| 臺大學術典藏 |
2021-03-18T03:23:32Z |
Clinicopathologic Characterization of GREB1 -rearranged Uterine Sarcomas With Variable Sex-Cord Differentiation
|
Lee C.-H.; Kao Y.-C.; Lee W.-R.; Hsiao Y.-W.; Lu T.-P.; Chu C.-Y.; Lin Y.-J.; Huang H.-Y.; Hsieh T.-H.; Liu Y.-R.; Liang C.-W.; WEI-WU CHEN; Yip S.; Lum A.; Kuo K.-T.; Jeng Y.-M.; Yu S.-C.; Chung Y.-C.; Lee J.-C. |
| 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
|
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
|
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 |
2021-03-08T08:06:07Z |
Loss of SFRP1 expression is a key progression event in gastrointestinal stromal tumor pathogenesis
|
Liang C.-W.; Yang C.-Y.; Flavin R.; Fletcher J.A.; Lu T.-P.; I-RUE LAI; Li Y.-I.; Chang Y.-L.; Lee J.-C. |
| 臺大學術典藏 |
2021-03-08T06:51:49Z |
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.;Lin L.-Y.;Yu C.-C.;Ho L.-T.;Huang H.-C.;Chen C.-Y.J.;Lu T.-P.;Liang-Chuan Lai;Yeh S.-F.S.;Lai L.-P.;Chuang E.Y.;Rivolta I.;Antzelevitch C.; Juang J.-M.J.; Binda A.; Lee S.-J.; Hwang J.-J.; 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.; Liang-Chuan Lai; Yeh S.-F.S.; Lai L.-P.; Chuang E.Y.; Rivolta I.; Antzelevitch C. |
| 臺大學術典藏 |
2021-02-18T08:38:01Z |
Long-term changes of gut microbiota, antibiotic resistance, and metabolic parameters after Helicobacter pylori eradication: a multicentre, open-label, randomised trial
|
Liou J.-M.; CHIEN-CHUAN CHEN; Chang C.-M.; Fang Y.-J.; Bair M.-J.; Chen P.-Y.; Chang C.-Y.; Hsu Y.-C.; Chen M.-J.; Chien-Chuan Chen; Lee J.-Y.; Yang T.-H.; Luo J.-C.; Chen C.-Y.; Hsu W.-F.; Chen Y.-N.; Wu J.-Y.; Lin J.-T.; Lu T.-P.; Chuang E.Y.; El-Omar E.M.; Wu M.-S.; Taiwan Gastrointestinal Disease; Helicobacter Consortium |
| 臺大學術典藏 |
2021-02-05T07:26:11Z |
Clinical Relevance of Liver Kinase B1(LKB1) Protein and Gene Expression in Breast Cancer
|
Chen I.-C.; Chang Y.-C.; Lu Y.-S.; KUEI-PIN CHUNG; Huang C.-S.; Lu T.-P.; Kuo W.-H.; Wang M.-Y.; Kuo K.-T.; Wu P.-F.; Hsueh T.-H.; Shen C.-Y.; Lin C.-H.; Cheng A.-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
|
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 |
2021-02-05T06:29:20Z |
A 4-lncRNA scoring system for prognostication of adult myelodysplastic syndromes
|
Yao C.-Y.;Chen C.-H.;Huang H.-H.;Hou H.-A.;Lin C.-C.;Tseng M.-H.;Kao C.-J.;Lu T.-P.;Wen-Chien Chou;Tien H.-F.; Yao C.-Y.; Chen C.-H.; Huang H.-H.; Hou H.-A.; Lin C.-C.; Tseng M.-H.; Kao C.-J.; Lu T.-P.; WEN-CHIEN CHOU; Tien H.-F. |
| 臺大學術典藏 |
2021-02-04T08:18:22Z |
Transcriptome changes in relation to manic episode
|
Lee Y.-C.;Chao Y.-L.;Chang C.-E.;Hsieh M.-H.;Liu K.-T.;Hsi-Chung Chen;Lu M.-L.;Chen W.-Y.;Chen C.-H.;Tsai M.-H.;Lu T.-P.;Huang M.-C.;Kuo P.-H.; Lee Y.-C.; Chao Y.-L.; Chang C.-E.; Hsieh M.-H.; Liu K.-T.; HSI-CHUNG CHEN; Lu M.-L.; Chen W.-Y.; Chen C.-H.; Tsai M.-H.; Lu T.-P.; Huang M.-C.; Kuo P.-H. |
| 臺大學術典藏 |
2021-02-02T02:20:44Z |
Altered gut microbiota and inflammatory cytokine responses in patients with Parkinson's disease
|
Lin C.-H.; Chen C.-C.; Chiang H.-L.; Liou J.-M.; Chang C.-M.; Lu T.-P.; Chuang E.Y.; Tai Y.-C.; Cheng C.; Lin H.-Y.; MING-SHIANG WU |
| 臺大學術典藏 |
2021-02-02T02:20:43Z |
Long-term changes of gut microbiota, antibiotic resistance, and metabolic parameters after Helicobacter pylori eradication: a multicentre, open-label, randomised trial
|
