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Showing items 56-80 of 136  (6 Page(s) Totally)
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Institution Date Title Author
國家衛生研究院 2013-07-08 Inside Cover: 1-arylsulfonyl-5-(N-hydroxyacrylamide)indolines histone deacetylase inhibitors are potent cytokine release suppressors(ChemBioChem 10/2013) Lee, HY;Yang, CR;Lai, MJ;Huang, HL;Hsieh, YL;Liu, YM;Yeh, TK;Li, YH;Mehndiratta, S;Teng, CM;Liou, JP
國家衛生研究院 2013-07 MPT0B098, a novel microtubule inhibitor that destabilizes the hypoxia-inducible factor-1 alpha mRNA through decreasing nuclear-cytoplasmic translocation of RNA-binding protein HuR Cheng, YC;Liou, JP;Kuo, CC;Lai, WY;Shih, KH;Chang, CY;Pan, WY;Tseng, JT;Chang, JY
國家衛生研究院 2013-04 MPT0G066, a novel microtubule-destabilizing agent, induces cell apoptosis and potentiates antineoplastic effects of cisplatin in human ovarian cancer cells in vitro and in vivo Chen, CH;Li, YC;Chang, LH;Liou, JP;Pan, SL;Teng, CM
國家衛生研究院 2013-03-12 A novel synthetic microtubule inhibitor, MPT0B214 exhibits antitumor activity in human tumor cells through mitochondria-dependent intrinsic pathway Chiang, NJ;Lin, CI;Liou, JP;Kuo, CC;Chang, CY;Chen, LT;Chang, JY
國家衛生研究院 2013-02 Azatyrosinamides: Novel RAS-related anticancer agents Wang, CL;Lee, O;Huang, CF;Li, EIC;Teng, CM;Pan, SL;Lian, JF;Chang, FS;Liou, JP;Wang, HP
臺北醫學大學 2013 Di- and Tripeptide Mimetic Prodrugs of Levodopa: Systemic and Brain Bioavailability of D-Phenylglycine-L-Dopa, a Sustained Dopamine Releasing Prodrug CL, Wang;YB, Fan;Lee, SE;Lian, JF;Liou, JP;Wang, HP
臺北醫學大學 2013 Histone deacetylase inhibition improved cardiac functions with direct antifibrotic activity in heart failure Kao, YH;Liou, JP;Chung, CC;Lien, GS;Kuo, CC;Chen, SA;Chen, YJ
臺北醫學大學 2013 Di- and Tripeptide Mimetic Prodrugs of Levodopa: Systemic and Brain Bioavailability of D-Phenylglycine-L-Dopa, a Sustained Dopamine Releasing Prodrug Wang, CL;Fan, YB;Lee, SE;Lian, JF;Liou, JP;Wang, HP
臺北醫學大學 2013 Evaluation of the safety and efficacy of warfarin in Taiwanese patients Kuo, LN;Liou, JP;Chen, HY;Chiang, YC;Wu, MT
臺北醫學大學 2013 A novel synthetic microtubule inhibitor, MPT0B214 exhibits antitumor activity in human tumor cells through mitochondria-dependent intrinsic pathway Chiang, NJ;Lin, CI;Liou, JP;Kuo, CC;Chang, CY;Chen, LT;Chang, JY
臺北醫學大學 2013 MPT0B098, a novel microtubule inhibitor that destabilizes the hypoxia-inducible factor-1α mRNA through decreasing nuclear-cytoplasmic translocation of RNA-binding protein HuR Cheng, YC;Liou, JP;Kuo, CC;Lai, WY;Shih, KH;Chang, CY;Pan, WY;Tseng, JT;Chang, JY.
