| 臺大學術典藏 |
2021-04-15T07:52:55Z |
Induction of endoplasmic reticulum stress and apoptosis by a marine prostanoid in human hepatocellular carcinoma
|
Chiang P.-C.; Chien C.-L.; Pan S.-L.; WEN-PIN CHEN; Teng C.-M.; Shen Y.-C.; Guh J.-H. |
| 臺大學術典藏 |
2021-02-02T00:43:15Z |
Anti-angiogenic effects and mechanism of prazosin
|
Liao C.-H.; Guh J.-H.; Chueh S.-C.; HONG-JENG YU |
| 臺大學術典藏 |
2021-02-02T00:43:06Z |
Erratum: Anti-angiogenic effects and mechanism of prazosin (The Prostate (2011) 71 (976-984))
|
Liao C.-H.; Guh J.-H.; Chueh S.-C.; HONG-JENG YU |
| 臺大學術典藏 |
2021-01-29T03:17:24Z |
A unique amidoanthraquinone derivative displays antiproliferative activity against human hormone-refractory metastatic prostate cancers through activation of LKB1-AMPK-mTOR signaling pathway
|
Hsu J.-L.;Shih-Ping Liu;Lee C.-C.;Hsu L.-C.;Ho Y.-F.;Huang H.-S.;Guh J.-H.; Hsu J.-L.; SHIH-PING LIU; Lee C.-C.; Hsu L.-C.; Ho Y.-F.; Huang H.-S.; Guh J.-H. |
| 臺大學術典藏 |
2021-01-29T03:17:21Z |
A novel small molecule hybrid of vorinostat and DACA displays anticancer activity against human hormone-refractory metastatic prostate cancer through dual inhibition of histone deacetylase and topoisomerase i
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Yu C.-C.;Pan S.-L.;Chao S.-W.;Shih-Ping Liu;Hsu J.-L.;Yang Y.-C.;Li T.-K.;Huang W.-J.;Guh J.-H.; Yu C.-C.; Pan S.-L.; Chao S.-W.; SHIH-PING LIU; Hsu J.-L.; Yang Y.-C.; Li T.-K.; Huang W.-J.; Guh J.-H. |
| 臺大學術典藏 |
2021-01-29T03:17:19Z |
KUD773, a phenylthiazole derivative, displays anticancer activity in human hormone-refractory prostate cancers through inhibition of tubulin polymerization and anti-Aurora a activity
|
Yu C.-C.;Shih-Ping Liu;Hsu J.-L.;Hsu J.T.A.;Kudryavtsev K.;Guh J.-H.; Yu C.-C.; SHIH-PING LIU; Hsu J.-L.; Hsu J.T.A.; Kudryavtsev K.; Guh J.-H. |
| 臺大學術典藏 |
2021-01-29T03:17:19Z |
Repurposing of phentolamine as a potential anticancer agent against human castration-resistant prostate cancer: A central role on microtubule stabilization and mitochondrial apoptosis pathway
|
Ho C.-H.;Hsu J.-L.;Shih-Ping Liu;Hsu L.-C.;Chang W.-L.;Chao C.C.-K.;Guh J.-H.; Ho C.-H.; Hsu J.-L.; SHIH-PING LIU; Hsu L.-C.; Chang W.-L.; Chao C.C.-K.; Guh J.-H. |
| 臺大學術典藏 |
2021-01-29T03:17:17Z |
Non-immunosuppressive triazole-based small molecule induces anticancer activity against human hormone-refractory prostate cancers: The role in inhibition of PI3K/AKT/mTOR and c-Myc signaling pathways
|
Leu W.-J.; Swain S.P.; Chan S.-H.; Hsu J.-L.; SHIH-PING LIU; Chan M.-L.; Yu C.-C.; Hsu L.-C.; Chou Y.-L.; Chang W.-L.; Hou D.-R.; Guh J.-H. |
| 臺大學術典藏 |
2021-01-29T03:17:15Z |
