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Showing items 151-200 of 354  (8 Page(s) Totally)
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Institution Date Title Author
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.
臺大學術典藏 2020-11-30T07:35:52Z Genetic polymorphisms of a novel vascular susceptibility gene, ninjurin2 (NINJ2), are associated with a decreased risk of Alzheimer's disease Lin K.-P.; Chen S.-Y.; Lai L.-C.; Huang Y.-L.; JEN-HAU CHEN; Chen T.-F.; Sun Y.; Wen L.-L.; Yip P.-K.; Chu Y.-M.; Chen W.J.; Chen Y.-C.
臺大學術典藏 2020-11-30T07:35:51Z Genetic polymorphisms of nerve growth factor receptor (NGFR) and the risk of Alzheimer's disease Cheng H.-C.;Sun Y.;Lai L.-C.;Chen S.-Y.;Lee W.-C.;Jen-Hau Chen;Chen T.-F.;Chen H.-H.;Wen L.-L.;Yip P.-K.;Chu Y.-M.;Chen W.J.;Chen Y.-C.; Cheng H.-C.; Sun Y.; Lai L.-C.; Chen S.-Y.; Lee W.-C.; JEN-HAU CHEN; Chen T.-F.; Chen H.-H.; Wen L.-L.; Yip P.-K.; Chu Y.-M.; Chen W.J.; Chen Y.-C.
臺大學術典藏 2020-11-30T07:35:51Z Genetic polymorphisms of clusterin gene are associated with a decreased risk of Alzheimer's disease Lin Y.-L.; Chen S.-Y.; Lai L.-C.; JEN-HAU CHEN; Yang S.-Y.; Huang Y.-L.; Chen T.-F.; Sun Y.; Wen L.-L.; Yip P.-K.; Chu Y.-M.; Chen W.J.; Chen Y.-C.
臺大學術典藏 2020-11-30T07:35:51Z Sequence variants of interleukin 6 (IL-6) are significantly associated with a decreased risk of late-onset Alzheimer's disease Chen S.-Y.; Chen T.-F.; Lai L.-C.; JEN-HAU CHEN; Sun Y.; Wen L.-L.; Yip P.-K.; Chu Y.-M.; Chen Y.-C.
臺大學術典藏 2020-11-30T07:35:50Z The authors' reply Chen Y.-C.; Chen S.-Y.; Lai L.-C.; JEN-HAU CHEN
臺大學術典藏 2020-11-30T07:35:44Z Impacts of Kidney Dysfunction and Cerebral Cortical Thinning on Cognitive Change in Elderly Population Chen C.-H.;Chen Y.-F.;Tsai P.-H.;Chiou J.-M.;Lai L.-C.;Chen T.-F.;Hung H.;Jen-Hau Chen;Chen Y.-C.; Chen C.-H.; Chen Y.-F.; Tsai P.-H.; Chiou J.-M.; Lai L.-C.; Chen T.-F.; Hung H.; JEN-HAU CHEN; Chen Y.-C.
臺大學術典藏 2020-11-19T08:19:30Z Genetic polymorphisms of nerve growth factor receptor (NGFR) and the risk of Alzheimer's disease Cheng H.-C.; Sun Y.; Lai L.-C.; Chen S.-Y.; WEN-CHUNG LEE; Chen J.-H.; Chen T.-F.; Chen H.-H.; Wen L.-L.; Yip P.-K.; Chu Y.-M.; Chen W.J.; Chen Y.-C.
臺大學術典藏 2020-11-17T02:45:38Z Distinct Signaling Pathways After Higher or Lower Doses of Radiation in Three Closely Related Human Lymphoblast Cell Lines TZU-PIN LU; Lai L.-C.; Lin B.-I.; Chen L.-H.; Hsiao T.-H.; Liber H.L.; Cook J.A.; Mitchell J.B.; Tsai M.-H.; Chuang E.Y.
臺大學術典藏 2020-11-17T02:45:37Z Down-regulation of NDRG1 promotes migration of cancer cells during reoxygenation Chuang E.Y.; Lee C.-Y.; TZU-PIN LU; Sher Y.-P.; Tsai M.-H.; Chen K.-C.; Su Y.-Y.; Lai L.-C.
