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Shuangshuang Xiong

Showing results (1-10 of 9) with videos related to

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IEEE Transactions on Neural Networks and Learning Systems|June 25, 2021
Data-Driven Formation Control for Unknown MIMO Nonlinear Discrete-Time Multi-Agent Systems With Sensor FaultShuangshuang Xiong, Zhongsheng Hou
IEEE Transactions on Neural Networks and Learning Systems|December 28, 2020
Model-Free Adaptive Control for Unknown MIMO Nonaffine Nonlinear Discrete-Time Systems With Experimental ValidationShuangshuang Xiong, Zhongsheng Hou
European Journal of Medicinal Chemistry|April 8, 2024
Dual-target inhibitors based on ERα: Novel therapeutic approaches for endocrine resistant breast cancerShuangshuang Xiong, Ke Song, Hua Xiang, et al.
Angewandte Chemie (International Ed. in English)|March 17, 2026
Intramolecular Silylarylation of α-Olefins Enabled by Disulfide Co-Catalysis and Maintained by Proton-into-Silylium InterconversionShuangshuang Xiong, Sijie Yuan, Junru Li, et al.
Journal of Medicinal Chemistry|February 20, 2024
Discovery and Proof of Concept of Potent Dual Polθ/PARP Inhibitors for Efficient Treatment of Homologous Recombination-Deficient TumorsLuyu Ma, Wei Chen, Ming Yang, et al.
Journal of Medicinal Chemistry|March 21, 2025
Discovery of a Highly Potent and Selective Tyrosine Kinase 2 (TYK2) Degrader with In Vivo Therapeutic Efficacy in a Murine Psoriasis ModelShuangshuang Xiong, Jiaqi Yang, Ming Yang, et al.
Bioorganic Chemistry|November 14, 2022
Novel 6-amino-1,3,5-triazine derivatives as potent BTK inhibitors: structure-activity relationship (SAR) analysis and preliminary mechanism investigationMaoxu Xiao, Meiqi Zhu, Shuangjie Wu, et al.
Bioorganic Chemistry|March 16, 2023
Structural optimization of tetrahydroisoquinoline-hydroxamate hybrids as potent dual ERα degraders and HDAC inhibitorsShuangshuang Xiong, Xin Wang, Meiqi Zhu, et al.
Bioorganic Chemistry|October 23, 2023
X-ray crystallography study and optimization of novel benzothiophene analogs as potent selective estrogen receptor covalent antagonists (SERCAs) with improved potency and safety profilesChengfeng Bai, Yang Lv, Shuangshuang Xiong, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
IEEE Transactions on Neural Networks and Learning Systems|June 25, 2021
Data-Driven Formation Control for Unknown MIMO Nonlinear Discrete-Time Multi-Agent Systems With Sensor FaultShuangshuang Xiong, Zhongsheng Hou
IEEE Transactions on Neural Networks and Learning Systems|December 28, 2020
Model-Free Adaptive Control for Unknown MIMO Nonaffine Nonlinear Discrete-Time Systems With Experimental ValidationShuangshuang Xiong, Zhongsheng Hou
European Journal of Medicinal Chemistry|April 8, 2024
Dual-target inhibitors based on ERα: Novel therapeutic approaches for endocrine resistant breast cancerShuangshuang Xiong, Ke Song, Hua Xiang, et al.
Angewandte Chemie (International Ed. in English)|March 17, 2026
Intramolecular Silylarylation of α-Olefins Enabled by Disulfide Co-Catalysis and Maintained by Proton-into-Silylium InterconversionShuangshuang Xiong, Sijie Yuan, Junru Li, et al.
Journal of Medicinal Chemistry|February 20, 2024
Discovery and Proof of Concept of Potent Dual Polθ/PARP Inhibitors for Efficient Treatment of Homologous Recombination-Deficient TumorsLuyu Ma, Wei Chen, Ming Yang, et al.
Journal of Medicinal Chemistry|March 21, 2025
Discovery of a Highly Potent and Selective Tyrosine Kinase 2 (TYK2) Degrader with In Vivo Therapeutic Efficacy in a Murine Psoriasis ModelShuangshuang Xiong, Jiaqi Yang, Ming Yang, et al.
Bioorganic Chemistry|November 14, 2022
Novel 6-amino-1,3,5-triazine derivatives as potent BTK inhibitors: structure-activity relationship (SAR) analysis and preliminary mechanism investigationMaoxu Xiao, Meiqi Zhu, Shuangjie Wu, et al.
Bioorganic Chemistry|March 16, 2023
Structural optimization of tetrahydroisoquinoline-hydroxamate hybrids as potent dual ERα degraders and HDAC inhibitorsShuangshuang Xiong, Xin Wang, Meiqi Zhu, et al.
Bioorganic Chemistry|October 23, 2023
X-ray crystallography study and optimization of novel benzothiophene analogs as potent selective estrogen receptor covalent antagonists (SERCAs) with improved potency and safety profilesChengfeng Bai, Yang Lv, Shuangshuang Xiong, et al.
Pageof 1