Enantiomerically pure β-dipeptide derivative induces anticancer activity against human hormone-refractory prostate cancer through both PI3K/Akt-dependent and -independent pathways
|
Chan M.-L.;Yu C.-C.;Hsu J.-L.;Leu W.-J.;Chan S.-H.;Hsu L.-C.;Shih-Ping Liu;Ivantcova P.M.;Dogan ?.;Br?Se S.;Kudryavtsev K.V.;Guh J.-H.; Chan M.-L.; Yu C.-C.; Hsu J.-L.; Leu W.-J.; Chan S.-H.; Hsu L.-C.; SHIH-PING LIU; Ivantcova P.M.; Dogan ?.; Br?se S.; Kudryavtsev K.V.; Guh J.-H. |
| 臺大學術典藏 |
2021-01-29T03:17:14Z |
Para-toluenesulfonamide induces anti-tumor activity through Akt-dependent and -independent mTOR/p70S6K pathway: Roles of lipid raft and cholesterol contents
|
Hsu J.-L.;Leu W.-J.;Hsu L.-C.;Shih-Ping Liu;Zhong N.-S.;Guh J.-H.; Hsu J.-L.; Leu W.-J.; Hsu L.-C.; SHIH-PING LIU; Zhong N.-S.; Guh J.-H. |
| 臺大學術典藏 |
2021-01-29T03:17:13Z |
Phosphodiesterase type 5 (PDE5) inhibitors sensitize topoisomerase II inhibitors in killing prostate cancer through PDE5-independent impairment of HR and NHEJ DNA repair systems
|
Chang J.-F.;Hsu J.-L.;Sheng Y.-H.;Leu W.-J.;Yu C.-C.;Chan S.-H.;Chan M.-L.;Hsu L.-C.;Shih-Ping Liu;Guh J.-H.; Chang J.-F.; Hsu J.-L.; Sheng Y.-H.; Leu W.-J.; Yu C.-C.; Chan S.-H.; Chan M.-L.; Hsu L.-C.; SHIH-PING LIU; Guh J.-H. |
| 臺大學術典藏 |
2021-01-29T03:17:11Z |
Phosphodiesterase Type 5 Inhibitors Synergize Vincristine in Killing Castration-Resistant Prostate Cancer Through Amplifying Mitotic Arrest Signaling
|
Hsu J.-L.; Leu W.-J.; Hsu L.-C.; Ho C.-H.; SHIH-PING LIU; Guh J.-H. |
| 臺大學術典藏 |
2020-12-28T05:56:09Z |
A unique P-glycoprotein interacting agent displays anticancer activity against hepatocellular carcinoma through inhibition of GRP78 and mTOR pathways
|
Guh J.-H.; Bastow K.F.; Lee K.-H.; Nakagawa-Goto K.; Yu C.-C.; Chiang P.-C.; TING-CHUN KUO |
| 臺大學術典藏 |
2020-12-28T05:56:09Z |
WJ9708012 exerts anticancer activity through PKC-α related crosstalk of mitochondrial and endoplasmic reticulum stresses in human hormone-refractory prostate cancer cells
|
TING-CHUN KUO; Huang W.-J.; Guh J.-H. |
| 臺大學術典藏 |
2020-06-22T07:36:56Z |
The combination of MK-2206 and WZB117 exerts a synergistic cytotoxic effect against breast cancer cells
|
Li Y.-L.;Weng H.-C.;Hsu J.-L.;Shu-Wha Lin;Guh J.-H.;Hsu L.-C.; Li Y.-L.; Weng H.-C.; Hsu J.-L.; SHU-WHA LIN; Guh J.-H.; Hsu L.-C. |
| 臺大學術典藏 |
2020-02-27T01:50:16Z |
Induction of endoplasmic reticulum stress and apoptosis by a marine prostanoid in human hepatocellular carcinoma
|
Chiang P.-C.;Chung-Liang Chien;Pan S.-L.;Chen W.-P.;Teng C.-M.;Shen Y.-C.;Guh J.-H.; Chiang P.-C.; CHUNG-LIANG CHIEN; Pan S.-L.; Chen W.-P.; Teng C.-M.; Shen Y.-C.; Guh J.-H. |
