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Showing items 151-160 of 232  (24 Page(s) Totally)
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Institution Date Title Author
臺大學術典藏 2021-01-15T02:46:15Z The Development of Maillard Reaction, and Advanced Glycation End Product (AGE)-Receptor for AGE (RAGE) Signaling Inhibitors as Novel Therapeutic Strategies for Patients with AGE-Related Diseases Shen C.-Y.; Lu C.-H.; Wu C.-H.; Li K.-J.; Kuo Y.-M.; SONG-CHOU HSIEH; Yu C.-L.
臺大學術典藏 2021-01-15T02:46:14Z Aberrant non-coding rna expression in patients with systemic lupus erythematosus: Consequences for immune dysfunctions and tissue damage Tsai C.-Y.; Shen C.-Y.; Liu C.-W.; SONG-CHOU HSIEH; Liao H.-T.; Li K.-J.; Lu C.-S.; Lee H.-T.; Lin C.-S.; Wu C.-H.; Kuo Y.-M.; Yu C.-L.
臺大學術典藏 2021-01-06T03:58:49Z Acquisition and cure of autoimmune disease following allogeneic hematopoietic stem cell transplantation Hou H.-A.; JIH-LUH TANG; Hsu S.-C.; Yu C.-L.; Chen Y.-C.; Yao M.
臺大學術典藏 2020-12-24T02:04:05Z Antenatal treatment of chylothorax and cystic hygroma with OK-432 in nonimmune hydrops fetalis Chen M.;Chen C.-P.;Shih J.-C.;Hung-Chieh Chou;Yu C.-L.;Wang B.-T.;Hsieh C.-Y.; Chen M.; Chen C.-P.; Shih J.-C.; HUNG-CHIEH CHOU; Yu C.-L.; Wang B.-T.; Hsieh C.-Y.
臺大學術典藏 2020-12-22T03:29:51Z Rapid detection of β-globin gene (HBB) mutations coupling heteroduplex and primer-extension analysis by DHPLC Su Y.-N.;Lee C.-N.;Hung C.-C.;Chen C.-A.;Cheng W.-F.;Po-Nien Tsao;Yu C.-L.;Hsieh F.-J.; Su Y.-N.; Lee C.-N.; Hung C.-C.; Chen C.-A.; Cheng W.-F.; PO-NIEN TSAO; Yu C.-L.; Hsieh F.-J.
臺大學術典藏 2020-12-22T03:29:45Z Quantitative analysis of SMN1 and SMN2 genes based on DHPLC: A highly efficient and reliable carrier-screening test Su Y.-N.;Hung C.-C.;Li H.;Lee C.-N.;Cheng W.-F.;Po-Nien Tsao;Chang M.-C.;Yu C.-L.;Hsieh W.-S.;Lin W.-L.;Hsu S.-M.; Su Y.-N.; Hung C.-C.; Li H.; Lee C.-N.; Cheng W.-F.; PO-NIEN TSAO; Chang M.-C.; Yu C.-L.; Hsieh W.-S.; Lin W.-L.; Hsu S.-M.
臺大學術典藏 2020-12-18T08:38:30Z Disseminated mycobacterium abscessus infection and showerheads, Taiwan Kuo Y.-M.;Cheng A.;Wu P.-C.;Hsieh S.-C.;Hsieh S.-M.;Po-Ren Hsueh;Yu C.-L.; Kuo Y.-M.; Cheng A.; Wu P.-C.; Hsieh S.-C.; Hsieh S.-M.; PO-REN HSUEH; Yu C.-L.
臺大學術典藏 2020-12-16T02:26:16Z Debate in newborn screening for metabolic disorders in Taiwan - A voluntary screening? Mandatory screening? Or both? Wuh-Liang Hwu;Yu C.-L.; WUH-LIANG HWU; Yu C.-L.
臺大學術典藏 2020-12-16T02:26:08Z Six novel NPC1 mutations in Chinese patients with Niemann-Pick disease type C Yang C.-C.;Su Y.-N.;Chiou P.-C.;Fietz M.J.;Yu C.-L.;Wuh-Liang Hwu;Lee M.-J.; Yang C.-C.; Su Y.-N.; Chiou P.-C.; Fietz M.J.; Yu C.-L.; WUH-LIANG HWU; Lee M.-J.
臺大學術典藏 2020-12-16T02:26:06Z Identification of forty-five novel and twenty-three known NF1 mutations in Chinese patients with neurofibromatosis type 1. Lee M.J.;Su Y.N.;You H.L.;Chiou S.C.;Lin L.C.;Yang C.C.;Lee W.C.;Wuh-Liang Hwu;Hsieh F.J.;Stephenson D.A.;Yu C.L.; Lee M.J.; Su Y.N.; You H.L.; Chiou S.C.; Lin L.C.; Yang C.C.; Lee W.C.; WUH-LIANG HWU; Hsieh F.J.; Stephenson D.A.; Yu C.L.

Showing items 151-160 of 232  (24 Page(s) Totally)
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