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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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顯示項目 602801-602825 / 2347236 (共93890頁)
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機構 日期 題名 作者
臺大學術典藏 2018-09-10T15:18:46Z Mutation genotypes of RNF213 gene from moyamoya patients in Taiwan Lee, M.-J. and Chen, Y.-F. and Fan, P.-C. and Wang, K.-C. and Wang, K. and Wang, J. and Kuo, M.-F.; Lee, Ming-Jen;Chen, Ya-Fang;Fan, Pi-Chuan;Wang, Kuo-Chuan;Wang, Kai;Wang, Jinyuan;Kuo, Meng-Fai; 陳雅芳;范碧娟;郭夢菲;李銘仁;王國川; MENG-FAI KUO; Lee, Ming-Jen; Chen, Ya-Fang; KUOCHUAN WANG; PI-CHUAN FAN; Fan, Pi-Chuan; YA-FANG CHEN; Wang, Kuo-Chuan; Wang, Kai; Wang, Jinyuan
臺大學術典藏 2020-03-03T02:33:27Z Mutation genotypes of RNF213 gene from moyamoya patients in Taiwan MING-JEN LEE; Chen Y.-F.; Fan P.-C.; Wang K.-C.; Wang K.; Wang J.; Kuo M.-F.
臺大學術典藏 2015 Mutation genotypes of RNF213 gene from moyamoya patients in Taiwan Kuo M.-F.; Wang K.; Wang J.; KUOCHUAN WANG; Fan P.-C.; Chen Y.-F.; Lee M.-J.; Lee M.-J.;Chen Y.-F.;Fan P.-C.;Kuochuan Wang;Wang K.;Wang J.;Kuo M.-F.
臺大學術典藏 2020-12-21T01:58:19Z Mutation genotypes of RNF213 gene from moyamoya patients in Taiwan Kuo M.-F.; Wang J.; Wang K.; Wang K.-C.; PI-CHUAN FAN; Chen Y.-F.; Lee M.-J.; Lee M.-J.;Chen Y.-F.;Pi-Chuan Fan;Wang K.-C.;Wang K.;Wang J.;Kuo M.-F.
臺大學術典藏 2020-01-03T06:13:22Z Mutation in cyl operon alters hemolytic phenotypes of Streptococcus agalactiae Chou C.C.;Lin M.C.;Su F.J.;Chen M.M.; Chou C.C.; Lin M.C.; Su F.J.; Chen M.M.; CHIN-CHENG CHOU
臺大學術典藏 2020-01-03T06:13:52Z Mutation in cyl operon alters hemolytic phenotypes of Streptococcus agalactiae Chou C.C.;Lin M.C.;Su F.J.;Chen M.M.; Chou C.C.; Lin M.C.; Su F.J.; Chen M.M.; MEEI-MEI CHEN
國家衛生研究院 2004-09 Mutation in enterovirus 71 capsid protein VP1 confers resistance to the inhibitory effects of pyridyl imidazolidinone Shih, SR; Tsai, MC; Tseng, SN; Won, KF; Shia, KS; Li, WT; Chern, JH; Chen, GW; Lee, CC; Lee, YC; Peng, KC; Chao, YS
中國醫藥大學 2002.03 Mutation in the FGFR2 gene in a Taiwanese patient with Beare-Stevenson cutis gyrata syndrome (Wang TJ); (Huang CB); 蔡輔仁(Fuu-Jen Tsai); 鄔哲源; (Lai RB); (Hsiao M)
中國醫藥大學 2002.03 Mutation in the FGFR2 gene in a Taiwanese patient with Beare-Stevenson cutis gyrata syndrome (Wang TJ); (Huang CB); 蔡輔仁(Fuu-Jen Tsai); 鄔哲源; (Lai RB); (Hsiao M)
中國醫藥大學 2002 Mutation in the FGFR2 gene in a Taiwanese patient with Beare-Stevenson cutis gyrata syndrome Wang, TJ; Huang, CB; Tsai, FJ; Wu, JY; Lai, RB; Hsiao, M
中國醫藥大學 2002 Mutation in the FGFR2 gene in a Taiwanese patient with Beare-Stevenson cutis gyrata syndrome Wang, TJ; Huang, CB; Tsai, FJ; Wu, JY; Lai, RB; Hsiao, M
國家衛生研究院 2005-05-15 Mutation in the tyrosine kinase domain of epidermal growth factor receptor is a predictive and prognostic factor for gefitinib treatment in patients with non-small cell lung cancer Chou, TY; Chiu, CH; Li, LH; Hsiao, CY; Tzen, CY; Chang, KT; Chen, YM; Perng, RP; Tsai, SF; Tsai, CM
國家衛生研究院 2005-06 Mutation in the tyrosine kinase domain of epidermal growth factor receptor is a predictive and prognostic factor for gefitinib treatment in patients with non-small cell lung cancer Tsai, CM;Chiu, CH;Chou, TY;Li, LH;Hsiao, CY;Chen, M;Perng, RP;Tsai, SF
