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Institution Date Title Author
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.
臺大學術典藏 2019-12-05T06:26:50Z 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.;Hsien-Ching Chiu;Jee S.-H.; Sheen Y.-S.; Chu C.-Y.; Lin P.-J.; Liaw S.-H.; HSIEN-CHING CHIU; Jee S.-H.
國立臺灣大學 2007-01 Mutation of keratin 9 (R163W) in a family with epidermolytic palmoplantar keratoderma and knuckle pads. Sheen, YS; Chu, CY; Lin, PJ; Liaw, SH; Chiu, HC; Jee, SH
慈濟大學 1996 Mutation of Lysines in a Plasminogen Binding Region of Streptokinase Identifies Residues Important for Generating a Functional Activator Complex Lin, Lee-Fong;Oeun, Saravuth;Houng, Aiilyan;Reed, Guy L.
國立臺灣大學 2008 Mutation of Mitochondrial DNA G13513a Presenting with Leigh Syndrome, Wolff-Parkinson-White Syndrome and Cardiomyopathy 王緖斌; 翁妏謹; 李妮鍾; 胡務亮; 范碧娟; 李旺祚; WANG, SHI-BING; WENG, WEN-CHIN; LEE, NI-CHUNG; HWU, WUH-LIANG; FAN, PI-CHUAN; LEE, WANG-TSO
臺大學術典藏 2020-12-09T01:38:40Z Mutation of Mitochondrial DNA G13513A Presenting with Leigh Syndrome, Wolff-Parkinson-White Syndrome and Cardiomyopathy Wang S.-B.;Weng W.-C.;Ni-Chung Lee;Hwu W.-L.;Fan P.-C.;Lee W.-T.; Wang S.-B.; Weng W.-C.; NI-CHUNG LEE; Hwu W.-L.; Fan P.-C.; Lee W.-T.
臺大學術典藏 2020-12-16T02:25:55Z Mutation of Mitochondrial DNA G13513A Presenting with Leigh Syndrome, Wolff-Parkinson-White Syndrome and Cardiomyopathy Wang S.-B.;Weng W.-C.;Lee N.-C.;Wuh-Liang Hwu;Fan P.-C.;Lee W.-T.; Wang S.-B.; Weng W.-C.; Lee N.-C.; WUH-LIANG HWU; Fan P.-C.; Lee W.-T.
臺大學術典藏 2020-12-18T02:21:52Z Mutation of Mitochondrial DNA G13513A Presenting with Leigh Syndrome, Wolff-Parkinson-White Syndrome and Cardiomyopathy Wang S.-B.;Weng W.-C.;Lee N.-C.;Hwu W.-L.;Fan P.-C.;Wang-Tso Lee; Wang S.-B.; Weng W.-C.; Lee N.-C.; Hwu W.-L.; Fan P.-C.; WANG-TSO LEE
臺大學術典藏 2008 Mutation of Mitochondrial DNA G13513A Presenting with Leigh Syndrome, Wolff-Parkinson-White Syndrome and Cardiomyopathy Wang S.-B.; Weng W.-C.; Lee N.-C.; Hwu W.-L.; PI-CHUAN FAN; Lee W.-T.
臺大學術典藏 2021-01-05T06:41:17Z Mutation of Mitochondrial DNA G13513A Presenting with Leigh Syndrome, Wolff-Parkinson-White Syndrome and Cardiomyopathy Wang S.-B.;Wen-Chin Weng;Lee N.-C.;Hwu W.-L.;Fan P.-C.;Lee W.-T.; Wang S.-B.; WEN-CHIN WENG; Lee N.-C.; Hwu W.-L.; Fan P.-C.; Lee W.-T.
中山醫學大學 2000 Mutation of p53 gene codon 63 in saliva as a molecular marker for oral squamous cell carcinomas. Liao, PH; Chang, YC; Huang, MF; Tai, KW; Chou, MY
臺大學術典藏 2018-09-10T04:05:49Z Mutation of p53 gene in hepatocellular carcinoma in Taiwan Sheu, J.-C.; Sheu, J.-C.; HSUAN-SHU LEE et al.
臺大學術典藏 2018-09-10T04:04:36Z Mutation of p53 gene in hepatocellular carcinoma in Taiwan Sheu, J.-C. and Huang, G.-T. and Lee, P.-H. and Chung, J.-C. and Chou, H.-C. and Lai, M.-Y. and Wang, J.-T. and Lee, H.-S. and Shih, L.-N. and Yang, P.-M. and Wang, T.-H. and Chen, D.-S.; PO-HUANG LEE
臺大學術典藏 2021-02-02T06:41:28Z Mutation of p53 gene in Hepatocellular Carcinoma in Taiwan Sheu J.-C.; Huang G.-T.; Chung J.-C.; Chou H.-C.; Lai M.-Y.; Wang J.-T.; Lee, Hsuan-Shu; Shih L.-N.; Yang P.-M.; Wang T.-H.; Chen D.-S.
臺大學術典藏 2021-04-22T06:57:09Z Mutation of p53 gene in Hepatocellular Carcinoma in Taiwan Sheu J.-C.; Huang G.-T.; Chung J.-C.; Chou H.-C.; Lai M.-Y.; Wang J.-T.; Lee H.-S.; Shih L.-N.; PEI-MING YANG; Wang T.-H.; Chen D.-S.

Showing items 603171-603195 of 2348419  (93937 Page(s) Totally)
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