臺大學術典藏 2020-11-17T02:45:37Z Concurrent analysis of copy number variations and expression profiles to identify genes associated with tumorigenesis and survival outcome in lung adenocarcinoma Tzu-Pin Lu ;Chen P.-C.;Lai L.-C.;Tsai M.-H.;Hsiao C.K.;Chuang E.Y.; TZU-PIN LU; Chen P.-C.; Lai L.-C.; Tsai M.-H.; Hsiao C.K.; Chuang E.Y.
臺大學術典藏 2020-11-17T02:45:37Z Concurrent analysis of copy number variation and gene expression: Application in paired non-smoking female lung cancer patients Chen P.-C.; Chang J.-C.;Lai L.-C.;Tzu-Pin Lu ;Tsai M.-H.;Chuang E.Y.;Hsiao C.K.;Chen P.-C.; Chang J.-C.; Lai L.-C.; TZU-PIN LU; Tsai M.-H.; Chuang E.Y.; Hsiao C.K.
臺大學術典藏 2020-11-17T02:45:37Z Identification of a novel biomarker, SEMA5A, for non-small cell lung carcinoma in nonsmoking women TZU-PIN LU; Tsai M.-H.; Lee J.-M.; Hsu C.-P.; Chen P.-C.; Lin C.-W.; Shih J.-Y.; Yang P.-C.; Hsiao C.K.; Lai L.-C.; Chuang E.Y.
臺大學術典藏 2020-11-17T02:45:36Z MiRSystem: An integrated system for characterizing enriched functions and pathways of microRNA targets Tzu-Pin Lu ;Lee C.-Y.;Tsai M.-H.;Chiu Y.-C.;Hsiao C.K.;Lai L.-C.;Chuang E.Y.; TZU-PIN LU; Lee C.-Y.; Tsai M.-H.; Chiu Y.-C.; Hsiao C.K.; Lai L.-C.; Chuang E.Y.
臺大學術典藏 2020-11-17T02:45:36Z Integrated analyses of copy number variations and gene expression in lung adenocarcinoma TZU-PIN LU; Lai L.-C.; Tsai M.-H.; Chen P.-C.; Hsu C.-P.; Lee J.-M.; Hsiao C.K.; Chuang E.Y.
臺大學術典藏 2020-11-17T02:45:36Z Expression and functions of semaphorins in cancer TZU-PIN LU; Tsai M.-H.; Hsiao C.K.; Lai L.-C.; Chuang E.Y.
臺大學術典藏 2020-11-17T02:45:35Z Identification of gene expression biomarkers for predicting radiation exposure Tzu-Pin Lu;Hsu Y.-Y.;Lai L.-C.;Tsai M.-H.;Chuang E.Y.; TZU-PIN LU; Hsu Y.-Y.; Lai L.-C.; Tsai M.-H.; Chuang E.Y.
臺大學術典藏 2020-11-17T02:45:35Z Concurrent analysis of copy number variation and gene expression: Application in paired non-smoking female lung cancer patients Chen P.-C.;Tzu-Pin Lu;Chang J.-C.;Lai L.-C.;Tsai M.-H.;Hsiao C.K.;Chuang E.Y.; Chen P.-C.; TZU-PIN LU; Chang J.-C.; Lai L.-C.; Tsai M.-H.; Hsiao C.K.; Chuang E.Y.
臺大學術典藏 2020-11-17T02:45:34Z Utilizing multiple in silico analyses to identify putative causal SCN5A variants in brugada syndrome Lin J.-L.; Chiang F.-T.; Yeh S.S.-F.; Chen W.-P.; Chuang E.Y.; Lai L.-P.; Hwang J.-J.; Juang J.-M.J.;Tzu-Pin Lu;Lai L.-C.;Hsueh C.-H.;Liu Y.-B.;Tsai C.-T.;Lin L.-Y.;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.; Juang J.-M.J.; TZU-PIN LU; Lai L.-C.; Hsueh C.-H.; Liu Y.-B.; Tsai C.-T.; Lin L.-Y.; Yu C.-C.
