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"ming jen lee"的相關文件
顯示項目 56-105 / 123 (共3頁)
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| 臺大學術典藏 |
2020-03-03T02:33:28Z |
A novel XK gene mutation in a Taiwanese family with McLeod syndrome
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Chen P.-Y.; Lai S.-C.; Yang C.-C.; MING-JEN LEE; Chiu Y.-H.; Yan S.-H.; Lu C.-S.; Yeh T.-H. |
| 臺大學術典藏 |
2020-03-03T02:33:28Z |
A case of familial amyloidotic polyneuropathy with a rare Phe33Leu mutation in the TTR gene
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Chen C.-H.; Huang C.-W.; MING-JEN LEE |
| 臺大學術典藏 |
2020-03-03T02:33:28Z |
BST1 rs11724635 interacts with environmental factors to increase the risk of Parkinson's disease in a Taiwanese population
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Chen M.-L.; Lin C.-H.; MING-JEN LEE; Wu R.-M. |
| 臺大學術典藏 |
2020-03-03T02:33:27Z |
Microglia-derived cytokines/chemokines are involved in the enhancement of LPS-induced loss of nigrostriatal dopaminergic neurons in DJ-1 knockout mice
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Chien C.-H.; MING-JEN LEE; Liou H.-C.; Liou H.-H.; Fu W.-M. |
| 臺大學術典藏 |
2020-03-03T02:33:27Z |
The temporal profiles of changes in nerve excitability indices in familial amyloid polyneuropathy
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Lai H.-J.; Chiang Y.-W.; Yang C.-C.; Hsieh S.-T.; Chao C.-C.; MING-JEN LEE; Kuo C.-C. |
| 臺大學術典藏 |
2020-03-03T02:33:27Z |
Increased histone deacetylase activity involved in the suppressed invasion of cancer cells survived from ALA-mediated photodynamic treatment
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Li P.-T.; Tsai Y.-J.; MING-JEN LEE; Chen C.-T. |
| 臺大學術典藏 |
2020-03-03T02:33:27Z |
Mutation genotypes of RNF213 gene from moyamoya patients in Taiwan
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MING-JEN LEE; Chen Y.-F.; Fan P.-C.; Wang K.-C.; Wang K.; Wang J.; Kuo M.-F. |
| 臺大學術典藏 |
2020-03-03T02:33:27Z |
Local immunosuppressive microenvironment enhances migration of melanoma cells to lungs in DJ-1 knockout mice
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Chien C.-H.; MING-JEN LEE; Liou H.-C.; Liou H.-H.; Fu W.-M. |
| 臺大學術典藏 |
2020-03-03T02:33:26Z |
Burning pain: Axonal dysfunction in erythromelalgia
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Farrar M.A.; MING-JEN LEE; Howells J.; Andrews P.I.; Lin C.S.-Y. |
| 臺大學術典藏 |
2020-03-03T02:33:26Z |
Doxycycline potentiates antitumor effect of 5-aminolevulinic acid-mediated photodynamic therapy in malignant peripheral nerve sheath tumor cells
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MING-JEN LEE; Hung S.-H.; Huang M.-C.; Tsai T.; Chen C.-T. |
| 臺大學術典藏 |
2020-03-03T02:33:26Z |
Growth hormone is increased in the lungs and enhances experimental lung metastasis of melanoma in DJ-1 KO mice
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Chien C.-H.; MING-JEN LEE; Liou H.-C.; Liou H.-H.; Fu W.-M. |
| 臺大學術典藏 |
2020-03-03T02:33:26Z |
The Biophysical Basis Underlying Gating Changes in the p.V1316A Mutant Nav1.7 Channel and the Molecular Pathogenesis of Inherited Erythromelalgia
