| 國立成功大學 |
2017-07 |
Pharmacokinetics and protein binding of MPT0B292
|
Tien;Yu-En;Li;Chan-Jung;Liou;Jing-Ping;Chang;Jang-Yang;Huang;Jin-Ding |
| 國立成功大學 |
2017-07 |
Characteristics of GaN-Based LEDs With Hybrid Microhole Arrays and SiO2 Microspheres/Nanoparticles Structures
|
Liou;Jian-Kai;Chan;Yi-Chun;Chen;Wei-Cheng;Chang;Ching-Hong;Chen;Chun-Yen;Tsai;Jung-Hui;Liu;Wen-Chau |
| 國立成功大學 |
2017-06 |
Performance Enhancement of GaN-Based Light-Emitting Diodes by Using Transparent Ag Metal Line Patterns
|
Hsu;Chi-Shiang;Chen;Sheng-Yi;Liou;Jian-Kai;Chen;Wei-Cheng;Chang;Ching-Hong;Chen;Chun-Yen;Cheng;Shiou-Ying;Guo;Der-Feng;Liu;Wen-Chau |
| 國立成功大學 |
2017-01-18 |
An Arbitrary Color Light Emitter
|
Tan;Wei-Chun;Chen;Yu-Chi;Liou;Yi-Rou;Hu;Han-Wen;Hofmann;Mario;Chen;Yang-Fang |
| 國立成功大學 |
2017 |
Weierstrass cycles in moduli spaces and the Krichever map
|
Liou;(Frank), Jia-Ming;Schwarz;Albert |
| 臺北醫學大學 |
2015 |
1-Arylsulfonyl-5-(N-hydroxyacrylamide)tetrahydroquinolines as potent histone deacetylase inhibitors suppressing the growth of prostate cancer cells
|
Liu;Y.M.;Lee;H.Y.;Chen;C.H.;Lee;C.H.;Wang;L.T.;Pan;S.L.;Lai;M.J.;Yeh;T.K.;Liou;J.P. |
| 臺北醫學大學 |
2015 |
1-Arylsulfonyl-5-(N-hydroxyacrylamide)tetrahydroquinolines as potent histone deacetylase inhibitors suppressing the growth of prostate cancer cells
|
Liu;Y, M.;Lee;H, Y.;Chen;C, H.;Lee;C, H.;Wang;L, T.;Pan;S, L.;Lai;M, J.;Yeh;T, K.;Liou;J, P. |
| 臺北醫學大學 |
2014 |
A novel action mechanism for MPT0G013, a derivative of arylsulfonamide, inhibits tumor angiogenesis through up-regulation of TIMP3 expression
|
Wang;C, Y.;Liou;J, P;Tsai;A, C;Lai;M, J.;Liu;Y, M.;Lee;H, Y.;Wang;J, C.;Pan;S, L.;Teng;C, M. |
| 臺北醫學大學 |
2014 |
Effect of C7-substitution of 1-arylsulfonyl-5-(N-hydroxyacrylamide)indolines on the selectivity towards a subclass of histone deacetylases
|
Lee;H, Y.;Wang;L, T.;Li;Y, H.;Pan;S, L.;Chen;Y, L;Teng;C, M.;Liou;J, P. |
| 臺北醫學大學 |
2014 |
A novel action mechanism for MPT0G013, a derivative of arylsulfonamide, inhibits tumor angiogenesis through up-regulation of TIMP3 expression
|
Wang;C.Y.;Liou;J.P;Tsai;A.C;Lai;M.J.;Liu;Y.M.;Lee;H.Y.;Wang;J.C.;Pan;S.L.;Teng;C.M. |
| 臺北醫學大學 |
2014 |
Effect of C7-substitution of 1-arylsulfonyl-5-(N-hydroxyacrylamide)indolines on the selectivity towards a subclass of histone deacetylases
|
Lee;H.Y.;Wang;L.T.;Li;Y.H.;Pan;S.L.;Chen;Y.L;Teng;C.M.;Liou;J.P. |
| 臺北醫學大學 |
2013 |
The HDAC inhibitor, MPT0E028, enhances erlotinib-induced cell death in EGFR-TKI-resistant NSCLC cells
|
Chen;M, C.;Chen;C, H.;Wang;J, C.;Tsai;A, C.;Liou;J, P.;Pan;S, L.;Teng;C, M. |
| 臺北醫學大學 |
2013 |
The HDAC inhibitor, MPT0E028, enhances erlotinib-induced cell death in EGFR-TKI-resistant NSCLC cells
|
Chen;M.C.;Chen;C.H.;Wang;J.C.;Tsai;A.C.;Liou;J.P.;Pan;S.L.;Teng;C.M. |
| 臺北醫學大學 |
2012 |