臺大學術典藏 2020-11-17T02:45:34Z Identification of genes with consistent methylation levels across different human tissues Tzu-Pin Lu;Chen K.T.;Tsai M.-H.;Kuo K.-T.;Hsiao C.K.;Lai L.-C.;Chuang E.Y.; TZU-PIN LU; Chen K.T.; Tsai M.-H.; Kuo K.-T.; Hsiao C.K.; Lai L.-C.; Chuang E.Y.
臺大學術典藏 2020-11-17T02:45:34Z Comparisons and performance evaluations of RNA-seq alignment tools Wang W.-A.;Wu C.-T.;Tzu-Pin Lu;Tsai M.-H.;Lai L.-C.;Chuang E.Y.; Wang W.-A.; Wu C.-T.; TZU-PIN LU; Tsai M.-H.; Lai L.-C.; Chuang E.Y.
臺大學術典藏 2020-11-17T02:45:33Z Disease-targeted sequencing of ion channel genes identifies de novo mutations in patients with non-familial Brugada syndrome Chuang E.Y.; Lin J.-L.; Juang J.-M.J.;Tzu-Pin Lu;Lai L.-C.;Ho C.-C.;Liu Y.-B.;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.; Juang J.-M.J.; TZU-PIN LU; Lai L.-C.; Ho C.-C.; Liu Y.-B.; Tsai C.-T.; Lin L.-Y.; Yu C.-C.; Chen W.-J.; Chiang F.-T.; Yeh S.-F.S.; Lai L.-P.
臺大學術典藏 2020-11-17T02:45:33Z SNP rs10248565 in HDAC9 as a novel genomic aberration biomarker of lung adenocarcinoma in non-smoking women Lai L.-C.;Tsai M.-H.;Chen P.-C.;Chen L.H.;Hsiao J.-H.;Chen S.-K.;Tzu-Pin Lu;Lee J.-M.;Hsu C.-P.;Hsiao C.K.;Chuang E.Y.; Lai L.-C.; Tsai M.-H.; Chen P.-C.; Chen L.H.; Hsiao J.-H.; Chen S.-K.; TZU-PIN LU; Lee J.-M.; Hsu C.-P.; Hsiao C.K.; Chuang E.Y.
臺大學術典藏 2020-11-17T02:45:32Z Putative effectors for prognosis in lung adenocarcinoma are ethnic and gender specific Woolston A.;Sintupisut N.;Tzu-Pin Lu;Lai L.-C.;Tsai M.-H.;Chuang E.Y.;Yeang C.-H.; Woolston A.; Sintupisut N.; TZU-PIN LU; Lai L.-C.; Tsai M.-H.; Chuang E.Y.; Yeang C.-H.
臺大學術典藏 2020-11-17T02:45:32Z Identification of regulatory SNPs associated with genetic modifications in lung adenocarcinoma Bioinformatics Tzu-Pin Lu;Hsiao C.K.;Lai L.-C.;Tsai M.-H.;Hsu C.-P.;Lee J.-M.;Chuang E.Y.; TZU-PIN LU; Hsiao C.K.; Lai L.-C.; Tsai M.-H.; Hsu C.-P.; Lee J.-M.; Chuang E.Y.
臺大學術典藏 2020-11-17T02:45:30Z 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.;Tzu-Pin Lu;Lai L.-C.;Chen Y.;Tien H.-F.;Chuang E.Y.; Chiu Y.-C.; Tsai M.-H.; Chou W.-C.; Liu Y.-C.; Kuo Y.-Y.; Hou H.-A.; TZU-PIN LU; Lai L.-C.; Chen Y.; Tien H.-F.; Chuang E.Y.
臺大學術典藏 2020-11-17T02:45:29Z Development of a prediction model for radiosensitivity using the expression values of genes and long non-coding RNAs Wang W.-A.;Lai L.-C.;Tsai M.-H.;Tzu-Pin Lu;Chuang E.Y.; Wang W.-A.; Lai L.-C.; Tsai M.-H.; TZU-PIN LU; Chuang E.Y.
臺大學術典藏 2020-11-17T02:45:29Z Differential network analysis reveals the genome-wide landscape of estrogen receptor modulation in hormonal cancers Hsiao T.-H.;Chiu Y.-C.;Hsu P.-Y.;Tzu-Pin Lu;Lai L.-C.;Tsai M.-H.;Huang T.H.-M.;Chuang E.Y.;Chen Y.; Hsiao T.-H.; Chiu Y.-C.; Hsu P.-Y.; TZU-PIN LU; Lai L.-C.; Tsai M.-H.; Huang T.H.-M.; Chuang E.Y.; Chen Y.
