| 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 |
2020-09-23T08:35:47Z |
Mutation genotypes of RNF213 gene from moyamoya patients in Taiwan
|
Lee M.-J.; YA-FANG CHEN; Fan P.-C.; Wang K.-C.; 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 |
