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Institution Date Title Author
國立交通大學 2014-12-08T15:23:48Z "Mutated Thermostable Direct Hemolysin from Grimontia hollisae Affects Its Hemolytic Activity, Membrane Binding, and Protein Quaternary Structure" Wu, Tung-Kung; Huang, Wan-Ting
國立成功大學 2021-03-26 Mutant glucocorticoid receptor binding elements on the interleukin-6 promoter regulate dexamethasone effects Chang;Wen-Teng;Hong;Ming-Yuan;Chen;Chien-Liang;Hwang;Chi-Yuan;Tsai;Cheng-Chieh;Chuang;Chia-Chang
國立成功大學 2016-05-01 Mutant Interferon-gamma receptor 1 lacking cytoplasmic domain may transduces signals leading to mycobacterial susceptibility Shieh, Chi-Chang K.; Chiu, Darren Jianjhih; Chiang, Kuo-Ming; Yen, C-L
輔英科技大學 2002-10-01 Mutant K-ras oncogene regulates steroidogenesis of normal human adrenocortical cells by the RAF-MEK-MAPK pathway. C-H Wu;Y-F Chen;J-Y Wang; M-C Hsieh;C-S Yeh;S-T Lian;S-J Shin;S-R Lin
國立成功大學 2003-06 Mutant K-ras2 in serum Andreyev, H. J. N.; Benamouzig, R.; Beranek, M.; Clarke, P.; Cunningham, D.; Norman, A. R.; Giaretti, W.; De Goeij, A. F. P. M.; Iacopetta, B. J.; Jullian, E.; Krtolica, K.; Lee, J. Q.; Wang, Shan-Tair; Lees, N.; Al-Mulla, F.; Muller, O.; Pauly, M.; Pricolo, V.; Russo, A.; Troungos, C.; Urosevic, N.; Ward, R.
國家衛生研究院 2017-09 Mutant KIT translocates into the nucleus and induces NFKBIB expression that leads to KIT expression in imatinib-resistant gastrointestinal stromal tumors Hsueh, YS;Chang, HH;Shan, YS;Sun, HS;Fletcher, JA;Li, CF;Chen, LT
國立成功大學 2018 Mutant KRAS promotes liver metastasis of colorectal cancer, in part, by upregulating the MEK-Sp1-DNMT1-miR-137-YB-1-IGF-IR signaling pathway Chu, P.-C.;Lin, P.-C.;Wu, H.-Y.;Lin, K.-T.;Wu, C.;Bekaii-Saab, T.;Lin, Y.-J.;Lee, C.-T.;Lee, J.-C.;Chen, Chen C.-S.
國家衛生研究院 2018-11-22 Mutant Kras-induced upregulation of CD24 enhances prostate cancer stemness and bone metastasis Weng, CC;Ding, PY;Liu, YH;Hawse, JR;Subramaniam, M;Wu, CC;Lin, YC;Chen, CY;Hung, WC;Cheng, KH
臺大學術典藏 2019-05-03T07:57:40Z Mutant p53 amplifies a dynamin-1/APPL1 endosome feedback loop that regulates recycling and migration Ping-Hung Chen; PING-HUNG CHEN
臺大學術典藏 2019-08-20T06:57:10Z Mutant p53 amplifies a dynamin-1/APPL1 endosome feedback loop that regulates recycling and migration Mettlen, Marcel; Grossman, Heather M; Schmid, Sandra L; PING-HUNG CHEN; Lakoduk, Ashley M;Roudot, Philippe;Mettlen, Marcel;Grossman, Heather M;Schmid, Sandra L;Ping-Hung Chen; Lakoduk, Ashley M; Roudot, Philippe
中山醫學大學 2015 Mutant p53 confers chemoresistance in non-small cell lung cancer by upregulating Nrf2 Tung, M.-C.;Lin, P.-L.;Wang, Y.-C.;He, T.-Y.;Lee, M.-C.;Yeh, S.-D.;Chen, Chen C.-Y.;Lee, H.
國立成功大學 2022 Mutant Prevention Concentrations of Ciprofloxacin and Levofloxacin and Target Gene Mutations of Fluoroquinolones in Elizabethkingia anophelis Lin, I.-F.;Lai, C.-H.;Lin, S.-Y.;Lee, C.-C.;Lee, N.-Y.;Liu, P.-Y.;Yang, C.-H.;Huang, Y.-H.;Lin, J.-N.