Anticancer Activity of MPT0E028, a Novel Potent Histone Deacetylase Inhibitor, in Human Colorectal Cancer HCT116 Cells In Vitro and In Vivo
|
HL, Huang;HY, Lee;AC, Tsai;CY, Peng;MJ, Lai;Wang;JC;SL, Pan;CM, Teng;Liou;JP |
| 臺北醫學大學 |
2012 |
Synthesis and Biological Evaluation of 1-Arylsulfonyl-5-(N-hydroxyacrylamide) indoles as Potent Histone Deacetylase Inhibitors with Antitumor Activity in vivo
|
Lai;M, J.;Huang;H, L.;Pan;S, L.;Liu;Y, M.;Peng;C, Y.;Lee;H, Y.;Yeh;T, K.;Hung;P, H.;Teng;C, M.;Chen;S, H.;Chuang;H, Y.;Liou;J, P. |
| 臺北醫學大學 |
2012 |
Anticancer Activity of MPT0E028, a Novel Potent Histone Deacetylase Inhibitor, in Human Colorectal Cancer HCT116 Cells In Vitro and In Vivo
|
Huang, HL;Lee, HY;Tsai, AC;Peng, CY;Lai, MJ;Wang;JC;Pan, SL;Teng, CM;Liou;JP |
| 臺北醫學大學 |
2012 |
Synthesis and Biological Evaluation of 1-Arylsulfonyl-5-(N-hydroxyacrylamide) indoles as Potent Histone Deacetylase Inhibitors with Antitumor Activity in vivo
|
Lai;M.J.;Huang;H.L.;Pan;S.L.;Liu;Y.M.;Peng;C.Y.;Lee;H.Y.;Yeh;T.K.;Hung;P.H.;Teng;C.M.;Chen;S.H.;Chuang;H.Y.;Liou;J.P. |
| 國立臺灣海洋大學 |
2011-11 |
Mechanical and Tribological Properties of CNx-Coated Cemented WC Substrates with a Si Interlayer
|
Chou;C.-C.*;Chu;Y.-C.;Lee;J.-W.;Liou;C.-Y.;; 周昭昌 |
| 臺北醫學大學 |
2011 |
2-Amino-3,4,5-Trimethoxybenzophenones as Potent Tubulin Polymerization Inhibitors
|
Chuang;H, Y.;Chang;J, Y.;Lai;M, J.;Kuo;C, C. C.;Lee;H, Y.;Hsieh;H, P.;Chen;Y, J.;Chen;L, T.;Pan;W, Y.;Liou;J, P. |
| 臺北醫學大學 |
2011 |
Synthesis and biological evaluation of 1-(4'-Indolyl and 6'-Quinolinyl) indoles as a new class of potent anticancer agents
|
Lai;M, J.;Chang;J, Y.;Lee;H, Y.;Kuo;C, C. C.;Lin;M, H.;Hsieh;H, P.;Chang;C, Y.;Wu;J, S.;Wu;S, Y.;Shey;K, S.;Liou;J, P. |
| 臺北醫學大學 |
2011 |
Synthesis and Biological Evaluation of 4-Aroyl-6,7,8-Trimethoxyquinolines as a Novel Class of Anticancer Agents
|
Hsieh;C, C. C.;Lee;H, Y.;Nien;C, Y.;Kuo;C, C. C.;Chang;C, Y.;Chang;J, Y.;Liou;J, P. |
| 臺北醫學大學 |
2011 |
2-Amino-3,4,5-Trimethoxybenzophenones as Potent Tubulin Polymerization Inhibitors
|
Chuang;H.Y.;Chang;J.Y.;Lai;M.J.;Kuo;C.C.;Lee;H.Y.;Hsieh;H.P.;Chen;Y.J.;Chen;L.T.;Pan;W.Y.;Liou;J.P. |
| 臺北醫學大學 |
2011 |
Concise syntheses of N-aryl-5,6,7-trimethoxyindoles as antimitotic and vascular disrupting agents: application of the copper-mediated Ullmann-type arylation
|
Lee;H.Y.;Chang;J.Y.;Chang;L.Y.;Lai;W.Y.;Lai;M.J.;Shih;K.H.;Kuo;C.C.;Hsieh;H.P.;Chang;C.Y.;Liou;J.P. |
| 臺北醫學大學 |
2011 |
Synthesis and biological evaluation of 1-(4'-Indolyl and 6'-Quinolinyl) indoles as a new class of potent anticancer agents
|
Lai;M.J.;Chang;J.Y.;Lee;H.Y.;Kuo;C.C.;Lin;M.H.;Hsieh;H.P.;Chang;C.Y.;Wu;J.S.;Wu;S.Y.;Shey;K.S.;Liou;J.P. |
| 臺北醫學大學 |
2011 |
Synthesis and Biological Evaluation of 4-Aroyl-6,7,8-Trimethoxyquinolines as a Novel Class of Anticancer Agents
|
Hsieh;C.C.;Lee;H.Y.;Nien;C.Y.;Kuo;C.C.;Chang;C.Y.;Chang;J.Y.;Liou;J.P. |
