Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Hao-Yang Feng"'
Autor:
Xiao-zuo Zhang, Hai-qin Huo, Yu-qing Zhu, Hao-yang Feng, Jiao Jiao, Jian-xin Tan, Yan Wang, Ping Hu, Zheng-feng Xu
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 16 (2022)
The ability of human pluripotent stem cells (hPSCs) to specialize in neuroepithelial tissue makes them ideal candidates for use in the disease models of neural tube defects. In this study, we cultured hPSCs in suspension with modified neural inductio
Externí odkaz:
https://doaj.org/article/51efcc5ad61242039f85a77c5902f5a1
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Hao‐Yang Feng, Fengchang Qiao, Jianxin Tan, Xiaozuo Zhang, Ping Hu, Yun Stone Shi, Zhengfeng Xu
Publikováno v:
Journal of clinical laboratory analysis. 36(2)
Proline-rich transmembrane protein 2 (PRRT2) is a neuron-specific protein associated with seizures, dyskinesia, and intelligence deficit. Previous studies indicate that PRRT2 regulates neurotransmitter release from presynaptic membranes. However, PRR
Autor:
Yan Wang, Fengchang Qiao, Qing-Qing Li, Hao-Yang Feng, Jia-Hui Sun, Ya-Ping Zhou, Qi-Gang Zhou, Tingting Liu, Dan Wu, Xiao-Yu Teng, Zhengfeng Xu, Yan-Yu Zang, Jiang Chen, Ping Hu, Yun Stone Shi
Publikováno v:
CNS Neuroscience & Therapeutics
Aims This study aimed to explore the pathomechanism of a mutation on the leucine‐rich glioma inactivated 1 gene (LGI1) identified in a family having autosomal dominant lateral temporal lobe epilepsy (ADLTE), using a precise knock‐in mouse model.
Autor:
Qing-Qing Li, Jiang Chen, Ping Hu, Min Jia, Jia-Hui Sun, Hao-Yang Feng, Feng-Chang Qiao, Yan-Yu Zang, Yong-Yun Shi, Guiquan Chen, Nengyin Sheng, Yun Xu, Jian-Jun Yang, Zhengfeng Xu, Yun Stone Shi
Publikováno v:
Molecular psychiatry. 27(8)
N-methyl-D-aspartic acid type glutamate receptors (NMDARs) play critical roles in synaptic transmission and plasticity, the dysregulation of which leads to cognitive defects. Here, we identified a rare variant in the NMDAR subunit GluN2A (K879R) in a
Autor:
Qing-Qing, Li, Jiang, Chen, Ping, Hu, Min, Jia, Jia-Hui, Sun, Hao-Yang, Feng, Feng-Chang, Qiao, Yan-Yu, Zang, Yong-Yun, Shi, Guiquan, Chen, Nengyin, Sheng, Yun, Xu, Jian-Jun, Yang, Zhengfeng, Xu, Yun Stone, Shi
Publikováno v:
Molecular Psychiatry. 27:3115-3115