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Xiuli Zhao

Showing results (221-230 of 245) with videos related to

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European Journal of Pain (London, England)|February 12, 2011
Dynamic temporal and spatial regulation of mu opioid receptor expression in primary afferent neurons following spinal nerve injuryChun-Yi Lee, Federico M Perez, Wei Wang, et al.
Zhongguo Zhong Xi Yi Jie He Za Zhi Zhongguo Zhongxiyi Jiehe Zazhi = Chinese Journal of Integrated Traditional and Western Medicine|April 15, 2006
[Clinical study on effect of fluoxetine combined with Chinese medicine or tibetan drugs in treating senile depression in plateau district]Hong-Wu Zhang, Chun-Ying Wang, Hui-Ning Xu, et al.
Human Genetics|June 28, 2006
A novel deletion in TNNI2 causes distal arthrogryposis in a large Chinese family with marked variability of expressionMiao Jiang, Xiuli Zhao, Weitian Han, et al.
Biomaterials|February 26, 2022
Branched PEG-modification: A new strategy for nanocarriers to evade of the accelerated blood clearance phenomenon and enhance anti-tumor efficacyMin Liu, Jie Li, Dan Zhao, et al.
Biomaterials|September 10, 2014
Enhanced effect of pH-sensitive mixed copolymer micelles for overcoming multidrug resistance of doxorubicinLipeng Qiu, Mingxi Qiao, Qing Chen, et al.
European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences|April 10, 2024
First-in-human study on pharmacokinetics, safety, and tolerability of single and multiple escalating doses of PA9159 nasal spray, a highly potent glucocorticoid in healthy Chinese volunteersShaojie Guo, Yingchun Hu, Chengshuo Wang, et al.
Genes|April 26, 2025
The Spectra of Pathogenic Variants and Phenotypes in a Chinese Cohort of 298 Families with Osteogenesis ImperfectaSiji Zhou, Xiuzhi Ren, Yixuan Cao, et al.
Human Mutation|March 24, 2009
Mutations of the EPHA2 receptor tyrosine kinase gene cause autosomal dominant congenital cataractTianxiao Zhang, Rui Hua, Wei Xiao, et al.
Research (Washington, D.C.)|July 8, 2025
Daurisoline Modulates the TBK1-Dependent Type I Interferon Pathway to Boost Anti-tumor Immunity via Targeting of LRP1Borui Tang, Yuting Wang, Liping Li, et al.
Frontiers in Genetics|October 23, 2020
Genotypic and Phenotypic Analysis in Chinese Cohort With Autosomal Recessive Osteogenesis ImperfectaShan Li, Yixuan Cao, Han Wang, et al.
Pageof 25

Showing results (221-230 of 245) with videos related to

Sort By:
Pageof 25
European Journal of Pain (London, England)|February 12, 2011
Dynamic temporal and spatial regulation of mu opioid receptor expression in primary afferent neurons following spinal nerve injuryChun-Yi Lee, Federico M Perez, Wei Wang, et al.
Zhongguo Zhong Xi Yi Jie He Za Zhi Zhongguo Zhongxiyi Jiehe Zazhi = Chinese Journal of Integrated Traditional and Western Medicine|April 15, 2006
[Clinical study on effect of fluoxetine combined with Chinese medicine or tibetan drugs in treating senile depression in plateau district]Hong-Wu Zhang, Chun-Ying Wang, Hui-Ning Xu, et al.
Human Genetics|June 28, 2006
A novel deletion in TNNI2 causes distal arthrogryposis in a large Chinese family with marked variability of expressionMiao Jiang, Xiuli Zhao, Weitian Han, et al.
Biomaterials|February 26, 2022
Branched PEG-modification: A new strategy for nanocarriers to evade of the accelerated blood clearance phenomenon and enhance anti-tumor efficacyMin Liu, Jie Li, Dan Zhao, et al.
Biomaterials|September 10, 2014
Enhanced effect of pH-sensitive mixed copolymer micelles for overcoming multidrug resistance of doxorubicinLipeng Qiu, Mingxi Qiao, Qing Chen, et al.
European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences|April 10, 2024
First-in-human study on pharmacokinetics, safety, and tolerability of single and multiple escalating doses of PA9159 nasal spray, a highly potent glucocorticoid in healthy Chinese volunteersShaojie Guo, Yingchun Hu, Chengshuo Wang, et al.
Genes|April 26, 2025
The Spectra of Pathogenic Variants and Phenotypes in a Chinese Cohort of 298 Families with Osteogenesis ImperfectaSiji Zhou, Xiuzhi Ren, Yixuan Cao, et al.
Human Mutation|March 24, 2009
Mutations of the EPHA2 receptor tyrosine kinase gene cause autosomal dominant congenital cataractTianxiao Zhang, Rui Hua, Wei Xiao, et al.
Research (Washington, D.C.)|July 8, 2025
Daurisoline Modulates the TBK1-Dependent Type I Interferon Pathway to Boost Anti-tumor Immunity via Targeting of LRP1Borui Tang, Yuting Wang, Liping Li, et al.
Frontiers in Genetics|October 23, 2020
Genotypic and Phenotypic Analysis in Chinese Cohort With Autosomal Recessive Osteogenesis ImperfectaShan Li, Yixuan Cao, Han Wang, et al.
Pageof 25