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Yue Qiu

Showing results (571-580 of 939) with videos related to

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ACS Nano|October 20, 2020
Precise Synthesis of Fe-N<sub>2</sub> Sites with High Activity and Stability for Long-Life Lithium-Sulfur BatteriesYue Qiu, Lishuang Fan, Maoxu Wang, et al.
Carbohydrate Polymers|July 22, 2022
Hot extrusion 3D printing technologies based on starchy food: A reviewJianyou Zhang, Yan Li, Yanping Cai, et al.
Amino Acids|September 21, 2016
Cell-penetrating peptides induce apoptosis and necrosis through specific mechanism and cause impairment of Na<sup>+</sup>-K<sup>+</sup>-ATPase and mitochondriaYue Qiu, Qianwen Yu, Kairong Shi, et al.
Cell Proliferation|May 6, 2021
Maternal sevoflurane exposure induces temporary defects in interkinetic nuclear migration of radial glial progenitors in the fetal cerebral cortex through the Notch signalling pathwayMing Jiang, Tianxiang Tang, Xinyue Liang, et al.
Chemical Communications (Cambridge, England)|December 5, 2025
High-quality deep-blue CsPbBr<sub>3</sub> quantum rods toward stable white light-emitting diodesWei Shen, Wei Zhao, Zhongyi Yang, et al.
European Geriatric Medicine|May 2, 2025
Validation of the hospital frailty risk score in ChinaYue Qiu, Weiqing Xiong, Xinyue Fang, et al.
Chinese Journal of Traumatology = Zhonghua Chuang Shang Za Zhi|January 6, 2006
The experimental study of genetic engineering human neural stem cells mediated by lentivirus to express multigenePei-qiang Cai, Xun Tang, Yue-qiu Lin, et al.
Journal of Translational Medicine|June 18, 2025
Effects of antibiotic exposure on risks of colorectal tumors: a systematic review and meta-analysisYi-Cheng Liu, Xiang-Yi Tang, Ji-Xuan Lang, et al.
Journal of Human Genetics|January 9, 2019
A rare deep intronic mutation of PKHD1 gene, c.8798-459 C > A, causes autosomal recessive polycystic kidney disease by pseudoexon activationJing Chen, Na Ma, Xiaomeng Zhao, et al.
Journal of Assisted Reproduction and Genetics|November 14, 2019
Analysis of molecular cytogenetic features and PGT-SR for two infertile patients with small supernumerary marker chromosomesDehua Cheng, Shimin Yuan, Duo Yi, et al.
Pageof 94

Showing results (571-580 of 939) with videos related to

Sort By:
Pageof 94
ACS Nano|October 20, 2020
Precise Synthesis of Fe-N<sub>2</sub> Sites with High Activity and Stability for Long-Life Lithium-Sulfur BatteriesYue Qiu, Lishuang Fan, Maoxu Wang, et al.
Carbohydrate Polymers|July 22, 2022
Hot extrusion 3D printing technologies based on starchy food: A reviewJianyou Zhang, Yan Li, Yanping Cai, et al.
Amino Acids|September 21, 2016
Cell-penetrating peptides induce apoptosis and necrosis through specific mechanism and cause impairment of Na<sup>+</sup>-K<sup>+</sup>-ATPase and mitochondriaYue Qiu, Qianwen Yu, Kairong Shi, et al.
Cell Proliferation|May 6, 2021
Maternal sevoflurane exposure induces temporary defects in interkinetic nuclear migration of radial glial progenitors in the fetal cerebral cortex through the Notch signalling pathwayMing Jiang, Tianxiang Tang, Xinyue Liang, et al.
Chemical Communications (Cambridge, England)|December 5, 2025
High-quality deep-blue CsPbBr<sub>3</sub> quantum rods toward stable white light-emitting diodesWei Shen, Wei Zhao, Zhongyi Yang, et al.
European Geriatric Medicine|May 2, 2025
Validation of the hospital frailty risk score in ChinaYue Qiu, Weiqing Xiong, Xinyue Fang, et al.
Chinese Journal of Traumatology = Zhonghua Chuang Shang Za Zhi|January 6, 2006
The experimental study of genetic engineering human neural stem cells mediated by lentivirus to express multigenePei-qiang Cai, Xun Tang, Yue-qiu Lin, et al.
Journal of Translational Medicine|June 18, 2025
Effects of antibiotic exposure on risks of colorectal tumors: a systematic review and meta-analysisYi-Cheng Liu, Xiang-Yi Tang, Ji-Xuan Lang, et al.
Journal of Human Genetics|January 9, 2019
A rare deep intronic mutation of PKHD1 gene, c.8798-459 C > A, causes autosomal recessive polycystic kidney disease by pseudoexon activationJing Chen, Na Ma, Xiaomeng Zhao, et al.
Journal of Assisted Reproduction and Genetics|November 14, 2019
Analysis of molecular cytogenetic features and PGT-SR for two infertile patients with small supernumerary marker chromosomesDehua Cheng, Shimin Yuan, Duo Yi, et al.
Pageof 94