Liou J.-M.; Chen C.-C.; Chang C.-M.; Fang Y.-J.; Bair M.-J.; Chen P.-Y.; Chang C.-Y.; Hsu Y.-C.; Chen M.-J.; Chen C.-C.; Lee J.-Y.; Yang T.-H.; Luo J.-C.; Chen C.-Y.; Hsu W.-F.; Chen Y.-N.; Wu J.-Y.; Lin J.-T.; Lu T.-P.; Chuang E.Y.; El-Omar E.M.; MING-SHIANG WU; Taiwan Gastrointestinal Disease; Helicobacter Consortium |
| 臺大學術典藏 |
2021-02-02T02:20:38Z |
Comparison of DNA stabilizers and storage conditions on preserving fecal microbiota profiles
|
Chen C.-C.; Wu W.-K.; Chang C.-M.; Panyod S.; Lu T.-P.; Liou J.-M.; Fang Y.-J.; Chuang E.Y.; MING-SHIANG WU |
| 臺大學術典藏 |
2021-01-08T01:57:15Z |
Sp110 polymorphisms are genetic markers for vulnerability to latent and active tuberculosis infection in Taiwan
|
Yan B.-S.; Chang S.-Y.; Chen M.-L.; MENG-RUI LEE; Liang Y.-C.; Lu T.-P.; Wang J.-Y. |
| 臺大學術典藏 |
2021-01-04T12:12:29Z |
Prognostic significance of NPM1 mutation-modulated microRNA-mRNA regulation in acute myeloid leukemia
|
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. |
| 國立成功大學 |
2021 |
Incidence of chronic thromboembolic pulmonary hypertension in Taiwan
|
Liu, H.-Y.;Lu, T.-P.;Tao, C.-W.;Wu, Y.-J.;Huang, W.-C.;Hsu, C.-H.;Liao, W.-C.;Hsu, Hsu H.-H.;Lin, M.-C.;Yu, C.-J. |
| 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 |
2020-12-30T07:47:47Z |
Impact of ancestral differences and reassessment of the classification of previously reported pathogenic variants in patients with brugada syndrome in the genomic era: A SADS-TW BrS registry
|
Chen C.-Y.J.; Lu T.-P.; Lin L.-Y.; YEN BIN LIU; Ho L.-T.; Huang H.-C.; Lai L.-P.; Hwang J.-J.; Yeh S.-F.S.; Wu C.-K.; Juang J.-M.J.; Antzelevitch C. |
| 臺大學術典藏 |
2020-12-30T07:47:46Z |
Validation and disease risk assessment of previously reported genome-wide genetic variants associated with brugada syndrome: SADS-TW BrS registry
|
Jyh-Ming J.-J.; YEN BIN LIU; 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 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 |
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 |
2020-12-29T08:11:10Z |
Preoperative sarcopenia is associated with poor overall survival in pancreatic cancer patients following pancreaticoduodenectomy
|
Chen B.-B.; Wang Y.-H.; Lu T.-P.; CHIEN-HUI WU; Tien Y.-W.; Peng Y.-C. |
| 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 |
2020-12-28T12:03:50Z |
Genome-wide methylation profiles in coronary artery ectasia
|
Lu T.-P.; Chuang N.-C.; Cheng C.-Y.; Hsu C.-A.; Wang Y.-C.; Lin Y.-H.; Lee J.-K.; Wu C.-K.; HWANG, JUEY-JEN; Lin L.-Y.; Yeh S.-F.S.; Chien K.-L.; Juang J.-M.J. |
| 臺大學術典藏 |
2020-12-28T12:03:29Z |
Impact of ancestral differences and reassessment of the classification of previously reported pathogenic variants in patients with brugada syndrome in the genomic era: A SADS-TW BrS registry
|
Chen C.-Y.J.; Lu T.-P.; Lin L.-Y.; Liu Y.-B.; Ho L.-T.; Huang H.-C.; Lai L.-P.; HWANG, JUEY-JEN; Yeh S.-F.S.; Wu C.-K.; Juang J.-M.J.; Antzelevitch C. |
| 臺大學術典藏 |
2020-12-28T12:03:19Z |
Validation and disease risk assessment of previously reported genome-wide genetic variants associated with brugada syndrome: SADS-TW BrS registry
|
Lin J.-L.; Yang D.-H.; Chuang J.-Y.; Sherri Yeh S.-F.; Chen J.-J.; Liao M.-T.; Jyh-Ming J.-J.; 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.; Lu T.-P.; Chuang E.Y.; Ackerman M.J. |
| 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 |
2020-12-28T10:52:56Z |
Impact of ancestral differences and reassessment of the classification of previously reported pathogenic variants in patients with brugada syndrome in the genomic era: A SADS-TW BrS registry