臺北醫學大學 2014 Mutants TP53 p.R273H and p.R273C but not p.R273G Enhance Cancer Cell Malignancy Li, J;Yang, L;Gaur, S;Zhang, K;Wu, X;Yuan, YC;Li, H;Hu, S;Weng, Y;Yen, Y
國立交通大學 2020-07-01T05:22:08Z Mutated Human P-Selectin Glycoprotein Ligand-1 and Viral Protein-1 of Enterovirus 71 Interactions on Au Nanoplasmonic Substrate for Specific Recognition by Surface-Enhanced Raman Spectroscopy Sivashanmugan, Kundan; Lee, Han; Liao, Jiunn-Der; Wang, Chen-Chu; Lin, Chen-Hsueh; Yang, Yuh-Shyong; Sitjar, Jaya
國立成功大學 2020-04 Mutated Human P-Selectin Glycoprotein Ligand-1 and Viral Protein-1 of Enterovirus 71 Interactions on Au Nanoplasmonic Substrate for Specific Recognition by Surface-Enhanced Raman Spectroscopy Sivashanmugan;Kundan;Lee;Han;Liao;Jiunn-Der;Wang;Chen-Chu;Lin;Chen-Hsueh;Yang;Yuh-Shyong;Sitjar;Jaya
國立交通大學 2019-04-02T05:58:12Z Mutated Thermostable Direct Hemolysin from Grimontia hollisae Affects Its Hemolytic Activity, Membrane Binding, and Protein Quaternary Structure Wu, Tung-Kung; Huang, Wan-Ting
國立成功大學 2007-01 Mutation analyses of COL7A1 gene in three Taiwanese patients with severe recessive dystrophic epidermolysis bullosa Chao, Sheau-Chiou; Lee, Julia Yu-Yun
國立臺灣大學 2010 Mutation Analysis and Characterization of Alternative Splice Variants of the Wilson Disease Gene Atp7b 萬磊; 蔡長海; 許欽木; 黃錦章; 楊智超; 廖秋菊; 吳錦景; 許妤安; 李正淳; 劉素卿; 林瑋德; 蔡輔仁; WAN, LEI; TSAI, CHANG-HAI; HSU, CHIN-MOO; HUANG, CHIN-CHANG; YANG, CHIH-CHAO; LIAO, CHIU-CHU; WU, CHIN-CHING; HSU, YU-AN; LEE, CHENG-CHUN; LIU, SU-CHING; LIN, WEI-DE; TSAI, FUU-JEN
中國醫藥大學 2010-11 Mutation analysis and characterization of alternative splice variants of the Wilson disease gene ATP7B 萬磊(Lei Wan); 蔡長海(Chang-Hai Tsai); 許欽木(Chin-Moo Hsu); (Chin-Chang Huang); (Chih-Chao Yang); 廖秋菊(Chiu-Chu Liao); 吳錦景(Chin-Ching Wu); (Yu-An Hsu); 李正淳(Cheng-Chun Lee); 劉素卿(Su-Ching Liu); 林瑋德(Wei-De Lin); 蔡輔仁(Fuu-Jen Tsai)*
臺大學術典藏 2018-09-10T08:05:14Z Mutation analysis and characterization of alternative splice variants of the Wilson disease gene ATP7B Wan, L.;Tsai, C.-H.;Hsu, C.-M.;Huang, C.-C.;Yang, C.-C.;Liao, C.-C.;Wu, C.-C.;Hsu, Y.-A.;Lee, C.-C.;Liu, S.-C.;Lin, W.-D.;Tsai, F.-J.; Chih-Chao Yang
亞洲大學 2010-11 Mutation analysis and characterization of alternative splice variants of the Wilson disease gene ATP7B. 萬磊;Wan, Lei;Tsai, FJ
中國醫藥大學 1998 Mutation analysis in fibroblast growth factor receptor genes: Chinese data Lin, SP; Tsai, FJ; Wu, JY; Peng, CT; Tsai, CH
國立成功大學 2001-06 Mutation analysis in the family of a Taiwanese boy with with epidermolysis bullosa simplex Dowling-Meara Ning, C. C.; Chao, Sheau-Chiou; Uitto, J; Shieh, C. C.; Lee, Julia Yu-Yun
亞洲大學 2001-12 Mutation analysis of a family with hereditary hemorrhagic telangiectasia associated with hepatic arteriovenous malformation Wei-De Lin;Wu,Jer-Yuarn;Tsai,Fuu-Jen;Lee,Chun-Cheng;Chang-Hai Tsai
