| 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. |
| 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
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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
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Tsai M.-H.; Lai L.-C.; Chiang L.-M.; JYH-MING JIMMY JUANG; Chattopadhyay A.; Lee C.-Y.; Lu T.-P.; Chuang E.Y. |
| 臺大學術典藏 |
2020-12-28T07:56:37Z |
GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death
|
Huang H.-C.; Yu C.-C.; Ho L.-T.; Liu Y.-B.; Lin L.-Y.; Chen W.-J.; Hwang J.-J.; JYH-MING JIMMY JUANG; Binda A.; Lee S.-J.; 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 |
2020-12-25T08:38:37Z |
Quantification of contractile mechanics in the rat heart from ventricular pressure alone
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Chang K.-C.; Chen Y.-S.; Yu H.-Y.; Wang C.-H.; Chang R.-W.; Chang C.-Y.; Wu M.-S.; HSIEN-LI KAO; Lai L.-C.; Young T.-H. |
| 臺大學術典藏 |
2020-12-25T08:38:35Z |
Defects in vascular mechanics due to aging in rats: Studies on arterial wave properties from a single aortic pressure pulse
|
Chang K.-C.; Wang C.-H.; Lai L.-C.; HSIEN-LI KAO; Cheng Y.-J.; Wu M.-S.; Chang C.-Y.; Chang R.-W.; Hsu S.-H. |
| 臺大學術典藏 |
2020-12-24T08:38:19Z |
Methylation in pericytes after acute injury promotes chronic kidney disease
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Lin S.-L.; Chen Y.-M.; Chu T.-S.; Yang K.-C.; Lai L.-C.; Schrimpf C.; WEN-CHIH CHIANG; Lai C.-F.; Wei S.-Y.; Chou Y.-H.;Pan S.-Y.;Shao Y.-H.;Shih H.-M.;Wei S.-Y.;Lai C.-F.;Wen-Chih Chiang;Schrimpf C.;Yang K.-C.;Lai L.-C.;Chen Y.-M.;Chu T.-S.;Lin S.-L.; Chou Y.-H.; Pan S.-Y.; Shao Y.-H.; Shih H.-M. |
| 臺大學術典藏 |
2020-12-24T08:11:48Z |
Systolic aortic pressure-time area is a useful index describing arterial wave properties in rats with diabetes
|
Lin F.-Y.; Chen Y.-S.; Luo J.-M.; Yu H.-Y.; MING-SHIOU WU; Chang C.-Y.; Chang R.-W.; Lai L.-C.; Wang C.-H.; Chang K.-C. |
| 臺大學術典藏 |
2020-12-24T08:11:46Z |
Quantification of contractile mechanics in the rat heart from ventricular pressure alone
|
Wang C.-H.; Wang C.-H.;Chang R.-W.;Chang C.-Y.;Ming-Shiou Wu;Kao H.-L.;Lai L.-C.;Young T.-H.;Yu H.-Y.;Chen Y.-S.;Chang K.-C.; Chang R.-W.; Chang C.-Y.; MING-SHIOU WU; Kao H.-L.; Lai L.-C.; Young T.-H.; Yu H.-Y.; Chen Y.-S.; Chang K.-C. |
| 臺大學術典藏 |
2020-12-24T08:11:45Z |
Defects in vascular mechanics due to aging in rats: Studies on arterial wave properties from a single aortic pressure pulse
|
Chang K.-C.; Chang C.-Y.;Chang R.-W.;Hsu S.-H.;Ming-Shiou Wu;Cheng Y.-J.;Kao H.-L.;Lai L.-C.;Wang C.-H.;Chang K.-C.; Chang C.-Y.; Chang R.-W.; Hsu S.-H.; MING-SHIOU WU; Cheng Y.-J.; Kao H.-L.; Lai L.-C.; Wang C.-H. |
| 臺大學術典藏 |
2020-12-24T06:30:18Z |
Methylation in pericytes after acute injury promotes chronic kidney disease
|
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.; YUNG-MING CHEN; Chu T.-S.; Lin S.-L. |
| 臺大學術典藏 |
2020-12-22T03:29:15Z |
SHANK3 Regulates Intestinal Barrier Function Through Modulating ZO-1 Expression Through the PKC?-dependent Pathway
|
Ni Y.-H.; Shun C.-T.; Chuang E.Y.; Hsiao J.-H.; Yu L.C.H.; Lai L.-C.; Tung C.-C.; Weng M.-T.; PO-NIEN TSAO; Yang-Yen H.-F.; Wei S.-C.; Wei S.-C.;Yang-Yen H.-F.;Po-Nien Tsao;Weng M.-T.;Tung C.-C.;Yu L.C.H.;Lai L.-C.;Hsiao J.-H.;Chuang E.Y.;Shun C.-T.;Ni Y.-H.;Xavier R.J.;Podolsky D.K.;Yen J.J.Y.;Wong J.-M.; Xavier R.J.; Podolsky D.K.; Yen J.J.Y.; Wong J.-M. |
| 臺大學術典藏 |
2020-12-21T08:16:30Z |
Disease-targeted sequencing of ion channel genes identifies de novo mutations in patients with non-familial Brugada syndrome
|
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.; WEN-JONE CHEN; Chiang F.-T.; Yeh S.-F.S.; Lai L.-P.; Chuang E.Y. |
| 臺大學術典藏 |
2020-12-04T07:44:55Z |
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 |
2020-12-04T07:44:54Z |
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.; 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 |
2020-12-04T07:44:29Z |
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 |
2020-12-02T02:34:15Z |
Identification of a novel biomarker, SEMA5A, for non-small cell lung carcinoma in nonsmoking women
|
Lu T.-P.;Tsai M.-H.;Lee J.-M.;Hsu C.-P.;Chen P.-C.;Lin C.-W.;Shih J.-Y.;Pan-Chyr Yang;Hsiao C.K.;Lai L.-C.;Chuang E.Y.; Lu T.-P.; Tsai M.-H.; Lee J.-M.; Hsu C.-P.; Chen P.-C.; Lin C.-W.; Shih J.-Y.; PAN-CHYR YANG; Hsiao C.K.; Lai L.-C.; Chuang E.Y. |
| 臺大學術典藏 |
2020-11-30T08:41:57Z |
Genetic polymorphisms of a novel vascular susceptibility gene, ninjurin2 (NINJ2), are associated with a decreased risk of Alzheimer's disease
|
KUN-PEI LIN; Chen S.-Y.; Lai L.-C.; Huang Y.-L.; Chen J.-H.; Chen T.-F.; Sun Y.; Wen L.-L.; Yip P.-K.; Chu Y.-M.; Chen W.J.; Chen Y.-C. |
