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Showing items 266-315 of 330  (7 Page(s) Totally)
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Institution Date Title Author
國家衛生研究院 2008-02 A novel peroxisome proliferator-activated receptor alpha/gamma agonist, BPR1H0101, inhibits topoisomerase II catalytic activity in human cancer cells Kao, YH; Hsieh, HP; Chitlimalla, SK; Pan, WY; Kuo, CC; Tsai, YC; Lin, WH; Chuang, SE; Chang, JY
臺北醫學大學 2008 Discovery of 4-Amino and 4-Hydroxy-1-Aroylindoles as Potent Tubulin Polymerization Inhibitors 劉景平; Liou JP; Wu ZY; Kuo CC; Chang CY; Lu PY; Chen CM; Hsieh HP; Chang JY
臺北醫學大學 2008 Synthesis and Structure-Activity Relationships of 2-Amino and 2-Hydroxy-1-Aroylnaphthalenes as Potent Antitubulin Agents 劉景平; Reddy GR; Kuo CC; Tan UK; Coumar MS; Chang CY; Lai MJ; Wu SY; Chang JY; Liou JP; Hsieh HP
國家衛生研究院 2007-11-15 Tamoxifen accelerates proteasomal degradation of O-6-methylguanine DNA methyltransferase in human cancer cells Kuo, CC; Liu, JF; Shiah, HS; Ma, LC; Chang, JY
國家衛生研究院 2007-11 Effects of CpG-B ODN on the protein expression profile of swine PBMC Nagarajan, G; Kuo, CC; Liang, CM; Chen, CM; Liang, SM
國家衛生研究院 2007-10 A novel oral indoline-sulfonamide agent, N-[1-(4-Methoxy-benzenesulfonyl)-2,3-dihydro-1H-indol-7-yl]-Isonicotinamide (J30), exhibits potent activity against human cancer cells in vitro and in vivo through the disruption of microtubule Liou, JP; Hsu, KS; Kuo, CC; Chang, CY; Chang, JY
國家衛生研究院 2007-09-06 4-and 5-aroylindoles as novel classes of potent antitubulin agents Liou, JP; Wu, CY; Hsieh, HP; Chang, CY; Chen, CM; Kuo, CC; Chang, JY
國立臺灣大學 2007-09 Extracellular proton-modulated pore-blocking effects of the anticonvulsant felbamate on NMDA channel. Chang, HR; Kuo, CC.
國家衛生研究院 2007-07-31 Combined modalities of resistance in an oxaliplatin-resistant human gastric cancer cell line with enhanced sensitivity to 5-fluorouracil Chen, CC; Chen, LT; Tsou, TC; Pan, WY; Kuo, CC; Liu, JF; Yeh, SC; Tsai, FY; Hsieh, HP; Chang, JY
國立臺灣大學 2007-07 Characterization of the Gating Conformational Changes in the Felbamate Binding Site in NMDA Channels. Chang, HR; Kuo, CC.
國家衛生研究院 2007-05 Involvement of heat shock protein (Hsp)90 beta but not Hsp90 alpha in antiapoptotic effect of CpG-B oligodeoxynucleotide Kuo, CC;Liang, CM;Lai, CY;Liang, SM
國立臺灣大學 2007-04 A hydrophobic element secures S4 voltage sensor in position in resting Shaker K channels. Yang, YC; Own, CJ; Kuo, CC.