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Huang C.-W.; Lai H.-J.; Huang P.-Y.; MING-JEN LEE; Kuo C.-C. |
| 臺大學術典藏 |
2020-03-03T02:33:26Z |
A single nucleotide TDP-43 mutation within a Taiwanese family: A multifaceted demon
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Cheng Y.-W.; MING-JEN LEE; Chen T.-F.; Cheng T.-W.; Lai Y.-M.; Hua M.-S.; Chiu M.-J. |
| 臺大學術典藏 |
2020-03-03T02:33:25Z |
Cardiac manifestations and prognostic implications of hereditary transthyretin amyloidosis associated with transthyretin Ala97Ser
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Lai H.-J.; Huang K.-C.; Liang Y.-C.; Chien K.-L.; MING-JEN LEE; Hsieh S.-T.; Chao C.-C.; Yang C.-C. |
| 臺大學術典藏 |
2020-03-03T02:33:25Z |
Detrimental effects of intracerebral haemorrhage on patients with CADASIL harbouring NOTCH3 R544C mutation
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Chen C.-H.; Tang S.-C.; Cheng Y.-W.; Tsai H.-H.; Chi N.-F.; Sung P.-S.; Yeh H.-L.; Lien L.-M.; Lin H.-J.; MING-JEN LEE; Hu C.-J.; Chiou H.-Y.; Jeng J.-S. |
| 臺大學術典藏 |
2020-03-03T02:33:25Z |
Calebin-A induced death of malignant peripheral nerve sheath tumor cells by activation of histone acetyltransferase
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MING-JEN LEE; Tsai Y.-J.; Lin M.-Y.; You H.-L.; Kalyanam N.; Ho C.-T.; Pan M.-H. |
| 臺大學術典藏 |
2020-03-03T02:33:25Z |
Antagonism of proteasome inhibitor-induced heme oxygenase-1 expression by PINK1 mutation
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Sheng X.-J.; Tu H.-J.; Chien W.-L.; Kang K.-H.; Lu D.-H.; Liou H.-H.; MING-JEN LEE; Fu W.-M. |
| 臺大學術典藏 |
2020-03-03T02:33:24Z |
Anomalous enhancement of resurgent Na+ currents at high temperatures by SCN9A mutations underlies the episodic heat-enhanced pain in inherited erythromelalgia
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Huang C.-W.; Lai H.-J.; Huang P.-Y.; MING-JEN LEE; Kuo C.-C. |
| 臺大學術典藏 |
2019-12-01 |
Anomalous enhancement of resurgent Na+ currents at high temperatures by SCN9A mutations underlies the episodic heat-enhanced pain in inherited erythromelalgia
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Huang, Po Yuan; CHUNG-CHIN KUO; MING-JEN LEE; Lai, Hsing Jung; Huang, Chiung Wei; Huang, Po Yuan;CHUNG-CHIN KUO;MING-JEN LEE;Lai, Hsing Jung;Huang, Chiung Wei |
| 臺大學術典藏 |
2019-10-02T06:38:46Z |
Cardiac manifestations and prognostic implications of hereditary transthyretin amyloidosis associated with transthyretin Ala97Ser
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CHI-CHAO CHAO;MING-JEN LEE;Huang, Kuan Chih;Liang, Yun Chieh;Lai, Hsing Jung;Chih-Chao Yang;SUNG-TSANG HSIEH;KUO-LIONG CHIEN; KUO-LIONG CHIEN; SUNG-TSANG HSIEH; Chih-Chao Yang; Lai, Hsing Jung; Liang, Yun Chieh; Huang, Kuan Chih; MING-JEN LEE; CHI-CHAO CHAO |
| 臺大學術典藏 |
2019-07-23T01:51:05Z |
Calebin-A induced death of malignant peripheral nerve sheath tumor cells by activation of histone acetyltransferase
