| 國立成功大學 |
2023 |
Anticancer polypyrrole-polyethylenimine drug-free nanozyme for precise B-cell lymphoma therapy
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Nguyen, T.T.;Chuang, E.-Y.;Chen, Y.-P.;Tseng, P.-C.;Jhan, M.-K.;Lai, C.-Y.;Wang, Y.-T.;Hung, Y.-P.;Changou, Changou C.A.;Lee, C.-M.;Chen, Chen C.-L.;Lin, C.-F. |
| 臺大學術典藏 |
2022-09-20T06:49:21Z |
Utilizing multiple in silico analyses to identify putative causal SCN5A variants in brugada syndrome
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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 |
2022-09-20T06:49:08Z |
Genome-wide screening identifies a KCNIP1 copy number variant as a genetic predictor for atrial fibrillation
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Tsai C.-T.; Hsieh C.-S.; Chang S.-N.; Chuang E.Y.; Ueng K.-C.; Tsai C.-F.; Lin T.-H.; Wu C.-K.; Lee J.-K.; Lin L.-Y.; Wang Y.-C.; Yu C.-C.; Lai L.-P.; Tseng C.-D.; HWANG, JUEY-JEN; Chiang F.-T.; Lin J.-L. |
| 臺大學術典藏 |
2022-09-20T06:48:42Z |
Global expression profiling identifies a novel hyaluronan synthases 2 gene in the pathogenesis of lower extremity varicose veins
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Hsieh C.-S.; Tsai C.-T.; Chen Y.-H.; Chang S.-N.; HWANG, JUEY-JEN; Chuang E.Y.; Wu I.-H. |
| 臺大學術典藏 |
2022-09-20T06:48:40Z |
Genome-Wide copy number variation association study of Atrial Fibrillation related Thromboembolic Stroke
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Hsieh C.-S.; Huang P.-S.; Chang S.-N.; Wu C.-K.; HWANG, JUEY-JEN; Chuang E.Y.; Tsai C.-T. |
| 臺大學術典藏 |
2022-09-20T06:48:31Z |
GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death
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Juang J.-M.J.; Binda A.; Lee S.-J.; HWANG, JUEY-JEN; Chen W.-J.; Liu Y.-B.; 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 |
2022-09-20T06:48:31Z |
Prevalence of sudden arrhythmic death syndrome-related genetic mutations in an Asian cohort of whole genome sequence
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Huang P.-S.; Hsieh C.-S.; Chang S.-N.; Chen J.-J.; Chiu F.-C.; Wu C.-K.; HWANG, JUEY-JEN; Chuang E.Y.; Tsai C.-T. |
| 臺大學術典藏 |
2022-09-20T06:48:30Z |
Validation and Disease Risk Assessment of Previously Reported Genome-Wide Genetic Variants Associated With Brugada Syndrome: SADS-TW BrS Registry
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Jimmy Juang J.-M.; Liu Y.-B.; Julius Chen C.-Y.; Yu Q.-Y.; Chattopadhyay A.; Lin L.-Y.; Chen W.-J.; Yu C.-C.; Huang H.-C.; Ho L.-T.; Lai L.-P.; HWANG, JUEY-JEN; Lin T.-T.; Liao M.-T.; Chen J.-J.; Sherri Yeh S.-F.; Chuang J.-Y.; Yang D.-H.; Lin J.-L.; Lu T.-P.; Chuang E.Y.; Ackerman M.J. |
| 臺大學術典藏 |
2022-09-20T06:48:20Z |
An Artificial Intelligence-Enabled ECG Algorithm for the Prediction and Localization of Angiography-Proven Coronary Artery Disease
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Huang P.-S.; Tseng Y.-H.; Tsai C.-F.; Chen J.-J.; Yang S.-C.; Chiu F.-C.; Chen Z.-W.; HWANG, JUEY-JEN; Chuang E.Y.; Wang Y.-C.; Tsai C.-T. |
| 臺大學術典藏 |
2022-09-20T06:48:19Z |
The Gut Microbiome, Seleno-Compounds, and Acute Myocardial Infarction
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Chiu F.-C.; Tsai C.-F.; Huang P.-S.; Shih C.-Y.; Tsai M.-H.; HWANG, JUEY-JEN; Wang Y.-C.; Chuang E.Y.; Tsai C.-T.; Chang S.-N. |
| 臺大學術典藏 |
2022-09-06T07:43:40Z |
Duodenal ulcer-related antigens from Helicobacter pylori: Immunoproteome and protein microarray approaches
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Lin Y.-F.; Chen C.-Y.; Tsai M.-H.; MING-SHIANG WU; Wang Y.-C.; Chuang E.Y.; Lin J.-T.; Yang P.-C.; Chow L.-P. |
| 臺大學術典藏 |
2022-09-06T02:42:26Z |
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.; LIAN-YU LIN; Yu C.-C.; Hwang J.-J.; 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 |
2022-09-06T02:42:23Z |
Disease-targeted sequencing of ion channel genes identifies de novo mutations in patients with non-familial Brugada syndrome
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Juang J.-M.J.; Lu T.-P.; Lai L.-C.; Ho C.-C.; Liu Y.-B.; Tsai C.-T.; LIAN-YU LIN; 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 |
