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Institution Date Title Author
臺大學術典藏 2018-09-10T06:40:10Z Hereditary neuropathy with liability to pressure palsies: A clinical and electrophysiological study Cheng, M.-L. and Jeng, J.-S. and Sung, S.-F. and Chang, Y.-C. and Huang, C.-C. and Chen R.-, C. and Hsieh, S.-T.; SUNG-TSANG HSIEH
臺大學術典藏 2020-03-02T08:11:33Z Hereditary neuropathy with liability to pressure palsies: A clinical and electrophysiological study Cheng M.-L.;Jeng J.-S.;Sung S.-F.;Chang Y.-C.;Huang C.-C.;Chen R.- C.;Sung-Tsang Hsieh; Cheng M.-L.; Jeng J.-S.; Sung S.-F.; Chang Y.-C.; Huang C.-C.; Chen R.- C.; SUNG-TSANG HSIEH
臺大學術典藏 2020-03-03T03:46:14Z Hereditary neuropathy with liability to pressure palsies: A clinical and electrophysiological study Cheng M.-L.; JIANN-SHING JENG; Sung S.-F.; Chang Y.-C.; Huang C.-C.; Chen R.- C.; Hsieh S.-T.
臺大學術典藏 2020-11-03T11:45:23Z Hereditary neuropathy with liability to pressure palsies: A clinical and electrophysiological study Cheng M.-L.;Jiann-Shing Jeng;Sung S.-F.;Chang Y.-C.;Huang C.-C.;Chen R.- C.;Hsieh S.-T.; Cheng M.-L.; JIANN-SHING JENG; Sung S.-F.; Chang Y.-C.; Huang C.-C.; Chen R.- C.; Hsieh S.-T.
國立臺灣大學 1991 Hereditary Pancreatitis in a Chinese Family 林肇堂; Wang, T. H.; 陳定信; Lin, Jaw-Town; Wang, T. H.; Chen, Ding-Shinn
國立臺灣大學 1994 Hereditary Progressive Dystonia with Marked Diurnal Fluctuation (Segawa Syndrome) in Taiwan 王本榮; 楊千立; 胡務亮; 沈友仁; WANG, PEN-JUNG; KO, YOU-MIN; YOUNG, CHAINLLIE; HWU, WUH-LIANG; SHEN, YU-ZEN
臺大學術典藏 2020-12-16T02:26:30Z Hereditary progressive dystonia with marked diurnal fluctuation (Segawa syndrome) in Taiwan Wang P.-J.; Ko Y.-M.; Young C.; WUH-LIANG HWU; Shen Y.-Z.
臺大學術典藏 2020-12-16T02:26:33Z Hereditary progressive dystonia with marked diurnal fluctuation: report of a case. WUH-LIANG HWU; Wang P.J.; Shen Y.Z.
國立臺灣大學 1989 Hereditary Progressive Dystonia with Marked Diurnal Fluctuation:Report of A Case 王本榮; Shen, Y. Z.; 胡務亮; Wang, Pen-Jung; Shen, Y. Z.; Hwu, Wuh-Liang
國立臺灣大學 1989 Hereditary Progrressive Dystonia with Marked Diurnal Fluctuation, Report of a Case 胡務亮; Wang, P. J.; Shen, Y. Z.; Hwu, Wuh-Liang; Wang, P. J.; Shen, Y. Z.
臺大學術典藏 2018-09-10T04:25:34Z Hereditary sensory neuropathy is caused by a mutation in the delta subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct4) gene Lee, M.-J. and Stephenson, D.A. and Groves, M.J. and Sweeney, M.G. and Davis, M.B. and An, S.-F. and Houlden, H. and Salih, M.A.M. and Timmerman, V. and de Jonghe, P. and Auer-Grumbach, M. and Di Maria, E. and Scaravilli, F. and Wood, N.W. and Reilly, M.M.; MING-JEN LEE
臺大學術典藏 2020-03-03T02:33:36Z Hereditary sensory neuropathy is caused by a mutation in the delta subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct4) gene MING-JEN LEE; Stephenson D.A.; Groves M.J.; Sweeney M.G.; Davis M.B.; An S.-F.; Houlden H.; Salih M.A.M.; Timmerman V.; de Jonghe P.; Auer-Grumbach M.; Di Maria E.; Scaravilli F.; Wood N.W.; Reilly M.M.
