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Xiaoqin Fu

Showing results (41-50 of 52) with videos related to

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Frontiers in Physiology|November 21, 2022
RNA-seq and qRT-PCR analyses reveal the physiological response to acute hypoxia and reoxygenation in <i>Epinephelus coioides</i>Xingxing Lai, Zhongxuan Zhong, Bing Lin, et al.
Experimental Neurology|July 2, 2020
Protective effects of FGF10 on neurovascular unit in a rat model of neonatal hypoxic-ischemic brain injuryMingchu Fang, Shishuang Jiang, Jianghu Zhu, et al.
Mikrochimica Acta|September 20, 2025
Smartphone electrochemical sensor based on laser-induced graphene integrated electrode for on-site sulfadimidine detection in beef and milkQian Zeng, Yangping Wen, Weiqiang Li, et al.
Food & Function|February 18, 2021
Neuroprotective effect of apigenin against hypoxic-ischemic brain injury in neonatal rats <i>via</i> activation of the PI3K/Akt/Nrf2 signaling pathwayChangchang Fu, Yihui Zheng, Kun Lin, et al.
Neurobiology of Disease|February 29, 2024
Clock knockout in inhibitory neurons reduces predisposition to epilepsy and influences anxiety-like behaviors in miceLu Deng, Hong Jiang, Jingjing Lin, et al.
Molecular Cell|August 4, 2012
Molecular basis for specific regulation of neuronal kinesin-3 motors by doublecortin family proteinsJudy S Liu, Christian R Schubert, Xiaoqin Fu, et al.
Journal of Visualized Experiments : Jove|June 22, 2026
No Significant Direct Causal Association Between TNF Pathway Biomarkers and Hip Fracture Risk: A Study Based on Real-World DataPeng Xiao, Bingqi Wei, Guilong Zhang, et al.
Molecular Biology of the Cell|January 6, 2021
Doublecortin facilitates the elongation of the somatic Golgi apparatus into proximal dendritesPeijun Li, Luyao Li, Binyuan Yu, et al.
Neuroscience|July 4, 2024
The de novo missense mutation F224S in GABRB2, identified in epileptic encephalopathy and developmental delay, impairs GABA<sub>A</sub>R functionPing-Ping Li, Yue-Yuan Zhou, Li Gao, et al.
Human Molecular Genetics|October 4, 2017
TUBB4A mutations result in specific neuronal and oligodendrocytic defects that closely match clinically distinct phenotypesJulian Curiel, Guillermo Rodríguez Bey, Asako Takanohashi, et al.
Pageof 6

Showing results (41-50 of 52) with videos related to

Sort By:
Pageof 6
Frontiers in Physiology|November 21, 2022
RNA-seq and qRT-PCR analyses reveal the physiological response to acute hypoxia and reoxygenation in <i>Epinephelus coioides</i>Xingxing Lai, Zhongxuan Zhong, Bing Lin, et al.
Experimental Neurology|July 2, 2020
Protective effects of FGF10 on neurovascular unit in a rat model of neonatal hypoxic-ischemic brain injuryMingchu Fang, Shishuang Jiang, Jianghu Zhu, et al.
Mikrochimica Acta|September 20, 2025
Smartphone electrochemical sensor based on laser-induced graphene integrated electrode for on-site sulfadimidine detection in beef and milkQian Zeng, Yangping Wen, Weiqiang Li, et al.
Food & Function|February 18, 2021
Neuroprotective effect of apigenin against hypoxic-ischemic brain injury in neonatal rats <i>via</i> activation of the PI3K/Akt/Nrf2 signaling pathwayChangchang Fu, Yihui Zheng, Kun Lin, et al.
Neurobiology of Disease|February 29, 2024
Clock knockout in inhibitory neurons reduces predisposition to epilepsy and influences anxiety-like behaviors in miceLu Deng, Hong Jiang, Jingjing Lin, et al.
Molecular Cell|August 4, 2012
Molecular basis for specific regulation of neuronal kinesin-3 motors by doublecortin family proteinsJudy S Liu, Christian R Schubert, Xiaoqin Fu, et al.
Journal of Visualized Experiments : Jove|June 22, 2026
No Significant Direct Causal Association Between TNF Pathway Biomarkers and Hip Fracture Risk: A Study Based on Real-World DataPeng Xiao, Bingqi Wei, Guilong Zhang, et al.
Molecular Biology of the Cell|January 6, 2021
Doublecortin facilitates the elongation of the somatic Golgi apparatus into proximal dendritesPeijun Li, Luyao Li, Binyuan Yu, et al.
Neuroscience|July 4, 2024
The de novo missense mutation F224S in GABRB2, identified in epileptic encephalopathy and developmental delay, impairs GABA<sub>A</sub>R functionPing-Ping Li, Yue-Yuan Zhou, Li Gao, et al.
Human Molecular Genetics|October 4, 2017
TUBB4A mutations result in specific neuronal and oligodendrocytic defects that closely match clinically distinct phenotypesJulian Curiel, Guillermo Rodríguez Bey, Asako Takanohashi, et al.
Pageof 6