| 臺大學術典藏 |
2020-12-30T08:47:43Z |
Disease-targeted sequencing of ion channel genes identifies de novo mutations in patients with non-familial Brugada syndrome
|
Lin J.-L.; Chuang E.Y.; Lai L.-P.; Juang J.-M.J.; Lu T.-P.; Lai L.-C.; Ho C.-C.; Liu Y.-B.; CHIA-TI TSAI; Lin L.-Y.; Yu C.-C.; Chen W.-J.; Chiang F.-T.; Yeh S.-F.S. |
| 臺大學術典藏 |
2020-12-30T07:47:50Z |
Utilizing multiple in silico analyses to identify putative causal SCN5A variants in brugada syndrome
|
Chuang E.Y.; Lai L.-P.; Lin J.-L.; Juang J.-M.J.; Lu T.-P.; Lai L.-C.; Hsueh C.-H.; YEN BIN LIU; Tsai C.-T.; Lin L.-Y.; Yu C.-C.; Hwang J.-J.; Chiang F.-T.; Yeh S.S.-F.; Chen W.-P. |
| 臺大學術典藏 |
2020-12-30T07:47:49Z |
Disease-targeted sequencing of ion channel genes identifies de novo mutations in patients with non-familial Brugada syndrome
|
Juang J.-M.J.; Lu T.-P.; Lai L.-C.; Ho C.-C.; YEN BIN LIU; Tsai C.-T.; Lin L.-Y.; Yu C.-C.; Chen W.-J.; Chiang F.-T.; Yeh S.-F.S.; Lai L.-P.; Chuang E.Y.; Lin J.-L. |
| 臺大學術典藏 |
2020-12-30T07:47:44Z |
GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death
|
Juang J.-M.J.; Binda A.; Lee S.-J.; Hwang J.-J.; Chen W.-J.; YEN BIN LIU; Lin L.-Y.; Yu C.-C.; Ho L.-T.; Huang H.-C.; Chen C.-Y.J.; Lu T.-P.; Lai L.-C.; Yeh S.-F.S.; Lai L.-P.; Chuang E.Y.; Rivolta I.; Antzelevitch C. |
| 臺大學術典藏 |
2020-12-30T02:43:32Z |
Colonization With Multidrug-Resistant Organisms Among Healthy Adults in the Community Setting: Prevalence, Risk Factors, and Composition of Gut Microbiome
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SHAN-CHWEN CHANG; Wang J.-T.; Wang S.-S.; Chen H.-C.; Chou Y.-H.; Lin K.-Y.; Lai L.-C.; Chen Y.-A.; Huang Y.-S. |
| 臺大學術典藏 |
2020-12-29T08:15:53Z |
MiR-338-5p inhibits cell proliferation, colony formation, migration and cisplatin resistance in esophageal squamous cancer cells by targeting FERMT2
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Hsieh, Y.-C.; Chen, L.-H.; Lin, W.-C.; Lin, W.-C.;Chen, L.-H.;Hsieh, Y.-C.;Yang, P.-W.;Lai, L.-C.;Chuang, E.Y.;Lee, J.-M.;Tsai, M.-H.; Yang, P.-W.; Lai, L.-C.; Chuang, E.Y.; Lee, J.-M.; Tsai, M.-H.; LI-HAN CHEN |
| 臺大學術典藏 |
2020-12-28T12:04:03Z |
Utilizing multiple in silico analyses to identify putative causal SCN5A variants in brugada syndrome
|
Juang J.-M.J.; Lu T.-P.; Lai L.-C.; Hsueh C.-H.; Liu Y.-B.; Tsai C.-T.; Lin L.-Y.; Yu C.-C.; HWANG, JUEY-JEN; Chiang F.-T.; Yeh S.S.-F.; Chen W.-P.; Chuang E.Y.; Lai L.-P.; Lin J.-L. |
| 臺大學術典藏 |
2020-12-28T12:03:16Z |
GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death
|
Antzelevitch C.; Rivolta I.; Chuang E.Y.; Lai L.-P.; Yeh S.-F.S.; Lai L.-C.; Lu T.-P.; Huang H.-C.; Chen C.-Y.J.; Ho L.-T.; Yu C.-C.; Lin L.-Y.; Liu Y.-B.; Juang J.-M.J.; Binda A.; Lee S.-J.; HWANG, JUEY-JEN; Chen W.-J. |
| 臺大學術典藏 |
2020-12-28T10:52:54Z |
GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death
|
Binda A.; Juang J.-M.J.; Lee S.-J.; Hwang J.-J.; Chen W.-J.; Liu Y.-B.; Lin L.-Y.; Yu C.-C.; Ho L.-T.; HUI-CHUN HUANG; Chen C.-Y.J.; Lu T.-P.; Lai L.-C.; Yeh S.-F.S.; Lai L.-P.; Chuang E.Y.; Rivolta I.; Antzelevitch C. |
| 臺大學術典藏 |
2020-12-28T10:02:42Z |
Utilizing multiple in silico analyses to identify putative causal SCN5A variants in brugada syndrome
|
Liu Y.-B.; Tsai C.-T.; Lin L.-Y.; CHIH-CHIEH YU; Hwang J.-J.; Chiang F.-T.; Yeh S.S.-F.; Chen W.-P.; Chuang E.Y.; Lai L.-P.; Lin J.-L.; Juang J.-M.J.; Lu T.-P.; Lai L.-C.; Hsueh C.-H. |
