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显示项目 603071-603095 / 2348419 (共93937页)
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机构 日期 题名 作者
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 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

显示项目 603071-603095 / 2348419 (共93937页)
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每页显示[10|25|50]项目