2022-09-06T02:42:21Z |
Next-generation sequencing of nine atrial fibrillation candidate genes identified novel de novo mutations in patients with extreme trait of atrial fibrillation
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Tsai C.-T.; Hsieh C.-S.; Chang S.-N.; Chuang E.Y.; Juang J.-M.J.; LIAN-YU LIN; Lai L.-P.; Hwang J.-J.; Chiang F.-T.; Lin J.-L. |
| 臺大學術典藏 |
2022-09-06T02:42:15Z |
Genome-wide screening identifies a KCNIP1 copy number variant as a genetic predictor for atrial fibrillation
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Tsai C.-T.; Hsieh C.-S.; Chang S.-N.; Chuang E.Y.; Ueng K.-C.; Tsai C.-F.; Lin T.-H.; Wu C.-K.; Lee J.-K.; LIAN-YU LIN; Wang Y.-C.; Yu C.-C.; Lai L.-P.; Tseng C.-D.; Hwang J.-J.; Chiang F.-T.; Lin J.-L. |
| 臺大學術典藏 |
2022-09-06T02:41:47Z |
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.; Liu Y.-B.; LIAN-YU LIN; 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 |
2022-09-06T02:41:46Z |
Validation and Disease Risk Assessment of Previously Reported Genome-Wide Genetic Variants Associated With Brugada Syndrome: SADS-TW BrS Registry
|
Jimmy Juang J.-M.; Liu Y.-B.; Julius Chen C.-Y.; Yu Q.-Y.; Chattopadhyay A.; LIAN-YU LIN; Chen W.-J.; Yu C.-C.; Huang H.-C.; Ho L.-T.; Lai L.-P.; Hwang J.-J.; Lin T.-T.; Liao M.-T.; Chen J.-J.; Sherri Yeh S.-F.; Chuang J.-Y.; Yang D.-H.; Lin J.-L.; Lu T.-P.; Chuang E.Y.; Ackerman M.J. |
| 臺大學術典藏 |
2022-08-12T06:27:51Z |
Comparison of triple negative breast cancer between Asian and western data sets
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Chen L.H.; Lai L.-C.; Hsiao C.K.; Chen P.-C.; Tsai M.-H.; Kuo W.-H.; KING-JEN CHANG; Chuang E.Y. |
| 臺大學術典藏 |
2022-08-12T06:27:46Z |
Identification of prognostic genes for recurrent risk prediction in triple negative breast cancer patients in Taiwan
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Chen L.H.; Kuo W.-H.; Tsai M.-H.; Chen P.-C.; Hsiao C.K.; Chuang E.Y.; Chang L.-Y.; Hsieh F.-J.; Lai L.-C.; KING-JEN CHANG |
| 臺大學術典藏 |
2022-08-12T06:27:41Z |
Molecular Characteristics and Metastasis Predictor Genes of Triple-Negative Breast Cancer: A Clinical Study of Triple-Negative Breast Carcinomas
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Kuo W.-H.; Chang Y.-Y.; Lai L.-C.; Tsai M.-H.; Hsiao C.K.; KING-JEN CHANG; Chuang E.Y. |
| 臺大學術典藏 |
2022-08-12T06:27:34Z |
Deregulated microRNAs in triple-negative breast cancer revealed by deep sequencing
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Chang Y.-Y.; Kuo W.-H.; Hung J.-H.; Lee C.-Y.; Lee Y.-H.; Chang Y.-C.; Lin W.-C.; Shen C.-Y.; Huang C.-S.; Hsieh F.-J.; Lai L.-C.; Tsai M.-H.; KING-JEN CHANG; Chuang E.Y. |
| 臺大學術典藏 |
2022-08-12T06:27:19Z |
Evolutionary trajectories and genomic divergence in localized breast cancers after ipsilateral breast tumor recurrence
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Wu C.-H.; Yeh H.-T.; Hsieh C.-S.; Huang C.-C.; Chattopadhyay A.; Chung Y.-C.; Tu S.-H.; Li Y.-H.; Lu T.-P.; Lai L.-C.; Hou M.-F.; KING-JEN CHANG; Tsai M.-H.; Chuang E.Y. |
| 臺大學術典藏 |
2022-07-28T02:34:32Z |
Extracellular domain of semaphorin 5A serves a tumor‑suppressing role by activating interferon signaling pathways in lung adenocarcinoma cells
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Chen M.-Z.; Su L.-Y.; Ko P.-H.; Hsu M.-H.; Chuang L.-L.; Chen L.-H.; Lu T.-P.; Chuang E.Y.; Chow L.-P.; Tsai M.-H.; Hsu H.-H.; LIANG-CHUAN LAI |
| 臺大學術典藏 |
2022-05-09T08:46:40Z |
Use of germline polymorphisms in predicting concurrent chemoradiotherapy response in esophageal cancer
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Chen P.-C.; YEN-CHING CHEN; Lai L.-C.; Tsai M.-H.; Chen S.-K.; Yang P.-W.; Lee Y.-C.; Hsiao C.K.; Lee J.-M.; Chuang E.Y. |
| 臺大學術典藏 |
2022-05-05T05:15:42Z |
Genetic loci associated with an earlier age at onset in multiplex schizophrenia
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Woolston A.L.; Hsiao P.-C.; Kuo P.-H.; Wang S.-H.; Lien Y.-J.; Liu C.-M.; Hwu H.-G.; Lu T.-P.; Chuang E.Y.; Chang L.-C.; Chen C.-H.; Wu J.-Y.; Tsuang M.T.; WEI J. CHEN |
