expression profiles of circRNA
Autor:
Xingyu, Pan, Jingrong, Zhao, Zhiying, Zhou, Jijun, Chen, Zhenxing, Yang, Yuxuan, Wu, Meizhu, Bai, Yang, Jiao, Yun, Yang, Xuye, Hu, Tianling, Cheng, Qianyun, Lu, Bin, Wang, Chang-Lin, Li, Ying-Jin, Lu, Lei, Diao, Yan-Qing, Zhong, Jing, Pan, Jianmin, Zhu, Hua-Sheng, Xiao, Zi-Long, Qiu, Jinsong, Li, Zefeng, Wang, Jingyi, Hui, Lan, Bao, Xu, Zhang
Publikováno v:
eLife
The congenital intellectual disability (ID)-causing gene mutations remain largely unclear, although many genetic variations might relate to ID. We screened gene mutations in Chinese Han children suffering from severe ID and found a single-nucleotide
Publikováno v:
Journal of Iron and Steel Research International. 24:18-26
COREX shaft furnace (SF) is a typical screw feeder with a storage container coupled with eight screw casings and screws. The structure of screw casing plays an important role in the moving behavior of burdens, stress distribution, abrasive wear of sc
Publikováno v:
Molecular Medicine Reports
Retinitis pigmentosa (RP) is a common form of inherited retinal degeneration that causes progressive loss of vision or adult blindness, characterized by the impairment of rod and cone photoreceptors. At present, mutations in >60 pathogenic genes have