臺大學術典藏 2020-11-17T02:45:27Z Identification of methylation-driven, differentially expressed STXBP6 as a novel biomarker in lung adenocarcinoma Lenka G.; Tsai M.-H.; Lin H.-C.; Hsiao J.-H.; Lee Y.-C.; TZU-PIN LU; Lee J.-M.; Hsu C.-P.; Lai L.-C.; Chuang E.Y.
臺大學術典藏 2020-11-17T02:45:27Z iGC-an integrated analysis package of gene expression and copy number alteration Lai Y.-P.;Wang L.-B.;Wang W.-A.;Lai L.-C.;Tsai M.-H.;Tzu-Pin Lu;Chuang E.Y.; Lai Y.-P.; Wang L.-B.; Wang W.-A.; Lai L.-C.; Tsai M.-H.; TZU-PIN LU; Chuang E.Y.
臺大學術典藏 2020-11-17T02:45:25Z ADAM9 promotes lung cancer progression through vascular remodeling by VEGFA, ANGPT2, and PLAT Lin C.-Y.; Cho C.-F.; Bai S.-T.; Liu J.-P.; Kuo T.-T.; Wang L.-J.; Lin Y.-S.; Lin C.-C.; Lai L.-C.; TZU-PIN LU; Hsieh C.-Y.; Chu C.-N.; Cheng D.-C.; Sher Y.-P.
臺大學術典藏 2020-11-17T02:45:24Z An automated microfluidic DNA microarray platform for genetic variant detection in inherited arrhythmic diseases Huang S.-H.;Chang Y.-S.;Juang J.-M.J.;Chang K.-W.;Tsai M.-H.;Tzu-Pin Lu;Lai L.-C.;Chuang E.Y.;Huang N.-T.; Huang S.-H.; Chang Y.-S.; Juang J.-M.J.; Chang K.-W.; Tsai M.-H.; TZU-PIN LU; Lai L.-C.; Chuang E.Y.; Huang N.-T.
臺大學術典藏 2020-11-17T02:45:24Z CellExpress: A comprehensive microarray-based cancer cell line and clinical sample gene expression analysis online system Lai L.-C.; Tsai M.-H.; TZU-PIN LU; Chuang E.Y.; Lee C.-Y.; Lee Y.-F.; Lee Y.-F.;Lee C.-Y.;Lai L.-C.;Tsai M.-H.;Tzu-Pin Lu;Chuang E.Y.
臺大學術典藏 2020-11-17T02:45:23Z Whole-genome de novo sequencing reveals unique genes that contributed to the adaptive evolution of the Mikado pheasant Lee C.-Y.;Hsieh P.-H.;Chiang L.-M.;Chattopadhyay A.;Li K.-Y.;Lee Y.-F.;Tzu-Pin Lu;Lai L.-C.;Lin E.-C.;Lee H.;Ding S.-T.;Tsai M.-H.;Chen C.-Y.;Chuang E.Y.; Lee C.-Y.; Hsieh P.-H.; Chiang L.-M.; Chattopadhyay A.; Li K.-Y.; Lee Y.-F.; TZU-PIN LU; Lai L.-C.; Lin E.-C.; Lee H.; Ding S.-T.; Tsai M.-H.; Chen C.-Y.; Chuang E.Y.
臺大學術典藏 2020-11-17T02:45:23Z The extracellular SEMA domain attenuates intracellular apoptotic signaling of semaphorin 6A in lung cancer cells Shen C.-Y.; Chang Y.-C.; Chen L.-H.; Lin W.-C.; Lee Y.-H.; Yeh S.-T.; Chen H.-K.; Fang W.; Hsu C.-P.; Lee J.-M.; TZU-PIN LU; Hsiao P.-W.; Lai L.-C.; Tsai M.-H.; Chuang E.Y.