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Ho, Chi Tang;MING-JEN LEE;Tsai, Yi Jane;Lin, May Yao;You, Huey Ling;MIN-HSIUNG PAN;Kalyanam, Nagabhushanam; Ho, Chi Tang; MING-JEN LEE; Tsai, Yi Jane; Lin, May Yao; You, Huey Ling; MIN-HSIUNG PAN; Kalyanam, Nagabhushanam; Ho, Chi Tang; MING-JEN LEE; Tsai, Yi Jane; Lin, May Yao; You, Huey Ling; MIN-HSIUNG PAN; Kalyanam, Nagabhushanam; MIN-HSIUNG PAN |
| 臺大學術典藏 |
2018-09-10T14:50:32Z |
A novel XK gene mutation in a Taiwanese family with McLeod syndrome
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Chen, P.-Y. and Lai, S.-C. and Yang, C.-C. and Lee, M.-J. and Chiu, Y.-H. and Yan, S.-H. and Lu, C.-S. and Yeh, T.-H.; MING-JEN LEE; Chih-Chao Yang |
| 臺大學術典藏 |
2018-09-10T14:50:32Z |
BST1 rs11724635 interacts with environmental factors to increase the risk of Parkinson's disease in a Taiwanese population
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Ruey-Meei Wu; Chin-Hsien Lin; MING-JEN LEE; Chen, M.-L. and Lin, C.-H. and Lee, M.-J. and Wu, R.-M. |
| 臺大學術典藏 |
2018-09-10T14:50:32Z |
A case of familial amyloidotic polyneuropathy with a rare Phe33Leu mutation in the TTR gene
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Chen, C.-H. and Huang, C.-W. and Lee, M.-J.; MING-JEN LEE |
| 臺大學術典藏 |
2018-09-10T09:48:48Z |
Microstructural integrity of cerebral fiber tracts in hereditary spastic paraparesis with SPG11 mutation
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Pan, M.-K. and Huang, S.-C. and Lo, Y.-C. and Yang, C.-C. and Cheng, T.-W. and Yang, C.-C. and Hua, M.-S. and Lee, M.-J. and Tseng, W.-Y.I.; Ming-Kai Pan; WEN-YIH TSENG; MING-JEN LEE |
| 臺大學術典藏 |
2018-09-10T09:44:16Z |
A Novel SCN9A Mutation Responsible for Primary Erythromelalgia and Is Resistant to the Treatment of Sodium Channel Blockers
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CHEN-TUNG YEN;MING-JEN LEE;Lee, M.-J.;Chen, C.-C.;Yen, C.-T.;Huang, P.-Y.;Wu, M.-T.; Wu, M.-T.; Huang, P.-Y.; Yen, C.-T.; Chen, C.-C.; Lee, M.-J.; MING-JEN LEE; CHEN-TUNG YEN |
| 臺大學術典藏 |
2018-09-10T09:40:35Z |
Molecular pathogenesis of neurofibromatosis type 1
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Lee, M.-J. and Etheridge, A. and Galas, D.J. and Wang, K.; MING-JEN LEE |
| 臺大學術典藏 |
2018-09-10T09:40:35Z |
The influences of reserpine and imipramine on the 5-HT2 receptor binding site and its coupled second messenger in rat cerebral cortex
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Lee, M.-J. and Wei, J.-W.; MING-JEN LEE |
| 臺大學術典藏 |
2018-09-10T09:40:35Z |
The influences of reserpine and imipramine on the 5-HT2 receptor binding site and its coupled second messenger in rat cerebral cortex.
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Lee, M.J. and Wei, J.W.; MING-JEN LEE |
| 臺大學術典藏 |
2018-09-10T09:40:19Z |
Overweight modulates APOE and APOA5 alleles on the risk of severe hypertriglyceridemia
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Lee, Ming-Jen;Chien, Kuo-Liong;Chen, Ming-Fong;Stephenson, Dennis A.;Su, Ta-Chen; Lee, Ming-Jen; TA-CHEN SU; Lee, Ming-Jen; Chien, Kuo-Liong; MING-FONG CHEN; MING-JEN LEE; Chen, Ming-Fong; KUO-LIONG CHIEN; Stephenson, Dennis A.; Stephenson, Dennis A.; Su, Ta-Chen; Su, Ta-Chen; Chien, Kuo-Liong |
