| 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) |
| 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. |
| 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 |
| 國立臺灣大學 |
1992 |
Mutation of P53 Gene in Hepatocellular Carcinoma in Taiwan
|
許金川; Lee, P. H.; Chung, J. C.; Chou, H. C.; Lai, M. Y.; Wang, J. T.; Lee, H. S.; Shih, L. N.; Yang, P. M.; Wang, T. H.; Chen, D. S.; Sheu, Jin-Chuan; Lee, P. H.; Chung, J. C.; Chou, H. C.; Lai, M. Y.; Wang, J. T.; Lee, H. S.; Shih, L. N.; Yang, P. M.; Wang, T. H.; Chen, D. S. |
| 臺大學術典藏 |
2019-09-02T08:58:49Z |
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, Jin-Town;Lee H.-S.;Shih L.-N.;Yang P.-M.;Wang T.-H.;Chen D.-S.; Sheu J.-C.; Huang G.-T.; Chung J.-C.; Chou H.-C.; Lai M.-Y.; Wang, Jin-Town; Lee H.-S.; Shih L.-N.; Yang P.-M.; Wang T.-H.; Chen D.-S. |
| 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. |
| 中山醫學大學 |
1995 |
Mutation of p53 gene on transformed C3H10T1 ／ 2 cells by N － nitroso Maillard reaction products
|
蘇文男; Su, Wen-Nan |
| 慈濟大學 |
2021 |
Mutation of the Carboxy-Terminal Processing Protease Gene in Acinetobacter baumannii and its Impact on Membrane Integrity and Virulence Properties
|
RakeshRoy |
| 臺大學術典藏 |
2018-09-10T04:13:04Z |
Mutation of the DR5/TRAIL receptor 2 gene is infrequent in hepatocellular carcinoma
|
Jeng, Y.-M. and Hsu, H.-C.; YUNG-MING JENG |
| 國立臺灣大學 |
2002 |
Mutation of the Dr5/Trail Receptor 2 Gene Is Infrequent in Hepatocellular Carcinoma
|
鄭永銘; 許輝吉; JENG, YUNG-MING; HSU, HEY-CHI |
| 臺大學術典藏 |
2020-03-06T08:25:41Z |
Mutation of the DR5/TRAIL receptor 2 gene is infrequent in hepatocellular carcinoma
|
Yung-Ming Jeng;Hsu H.-C.; YUNG-MING JENG; Hsu H.-C. |
| 國立成功大學 |
2016-08-12 |
Mutation of the Enterohemorrhagic Escherichia coli Core LPS Biosynthesis Enzyme RfaD Confers Hypersusceptibility to Host Intestinal Innate Immunity In vivo
|
Kuo, Cheng-Ju; Chen, Jenn-Wei; Chiu, Hao-Chieh; Teng, Ching-Hao; Hsu, Tai-I; Lu, Pei-Jung; Syu, Wan-Jr; Wang, Sin-Tian; Chou, Ting-Chen; Chen, Chang-Shi |
| 國立臺灣大學 |
2016 |
Mutation of the Enterohemorrhagic Escherichia coli Core LPS Biosynthesis Enzyme RfaD Confers Hypersusceptibility to Host Intestinal Innate Immunity In vivo
|
Kuo, Cheng-Ju; Chen, Jenn-Wei; Chiu, Hao-Chieh; Teng, Ching-Hao; Hsu, Tai-I; Lu, Pei-Jung; Syu, Wan-Jr; Wang, Sin-Tian; Chou, Ting-Chen; Chen, Chang-Shi; 邱浩傑 |
| 臺大學術典藏 |
2021-06-24T01:53:52Z |
Mutation of the enterohemorrhagic escherichia coli core LPS biosynthesis enzyme RfaD confers hypersusceptibility to host intestinal innate immunity in vivo