|
Chen C.-Y.J.; Lu T.-P.; Lin L.-Y.; Liu Y.-B.; Ho L.-T.; HUI-CHUN HUANG; Lai L.-P.; Hwang J.-J.; Yeh S.-F.S.; Wu C.-K.; Juang J.-M.J.; Antzelevitch C. |
| 臺大學術典藏 |
2020-12-28T10:52:55Z |
Validation and disease risk assessment of previously reported genome-wide genetic variants associated with brugada syndrome: SADS-TW BrS registry
|
Liu Y.-B.; Jyh-Ming J.-J.; Julius Chen C.-Y.; Yu Q.-Y.; Chattopadhyay A.; Lin L.-Y.; Chen W.-J.; Yu C.-C.; HUI-CHUN HUANG; 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 |
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 |
2020-12-28T07:56:45Z |
Genome-wide methylation profiles in coronary artery ectasia
|
JYH-MING JIMMY JUANG; Chien K.-L.; Lu T.-P.; Chuang N.-C.; Cheng C.-Y.; Hsu C.-A.; Wang Y.-C.; Lin Y.-H.; Lee J.-K.; Wu C.-K.; Hwang J.-J.; Lin L.-Y.; Yeh S.-F.S. |
| 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. |
| 臺大學術典藏 |
2020-12-28T07:56:41Z |
Impact of ancestral differences and reassessment of the classification of previously reported pathogenic variants in patients with brugada syndrome in the genomic era: A SADS-TW BrS registry
|
Liu Y.-B.; Lin L.-Y.; Lu T.-P.; Chen C.-Y.J.; Ho L.-T.; Huang H.-C.; Lai L.-P.; Hwang J.-J.; Yeh S.-F.S.; Wu C.-K.; JYH-MING JIMMY JUANG; Antzelevitch C. |
| 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 |
2020-12-21T08:16:30Z |
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 |
2020-12-04T07:44:42Z |
Genome-wide methylation profiles in coronary artery ectasia
|
Lu T.-P.; Chuang N.-C.; Cheng C.-Y.; Hsu C.-A.; Wang Y.-C.; Lin Y.-H.; Lee J.-K.; Wu C.-K.; Hwang J.-J.; LIAN-YU LIN; Yeh S.-F.S.; Chien K.-L.; Juang J.-M.J. |
| 臺大學術典藏 |
2020-12-04T07:44:36Z |
Impact of ancestral differences and reassessment of the classification of previously reported pathogenic variants in patients with brugada syndrome in the genomic era: A SADS-TW BrS registry
|
Chen C.-Y.J.; Lu T.-P.; LIAN-YU LIN; Liu Y.-B.; Ho L.-T.; Huang H.-C.; Lai L.-P.; Hwang J.-J.; Yeh S.-F.S.; Wu C.-K.; Juang J.-M.J.; Antzelevitch C. |
| 臺大學術典藏 |
2020-12-04T07:44:31Z |
Validation and disease risk assessment of previously reported genome-wide genetic variants associated with brugada syndrome: SADS-TW BrS registry
|
Yang D.-H.; Lin J.-L.; Lu T.-P.; Chuang E.Y.; Ackerman M.J.; Jyh-Ming J.-J.; 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. |
| 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 |
2020-12-02T11:04:31Z |
Genome-wide methylation profiles in coronary artery ectasia
|
Lu T.-P.; Chuang N.-C.; Cheng C.-Y.; Hsu C.-A.; Wang Y.-C.; Lin Y.-H.; Lee J.-K.; CHO-KAI WU; Hwang J.-J.; Lin L.-Y.; Yeh S.-F.S.; Chien K.-L.; Juang J.-M.J. |
| 臺大學術典藏 |
2020-12-02T11:04:29Z |
Impact of ancestral differences and reassessment of the classification of previously reported pathogenic variants in patients with brugada syndrome in the genomic era: A SADS-TW BrS registry
|
Chen C.-Y.J.; Lu T.-P.; Lin L.-Y.; Liu Y.-B.; Ho L.-T.; Huang H.-C.; Lai L.-P.; Hwang J.-J.; Yeh S.-F.S.; CHO-KAI WU; Juang J.-M.J.; Antzelevitch C. |
| 臺大學術典藏 |
2020-12-02T09:15:17Z |
Genome-wide methylation profiles in coronary artery ectasia
|
Lu T.-P.; Chuang N.-C.; Cheng C.-Y.; Hsu C.-A.; YI-CHIH WANG; Lin Y.-H.; Lee J.-K.; Wu C.-K.; Hwang J.-J.; Lin L.-Y.; Yeh S.-F.S.; Chien K.-L.; Juang J.-M.J. |
| 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. |