| 臺大學術典藏 |
2018-09-10T09:14:42Z |
PRRT2 mutations in paroxysmal kinesigenic dyskinesia with infantile convulsions in a Taiwanese cohort
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Lee, Y.-C. and Lee, M.-J. and Yu, H.-Y. and Chen, C. and Hsu, C.-H. and Lin, K.-P. and Liao, K.-K. and Chang, M.-H. and Liao, Y.-C. and Soong, B.-W.; MING-JEN LEE |
| 臺大學術典藏 |
2018-09-10T09:14:42Z |
The systems biology of neurofibromatosis type 1 - Critical roles for microRNA
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Lee, Ming-Jen;Cho, Ji-Hoon;Galas, David J.;Wang, Kai; Lee, M.-J. and Cho, J.-H. and Galas, D.J. and Wang, K.; 李銘仁; Lee, Ming-Jen; Hsu, Wei-Hsuan; MING-JEN LEE; Lee, Bao-Hong; Cho, Ji-Hoon; Pan, Tzu-Ming; Galas, David J.; Wang, Kai |
| 臺大學術典藏 |
2018-09-10T08:30:52Z |
Clinical phenotype of G206D mutation in the presenilin 1 gene in pathologically confirmed familial Alzheimer's disease
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Wu, Y.-Y. and Cheng, I.H.-J. and Lee, C.-C. and Chiu, M.-J. and Lee, M.-J. and Chen, T.-F. and Hsu, J.-L.; Ta-Fu Chen; Ming-Jang Chiu; MING-JEN LEE |
| 臺大學術典藏 |
2018-09-10T08:30:51Z |
Neurological complications of acute intermittent porphyria
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Kuo, H.-C. and Huang, C.-C. and Chu, C.-C. and Lee, M.-J. and Chuang, W.-L. and Wu, C.-L. and Wu, T. and Ning, H.-C. and Liu, C.-Y.; 郭弘周;黃錦章;朱俊哲;李銘仁;莊雯莉;吳東霖;甯孝真;劉智仰; KUO, HUNG-CHOU;HUANG, CHIN-CHANG;CHU, CHUN-CHE;LEE, MING-JEN;CHUANG, WEN-LI;WU, TONY T.;NING, HSIAO-CHEN;LIU, CHIH-YANG; MING-JEN LEE; Rand, D; Eng, JJ; Tang, PF; Jeng, JS; Hung, C; KUO, HUNG-CHOU; HUANG, CHIN-CHANG; CHU, CHUN-CHE; LEE, MING-JEN; CHUANG, WEN-LI; WU, TONY T.; NING, HSIAO-CHEN; LIU, CHIH-YANG |
| 臺大學術典藏 |
2018-09-10T08:30:51Z |
Purple pigments: The pathophysiology of acute porphyric neuropathy
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Lin, C.S.-Y. and Lee, M.-J. and Park, S.B. and Kiernan, M.C.; 李銘仁; Lin, Cindy S.-Y.; Lee, Ming-Jen; Park, Susanna B.; Kiernan, Matthew C.; MING-JEN LEE; Lin, Cindy S.-Y.; Lee, Ming-Jen; Park, Susanna B.; Kiernan, Matthew C. |
| 臺大學術典藏 |
2018-09-10T08:30:51Z |
rs5848 variant of progranulin gene is a risk of Alzheimer's disease in the Taiwanese population
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Lee, M.-J. and Chen, T.-F. and Cheng, T.-W. and Chiu, M.-J.; Lee, Ming-Jen;Chen, Ta-Fu;Cheng, Ting-Wen;Chiu, Ming-Jang; Lee, Ming-Jen; Ta-Fu Chen; Chen, Ta-Fu; MING-JEN LEE; Cheng, Ting-Wen; Ming-Jang Chiu; Chiu, Ming-Jang |
| 臺大學術典藏 |
2018-09-10T08:30:51Z |
Valosin-containing protein and neurofibromin interact to regulate dendritic spine density
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Wang, H.-F. and Shih, Y.-T. and Chen, C.-Y. and Chao, H.-W. and Lee, M.-J. and Hsueh, Y.-P.; MING-JEN LEE |
| 臺大學術典藏 |
2018-09-10T08:04:48Z |
Cerebral amyloid angiopathy in East and West
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陳右緯;李銘仁; Chen, Y.-W. and Lee, M.-J. and Smith, E.E.; Chen, Yu-Wei; Lee, Ming-Jen; Smith, Eric E.; MING-JEN LEE; Chen, Yu-Wei; Lee, Ming-Jen; Smith, Eric E. |