國家衛生研究院 2007-02-26 Cytotoxic and novel skeleton compounds from the heartwood of Chamaecyparis obtusa var. formosana Chien, SC; Chang, JY; Kuo, CC; Hsieh, CC; Yang, NS; Kuo, YH
國家衛生研究院 2007-01 D-501036, a novel selenophene-based triheterocycle derivative, exhibits potent in vitro and in vivo antitumoral activity which involves DNA damage and ataxia telangiectasia-mutated nuclear protein kinase activation Juang, SH;Lung, CC;Hsu, PC;Hsu, KS;Li, YC;Hong, PC;Shiah, HS;Kuo, CC;Huang, CW;Wang, YC;Huang, L;Chen, TS;Chen, SF;Fu, KC;Hsu, CL;Lin, MJ;Chang, CJ;Ashendel, CL;Chan, TCK;Chou, KM;Chang, JY
臺北醫學大學 2007 4- and 5-Aroylindoles as Novel Classes of Potent Antitubulin Agents. 劉景平; Liou JP; Wu CY; Hsieh HP; Chang CY; Chen CM; Kuo CC; Chang JY
臺北醫學大學 2007 A novel oral indoline-sulfonamide agent; J30; exhibits potent activity against human cancer cells in vitro and in vivo through the disruption of microtubule. 劉景平; Liou JP; Hsu KS; Kuo CC; Chang CY; Chang JY;
國家衛生研究院 2006-11-27 C-35 terpenoids from the bark of Calocedrus macrolepis var. formosana with activity against human cancer cell lines Hsieh, CL; Tseng, MH; Shao, YY; Chang, JY; Kuo, CC; Chang, CY; Kuo, YH
國家衛生研究院 2006-11-16 7-aroyl-aminoindoline-1-sulfonamides as a novel class of potent antitubulin agents Chang, JY; Hsieh, HP; Chang, CY; Hsu, KS; Chiang, YF; Chen, CM; Kuo, CC; Liou, JP
國家衛生研究院 2006-11 Combined modalities of resistance in an oxaliplaitin-resistant human gastric cancer cell line with enhanced sensitivity Chen, LT;Chen, CC;Tsou, TC;Pan, WY;Kuo, CC;Liu, JF;Yeh, SC;Tsai, FY;Hsieh, HR;Chang, JY
國家衛生研究院 2006-11 D-501036, a novel selenophene-base triheterocycle derivative exhibits potent in vitro and in vivo anti-tumoral activity, which involves DNA-damage and ATM activation Lung, CC;Juang, SH;Hsu, PC;Hseu, KS;Li, YC;Hong, PC;Shiah, HS;Kuo, CC;Chang, CJ;Chang, JY
國家衛生研究院 2006-11 Tamoxifen induces degradation of the o6-methylguanine DNA methyltransferase protein via the ubiquitin-dependent proteosome pathway in human cancer cells Kuo, CC;Liu, JF;Chang, JY
國家衛生研究院 2006-10-19 2-amino and 2 '-aminocombretastatin derivatives as potent antimitotic agents Chang, JY; Yang, MF; Chang, CY; Chen, CM; Kuo, CC; Liou, JP
國家衛生研究院 2006-10 Structure-activity relationship studies of 3-aroylindoles as potent antimitotic agents Liou, JP;Mahindroo, N;Chang, CW;Guo, FM;Lee, SWH;Tan, UK;Yeh, TK;Kuo, CC;Chang, YW;Lu, PH;Tung, YS;Lin, KT;Chang, JY;Hsieh, HP
國立臺灣大學 2006-09 Electrophoresis of a finite cylinder positioned eccentrically along the axis of a long cylindrical pore Hsu, JP; Kuo, CC
臺大學術典藏 2006-09 Electrophoresis of a finite cylinder positioned eccentrically along the axis of a long cylindrical pore JYH-PING HSU; Kuo, CC; Jyh-Ping Hsu; Kuo, Cc
國立臺灣大學 2006-08 Electrophoresis of a toroid along the axis of a cylindrical pore Hsu, JP; Kuo, CC; Ku, MH
臺大學術典藏 2006-08 Electrophoresis of a toroid along the axis of a cylindrical pore Ku, MH; Kuo, CC; JYH-PING HSU; Jyh-Ping Hsu; Kuo, Cc; Ku, Mh
國家衛生研究院 2006-02 DNA repair enzyme, O-6-methylguanine DNA methyltransferase, modulates cytotoxicity of camptothecin-derived topoisomerase I inhibitors Kuo, CC; Liu, JF; Chang, JY
臺北醫學大學 2006 2-Amino and 2’-Aminocombretastatin Derivatives as Potential Antimitotic Agent 陳繼明; 劉景平; Chang JY; Yang MF; Chang CY; Chen CM; Kuo CC; Liou JP
臺北醫學大學 2006 7-Aroyl-aminoindoline-1-sulfonamides as a Novel Class of Potent Antitubulin Agents 劉景平; 陳繼明; Chang JY; Hsieh HP; Chang CY; Hsu KS; Chiang YF; Chen CM; Kuo CC; Liou JP*
臺北醫學大學 2006 Structure-Activity Relationship Studies of 3-Aroylindoles as Potent Antimitotic Agents 劉景平; Liou JP; Mahindroo N; Chang CW; Guo FM; Lee SW; Yeh TK; Tan UK; Kuo CC; Chang YW; Lu PH; Tung YS;
國立臺灣大學 2006 The effect of ultrasound stimulation versus bioreactors on neocartilage formation in tissue engineering scaffolds seeded with human chondrocytes in vitro. Hsu, SH; Kuo, CC; Whu, SW; Lin, CH; Tsai, CL
國立臺灣大學 2005-12 BOLD signals correlate with ensemble unit activities in rat's somatosensory cortex. Kuo, CC; Chen, JH; Tsai, CY; Liang, KC; Yen, CT
國立臺灣大學 2005-09 Comparison of anterior cingulate and primary somatosensory neuronal responses to noxious laser-heat stimuli in conscious, behaving rats. Kuo, CC; Yen, CT
國立臺灣大學 2005-05 An inactivation stabilizer of the Na+ channel acts as an opportunistic pore blocker modulated by external Na+. Yang, YC; Kuo, CC.
