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Showing items 1-10 of 190  (19 Page(s) Totally)
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Institution Date Title Author
臺北醫學大學 2015 MT-4 Suppresses Resistant Ovarian Cancer Growth through Targeting Tubulin and HSP27 Pai, HC;Kumar, S;Shen, CC;Liou, JP;Pan, SL;Teng, CM
臺北醫學大學 2015 Novel oral histone deacetylase inhibitor, MPT0E028, displays potent growth-inhibitory activity against human B-cell lymphoma in vitro and in vivo Huang, HL;Peng, CY;Lai, MJ;Chen, CH;Lee, HY;Wang, JC;Liou, JP;Pan, SL;Teng, CM.
中國醫藥大學 2014-12 Novel oral histone deacetylase inhibitor, MPT0E028, displays potent growth-inhibitory activity against human B-cell lymphoma in vitro and in vivo. (Huang HL);彭婕妤(Chieh-Yu Peng);(Lai MJ);(Chen CH);(Lee HY);(Wang JC);(Liou JP)*;(Pan SL)*;(Teng CM)*
國家衛生研究院 2014-04 Orally active microtubule-targeting agent, MPT0B271, for the treatment of human non-small cell lung cancer, alone and in combination with erlotinib Tsai, AC;Wang, CY;Liou, JP;Pai, HC;Hsiao, CJ;Chang, JY;Wang, JC;Teng, CM;Pan, SL
亞洲大學 2014-04 YC-1 inhibits proliferation of breast cancer cells by downregulating EZH2 expression via activation of c-Cbl and ERK Chang, LC;Chang, LC;Lin, HY;Lin, HY;Tsai, MT;Tsai, MT;鄒瑞煌;Chou, Ruey-Hwang;Lee, FY;Lee, FY;Teng, CM;Teng, CM;Hsieh, MT;Hsieh, MT;Hung, HY;Hung, HY;Huang LJ, ;余永倫;Kuo, SC;Kuo, SC;
臺北醫學大學 2014 NPRL-Z-1, as a new topoisomerase II poison, induces cell apoptosis and ROS generation in human renal carcinoma cells Wu, SY;Pan, SL;Xiao, ZY;Hsu, JL;Chen, MC;Lee, KH;Teng, CM
臺北醫學大學 2014 A novel class I HDAC inhibitor, MPT0G030, induces cell apoptosis and differentiation in human colorectal cancer cells via HDAC1/PKCδ and E-cadherin Wang, LT;Liou, JP;Li, YH;Liu, YM;Pan, SL;Teng, CM
臺北醫學大學 2014 Indolyl or Indolinyl hydroxamate compounds Chen, CS;Liou, JP;Liu, HJ;Hung, KS;Shan, PW;Chiu, WT;Teng, CM
臺北醫學大學 2014 In vitro and in vivo anti-tumour effects of MPT0B014, a novel derivative aroylquinoline, and in combination with erlotinib in human non-small-cell lung cancer cells Tsai, AC;Pai, HC;Wang, CY;Liou, JP;Teng, CM;Wang, JC;Pan, SL
臺北醫學大學 2014 Indole-3-ethylsulfamoylphenylacrylamides: Potent histone deacetylase inhibitors with anti-inflammatory activity Mehndiratta, S;Hsieh, YL;Liu, YM;Wang, AW;Lee, HY;Liang, LY;Kumar, S;Teng, CM;CR*, Yang;Liou, JP*.

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