| 國立成功大學 |
2023 |
Carboxyl-terminal modulator protein facilitates tumor metastasis in triple-negative breast cancer
|
Lin, C.-H.;Lin, W.-D.;Huang, Y.-C.;Chen, Y.-C.;Loh, Z.-J.;Ger, L.-P.;Lin, F.-C.;Li, H.-Y.;Cheng, H.-C.;Lee, K.-H.;Hsiao, M.;Lu, P.-J. |
| 臺大學術典藏 |
2021-01-06T03:39:11Z |
Significant association of XRCC4 single nucleotide polymorphisms with childhood leukemia in Taiwan
|
Wu K.-H.; Wang C.-H.; YUNG-LI YANG; Peng C.-T.; Lin W.-D.; Tsai F.-J.; Lin D.-T.; Bau D.-T. |
| 國立成功大學 |
2021 |
From simple and specific zymographic detections to the annotation of a fungus Daldinia caldariorum D263 that encodes a wide range of highly bioactive cellulolytic enzymes
|
Lin, M.-C.;Kuo, H.-W.;Kao, M.-R.;Lin, W.-D.;Li, C.-W.;Hung, K.-S.;Yang, S.-C.;Yu, S.-M.;Ho, T.-H.D. |
| 臺大學術典藏 |
2020-12-24T06:16:24Z |
Congenital generalized lipodystrophy in Taiwan
|
Hsu R.-H.; Lin W.-D.; Chao M.-C.; Hsiao H.-P.; Wong S.-L.; Chiu P.-C.; Chu S.-Y.; Ke Y.-Y.; Lau B.-H.; YIN-HSIU CHIEN; Hwu W.-L.; Tsai F.-J.; Wang C.-H.; Lee N.-C. |
| 臺大學術典藏 |
2020-12-21T01:58:21Z |
Molecular aspects of Dravet syndrome patients in Taiwan
|
Tsai F.-J.; Tsai C.-H.; Chou I.-C.; Tsai Y.; Lin W.-C.; Weng W.-C.; PI-CHUAN FAN; Chen S.-J.; Lin W.-D.;Chang K.-P.;Wang C.-H.;Chen S.-J.;Pi-Chuan Fan;Weng W.-C.;Lin W.-C.;Tsai Y.;Tsai C.-H.;Chou I.-C.;Tsai F.-J.; Lin W.-D.; Chang K.-P.; Wang C.-H. |
| 臺大學術典藏 |
2020-12-16T02:26:01Z |
Human gene mutations. Gene symbol: GLA. Disease: Fabry disease.
|
Lin W.D.;Wuh-Liang Hwu;Liu S.C.;Chen C.P.;Tsai F.J.; Lin W.D.; WUH-LIANG HWU; Liu S.C.; Chen C.P.; Tsai F.J. |
| 臺大學術典藏 |
2020-12-16T02:25:58Z |
Gene symbol: GLA. Disease: Fabry disease.
|
Lin W.D.;Wuh-Liang Hwu;Liu S.C.;Tsai F.J.; Lin W.D.; WUH-LIANG HWU; Liu S.C.; Tsai F.J. |
| 臺大學術典藏 |
2020-12-16T02:25:58Z |
Gene symbol: GCDH. Disease: Glutaricacidaemia I.
|
Lin W.D.;Wuh-Liang Hwu;Wang C.H.;Chen C.P.;Tsai F.J.; Lin W.D.; WUH-LIANG HWU; Wang C.H.; Chen C.P.; Tsai F.J. |
| 臺大學術典藏 |
2020-12-16T02:25:56Z |
Genetic analysis of mucopolysaccharidosis type VI in Taiwanese patients
|
Lin W.-D.;Lin S.-P.;Wang C.-H.;Wuh-Liang Hwu;Chuang C.-K.;Lin S.-J.;Tsai Y.;Chen C.-P.;Tsai F.-J.; Lin W.-D.; Lin S.-P.; Wang C.-H.; WUH-LIANG HWU; Chuang C.-K.; Lin S.-J.; Tsai Y.; Chen C.-P.; Tsai F.-J. |
| 臺大學術典藏 |
2020-12-16T02:25:46Z |
FOXL2 mutations in Taiwanese patients with blepharophimosis, ptosis, epicanthus inversus syndrome
|
Lin S.-P.; Chao M.-C.; Tsai Y.; Tsai F.-J.; Lin W.-D.;Chou I.-C.;Lee N.-C.;Wang C.-H.;Wuh-Liang Hwu;Lin S.-P.;Chao M.-C.;Tsai Y.;Tsai F.-J.; Lin W.-D.; Chou I.-C.; Lee N.-C.; Wang C.-H.; WUH-LIANG HWU |
