|
"tseng hy"的相关文件
显示项目 41-50 / 67 (共7页) << < 1 2 3 4 5 6 7 > >> 每页显示[10|25|50]项目
| 國家衛生研究院 |
2010-03 |
Synthesis and biological activities of 2-Amino-1-arylidenamino imidazoles as orally active anticancer agents
|
Li, WT;Hwang, DR;Song, JS;Chen, CP;Chuu, JJ;Hu, CB;Lin, HL;Huang, CL;Huang, CY;Tseng, HY;Lin, CC;Chen, TW;Lin, CH;Wang, HS;Shen, CC;Chang, CM;Chao, YS;Chen, CT |
| 國家衛生研究院 |
2009-07-15 |
Biochemistry, pharmacokinetics, and toxicology of a potent and selective DPP8/9 inhibitor
|
Wu, JJ;Tang, HK;Yeh, TK;Chen, CM;Shy, HS;Chu, YR;Chien, CH;Tsai, TY;Huang, YC;Huang, YL;Huang, CH;Tseng, HY;Jiaang, WT;Chao, YS;Chen, X |
| 國家衛生研究院 |
2008-04-01 |
A mammalian cell-based reverse two-hybrid system for functional analysis of 3C viral protease of human enterovirus 71
|
Lee, JC; Shih, SR; Chang, TY; Tseng, HY; Shih, YF; Yen, KJ; Chen, WC; Shie, JJ; Fang, JM; Liang, PH; Chao, YS; Hsu, JTA |
| 國家衛生研究院 |
2006-03 |
Anti-inflammatory mechanisms of phenanthroindolizidine alkaloids
|
Yang, CW; Chen, WL; Wu, PL; Tseng, HY; Lee, SJ |
| 國家衛生研究院 |
2005-04-15 |
Benzothiazolium compounds: Novel classes of inhibitors that suppress the nitric oxide production in RAW264.7 cells stimulated by LPS/IFN gamma
|
Tseng, HY; Wu, SH; Huang, WH; Wang, SF; Yang, YN; Mahindroo, N; Hsu, T; Jiaang, WT; Lee, SJ |
| 國家衛生研究院 |
2005-01-26- |
Tylophorine inhibits the expression of iNOS and COX-II through AP1 in RAW264.7 Cell Stimulated by LPS/IFNγ
|
Yang, CW;Chen, WL;Tseng, HY;Huang, YW;Wu, PL;Lee, SJ |
| 國立交通大學 |
2005-01-01 |
Self-induced transparency with transverse variations in resonant media by the power series approximation method
|
Cheng, BC; Tseng, HY; Chi, S |
| 元智大學 |
2005-01 |
Self-induced transparency with transverse variations in resonant media by the power series approximation method
|
祁甡; Cheng BC; Tseng HY |
| 國家衛生研究院 |
2004-09 |
Drug design of BPR0L075 as an anticancer agent
|
Hsieh, HP;Liou, JP;Chang, CW;Kuo, CC;Chang, YL;Kuo, FM;Tseng, HY;Pan, WY;Chen, CP;Yang, YN;Chen, CT;Lee, SJ;Chang, JY |
| 國家衛生研究院 |
2004-08-12 |
Concise synthesis and structure-activity relationships of combretastatin A-4 analogues, 1-aroylindoles and 3-aroylindoles, as novel classes of potent antitubulin agents
|
Liou, JP; Chang, YL; Kuo, FM; Chang, CW; Tseng, HY; Wang, CC; Yang, YN; Chang, JY; Lee, SJ; Hsieh, HP |
显示项目 41-50 / 67 (共7页) << < 1 2 3 4 5 6 7 > >> 每页显示[10|25|50]项目
|