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Institution	Date	Title	Author
臺大學術典藏	2021-03-11T04:29:31Z	Genome-wide screening identifies a KCNIP1 copy number variant as a genetic predictor for atrial fibrillation	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 J.-J.; FU-TIEN CHIANG; Lin J.-L.
臺大學術典藏	2021-03-08T06:51:49Z	MicroRNA-107 enhances radiosensitivity by suppressing granulin in PC-3 prostate cancer cells	Lo H.-C.;Hsu J.-H.;Liang-Chuan Lai;Tsai M.-H.;Chuang E.Y.; Lo H.-C.; Hsu J.-H.; Liang-Chuan Lai; Tsai M.-H.; Chuang E.Y.
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	2021-02-05T06:29:30Z	An mRNA expression signature for prognostication in de novo acute myeloid leukemia patients with normal karyotype	Chuang M.-K.; Chiu Y.-C.; WEN-CHIEN CHOU; Hou H.-A.; Tseng M.-H.; Kuo Y.-Y.; Chen Y.; Chuang E.Y.; Tien H.-F.
臺大學術典藏	2021-02-05T06:29:27Z	A 3-microRNA scoring system for prognostication in de novo acute myeloid leukemia patients	Chuang M.-K.; Chiu Y.-C.; WEN-CHIEN CHOU; Hou H.-A.; Chuang E.Y.; Tien H.-F.
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	2021-02-05T06:29:19Z	Prognostic impacts and dynamic changes of cohesin complex gene mutations in de novo acute myeloid leukemia	Tsai C.-H.;Hou H.-A.;Tang J.-L.;Kuo Y.-Y.;Chiu Y.-C.;Lin C.-C.;Liu C.-Y.;Tseng M.-H.;Lin T.-Y.;Liu M.-C.;Liu C.-W.;Lin L.-I.;Yao M.;Li C.-C.;Huang S.-Y.;Ko B.-S.;Hsu S.-C.;Lin C.-T.;Wu S.-J.;Chen C.-Y.;Tsay W.;Chuang E.Y.;Wen-Chien Chou;Tien H.-F.; Tsai C.-H.; Hou H.-A.; Tang J.-L.; Kuo Y.-Y.; Chiu Y.-C.; Lin C.-C.; Liu C.-Y.; Tseng M.-H.; Lin T.-Y.; Liu M.-C.; Liu C.-W.; Lin L.-I.; Yao M.; Li C.-C.; Huang S.-Y.; Ko B.-S.; Hsu S.-C.; Lin C.-T.; Wu S.-J.; Chen C.-Y.; Tsay W.; Chuang E.Y.; WEN-CHIEN CHOU; Tien H.-F.
臺大學術典藏	2021-02-02T02:22:06Z	Duodenal ulcer-related antigens from Helicobacter pylori: Immunoproteome and protein microarray approaches	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	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	2021-01-15T02:46:26Z	A whole genome methylation analysis of systemic lupus erythematosus: Hypomethylation of the IL10 and IL1R2 promoters is associated with disease activity	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	2021-01-06T03:58:25Z	Prognostic impacts and dynamic changes of cohesin complex gene mutations in de novo acute myeloid leukemia	Tsai C.-H.; Hou H.-A.; JIH-LUH TANG; Kuo Y.-Y.; Chiu Y.-C.; Lin C.-C.; Liu C.-Y.; Tseng M.-H.; Lin T.-Y.; Liu M.-C.; Liu C.-W.; Lin L.-I.; Yao M.; Li C.-C.; Huang S.-Y.; Ko B.-S.; Hsu S.-C.; Lin C.-T.; Wu S.-J.; Chen C.-Y.; Tsay W.; Chuang E.Y.; Chou W.-C.; Tien H.-F.
臺大學術典藏	2021-01-05T03:34:33Z	Prognostic impacts and dynamic changes of cohesin complex gene mutations in de novo acute myeloid leukemia	Kuo Y.-Y.; Tang J.-L.; Hou H.-A.; Tsai C.-H.; Tien H.-F.; Chou W.-C.; Chiu Y.-C.; Lin C.-C.; Liu C.-Y.; Tseng M.-H.; Lin T.-Y.; Liu M.-C.; Liu C.-W.; Lin L.-I.; MING YAO; Li C.-C.; Huang S.-Y.; Ko B.-S.; Hsu S.-C.; Lin C.-T.; Wu S.-J.; Chen C.-Y.; Tsay W.; Chuang E.Y.