|
Kuo C.-J.; Chen J.-W.; HAO-CHIEH CHIU; Teng C.-H.; Hsu T.-I.; Lu P.-J.; Syu W.-J.; Wang S.T.; Chou T.-C.; Chen C.-S. |
| 國立成功大學 |
2019-11-8 |
Mutation of the PTCH1 gene predicts recurrence of breast cancer
|
Wang;Chih-Yang;Chang;Yung-Chieh;Kuo;Yao-Lung;Lee;Kuo-Ting;Chen;Pai-Sheng;Cheung;Antonio, Chun Hei;Chang;Chih-Peng;Phan, Nam Nhut;Shen;Meng-Ru;Hsu;Hui-Ping |
| 國立成功大學 |
2019-12-1 |
Mutation of the PTCH1 gene predicts recurrence of breast cancer
|
徐慧萍; HSU, HUI-PING; Wang, Chih-Yang;Chang, Yung-Chieh;Kuo, Yao-Lung;Lee, Kuo-Ting;Chen, Pai-Sheng;Cheung, Chun Hei Antonio;Chang, Chih-Peng;Phan, Nam Nhut;Shen, Meng-Ru;Hsu, Hui-Ping |
| 國立臺灣大學 |
1989-06 |
Mutation of the Retinoblastoma Gene in a Human Prostate Carcinoma Cell Line
|
Bookstein, R.; 許金玉; Scully, P.; Lee, W. H.; Bookstein, R.; Shew, Jin-Yuh; Scully, P.; Lee, W. H. |
| 國立臺灣大學 |
2002 |
Mutation of the Sterol 27-Hydroxylase Gene (Cyp27a1) in a Taiwanese Family with Cerebrotendinous Xanthomatosis
|
葉炳強; YIP, PING-KEUNG |
| 臺大學術典藏 |
2018-09-10T04:05:42Z |
Mutation of the sterol 27-hydroxylase gene (CYP27A1) in a Taiwanese family with cerebrotendinous xanthomatosis [4]
|
Lee, M.-J. and Huang, Y.-C. and Sweeney, M.G. and Wood, N.W. and Reilly, M.M. and Yip, P.-K.; MING-JEN LEE |
| 臺大學術典藏 |
2020-03-03T02:33:36Z |
Mutation of the sterol 27-hydroxylase gene (CYP27A1) in a Taiwanese family with cerebrotendinous xanthomatosis [4]
|
MING-JEN LEE; Huang Y.-C.; Sweeney M.G.; Wood N.W.; Reilly M.M.; Yip P.-K. |
| 臺大學術典藏 |
2002 |
Mutation of the sterol 27-hydroxylase gene (CYP27A1) in a Taiwanese family with cerebrotendinous xanthomatosis [4]
|
Yip P.-K.; Reilly M.M.; Wood N.W.; Sweeney M.G.; Huang Y.-C.; MING-JEN LEE |
| 國家衛生研究院 |
2020-08 |
Mutation of the STK11 gene predicts recurrence of breast cancer
|
Wang, CY;Chang, YC;Kuo, YL;Lee, KT;Chen, PS;Cheung, CHA;Shen, CH;Chang, CP;Lai, MD;Shen, MR;Hsu, HP |
| 中山醫學大學 |
2009 |
Mutation ofgyrA andparC in clinical isolates ofAcinetobacter baumannii and its relationship with antimicrobial drugs resistance in Taiwan
|
Chien, Shang-Tao; Lin, Chun-Hsiu; Hsueh, Jui-Chen; Li, Pei-Ling; Hsu, Chao-Hsun; Chang, Shu-Hui; Chien, Hsin-I; Ben, Ren-Jy; Chang, Fu-Hsin; Hsu, Li-Sung |
| 中山醫學大學 |
2010 |
Mutation R184Q of connexin 26 in hearing loss patients has a dominant-negative effect on connexin 26 and connexin 30
|
Ching-Chyuan Su;Shuan-Yow Li;Mao-Chang Su;Wei-Chi Chen;Jiann-Jou Yang |