國立臺灣大學 2007-07 Mutation of a key residue in the T2SS ATPase uncouples ATP hydrolysis from protein translocation Shiue, S.-J.; Chien, I.-L.; Chan, N.-L.; Leu, W.-M.; Hu, N.-T
國立臺灣大學 2000 Mutation of Arabidopsis Plastid Phosphoglucose Isomerase Affects Leaf Starch Synthesis and Floral Initiation Yu, Tien-Shin; Lue, Wei-Ling; Wang, Shue-Mei; Chen, Jychian
國家衛生研究院 2009-09 Mutation of epidermal growth factor receptor is associated with MIG6 expression Nagashima, T;Ushikoshi-Nakayama, R;Suenaga, A;Ide, K;Yumoto, N;Naruo, Y;Takahashi, K;Saeki, Y;Taiji, M;Tanaka, H;Tsai, SF;Hatakeyama, M
國家衛生研究院 2009-09 Mutation of epidermal growth factor receptor is associated with MIG6 expression Nagashima, T;Ushikoshi-Nakayama, R;Suenaga, A;Ide, K;Yumoto, N;Naruo, Y;Takahashi, K;Saeki, Y;Taiji, M;Tanaka, H;Tsai, SF;Hatakeyama, M
國立成功大學 2008-04 Mutation of human plasminogen kringle 1-5 enhances anti-angiogenic action via increased interaction with integrin alpha(v)beta(3) Chang, Po-Chiao; Chang, Yu-Jia; Wu, Hua-Lin; Chang, Chin-Wei; Lin, Chung-I; Wang, Wei-Chih; Shi, Guey-Yueh
國立交通大學 2014-12-08T15:38:03Z Mutation of isoleucine 705 of the oxidosqualene-lanosterol cyclase from Saccharomyces cerevisiae affects lanosterol's C/D-ring cyclization and 17 alpha/beta-exocyclic side chain stereochemistry Wu, Tung-Kung; Chang, Yi-Chun; Liu, Yuan-Ting; Chang, Cheng-Hsiang; Wen, Hao-Yu; Li, Wen-Hsuan; Shie, Wen-Shiang
中國醫藥大學 2003 Mutation of IVS2-12A/C > G in combination with 707-714delGAGACTAC in the CYP21 gene is caused by deletion of the C4-CYP21 repeat module with steroid 21-hydroxylase deficiency Lee, HH; Chang, SF; Tsai, FJ; Tsai, LP; Lin, CY
中國醫藥大學 2003.06 Mutation of IVS2-12A/C > G in combination with 707-714delGAGACTAC in the CYP21 gene is caused by deletion of the C4-CYP21 repeat module with steroid 21-hydroxylase deficiency. (Lee HH); (Chang SF); 蔡輔仁(Fuu-Jen Tsai); (Tsai LP); (Lin CY)
中國醫藥大學 2003.06 Mutation of IVS2-12A/C > G in combination with 707-714delGAGACTAC in the CYP21 gene is caused by deletion of the C4-CYP21 repeat module with steroid 21-hydroxylase deficiency. (Lee HH); (Chang SF); 蔡輔仁(Fuu-Jen Tsai); (Tsai LP); (Lin CY)
臺北醫學大學 2003 Mutation of IVS2-12A/C>G together with 707-714delGAGACTAC in the CYP21 gene is caused by deletion of the C4-CYP21 repeat module with steroid 21-hydroxylase deficiency 張淑芬; Hsien-Hsiung Lee; Shwu-Fen Chang; Fuu-Jen Tsai; Li-Ping Tsai; Ching-Yu Lin
臺大學術典藏 2018-09-10T06:41:55Z Mutation of keratin 9 (R163W) in a family with epidermolytic palmoplantar keratoderma and knuckle pads Sheen, Y.-S.;Chu, C.-Y.;Lin, P.-J.;Liaw, S.-H.;Chiu, H.-C.;Jee, S.-H.; HSIEN-CHING CHIU; SHIOU-HWA JEE; CHIA-YU CHU; Yi-Shuan Sheen
臺大學術典藏 2019-12-04T08:44:13Z Mutation of keratin 9 (R163W) in a family with epidermolytic palmoplantar keratoderma and knuckle pads Sheen Y.-S.;Chia-Yu Chu;Lin P.-J.;Liaw S.-H.;Chiu H.-C.;Jee S.-H.; Sheen Y.-S.; CHIA-YU CHU; Lin P.-J.; Liaw S.-H.; Chiu H.-C.; Jee S.-H.

顯示項目 602801-602825 / 2347236 (共93890頁)
<< < 24108 24109 24110 24111 24112 24113 24114 24115 24116 24117 > >>
每頁顯示[10|25|50]項目