| 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 |
2020-02-06T10:53:26Z |
Synthesis and biological evaluation of anthra[1,9-cd]pyrazol-6(2H)-one scaffold derivatives as potential anticancer agents
|
Chen T.-C.;Guh J.-H.;Hsu H.-W.;Chen C.-L.;Lee C.-C.;Wu C.-L.;Lee Y.-R.;Jing-Jer Lin;Yu D.-S.;Huang H.-S.; Chen T.-C.; Guh J.-H.; Hsu H.-W.; Chen C.-L.; Lee C.-C.; Wu C.-L.; Lee Y.-R.; JING-JER LIN; Yu D.-S.; Huang H.-S. |
| 臺大學術典藏 |
2019 |
Design, synthesis and biological evaluation of tetracyclic azafluorenone derivatives with topoisomerase I inhibitory properties as potential anticancer agents
|
Chen T.-C.;Yu D.-S.;Chen S.-J.;Chen C.-L.;Lee C.-C.;Hsieh Y.-Y.;Chang L.-C.;Guh J.-H.;Jing-Jer Lin;Huang H.-S.; Huang H.-S.; JING-JER LIN; Guh J.-H.; Chang L.-C.; Hsieh Y.-Y.; Chen T.-C.; Yu D.-S.; Chen S.-J.; Chen C.-L.; Lee C.-C. |
| 臺大學術典藏 |
2018-09-10T15:27:37Z |
Design, synthesis and biological evaluation of tetracyclic azafluorenone derivatives with topoisomerase I inhibitory properties as potential anticancer agents
|
Chen, T.-C.;Yu, D.-S.;Chen, S.-J.;Chen, C.-L.;Lee, C.-C.;Hsieh, Y.-Y.;Chang, L.-C.;Guh, J.-H.;Lin, J.-J.;Huang, H.-S.; JIH-HWA GUH; JING-JER LIN |
| 臺大學術典藏 |
2018-09-10T15:26:46Z |
Menthols as Chiral Auxiliaries for Asymmetric Cycloadditive Oligomerization: Syntheses and Studies of β-Proline Hexamers
|
Kudryavtsev, K.V.;Ivantcova, P.M.;Muhle-Goll, C.;Churakov, A.V.;Sokolov, M.N.;Dyuba, A.V.;Arutyunyan, A.M.;Howard, J.A.K.;Yu, C.-C.;Guh, J.-H.;Zefirov, N.S.;Br\\Ase, S.; JIH-HWA GUH |
| 臺大學術典藏 |
2018-09-10T15:26:46Z |
Repurposing of nitroxoline as a potential anticancer agent against human prostate cancer - A crucial role on AMPK/mTOR signaling pathway and the interplay with Chk2 activation
|
Chang, W.-L.;Hsu, L.-C.;Leu, W.-J.;Chen, C.-S.;Guh, J.-H.; JIH-HWA GUH |
| 臺大學術典藏 |
2018-09-10T15:26:46Z |
Ring fusion strategy for synthesis and lead optimization of sulfur-substituted anthra[1,2-c[[1,2,5]thiadiazole-6,11-dione derivatives as promising scaffold of antitumor agents
|
Lee, Y.-R.;Chen, T.-C.;Lee, C.-C.;Chen, C.-L.;Ahmed Ali, A.A.;Tikhomirov, A.;Guh, J.-H.;Yu, D.-S.;Huang, H.-S.; JIH-HWA GUH |
| 臺大學術典藏 |
2018-09-10T15:26:46Z |
Structural studies and anticancer activity of a novel class of β-peptides
|
Kudryavtsev, K.V.;Yu, C.-C.;Ivantcova, P.M.;Polshakov, V.I.;Churakov, A.V.;Br\\Ase, S.;Zefirov, N.S.;Guh, J.-H.; JIH-HWA GUH |
| 臺大學術典藏 |
2018-09-10T15:26:46Z |
Tubulin-binding agents down-regulate matrix metalloproteinase-2 and -9 in human hormone-refractory prostate cancer cells - A critical role of Cdk1 in mitotic entry
|
Chang, W.-L.;Yu, C.-C.;Chen, C.-S.;Guh, J.-H.; JIH-HWA GUH |