中國醫藥大學 2001-12 Mutation analysis of a family with hereditary hemorrhagic telangiectasia associated with hepatic arteriovenous malformation 林瑋德(Wei-De Lin); 鄔哲源(Wu,Jer-Yuarn); 徐秀寶; 蔡輔仁(Tsai,Fuu-Jen)*; 李正淳(Lee,Chun-Cheng); 蔡長海
中國醫藥大學 2001 Mutation analysis of a family with hereditary hemorrhagic telangiectasia associated with hepatic arteriovenous malformation Lin, WD; Wu, JY; Hsu, HB; Tsai, FJ; Lee, CC; Tsai, CH
中國醫藥大學 2001 Mutation analysis of a family with hereditary hemorrhagic telangiectasia associated with hepatic arteriovenous malformation Lin, WD; Wu, JY; Hsu, HB; Tsai, FJ; Lee, CC; Tsai, CH
國家衛生研究院 2008-02 Mutation analysis of adenosine A2a receptor gene and interaction study with dopamine D2 receptor gene in schizophrenia Luu, SU; Liao, HM; Hung, TW; Liu, BY; Cheng, MC; Liao, DL; Chen, SJ; Chen, CH
臺北醫學大學 2005 MUTATION ANALYSIS OF ANDROGEN RECEPTOR GENE IN TAIWAN PROSTATE CANCER PATIENTS 陳冠州; Chen KC; Cheng CJ; Yan JH; Peng CC; Chiang HS; Hsieh HM
國立成功大學 2002-04 Mutation analysis of ATP2CI gene in Taiwanese patients with Hailey-Hailey disease Chao, Sheau-Chiou; Tsai, Ya-Ming; Yang, Mei-Hui
義守大學 2000-04 Mutation analysis of BCL 10 in acute myeloid leukaemia Liu Ta-Chih;Lin Pai-Mei;Chang Jan-Gowth;Lee Jing-Ping;Chen Tyen-Po;Sue Yu-Chieh;Lin Sheng-Fung
中國醫藥大學 2000 Mutation analysis of BCL 10 in acute myeloid leukaemia Liu, TC; Lin, PM; Chang, JG; Lee, JP; Chen, TP; Sue, YC; Lin, SF
中國醫藥大學 1998 Mutation analysis of Chinese patients with Wilson disease Tsai, FJ; Wu, JY; Chang, JG; Lin, SP; Peng, CT; Tsai, CH
中國醫藥大學 2001 Mutation analysis of Crouzon syndrome and identification of one novel mutation in Taiwanese patients Tsai, FJ; Yang, CF; Wu, JY; Tsai, CH; Lee, CC
中國醫藥大學 2001 Mutation analysis of Crouzon syndrome and identification of one novel mutation in Taiwanese patients Tsai, FJ; Yang, CF; Wu, JY; Tsai, CH; Lee, CC
亞洲大學 2006-02 Mutation Analysis of Crouzon Syndrome in Taiwanese Patients Chin-Ping Chang;Lei Wan;Chang-Hai Tsai;Cheng-Chun Lee;Fuu-Jen Tsai
中國醫藥大學 2006-02 Mutation Analysis of Crouzon Syndrome in Taiwanese Patients 張金萍(Chin-Ping Chang);萬磊(Lei Wan);蔡長海(Chang-Hai Tsai);(Cheng-Chun Lee);蔡輔仁(Fuu-Jen Tsai)*
中國醫藥大學 2003 Mutation analysis of CTNNB1 (beta-catenin) and AXINI, the components of Wnt pathway, in cervical carcinomas Su, TH; Chang, JG; Yeh, KT; Lin, TH; Lee, TP; Chen, JC; Lin, CC
中國醫藥大學 2003 Mutation analysis of CTNNB1 (beta-catenin) and AXINI, the components of Wnt pathway, in cervical carcinomas Su, TH; Chang, JG; Yeh, KT; Lin, TH; Lee, TP; Chen, JC; Lin, CC
國家衛生研究院 2006-10 Mutation analysis of DARPP-32 as a candidate gene for schizophrenia Li, CH; Liao, HM; Hung, TW; Chen, CH
臺大學術典藏 2020-03-05T03:20:31Z Mutation analysis of endothelin-B receptor gene in patients with Hirschsprung disease in Taiwan Lin Y.-C.;Lai H.-S.;Wen-Ming Hsu;Lee P.-I.;Chen H.-L.;Chang M.-H.; Lin Y.-C.; Lai H.-S.; WEN-MING HSU; Lee P.-I.; Chen H.-L.; Chang M.-H.
