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公開日期
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作者
來源出版物
scopus
WOS
全文
2011
Targeting energy metabolic and oncogenic signaling pathways in triple-negative breast cancer by a novel adenosine monophosphate-activated protein kinase (AMPK) activator
Lee K.-H.; Hsu E.-C.; JIH-HWA GUH
; Yang H.-C.; Wang D.; Kulp S.K.; Shapiro C.L.; Chen C.-S.
Journal of Biological Chemistry
89
90
2014
Terfenadine induces anti-proliferative and apoptotic activities in human hormone-refractory prostate cancer through histamine receptor-independent Mcl-1 cleavage and Bak up-regulation
Wang W.-T.; Chen Y.-H.; Hsu J.-L.; Leu W.-J.; Yu C.-C.; Chan S.-H.; Ho Y.-F.; LIH-CHING HSU
; JIH-HWA GUH
Naunyn-Schmiedeberg's Archives of Pharmacology
27
25
2005
Three new taxane diterpenoids from Taxus sumatrana
Shen Y.-C.; Cheng K.-C.; Lin Y.-C.; Cheng Y.-B.; Khalil A.T.; JIH-HWA GUH
; Chien C.-T.; Teng C.-M.; Chang Y.-T.
Journal of Natural Products
19
15
2013
Total synthesis of 14,21-diepi-squamocin-K
Liu C.-W.; Yeh T.-C.; Chen C.-H.; Yu C.-C.; Chen C.-S.; Hou D.-R.; JIH-HWA GUH
Tetrahedron
6
5
2011
Total synthesis of moniliformediquinone and calanquinone A as potent inhibitors for breast cancer
Thangaraj S.; Tsao W.-S.; Luo Y.-W.; Lee Y.-J.; Chang C.-F.; Lin C.-C.; Uang B.-J.; Yu C.-C.; JIH-HWA GUH
; Teng C.-M.
Tetrahedron
19
17
2015
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.; JIH-HWA GUH
Biochemical Pharmacology
19
19
2009
Tunicamycin induces resistance to camptothecin and etoposide in human hepatocellular carcinoma cells: Role of cell-cycle arrest and GRP78
Hsu J.-L.; Chiang P.-C.; JIH-HWA GUH
Naunyn-Schmiedeberg's Archives of Pharmacology
34
30
2004
Two new cytotoxic clerodane diterpenoids from Casearia membranacea
Shen Y.-C.; Wang L.-T.; Wang C.-H.; Khalil A.T.; JIH-HWA GUH
Chemical and Pharmaceutical Bulletin
35
35
2005
Two new sesquiterpene lactones from Ixeris chinensis
Khalil A.T.; Shen Y.-C.; JIH-HWA GUH
; Cheng S.-Y.
Chemical and Pharmaceutical Bulletin
16
14
2014
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.; LIH-CHING HSU
; Ho Y.-F.; Huang H.-S.; JIH-HWA GUH
Naunyn-Schmiedeberg's Archives of Pharmacology
13
12
2011
A unique P-glycoprotein interacting agent displays anticancer activity against hepatocellular carcinoma through inhibition of GRP78 and mTOR pathways
Kuo T.-C.; Chiang P.-C.; Yu C.-C.; Nakagawa-Goto K.; Bastow K.F.; Lee K.-H.; JIH-HWA GUH
Biochemical Pharmacology
18
15
2011
WJ9708012 exerts anticancer activity through PKC-α related crosstalk of mitochondrial and endoplasmic reticulum stresses in human hormone-refractory prostate cancer cells
Kuo T.-C.; Huang W.-J.; JIH-HWA GUH
Acta Pharmacologica Sinica
8
7
2008
WRC-213, an l-methionine-conjugated mitoxantrone derivative, displays anticancer activity with reduced cardiotoxicity and drug resistance: Identification of topoisomerase II inhibition and apoptotic machinery in prostate cancers
Hsiao C.-J.; TSAI-KUN LI
; Chan Y.-L.; LING-WEI HSIN
; Liao C.-H.; Lee C.-H.; Lyu P.-C.; JIH-HWA GUH
Biochemical Pharmacology
35
32
2005
YC-1 [3-(5′-hydroxymethyl-2′-furyl)-1-benzyl indazole] exhibits a novel antiproliferative effect and arrests the cell cycle in G 0-G1 in human hepatocellular carcinoma cells
Wang S.-W.; Pan S.-L.; JIH-HWA GUH
; Chen H.-L.; Huang D.-M.; Chang Y.-L.; Kuo S.-C.; Lee F.-Y.; Teng C.-M.
Journal of Pharmacology and Experimental Therapeutics
47
47
2005
YC-1 [3-(5′-hydroxymethyl-2′-furyl)-1-benzyl indazole] inhibits endothelial cell functions induced by angiogenic factors in vitro and angiogenesis in vivo models
Pan S.-L.; JIH-HWA GUH
; Peng C.-Y.; Wang S.-W.; Chang Y.-L.; Cheng F.-C.; Chang J.-H.; Kuo S.-C.; Lee F.-Y.; Teng C.-M.
Journal of Pharmacology and Experimental Therapeutics
55
53
2006
YC-1 [3-(5′-hydroxymethyl-2′-furyl)-1-benzyl indazole] inhibits neointima formation in balloon-injured rat carotid through suppression of expressions and activities of matrix metalloproteinases 2 and 9
Liu Y.-N.; Pan S.-L.; Peng C.-Y.; JIH-HWA GUH
; Huang D.-M.; Chang Y.-L.; Lin C.-H.; Pai H.-C.; Kuo S.-C.; Lee F.-Y.; Teng C.-M.
Journal of Pharmacology and Experimental Therapeutics
39
33
2008
YC-1 induces apoptosis of human renal carcinoma A498 cells in vitro and in vivo through activation of the JNK pathway
Wu S.Y.; Pan S.L.; Chen T.H.; Liao C.H.; Huang D.Y.; JIH-HWA GUH
; Chang Y.L.; Kuo S.C.; Lee F.Y.; Teng C.M.
British Journal of Pharmacology
25
25
2008
YC-1 induces heat shock protein 70 expression and prevents oxidized LDL-mediated apoptosis in vascular smooth muscle cells
Liu Y.-N.; Pan S.-L.; Peng C.-Y.; Huang D.-Y.; JIH-HWA GUH
; Kuo S.-C.; Lee F.-Y.; Teng C.-M.
Shock
12
10
2007
YC-1 inhibits HIF-1 expression in prostate cancer cells: Contribution of Akt/NF-κB signaling to HIF-1α accumulation during hypoxia
Sun H.-L.; Liu Y.-N.; Huang Y.-T.; Pan S.-L.; Huang D.-Y.; JIH-HWA GUH
; Lee F.-Y.; Kuo S.-C.; Teng C.-M.
Oncogene
162
158
2004
YC-1 prevents sodium nitroprusside-mediated apoptosis in vascular smooth muscle cells
Pan S.L.; JIH-HWA GUH
; Chang Y.L.; Kuo S.C.; Lee F.Y.; Teng C.M.
Cardiovascular Research
36
32