| 中國醫藥大學 |
2000 |
Mutation analysis of type 2 Gaucher disease in Taiwan Chinese and identification of two novel mutations.
|
Tsai, FJ; Wu, JY; Lin, SP; Chang, JG; Lee, CC; Tsai, CH |
| 中國醫藥大學 |
1998-11 |
Mutation analysis of Wilson disease in Taiwan and description of six new mutations
|
蔡長海(Chang-Hai Tsai)*; 蔡輔仁(Fuu-Jen Tsai); 鄔哲源; (Jang-Gowth Chang); 李正淳(Cheng-Chun Lee); (Shuan-Pei Lin); (Chi-Fan Yang); (Yuh-Jyh Jong); (Man-Chi Lo) |
| 國立成功大學 |
2003-06 |
Mutation analysis of X-linked hypohidrotic ectodermal dysplasia in a Taiwanese family
|
Chao, Sheau-Chiou; Chung, Ching-Hung; Yang, Chao-Chun; Yang, Mei-Hui; Lee, Julia Yu-Yun |
| 國立臺灣大學 |
2013 |
Mutation and Lineage Analysis of DNMT3A in BCR-ABL1-negative Chronic Myeloproliferative Neoplasms
|
Lin, Huan-Chau; Wang, Shu-Ching; Chen, Caleb Gon-Shen; Chang, Ming-Chih; Wang, Wei-Ting; Su, Nai-Wen; Cheng, Hung-I; Lin, Johnson; Chang, Yi-Fang; Hsieh, Ruey-Kuen; Chang, Chien-Chung; Hwang, Yuchi; Lim, Ken-Hong; Kuo, Yuan-Yeh; 郭遠燁 |
| 國立臺灣大學 |
2011 |
Mutation and Loss of Expression of Arid1a in Uterine Low-Grade Endometrioid Carcinoma
|
毛翠蓮; 鄭永銘; MAO, TSUI-LIEN; JENG, YUNG-MING |
| 臺大學術典藏 |
2018-09-10T08:42:59Z |
Mutation and loss of expression of ARID1A in uterine low-grade endometrioid carcinoma
|
YUNG-MING JENG; Guan, B. and Mao, T.-L. and Panuganti, P.K. and Kuhn, E. and Kurman, R.J. and Maeda, D. and Chen, E. and Jeng, Y.-M. and Wang, T.-L. and Shih, I.-M. |
| 臺大學術典藏 |
2020-03-06T08:25:18Z |
Mutation and loss of expression of ARID1A in uterine low-grade endometrioid carcinoma
|
Guan B. ;Mao T.-L. ;Panuganti P.K. ;Kuhn E. ;Kurman R.J. ;Maeda D. ;Chen E. ;Yung-Ming Jeng ;Wang T.-L. ;Shih I.-M.; Guan B.; Mao T.-L.; Panuganti P.K.; Kuhn E.; Kurman R.J.; Maeda D.; Chen E.; YUNG-MING JENG; Wang T.-L.; Shih I.-M. |
| 臺大學術典藏 |
2020-03-07T06:48:19Z |
Mutation and loss of expression of ARID1A in uterine low-grade endometrioid carcinoma
|
Wang T.-L.; Shih I.-M.; Jeng Y.-M.; Chen E.; Maeda D.; Kurman R.J.; Kuhn E.; Panuganti P.K.; TSUI-LIEN MAO; Guan B.; Guan B. ;Tsui-Lien Mao ;Panuganti P.K. ;Kuhn E. ;Kurman R.J. ;Maeda D. ;Chen E. ;Jeng Y.-M. ;Wang T.-L. ;Shih I.-M. |
| 臺大學術典藏 |
2020-03-05T12:32:52Z |
Mutation and loss of expression of ARID1A in uterine low-grade endometrioid carcinoma
|
Guan B.; TSUI-LIEN MAO; Panuganti P.K.; Kuhn E.; Kurman R.J.; Maeda D.; Chen E.; Jeng Y.-M.; Wang T.-L.; Shih I.-M. |
| 中國醫藥大學 |
2000-03 |
Mutation and recombination in the upstream homology box-flanked ospE-related genes of the Lyme disease spirochetes result in the development of new antigenic variants during infection
|
宋賢穎(Shian-Ying Sung)*; (McDowell, J. V.); (Carlyon, J. A.); (Marconi, R. T.)* |
| 國立交通大學 |
2014-12-08T15:45:41Z |
Mutation at non-cysteine positions eliminates the oxidation/reduction effect on the activity of phenol sulfotransferase.
|
Yang, YS |
| 國立交通大學 |
2014-12-08T15:45:33Z |
Mutation at noncysteine positions eliminates the oxidation/reduction effect on the activity of phenol sulfotransferase.
|
Yang, YS |
| 國立臺灣大學 |
2009 |
Mutation at the cargo-receptor binding site of Atg8 also affects its general autophagy regulation function
|
Ho, Kung-Hsien; Chang, Hsiang-En; Huang, Wei-Pang |
| 臺大學術典藏 |
2018-09-10T07:29:11Z |
Mutation at the cargo-receptor binding site of Atg8 also affects its general autophagy regulation function
|
Huang, Wei-Pang;Chang, Hsiang-En;Ho, Kung-Hsien;WEI-PANG HUANG;Huang, Wei-Pang;Chang, Hsiang-En;Ho, Kung-Hsien;Huang, W.-P.;Chang, H.-E.;Ho, K.-H.; Ho, K.-H.; Chang, H.-E.; Huang, W.-P.; Ho, Kung-Hsien; Chang, Hsiang-En; Huang, Wei-Pang; WEI-PANG HUANG; Ho, Kung-Hsien; Chang, Hsiang-En; Huang, Wei-Pang |
| 國立臺灣大學 |
2015 |
Mutation genotypes of RNF213 gene from moyamoya patients in Taiwan
|
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 |
| 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 |
| 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. |
