| 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. |
| 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. |