臺大學術典藏 2020-11-03T11:32:32Z Hereditary sensory neuropathy is caused by a mutation in the delta subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct4) gene Houlden H.; Salih M.A.M.; Timmerman V.; de Jonghe P.; Auer-Grumbach M.; Di Maria E.; Scaravilli F.; Wood N.W.; Reilly M.M.; Davis M.B.; An S.-F.; Sweeney M.G.; Groves M.J.; Stephenson D.A.; MING-JEN LEE
臺大學術典藏 2018-09-10T04:24:33Z Hereditary xanthinuria: report of two cases. Chu, T.S.; TZONG-SHINN CHU
臺大學術典藏 2021-07-20T03:15:56Z Hereditary xanthinuria: report of two cases. TZONG-SHINN CHU
國家衛生研究院 2011-12 Heregulin beta-1 induces loss of Cell-Cell contact and enhances expression of MUC1 at the cell surface in HCC2998 and MKN45-1 cells Okoshi, R;Shu, CL;Ihara, S;Fukui, Y
臺大學術典藏 2020-02-06T08:49:04Z Heregulin targets γ-catenin to the nucleolus by a mechanism dependent on the DF3/MUC1 oncoprotein Loda M.; Kufe D.; Li Y.;Wei-Hsuan Yu;Ren J.;Chen W.;Huang L.;Kharbanda S.;Loda M.;Kufe D.; Li Y.; WEI-HSUAN YU; Ren J.; Chen W.; Huang L.; Kharbanda S.
國立臺灣大學 2006 Herh Drug Rice Milk for Terminal Cancer Patients on Life Satisfaction Assessment 吳宗修; 邱泰源; 陳慶餘; 楊玲玲; WU, TSUNG-HSIU; CHIU, TAI-YUAN; CHEN, CHING-YU; YANG, L.-L.
亞洲大學 2016-01 Hericium erinaceus Inhibits TNF-?-Induced Angiogenesis and ROS Generation through Suppression of MMP-9/NF-?B Signaling and Activation of Nrf2-Mediated Antioxidant Genes in Human EA.hy926 Endothelial Cells Chang), 張竣維(Hebron C.;楊新玲*;Huang), 黃佩珍(Pei-Jane
亞洲大學 2016-01 Hericium erinaceus Inhibits TNF-?-Induced Angiogenesis and ROS Generation through Suppression of MMP-9/NF-?B Signaling and Activation of Nrf2-Mediated Antioxidant Genes in Human EA.hy926 Endothelial Cells 張竣維;Chang, Hebron C.;楊新玲*;黃佩珍;Huang, Pei-Jane
亞洲大學 2016-01 Hericium erinaceus Inhibits TNF-?-Induced Angiogenesis and ROS Generation through Suppression of MMP-9/NF-?B Signaling and Activation of Nrf2-Mediated Antioxidant Genes in Human EA.hy926 Endothelial Cells Huang;, 張竣維;Hebron C. Chang;楊新玲*;黃佩珍;Pei-Jane
中國醫藥大學 2016-01 Hericium erinaceus Inhibits TNF-?-Induced Angiogenesis and ROS Generation through Suppression of MMP-9/NF-?B Signaling and Activation of Nrf2-Mediated Antioxidant Genes in Human EA.hy926 Endothelial Cells (Hebron C. Chang);楊新玲(Yang Hsin-ling);(Jih-Hao Pan);(Mallikarjuna Korivi);(Jian-You Pan);(Meng-Chang Hsieh);趙蓓敏(Pei-Min Chao);(Pei-Jane Huang);蔡清讚(Tsai Ching-Tsan)*;許游章(You-Cheng Hseu)
亞洲大學 2015 Hericium erinaceus inhibits TNF-α-induced angiogenesis and ROS generation through suppression of MMP-9/NF-κB signaling and activation of Nrf2-mediated antioxidant genes in human endothelial cells 張竣維(Hebron, C.Chang)
亞洲大學 2015 Hericium erinaceus inhibits TNF-α-induced angiogenesis and ROS generation through suppression of MMP-9/NF-κB signaling and activation of Nrf2-mediated antioxidant genes in human endothelial cells Chang, 張竣維;Hebron C.
亞洲大學 2016-01 Hericium erinaceus inhibits TNF-α-induced angiogenesis and ROS generation through suppression of MMP-9/NF-κB signaling and activation of Nrf2-mediated antioxidant genes in human endothelial cells 張竣維;Chang, Hebron C.

Showing items 466121-466145 of 2348973  (93959 Page(s) Totally)
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