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Oncotarget|July 1, 2015
Epi-reevesioside F inhibits Na+/K+-ATPase, causing cytosolic acidification, Bak activation and apoptosis in glioblastomaJui-Ling Hsu, Fan-Lun Liu, Lih-Ching Hsu, et al.Bioorganic Chemistry|March 28, 2021
Inhibitor development of MTH1 via high-throughput screening with fragment based library and MTH1 substrate binding cavityCheng Peng, Yu-Hsuan Li, Chao-Wu Yu, et al.The Prostate|August 16, 2023
Mechanistic study of dual-function inhibitors targeting topoisomerase II and Rad51-mediated DNA repair pathway against castration-resistant prostate cancerYi-Chang Chiang, Wohn-Jenn Leu, Yi-Chin Chen, et al.Oncotarget|December 13, 2017
Enantiomerically pure β-dipeptide derivative induces anticancer activity against human hormone-refractory prostate cancer through both PI3K/Akt-dependent and -independent pathwaysMei-Ling Chan, Chia-Chun Yu, Jui-Ling Hsu, et al.Bioorganic Chemistry|September 8, 2025
Establishing a noncanonical zinc-binding group as a selective histone deacetylase inhibitor and possible novel anticancer agentHsuan-Chun Huang, Tse-Yu Chen, Tsung-Yu Yeh, et al.Oncotarget|October 22, 2016
Non-immunosuppressive triazole-based small molecule induces anticancer activity against human hormone-refractory prostate cancers: the role in inhibition of PI3K/AKT/mTOR and c-Myc signaling pathwaysWohn-Jenn Leu, Sharada Prasanna Swain, She-Hung Chan, et al.The Prostate|February 20, 2024
A novel HDAC6 inhibitor interferes microtubule dynamics and spindle assembly checkpoint and sensitizes cisplatin-induced apoptosis in castration-resistant prostate cancerPei-Chen Ye, Wohn-Jenn Leu, Tsung-Yu Yeh, et al.Nature Communications|June 20, 2023
Diploid and tetraploid genomes of Acorus and the evolution of monocotsLiang Ma, Ke-Wei Liu, Zhen Li, et al.Nature Plants|April 22, 2022
Genomes of leafy and leafless Platanthera orchids illuminate the evolution of mycoheterotrophyMing-He Li, Ke-Wei Liu, Zhen Li, et al.Pageof 5