English  |  正體中文  |  简体中文  |  Total items :0  
Visitors :  51969319    Online Users :  1017
Project Commissioned by the Ministry of Education
Project Executed by National Taiwan University Library
 
臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)
About TAIR

Browse By

News

Copyright

Related Links

"liou"

Return to Browse by Author
Sorting by Title Sort by Date

Showing items 101-124 of 124  (3 Page(s) Totally)
<< < 1 2 3 
View [10|25|50] records per page

Institution Date Title Author
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.
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. C.;Hsieh;H, P.;Chang;C, Y.;Liou;J, P.
元培科技大學 2008 Determination of Particulate-Bound Formaldehyde from Burning Incense by Solid Phase Microextraction Liou; Shiou-Wen; Chen; Cheng-Yao; Yang; Tzu-Ting.; Lin; Jia-Ming
臺北醫學大學 2006 Development of a RPLC-based Method for Measurement of Indoprofen Stability and Validation of the Method 吳安邦; 李仁愛; Liou; YB; Chen; FA; Lee; JA; Ho; HO; Wu; AB*;
國立政治大學 1997-01 Mortgage Prepayment in Taiwan 張金鶚;Liou

Showing items 101-124 of 124  (3 Page(s) Totally)
<< < 1 2 3 
View [10|25|50] records per page