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显示项目 603171-603180 / 2348419 (共234842页)
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机构 日期 题名 作者
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

显示项目 603171-603180 / 2348419 (共234842页)
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