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NingYu Wang

Showing results (71-80 of 96) with videos related to

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Journal of Chromatographic Science|June 20, 2012
Pharmacokinetic studies of a novel multikinase inhibitor for treating cancer by HPLC-UVXun Luo, Shuangzhi Li, Yongmei Xie, et al.
European Journal of Medicinal Chemistry|October 7, 2025
Design, synthesis and biological evaluation of 8-phenylquinazolin-2-amine derivatives as FLT3 covalent inhibitors targeting cysteine 828 in the ATP pocketWei Wei, Zuli Hu, Jiuyu Gao, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|December 16, 2014
A novel cinnamide YLT26 induces breast cancer cells apoptosis via ROS-mitochondrial apoptotic pathway in vitro and inhibits lung metastasis in vivoYing Xiong, Tinghong Ye, Mengyao Wang, et al.
Autism Research : Official Journal of the International Society for Autism Research|July 28, 2025
Fundus Peripapillary Vascular Changes in Autism Spectrum Disorder: A Cross-Sectional StudyYuexuan Wang, Yonglu Wang, Zhaoqi Zhu, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|June 5, 2016
A novel small-molecule YLT256 inhibits proliferation and induces apoptosis both in vitro and in vivo in solid tumorsHongxia Deng, Jun Zeng, Yongxia Zhu, et al.
European Journal of Medicinal Chemistry|November 23, 2021
Design, synthesis and biological evaluation of 7-((7H-pyrrolo[2,3-d]pyrimidin-4-yl)oxy)-2,3-dihydro-1H-inden-1-one derivatives as potent FAK inhibitors for the treatment of ovarian cancerWei Wei, Zhanzhan Feng, Zhihao Liu, et al.
European Journal of Medicinal Chemistry|December 1, 2023
Design and synthesis of the first PARP-1 and proteasome dual inhibitors to treat breast cancerHualong He, Wan Yang, Yaojie Shi, et al.
European Journal of Medicinal Chemistry|July 12, 2023
Design, synthesis and biological evaluation of indazole derivatives as selective covalent inhibitors of FGFR4 in wild-type and gatekeeper mutantsYingyue Yang, Xiaojie He, Zulong Li, et al.
Cerebral Cortex (New York, N.Y. : 1991)|July 20, 2022
Left frontal eye field encodes sound locations during passive listeningLiwei Sun, Chunlin Li, Songjian Wang, et al.
European Journal of Medicinal Chemistry|March 26, 2025
Design, synthesis and biological evaluation of 3-amino-6-(2-hydroxyphenyl)pyridazin-4-aryl derivatives as SMARCA2/4 degradersTianqiong Yang, Wei Wei, Qi Zhang, et al.
Pageof 10

Showing results (71-80 of 96) with videos related to

Sort By:
Pageof 10
Journal of Chromatographic Science|June 20, 2012
Pharmacokinetic studies of a novel multikinase inhibitor for treating cancer by HPLC-UVXun Luo, Shuangzhi Li, Yongmei Xie, et al.
European Journal of Medicinal Chemistry|October 7, 2025
Design, synthesis and biological evaluation of 8-phenylquinazolin-2-amine derivatives as FLT3 covalent inhibitors targeting cysteine 828 in the ATP pocketWei Wei, Zuli Hu, Jiuyu Gao, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|December 16, 2014
A novel cinnamide YLT26 induces breast cancer cells apoptosis via ROS-mitochondrial apoptotic pathway in vitro and inhibits lung metastasis in vivoYing Xiong, Tinghong Ye, Mengyao Wang, et al.
Autism Research : Official Journal of the International Society for Autism Research|July 28, 2025
Fundus Peripapillary Vascular Changes in Autism Spectrum Disorder: A Cross-Sectional StudyYuexuan Wang, Yonglu Wang, Zhaoqi Zhu, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|June 5, 2016
A novel small-molecule YLT256 inhibits proliferation and induces apoptosis both in vitro and in vivo in solid tumorsHongxia Deng, Jun Zeng, Yongxia Zhu, et al.
European Journal of Medicinal Chemistry|November 23, 2021
Design, synthesis and biological evaluation of 7-((7H-pyrrolo[2,3-d]pyrimidin-4-yl)oxy)-2,3-dihydro-1H-inden-1-one derivatives as potent FAK inhibitors for the treatment of ovarian cancerWei Wei, Zhanzhan Feng, Zhihao Liu, et al.
European Journal of Medicinal Chemistry|December 1, 2023
Design and synthesis of the first PARP-1 and proteasome dual inhibitors to treat breast cancerHualong He, Wan Yang, Yaojie Shi, et al.
European Journal of Medicinal Chemistry|July 12, 2023
Design, synthesis and biological evaluation of indazole derivatives as selective covalent inhibitors of FGFR4 in wild-type and gatekeeper mutantsYingyue Yang, Xiaojie He, Zulong Li, et al.
Cerebral Cortex (New York, N.Y. : 1991)|July 20, 2022
Left frontal eye field encodes sound locations during passive listeningLiwei Sun, Chunlin Li, Songjian Wang, et al.
European Journal of Medicinal Chemistry|March 26, 2025
Design, synthesis and biological evaluation of 3-amino-6-(2-hydroxyphenyl)pyridazin-4-aryl derivatives as SMARCA2/4 degradersTianqiong Yang, Wei Wei, Qi Zhang, et al.
Pageof 10