臺大學術典藏 2020-11-17T02:45:22Z VariED: The first integrated database of gene annotation and expression profiles for variants related to human diseases Juang J.-M.J.; Lai L.-C.; Tsai M.-H.; TZU-PIN LU; Chuang E.Y.; Lee C.-Y.;Chattopadhyay A.;Chiang L.-M.;Juang J.-M.J.;Lai L.-C.;Tsai M.-H.;Tzu-Pin Lu;Chuang E.Y.; Lee C.-Y.; Chattopadhyay A.; Chiang L.-M.
臺大學術典藏 2020-11-17T02:45:21Z AnamiR: Integrated analysis of MicroRNA and gene expression profiling Wang T.-T.;Lee C.-Y.;Lai L.-C.;Tsai M.-H.;Tzu-Pin Lu;Chuang E.Y.; Wang T.-T.; Lee C.-Y.; Lai L.-C.; Tsai M.-H.; TZU-PIN LU; Chuang E.Y.
臺大學術典藏 2020-11-17T02:45:20Z Using proteomic profiling to characterize protein signatures of different thymoma subtypes Fang W.; Chuang E.Y.; Zhu L.; Tsai M.-H.; TZU-PIN LU; Hsiao Y.-W.; Chen Y.-A.; Sun Q.-L.; Lai L.-C.; Lai L.-C.;Sun Q.-L.;Chen Y.-A.;Hsiao Y.-W.;Tzu-Pin Lu;Tsai M.-H.;Zhu L.;Chuang E.Y.;Fang W.
臺大學術典藏 2020-11-11T08:19:58Z Impacts of Kidney Dysfunction and Cerebral Cortical Thinning on Cognitive Change in Elderly Population CHIH-HAO CHEN; Chen Y.-F.; Tsai P.-H.; Chiou J.-M.; Lai L.-C.; Chen T.-F.; Hung H.; Chen J.-H.; Chen Y.-C.
臺大學術典藏 2020-11-03T11:20:40Z Genetic polymorphisms of a novel vascular susceptibility gene, ninjurin2 (NINJ2), are associated with a decreased risk of Alzheimer's disease Chen Y.-C.; Chen W.J.; Lin K.-P. ;Chen S.-Y. ;Lai L.-C. ;Huang Y.-L. ;Chen J.-H. ;Ta-Fu Chen ;Sun Y. ;Wen L.-L. ;Yip P.-K. ;Chu Y.-M. ;Chen W.J. ;Chen Y.-C.; Lin K.-P.; Chen S.-Y.; Lai L.-C.; Huang Y.-L.; Chen J.-H.; TA-FU CHEN; Sun Y.; Wen L.-L.; Yip P.-K.; Chu Y.-M.
臺大學術典藏 2020-10-26T11:34:42Z Disease-targeted sequencing of ion channel genes identifies de novo mutations in patients with non-familial Brugada syndrome Ho C.-C.; Lu T.-P.; Lai L.-C.; JYH-MING JIMMY JUANG; Liu Y.-B.; 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 2020-10-26T11:34:32Z 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 2020-10-26T11:34:29Z VariED: The first integrated database of gene annotation and expression profiles for variants related to human diseases Lee C.-Y.; Chattopadhyay A.; Chiang L.-M.; JYH-MING JIMMY JUANG; Lai L.-C.; Tsai M.-H.; Lu T.-P.; Chuang E.Y.
臺大學術典藏 2020-10-26T11:34:25Z GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death JYH-MING JIMMY JUANG; 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.; Lai L.-C.; Yeh S.-F.S.; Lai L.-P.; Chuang E.Y.; Rivolta I.; Antzelevitch C.
臺大學術典藏 2020-10-14T07:24:42Z SLCO3A1, a novel Crohn's disease-associated gene, regulates NF-κB activity and associates with intestinal perforation Wong J.-M.; Podolsky D.K.; Xavier R.J.; Wang C.-Y.; Tung C.-C.; Chen Y.; Shieh M.-J.; Ni Y.-H.; SHU-CHEN WEI; 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.
臺大學術典藏 2020-10-14T07:24:36Z SHANK3 Regulates Intestinal Barrier Function Through Modulating ZO-1 Expression Through the PKC?-dependent Pathway Tsao P.-N.; SHU-CHEN WEI; Yang-Yen H.-F.; Wong J.-M.; 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.

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