| 臺大學術典藏 |
2022-03-22T08:26:16Z |
An asymmetric 2,3-fluoranthene imide building block for regioregular semiconductors with aggregation-induced emission properties
|
Sun X;Liao M.-Y;Yu X;Wu Y.-S;Zhong C;Chueh C.-C;Li Z;Li Z.; Sun X; Liao M.-Y; Yu X; Wu Y.-S; Zhong C; Chueh C.-C; Li Z; Li Z.; CHU-CHEN CHUEH |
| 臺大學術典藏 |
2022-03-09T03:12:23Z |
AC-93253 iodide, a novel Src inhibitor, suppresses NSCLC progression by modulating multiple Src-related signaling pathways
|
Lai Y.-H.; Lin S.-Y.; Wu Y.-S.; HUEI-WEN CHEN; Chen J.J.W. |
| 臺大學術典藏 |
2022-02-15T06:22:51Z |
Mitochondrial UQCRC1 mutations cause autosomal dominant parkinsonism with polyneuropathy
|
Lin C.-H.; Tsai P.-.; Lin H.-Y.; Hattori N.; Funayama M.; Jeon B.; Sato K.; Abe K.; Mukai Y.; Takahashi Y.; Li Y.; Nishioka K.; Yoshino H.; Daida K.; Chen M.-L.; Cheng J.; Huang C.-Y.; Tzeng S.-R.; Wu Y.-S.; Lai H.-J.; Tsai H.-H.; Yen R.-F.; Lee N.-C.; Lo W.-C.; Hung Y.-C.; CHIH-CHIANG CHAN; Ke Y.-C.; Chao C.-C.; Hsieh S.-T.; Farrer M.; Wu R.-M. |
| 臺大學術典藏 |
2022-01-12T07:07:10Z |
Distinct clinico-biological features in AML patients with low allelic ratio FLT3-ITD: role of allogeneic stem cell transplantation in first remission
|
Tien F.-M.; Tsai C.-H.; Huang S.-C.; Liu J.-H.; Chen C.-Y.; Kuo Y.-Y.; Chuang Y.-K.; Tseng M.-H.; Peng Y.-L.; Liu M.-C.; Liu C.-W.; Liao X.-W.; Lin L.-I.; Wu Y.-S.; Hou M.-F.; Wu S.-J.; Hsu S.-C.; Ko B.-S.; Chou W.-C.; Yao M.; HSIN-AN HOU; Tang J.-L.; Tien H.-F. |
| 國立成功大學 |
2022 |
Carbon fibre-supported hierarchical NiCo layered double hydroxide nanosheets as non-enzymatic glucose sensors for sport drinks and serum
|
Lo, C.-T.;Wu, Y.-S.;Huang, S.-M.;Tsai, P.-J.;Lee, C.-L. |
| 國立成功大學 |
2022 |
The Moderator of Gamification of Physical Activities in Older Adults
|
Chen, H.-J.;Wu, Y.-S. |
| 國立成功大學 |
2022 |
Aesthetic Preference in the Composition Ratios of Graphic Designs
|
Wu, Y.-S. |
| 臺大學術典藏 |
2021-11-16T02:44:01Z |
Mitochondrial UQCRC1 mutations cause autosomal dominant parkinsonism with polyneuropathy
|
CHIN-HSIEN LIN; Tsai P.-.; Lin H.-Y.; Hattori N.; Funayama M.; Jeon B.; Sato K.; Abe K.; Mukai Y.; Takahashi Y.; Li Y.; Nishioka K.; Yoshino H.; Daida K.; Chen M.-L.; Cheng J.; Huang C.-Y.; Tzeng S.-R.; Wu Y.-S.; Lai H.-J.; Tsai H.-H.; Yen R.-F.; Lee N.-C.; Lo W.-C.; Hung Y.-C.; Chan C.-C.; Ke Y.-C.; Chao C.-C.; Hsieh S.-T.; Farrer M.; Wu R.-M. |
| 臺大學術典藏 |
2021-11-03T01:43:05Z |
Mitochondrial UQCRC1 mutations cause autosomal dominant parkinsonism with polyneuropathy
|
Lin C.-H.; Tsai P.-.; Lin H.-Y.; Hattori N.; Funayama M.; Jeon B.; Sato K.; Abe K.; Mukai Y.; Takahashi Y.; Li Y.; Nishioka K.; Yoshino H.; Daida K.; Chen M.-L.; Cheng J.; Huang C.-Y.; Tzeng S.-R.; Wu Y.-S.; Lai H.-J.; Tsai H.-H.; Yen R.-F.; Lee N.-C.; Lo W.-C.; Hung Y.-C.; Chan C.-C.; Ke Y.-C.; Chao C.-C.; Hsieh S.-T.; Farrer M.; RUEY-MEEI WU |
| 臺大學術典藏 |
2021-09-23T03:48:58Z |
Mitochondrial UQCRC1 mutations cause autosomal dominant parkinsonism with polyneuropathy
|
Lin C.-H.; Tsai P.-.; Lin H.-Y.; Hattori N.; Funayama M.; Jeon B.; Sato K.; Abe K.; Mukai Y.; Takahashi Y.; Li Y.; Nishioka K.; Yoshino H.; Daida K.; Chen M.-L.; Cheng J.; Huang C.-Y.; Tzeng S.-R.; Wu Y.-S.; Lai H.-J.; Tsai H.-H.; Yen R.-F.; Lee N.-C.; Lo W.-C.; Hung Y.-C.; Chan C.-C.; Ke Y.-C.; CHI-CHAO CHAO; Hsieh S.-T.; Farrer M.; Wu R.-M. |