臺大學術典藏	2021-01-05T00:56:28Z	Prognostic impacts and dynamic changes of cohesin complex gene mutations in de novo acute myeloid leukemia	Ko B.-S.; Huang S.-Y.; Li C.-C.; Tsai C.-H.; Hou H.-A.; Tang J.-L.; Kuo Y.-Y.; Chiu Y.-C.; Lin C.-C.; Liu C.-Y.; Tseng M.-H.; Lin T.-Y.; Liu M.-C.; Liu C.-W.; Lin L.-I.; Yao M.; Hsu S.-C.; Lin C.-T.; SHANG-JU WU; Chen C.-Y.; Tsay W.; Chuang E.Y.; Chou W.-C.; Tien H.-F.
臺大學術典藏	2021-01-04T12:12:34Z	An mRNA expression signature for prognostication in de novo acute myeloid leukemia patients with normal karyotype	HWEI-FANG TIEN; Chen Y.; Chuang E.Y.; Kuo Y.-Y.; Tseng M.-H.; Hou H.-A.; Chou W.-C.; Chiu Y.-C.; Chuang M.-K.
臺大學術典藏	2021-01-04T12:12:33Z	A 3-microRNA scoring system for prognostication in de novo acute myeloid leukemia patients	Chuang M.-K.; Chiu Y.-C.; Chou W.-C.; Hou H.-A.; Chuang E.Y.; HWEI-FANG TIEN
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.
臺大學術典藏	2020-12-30T08:47:48Z	Next-generation sequencing in the genetics of human atrial fibrillation	Hsieh C.-S.; Chuang E.Y.; Juang J.-M.J.; Hwang J.-J.; Tseng C.-D.; Chiang F.-T.; Lai L.-P.; Lin J.-L.; CHIA-TI TSAI
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	2020-12-30T08:47:41Z	Next-generation sequencing of nine atrial fibrillation candidate genes identified novel de novo mutations in patients with extreme trait of atrial fibrillation	Lin L.-Y.; Lai L.-P.; Hwang J.-J.; Chiang F.-T.; Lin J.-L.; CHIA-TI TSAI; Hsieh C.-S.; Chang S.-N.; Chuang E.Y.; Juang J.-M.J.
臺大學術典藏	2020-12-30T08:47:38Z	Genome-wide screening identifies a KCNIP1 copy number variant as a genetic predictor for atrial fibrillation	Chiang F.-T.; Lin J.-L.; Hwang J.-J.; Tseng C.-D.; CHIA-TI TSAI; 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.
臺大學術典藏	2020-12-30T08:47:32Z	Prevalence of sudden arrhythmic death syndrome-related genetic mutations in an Asian cohort of whole genome sequence	Chiu F.-C.; Wu C.-K.; Hwang J.-J.; Chuang E.Y.; CHIA-TI TSAI; Huang P.-S.; Hsieh C.-S.; Chang S.-N.; Chen J.-J.
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	2020-12-30T07:47:46Z	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	2020-12-29T08:15:53Z	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	2020-12-28T12:04:07Z	Next-generation sequencing in the genetics of human atrial fibrillation	Hsieh C.-S.; Chuang E.Y.; Juang J.-M.J.; HWANG, JUEY-JEN; Tseng C.-D.; Chiang F.-T.; Lai L.-P.; Lin J.-L.; Tsai C.-T.
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	2020-12-28T12:03:59Z	Next-generation sequencing of nine atrial fibrillation candidate genes identified novel de novo mutations in patients with extreme trait of atrial fibrillation	Tsai C.-T.; Hsieh C.-S.; Chang S.-N.; Chuang E.Y.; Juang J.-M.J.; Lin L.-Y.; Lai L.-P.; HWANG, JUEY-JEN; Chiang F.-T.; Lin J.-L.
臺大學術典藏	2020-12-28T12:03:54Z	Genome-wide screening identifies a KCNIP1 copy number variant as a genetic predictor for atrial fibrillation	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	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	2020-12-28T12:03:15Z	Prevalence of sudden arrhythmic death syndrome-related genetic mutations in an Asian cohort of whole genome sequence	Chiu F.-C.; Wu C.-K.; HWANG, JUEY-JEN; Chuang E.Y.; Tsai C.-T.; Huang P.-S.; Hsieh C.-S.; Chang S.-N.; Chen J.-J.
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	2020-12-28T08:14:22Z	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	2020-12-28T07:56:49Z	Next-generation sequencing of nine atrial fibrillation candidate genes identified novel de novo mutations in patients with extreme trait of atrial fibrillation	Lin L.-Y.; JYH-MING JIMMY JUANG; Chuang E.Y.; Chang S.-N.; Hsieh C.-S.; Tsai C.-T.; Lai L.-P.; Hwang J.-J.; Chiang F.-T.; Lin J.-L.
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	2020-12-28T07:56:37Z	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	2020-12-22T03:29:15Z	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.

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