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European Journal of Medicinal Chemistry|May 2, 2021
Ring-opening of five-membered heterocycles conjugated 4-isopropylresorcinol scaffold-based benzamides as HSP90 inhibitors suppressing tumor growth in vitro and in vivoYi-Min Liu, Huang-Ju Tu, Chueh-Heng Wu, et al.
Frontiers in Oncology|June 27, 2022
Plasma Circulating Tumor Epstein-Barr Virus for the Surveillance of Cancer Progression in Bone-Only Metastatic Nasopharyngeal CarcinomaGuo-Ying Liu, Wei-Xiong Xia, Zhuo-Fei Bi, et al.
Chembiochem : a European Journal of Chemical Biology|June 22, 2013
1-arylsulfonyl-5-(N-hydroxyacrylamide)indolines histone deacetylase inhibitors are potent cytokine release suppressorsHsueh-Yun Lee, Chia-Ron Yang, Mei-Jung Lai, et al.
European Journal of Medicinal Chemistry|September 20, 2017
1,4-Naphthoquinones as inhibitors of Itch, a HECT domain-E3 ligase, and tumor growth suppressors in multiple myelomaYi-Min Liu, Wei-Chun HuangFu, Han-Li Huang, et al.
World Journal of Gastroenterology|June 16, 2015
Low RASSF6 expression in pancreatic ductal adenocarcinoma is associated with poor survivalHui-Lin Ye, Dou-Dou Li, Qing Lin, et al.
Circulation Research|January 22, 2015
CXCL10/IP-10 is a biomarker and mediator for Kawasaki diseaseTai-Ming Ko, Ho-Chang Kuo, Jeng-Sheng Chang, et al.
European Journal of Medicinal Chemistry|July 20, 2020
Fluoropyrimidin-2,4-dihydroxy-5-isopropylbenzamides as antitumor agents against CRC and NSCLC cancer cellsWei-Cheng Wu, Yi-Min Liu, Yu-Hsuan Liao, et al.
European Journal of Medicinal Chemistry|November 27, 2018
1-Arylsulfonyl indoline-benzamides as a new antitubulin agents, with inhibition of histone deacetylaseMei-Jung Lai, Ritu Ojha, Mei-Hsiang Lin, et al.
Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi = Zhonghua Laodong Weisheng Zhiyebing Zazhi = Chinese Journal of Industrial Hygiene and Occupational Diseases|February 24, 2012
[The experimental study of suppressing silicosis fibrosis]Ze-ping Weng, Ji-jun Zhang, Wei-wei Liu, et al.
Journal of Medicinal Chemistry|March 24, 2012
Synthesis and biological evaluation of 1-arylsulfonyl-5-(N-hydroxyacrylamide)indoles as potent histone deacetylase inhibitors with antitumor activity in vivoMei-Jung Lai, Han-Li Huang, Shiow-Lin Pan, et al.
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