| 臺大學術典藏 |
2021-03-29T06:08:20Z |
Semaphorin 5A suppresses the proliferation and migration of lung adenocarcinoma cells
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Ko, P.-H.; Lenka, G.; Chen, Y.-A.; Chuang, E.Y.; Tsai, M.-H.; Sher, Y.-P.; Lai, L.-C.; ERIC YAO-YU CHUANG |
| 臺大學術典藏 |
2021-03-18T02:02:44Z |
SLCO3A1, a novel Crohn's disease-associated gene, regulates NF-κB activity and associates with intestinal perforation
|
Wei S.-C.;Tan Y.-Y.;Weng M.-T.;Lai L.-C.;Hsiao J.-H.;Chuang E.Y.;Chia-Tung Shun;Wu D.-C.;Kao A.-W.;Chuang C.-S.;Ni Y.-H.;Shieh M.-J.;Tung C.-C.;Chen Y.;Wang C.-Y.;Xavier R.J.;Podolsky D.K.;Wong J.-M.; Wei S.-C.; Tan Y.-Y.; Weng M.-T.; Lai L.-C.; Hsiao J.-H.; Chuang E.Y.; CHIA-TUNG SHUN; Wu D.-C.; Kao A.-W.; Chuang C.-S.; Ni Y.-H.; Shieh M.-J.; Tung C.-C.; Chen Y.; Wang C.-Y.; Xavier R.J.; Podolsky D.K.; Wong J.-M. |
| 臺大學術典藏 |
2021-03-18T02:02:29Z |
SHANK3 Regulates Intestinal Barrier Function Through Modulating ZO-1 Expression Through the PKC?-dependent Pathway
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Wei S.-C.;Yang-Yen H.-F.;Tsao P.-N.;Weng M.-T.;Tung C.-C.;Yu L.C.H.;Lai L.-C.;Hsiao J.-H.;Chuang E.Y.;Chia-Tung Shun;Ni Y.-H.;Xavier R.J.;Podolsky D.K.;Yen J.J.Y.;Wong J.-M.; Wei S.-C.; Yang-Yen H.-F.; Tsao P.-N.; Weng M.-T.; Tung C.-C.; Yu L.C.H.; Lai L.-C.; Hsiao J.-H.; Chuang E.Y.; CHIA-TUNG SHUN; Ni Y.-H.; Xavier R.J.; Podolsky D.K.; Yen J.J.Y.; Wong J.-M. |
| 臺大學術典藏 |
2021-03-11T04:29:40Z |
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 J.-J.;Fu-Tien Chiang;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.; Liu Y.-B.; Tsai C.-T.; Lin L.-Y.; Yu C.-C.; Hwang J.-J.; FU-TIEN CHIANG; Yeh S.S.-F.; Chen W.-P.; Chuang E.Y.; Lai L.-P.; Lin J.-L. |
| 臺大學術典藏 |
2021-03-11T04:29:38Z |
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.;Lin L.-Y.;Yu C.-C.;Chen W.-J.;Fu-Tien Chiang;Yeh S.-F.S.;Lai L.-P.;Chuang E.Y.;Lin J.-L.; Juang J.-M.J.; Lu T.-P.; Lai L.-C.; Ho C.-C.; Liu Y.-B.; Tsai C.-T.; Lin L.-Y.; Yu C.-C.; Chen W.-J.; FU-TIEN CHIANG; Yeh S.-F.S.; Lai L.-P.; Chuang E.Y.; Lin J.-L. |
| 臺大學術典藏 |
2021-02-05T06:29:24Z |
Prognostic significance of NPM1 mutation-modulated microRNA-mRNA regulation in acute myeloid leukemia
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Chiu Y.-C.; Tsai M.-H.; WEN-CHIEN CHOU; Liu Y.-C.; Kuo Y.-Y.; Hou H.-A.; Lu T.-P.; Lai L.-C.; Chen Y.; Tien H.-F.; Chuang E.Y. |
| 臺大學術典藏 |
2021-01-15T02:46:26Z |
A whole genome methylation analysis of systemic lupus erythematosus: Hypomethylation of the IL10 and IL1R2 promoters is associated with disease activity
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Lin S.-Y.; SONG-CHOU HSIEH; Lin Y.-C.; Lee C.-N.; Tsai M.-H.; Lai L.-C.; Chuang E.Y.; Chen P.-C.; Hung C.-C.; Chen L.-Y.; Hsieh W.S.; Niu D.-M.; Su Y.-N.; Ho H.-N. |