國家衛生研究院 2012-12 Application of Suzuki arylation, Sonogashira ethynylation and Rosenmund-von Braun cyanation in the exploration of substitution effects on the anticancer activity of 2-aroylquinolines Lee, HY;Lee, LW;Nien, CY;Kuo, CC;Lin, PY;Chang, CY;Chang, JY;Liou, JP
國家衛生研究院 2012-08-22 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
國家衛生研究院 2012-04 Synthesis and biological evaluation of 1-Arylsulfonyl-5-(N-hydroxyacrylamide)indoles as potent histone deacetylase inhibitors with antitumor activity in vivo Lai, MJ;Huang, HL;Pan, SL;Liu, YM;Peng, CY;Lee, HY;Yeh, TK;Huang, PH;Teng, CM;Chen, CS;Chuang, HY;Liou, JP
國家衛生研究院 2012-03-06 Indole compounds Hsieh, HP;Liou, JP;Chang, JY;Chang, CW
中國醫藥大學 2012-03 Synthesis and Biological Evaluation of 1-Arylsulfonyl-5-(N-hydroxyacrylamide)indoles as Potent Histone Deacetylase Inhibitors with Antitumor Activity in Vivo (Lai MJ);(Huang HL); (Pan SL);(Liu YM);彭婕妤(Chieh-Yu Peng);(Lee HY);(Yeh TK);(Huang PH); (Teng CM);(Chen CS);(Chuang HY);(Liou JP)*
臺北醫學大學 2012 Anti-Arthritic Effects of Magnolol in Human Interleukin 1b-Stimulated Fibroblast-Like Synoviocytes and in a Rat Arthritis Model Wang, JH;Shih, KS;Liou, JP;Wu, YM;ASY, Chang;Wang, KL;Tsai, CL;Yang, CR
臺北醫學大學 2012 ARYL SUBSTITUTED SULFONAMIDE COMPOUNDS AND THEIR USE AS ANTICANCER AGENTS Liou, JP;Chang, JY
國家衛生研究院 2011-12-22 5-Amino-2-aroylquinolines as highly potent tubulin polymerization inhibitors. Part 2. The impact of bridging groups at position C-2 Lee, HY;Chang, JY;Nien, CY;Kuo, CC;Shih, KH;Wu, CH;Chang, CY;Lai, WY;Liou, JP
國家衛生研究院 2011-09 Synthesis and biological evaluation of 1-(4′-Indolyl and 6′-Quinolinyl) indoles as a new class of potent anticancer agents Lai, MJ;Chang, JY;Lee, HY;Kuo, CC;Lin, MH;Hsieh, HP;Chang, CY;Wu, JS;Wu, SY;Shey, KS;Liou, JP
國家衛生研究院 2011-04-28 Scaffold-hopping strategy: Synthesis and biological evaluation of 5,6-Fused bicyclic heteroaromatics to identify orally bioavailable anticancer agents Tung, YS;Coumar, MS;Wu, YS;Shiao, HY;Chang, JY;Liou, JP;Shukla, P;Chang, CW;Chang, CY;Kuo, CC;Yeh, TK;Lin, CY;Wu, JS;Wu, SY;Liao, CC;Hsieh, HP
國家衛生研究院 2011-04-06 Indole compounds as inhibitors of tubulin polymerisation for the treatment of angiogenesis related disorders Hsieh, HP;Chang, JY;Liou, JP;Chang, CW
國家衛生研究院 2011-04 Concise syntheses of N-aryl-5,6,7-trimethoxyindoles as antimitotic and vascular disrupting agents: application of the copper-mediated Ullmann-type arylation Lee, HY;Chang, JY;Chang, LY;Lai, WY;Lai, MJ;Shih, KH;Kuo, CC;Chang, CY;Liou, JP
國家衛生研究院 2011-04 MPT0B098, a novel microtubule inhibitor, displays potent anti-angiogenic activity via destabilizing hypoxia-inducible factor-1alpha mRNA Cheng, YC;Liou, JP;Lai, WY;Chang, CY;Pan, WY;Kuo, CC;Chang, JY
國家衛生研究院 2011-03-07 Synthesis and biological evaluation of 4-aroyl-6,7,8-trimethoxyquinolines as a novel class of anticancer agents Hsieh, CC;Lee, HY;Nien, CY;Kuo, CC;Chang, CY;Chang, JY;Liou, JP

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