| 臺大學術典藏 |
2020-02-06T10:53:30Z |
Structure-based design, synthesis and biological evaluation of novel anthra[1,2-d]imidazole-6,11-dione homologues as potential antitumor agents
|
Chen T.-C.;Yu D.-S.;Huang K.-F.;Fu Y.-C.;Lee C.-C.;Chen C.-L.;Huang F.-C.;Hsieh H.-H.;Jing-Jer Lin;Huang H.-S.; Chen T.-C.; Yu D.-S.; Huang K.-F.; Fu Y.-C.; Lee C.-C.; Chen C.-L.; Huang F.-C.; Hsieh H.-H.; JING-JER LIN; Huang H.-S. |
| 臺大學術典藏 |
2020-02-06T10:53:30Z |
Structure-based design, synthesis and biological evaluation of novel anthra[1,2-d]imidazole-6,11-dione homologues as potential antitumor agents
|
Chen T.-C.;Yu D.-S.;Huang K.-F.;Fu Y.-C.;Lee C.-C.;Chen C.-L.;Huang F.-C.;Hsieh H.-H.;Jing-Jer Lin;Huang H.-S.; Chen T.-C.; Yu D.-S.; Huang K.-F.; Fu Y.-C.; Lee C.-C.; Chen C.-L.; Huang F.-C.; Hsieh H.-H.; JING-JER LIN; Huang H.-S. |
| 臺大學術典藏 |
2020-02-06T10:53:30Z |
Development and evaluation of novel phosphotyrosine mimetic inhibitors targeting the Src homology 2 domain of signaling lymphocytic activation molecule (SLAM) associated protein
|
Chu C.-Y.;Chang C.-P.;Chou Y.-T.;Handoko, Hu Y.-L.;Lo L.-C.;Jing-Jer Lin; Chu C.-Y.; Chang C.-P.; Chou Y.-T.; Handoko, Hu Y.-L.; Lo L.-C.; JING-JER LIN |
| 臺大學術典藏 |
2020-02-06T10:53:30Z |
Development and evaluation of novel phosphotyrosine mimetic inhibitors targeting the Src homology 2 domain of signaling lymphocytic activation molecule (SLAM) associated protein
|
Chu C.-Y.;Chang C.-P.;Chou Y.-T.;Handoko, Hu Y.-L.;Lo L.-C.;Jing-Jer Lin; Chu C.-Y.; Chang C.-P.; Chou Y.-T.; Handoko, Hu Y.-L.; Lo L.-C.; JING-JER LIN |
| 臺大學術典藏 |
2020-02-06T10:53:30Z |
Structure-based design, synthesis and evaluation of novel anthra[1,2-d]imidazole-6,11-dione derivatives as telomerase inhibitors and potential for cancer polypharmacology
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Huang H.-S.; JING-JER LIN; Guh J.-H.; Huang K.-F.; Huang F.-C.; Hsieh H.-H.; Lee C.-C.; Chen T.-C.; Chang D.-M.; Chen C.-L.; Chen C.-L.;Chang D.-M.;Chen T.-C.;Lee C.-C.;Hsieh H.-H.;Huang F.-C.;Huang K.-F.;Guh J.-H.;Jing-Jer Lin;Huang H.-S. |
| 臺大學術典藏 |
2020-02-06T10:53:30Z |
Structure-based design, synthesis and evaluation of novel anthra[1,2-d]imidazole-6,11-dione derivatives as telomerase inhibitors and potential for cancer polypharmacology
|
Huang H.-S.; JING-JER LIN; Guh J.-H.; Huang K.-F.; Huang F.-C.; Hsieh H.-H.; Lee C.-C.; Chen T.-C.; Chang D.-M.; Chen C.-L.; Chen C.-L.;Chang D.-M.;Chen T.-C.;Lee C.-C.;Hsieh H.-H.;Huang F.-C.;Huang K.-F.;Guh J.-H.;Jing-Jer Lin;Huang H.-S. |
| 臺大學術典藏 |
2020-02-06T10:53:29Z |
Conformational transition of a hairpin structure to G-quadruplex within the WNT1 gene promoter
|
Chang T.-C.; Kuo M.H.-J.;Wang Z.-F.;Tseng T.-Y.;Li M.-H.;Hsu S.-T.D.;Jing-Jer Lin;Chang T.-C.; Kuo M.H.-J.; Wang Z.-F.; Tseng T.-Y.; Li M.-H.; Hsu S.-T.D.; JING-JER LIN |
| 臺大學術典藏 |
2020-02-06T10:53:29Z |
Conformational transition of a hairpin structure to G-quadruplex within the WNT1 gene promoter
|
Chang T.-C.; Kuo M.H.-J.;Wang Z.-F.;Tseng T.-Y.;Li M.-H.;Hsu S.-T.D.;Jing-Jer Lin;Chang T.-C.; Kuo M.H.-J.; Wang Z.-F.; Tseng T.-Y.; Li M.-H.; Hsu S.-T.D.; JING-JER LIN |
| 臺大學術典藏 |
2020-02-06T10:53:29Z |
Direct evidence of mitochondrial G-quadruplex DNA by using fluorescent anti-cancer agents
|
Chang T.-C.; Lou P.-J.; Huang W.-C.;Tseng T.-Y.;Chen Y.-T.;Chang C.-C.;Wang Z.-F.;Wang C.-L.;Hsu T.-N.;Li P.-T.;Chen C.-T.;Jing-Jer Lin;Lou P.-J.;Chang T.-C.; Huang W.-C.; Tseng T.-Y.; Chen Y.-T.; Chang C.-C.; Wang Z.-F.; Wang C.-L.; Hsu T.-N.; Li P.-T.; Chen C.-T.; JING-JER LIN |
| 臺大學術典藏 |
2020-02-06T10:53:29Z |
Direct evidence of mitochondrial G-quadruplex DNA by using fluorescent anti-cancer agents
|
Chang T.-C.; Lou P.-J.; Huang W.-C.;Tseng T.-Y.;Chen Y.-T.;Chang C.-C.;Wang Z.-F.;Wang C.-L.;Hsu T.-N.;Li P.-T.;Chen C.-T.;Jing-Jer Lin;Lou P.-J.;Chang T.-C.; Huang W.-C.; Tseng T.-Y.; Chen Y.-T.; Chang C.-C.; Wang Z.-F.; Wang C.-L.; Hsu T.-N.; Li P.-T.; Chen C.-T.; JING-JER LIN |