| 臺大學術典藏 |
2021-01-12T03:32:02Z |
Methylation in pericytes after acute injury promotes chronic kidney disease
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Chou Y.-H.; Pan S.-Y.; Shao Y.-H.; Shih H.-M.; Wei S.-Y.; Lai C.-F.; Chiang W.-C.; Schrimpf C.; Yang K.-C.; Lai L.-C.; Chen Y.-M.; Chu T.-S.; SHUEI-LIONG LIN |
| 臺大學術典藏 |
2021-01-04T12:12:29Z |
Prognostic significance of NPM1 mutation-modulated microRNA-mRNA regulation in acute myeloid leukemia
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Chiu Y.-C.; Tsai M.-H.; Chou W.-C.; Liu Y.-C.; Kuo Y.-Y.; Hou H.-A.; Lu T.-P.; Lai L.-C.; Chen Y.; HWEI-FANG TIEN; Chuang E.Y. |
| 臺大學術典藏 |
2020-12-30T08:47:44Z |
Utilizing multiple in silico analyses to identify putative causal SCN5A variants in brugada syndrome
|
Chiang F.-T.; Hwang J.-J.; Lin L.-Y.; Yu C.-C.; CHIA-TI TSAI; Liu Y.-B.; Juang J.-M.J.; Lu T.-P.; Lai L.-C.; Hsueh C.-H.; Yeh S.S.-F.; Chen W.-P.; Chuang E.Y.; Lai L.-P.; Lin J.-L. |
| 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
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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
|
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. |
| 臺大學術典藏 |
2020-12-28T10:02:41Z |
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.; Liu Y.-B.; Tsai C.-T.; Lin L.-Y.; CHIH-CHIEH YU; 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 |
2020-12-28T08:14:22Z |
SLCO3A1, a novel Crohn's disease-associated gene, regulates NF-κB activity and associates with intestinal perforation
|
Wei S.-C.; Podolsky D.K.; Wong J.-M.; Tan Y.-Y.; Weng M.-T.; Lai L.-C.; Hsiao J.-H.; Chuang E.Y.; Shun C.-T.; Wu D.-C.; Kao A.-W.; Chuang C.-S.; YEN-HSUAN NI; Shieh M.-J.; Tung C.-C.; Chen Y.; Wang C.-Y.; Xavier R.J. |
| 臺大學術典藏 |
2020-12-28T08:14:12Z |
SHANK3 Regulates Intestinal Barrier Function Through Modulating ZO-1 Expression Through the PKC?-dependent Pathway
|
Shun C.-T.; YEN-HSUAN NI; Chuang E.Y.; Hsiao J.-H.; Lai L.-C.; Yu L.C.H.; Wei S.-C.; Yang-Yen H.-F.; Tsao P.-N.; Weng M.-T.; Tung C.-C.; Xavier R.J.; Podolsky D.K.; Yen J.J.Y.; Wong J.-M. |
| 臺大學術典藏 |
2020-12-28T07:56:42Z |
An automated microfluidic DNA microarray platform for genetic variant detection in inherited arrhythmic diseases
|
Huang S.-H.; Chang Y.-S.; JYH-MING JIMMY JUANG; Chang K.-W.; Tsai M.-H.; Lu T.-P.; Lai L.-C.; Chuang E.Y.; Huang N.-T. |
| 臺大學術典藏 |
2020-12-28T07:56:41Z |
VariED: The first integrated database of gene annotation and expression profiles for variants related to human diseases
|
Tsai M.-H.; Lai L.-C.; Chiang L.-M.; JYH-MING JIMMY JUANG; Chattopadhyay A.; Lee C.-Y.; Lu T.-P.; Chuang E.Y. |
