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教育部委託研究計畫      計畫執行:國立臺灣大學圖書館
 
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機構 日期 題名 作者
國家衛生研究院 2008-12-25 Synthesis and structure-activity relationships of 2-amino-1-aroylnaphthalene and 2-hydroxy-1-aroylnaphthalenes as potent antitubulin agents Reddy, GR;Kuo, CC;Tan, UK;Coumar, MS;Chang, CY;Chiang, YK;Lai, MJ;Yeh, JY;Wu, SY;Chang, JY;Liou, JP;Hsieh, HP
國立臺灣大學 2008-12 Highly-Aligned Electrospun Luminescent Nanofibers Prepared from Polyfluorene/PMMA Blends: Fabrication, Morphology, Photophysical Properties and Sensory Applications Kuo, CC; Wang, CT; Chen, WC
國家衛生研究院 2008-08 Transcriptional repression of O-6-methylguanine DNA methyltransferase gene rendering cells hypersensitive to N,N '-bis(2-chloroethyl)-N-nitrosurea in camptothecin-resistant cells Ma, LC; Kuo, CC; Liu, JF; Chen, LT; Chang, JY
國家衛生研究院 2008-07-24 Discovery of 4-amino and 4-hydroxy-1-aroylindoles as potent tubulin polymerization inhibitors Liou, JP; Wu, ZY; Kuo, CC; Chang, CY; Lu, PY; Chen, CM; Hsieh, HP; Chang, JY
國家衛生研究院 2008-05-01 The roles of Tyr91 and Lys162 in general acid-base catalysis in the pigeon NADP+-dependent malic enzyme Kuo, CC;Lin, KY;Hsu, YJ;Lin, SY;Lin, YT;Chang, GG;Chou, WY
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

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