國家衛生研究院 2005-02 Cytotoxic triterpenes from the aerial roots of Ficus microcarpa Chiang, YM; Chang, JY; Kuo, CC; Chang, CY; Kuo, YH
國家衛生研究院 2005-01 Four new 6-Nor-5(6 →7)abeo-abietane type diterpenes and antitumoral cytotoxic diterpene constituents from the bark of Taiwania cryptomerioides Chang, CI; Chang, JY; Kuo, CC; Pan, WY; Kuo, YH
臺北醫學大學 2005 Establishment of Taiwan hospital emergency incident comman system (T-HEICS). 邱文達; Kuo CC;Chiu WT;Tsai SH;
臺北醫學大學 2005 Establishment of Taiwan hospital emergency incident comman system (T-HEICS). 邱文達; Kuo CC;Chiu WT;Tsai SH;
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
國立臺灣大學 2004-08 Differential morphine effects on short- and long-latency laser-evoked cortical responses in the rat. Tsai, ML; Kuo, CC; Sun, WZ; Yen, CT
國家衛生研究院 2004-07-15 A novel bis-benzylidenecyclopentanone derivative, BPR0Y007, inducing a rapid caspase activation involving upregulation of Fas (CD95/APO-1) and wild-type p53 in human oral epidermoid carcinoma cells Juang, SH; Pan, WY; Kuo, CC; Liou, JP; Hung, YM; Chen, LT; Hsieh, HP; Chang, JY
國家衛生研究院 2004-07-01 BPR0L075, a novel synthetic indole compound with antimitotic activity in human cancer cells, exerts effective antitumoral activity in vivo Kuo, CC; Hsieh, HP; Pan, WY; Chen, CP; Lion, JP; Lee, SJ; Chang, YL; Chen, LT; Chen, CT; Chang, JY
國家衛生研究院 2004-07 Drug design for BPR0L075 as an anticancer agent Hsieh, HP;Liou, JP;W., CC;Kuo, CC;Chang, YL;Kuo, FM;Tseng, HY;Pan, WY;Chen, CP;Yang, YN;Chen, CT;Lee, SJ;Chang, JY
國立臺灣大學 2004-07 Block of tetrodotoxin-resistant Na+ channel pore by multivalent cations: gating modification and Na+ flow dependence. Kuo, CC; Chen, WY; Yang, YC.
國家衛生研究院 2004-02 Surfection: a new platform for transfected cell arrays Chang, FH; Lee, CH; Chen, MT; Kuo, CC; Chiang, YL; Hang, CY; Roffler, S
國立臺灣大學 2004-02 Use-dependent inhibition of the N-Methyl-D-aspartate currents by felbamate: a gating modifier with selective binding to the desensitized channels. Kuo, CC; Lin, BJ; Chang, HR; Hsieh, CP.
國家衛生研究院 2004-01-01 Salvinal, a novel microtubule inhibitor isolated from Salvia miltiorrhizae Bunge (Danshen), with antimitotic activity in multidrug-sensitive and -resistant human tumor cells Chang, JY; Chang, CY; Kuo, CC; Chen, LT; Wein, YS; Kuo, YH
國家衛生研究院 2004-01 Three new oleanane-type triterpenes from Ludwigia octovalvis with cytotoxic activity against two human cancer cell lines Chang, CI; Kuo, CC; Chang, JY; Kuo, YH
高雄醫學大學 2004 Salvinal; a novel microtubule inhibitor isolated from Salvia miltiorrhizae Bunge (Danshen); with antimitotic activity in multidrug-sensitive and -resistant human tumor cells.  張俊彥;陳立宗; Chang JY;Chang CY;Kuo CC;Chen LT;Wein YS;Kuo YH. 

Showing items 266-315 of 330  (7 Page(s) Totally)
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