國立臺灣大學 2008 Mutation Analysis of Endothelin-B Receptor Gene in Patients with Hirschsprung Disease in Taiwan 林裕誠; 賴鴻緒; 許文明; 李秉穎; 陳慧玲; 張美惠; LIN, YU-CHENG; LAI, HONG-SHIEE; HSU, WEN- MING; LEE, PING-ING; CHEN, HUEY-LING; CHANG, MEI-HWEI
臺大學術典藏 2018-09-10T07:10:02Z Mutation analysis of endothelin-B receptor gene in patients with Hirschsprung disease in Taiwan Lin, Y.-C. and Lai, H.-S. and Hsu, W.-M. and Lee, P.-I. and Chen, H.-L. and Chang, M.-H.; 林裕誠;賴鴻緒;許文明;李秉穎;陳慧玲;張美惠; LIN, YU-CHENG;LAI, HONG-SHIEE;HSU, WEN- MING;LEE, PING-ING;CHEN, HUEY-LING;CHANG, MEI-HWEI; PING-ING LEE; WEN-MING HSU; MEI-HWEI CHANG; HONG-SHIEE LAI; LIN, YU-CHENG; LAI, HONG-SHIEE; HSU, WEN- MING; LEE, PING-ING; CHEN, HUEY-LING; CHANG, MEI-HWEI
臺大學術典藏 2020-02-24T05:13:25Z Mutation analysis of endothelin-B receptor gene in patients with Hirschsprung disease in Taiwan Lin Y.-C.; HONG-SHIEE LAI; Hsu W.-M.; Lee P.-I.; Chen H.-L.; Chang M.-H.
臺大學術典藏 2020-03-10T03:30:32Z Mutation analysis of endothelin-B receptor gene in patients with Hirschsprung disease in Taiwan Hsu W.-M.; Lee P.-I.; HUEY-LING CHEN; Chang M.-H.; Lai H.-S.; Lin Y.-C.; Chang M.-H.;HUEY-LING CHEN;Lee P.-I.;Hsu W.-M.;Lai H.-S.;Lin Y.-C.
臺大學術典藏 2021-01-04T07:36:07Z Mutation analysis of endothelin-B receptor gene in patients with Hirschsprung disease in Taiwan Chen H.-L.; MEI-HWEI CHANG; Lee P.-I.; Hsu W.-M.; Lin Y.-C.; Lai H.-S.
臺大學術典藏 2008 Mutation analysis of endothelin-B receptor gene in patients with Hirschsprung disease in Taiwan Lin Y.-C.;Lai H.-S.;Hsu W.-M.;Ping-Ing Lee;Chen H.-L.;Chang M.-H.; Lin Y.-C.; Lai H.-S.; Hsu W.-M.; PING-ING LEE; Chen H.-L.; Chang M.-H.
國立臺灣大學 2006 Mutation Analysis of Gaucher Disease Patients in Taiwan: High Prevalence of the Recncii and L444p Mutations 許欽木; 蔡長梅; 李正淳; 胡務亮; 蔡輔仁; HSU, CHIN-MOO; TSAI, C-H; LEE, CHENG-CHUN; HWU, WUH-LIANG; TSAI, FUU-JEN
中國醫藥大學 2006-05 Mutation analysis of Gaucher disease patients in Taiwan: high prevalence of the RecNciI and L444P mutations 萬磊(Lei Wan); 許欽木(Hsu CM); 蔡長海; 李正淳(Lee,Chun-Cheng); 胡務亮(Hwu WL); 蔡輔仁(Tsai,Fuu-Jen)*
臺大學術典藏 2020-12-16T02:26:04Z Mutation analysis of Gaucher disease patients in Taiwan: High prevalence of the RecNciI and L444P mutations Wan L.;Hsu C.-M.;Tsai C.-H.;Lee C.-C.;Wuh-Liang Hwu;Tsai F.-J.; Wan L.; Hsu C.-M.; Tsai C.-H.; Lee C.-C.; WUH-LIANG HWU; Tsai F.-J.

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