| 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 |
| 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. |