| 臺大學術典藏 |
2018-09-10T08:04:48Z |
Clinical presentations and skin denervation in amyloid neuropathy due to transthyretin Ala97Ser
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Yang, N.C.-C. and Lee, M.-J. and Chao, C.-C. and Chuang, Y.-T. and Lin, W.-M. and Chang, M.-F. and Hsieh, P.-C. and Kan, H.-W. and Lin, Y.-H. and Yang, C.-C. and Chiu, M.-J. and Liou, H.-H. and Hsieh, S.-T.; CHI-CHAO CHAO; Horng-Huei Liou; SUNG-TSANG HSIEH; Ming-Jang Chiu; MING-JEN LEE; Chih-Chao Yang |
| 臺大學術典藏 |
2018-09-10T08:03:51Z |
The microRNA spectrum in 12 body fluids
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Weber, J.A. and Baxter, D.H. and Zhang, S. and Huang, D.Y. and Huang, K.H. and Lee, M.J. and Galas, D.J. and Wang, K.; KUO-HOW HUANG; MING-JEN LEE |
| 臺大學術典藏 |
2018-09-10T07:32:11Z |
Genotype-phenotype correlates in Taiwanese patients with early-onset recessive Parkinsonism
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Lee, M.-J. and Mata, I.F. and Lin, C.-H. and Tzen, K.-Y. and Lincoln, S.J. and Bounds, R. and Lockhart, P.J. and Hulihan, M.M. and Farrer, M.J. and Wu, R.-M.; 李銘仁;林靜嫻;曾凱元;吳瑞美; Lee, Ming-Jen; Mata, Ignacio F.; Lin, Chin-Hsien; Tzen, Kai-Yuan; Lincoln, Sarah J.; Bounds, Rebecca; Lockhart, Paul J.; Hulihan, Mary M.; Farrer, Matthew J.; Wu, Ruey-Meei; Ruey-Meei Wu; Chin-Hsien Lin; KAI-YUAN TZEN; MING-JEN LEE; Lee, Ming-Jen; Mata, Ignacio F.; Lin, Chin-Hsien; Tzen, Kai-Yuan; Lincoln, Sarah J.; Bounds, Rebecca; Lockhart, Paul J.; Hulihan, Mary M.; Farrer, Matthew J.; Wu, Ruey-Meei |
| 臺大學術典藏 |
2018-09-10T07:22:49Z |
Focal brain glucose hypermetabolism in myoclonus-dystonia syndrome caused by an epsilon-sarcoglycan gene mutation
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Tai, Chun-Hwei;Yen, Ruoh-Fan;Lin, Chin-Hsien;Yen, Kuo-Yang;Yip, Ping-Keung;Wu, Ruey-Meei;Lee, Ming-Jen; Tai, C.-H. and Yen, R.-F. and Lin, C.-H. and Yen, K.-Y. and Yip, P.-K. and Wu, R.-M. and Lee, M.-J.; Tai, Chun-Hwei; Ruey-Meei Wu; CHUN-HWEI TAI; Yen, Ruoh-Fan; Lin, Chin-Hsien; RUOH-FANG YEN; Chin-Hsien Lin; Yen, Kuo-Yang; Yip, Ping-Keung; MING-JEN LEE; Wu, Ruey-Meei; Lee, Ming-Jen |
| 臺大學術典藏 |
2018-09-10T07:22:27Z |
Longitudinal evaluation of an N-Ethyl-N-nitrosourea-created murine model with normal pressure hydrocephalus
|
李銘仁;陳燕惠;郭律廷;陳垣崇;洪舜郁;鄔哲源;張程; Lee, M.-J. and Chang, C.-P. and Lee, Y.-H. and Wu, Y.-C. and Tseng, H.-W. and Tung, Y.-Y. and Wu, M.-T. and Chen, Y.-H. and Kuo, L.-T. and Stephenson, D. and Hung, S.-L. and Wu, J.-Y. and Chang, C. and Chen, Y.-T. and Chern, Y.; Lee, Ming-Jen; Chang, Ching-Pang; Lee, Yi-Hsin; Wu, Yi-Chih; Tseng, Hsu-Wen; Tung, Yu-Ying; Wu, Min-Tzu; Chen, Yen-Hui; Kuo, Lu-Ting; Stephenson, Dennis; Hung, Shuen-Iu; Wu, Jer-Yuarn; Chang, Chen; Chen, Yuan-Tsong; Chern, Yijuang; ���P�f; Lu-Ting Kuo; MING-JEN LEE; Lee, Ming-Jen; Chang, Ching-Pang; Lee, Yi-Hsin; Wu, Yi-Chih; Tseng, Hsu-Wen; Tung, Yu-Ying; Wu, Min-Tzu; Chen, Yen-Hui; Kuo, Lu-Ting; Stephenson, Dennis; Hung, Shuen-Iu; Wu, Jer-Yuarn; Chang, Chen; Chen, Yuan-Tsong; Chern, Yijuang |
| 臺大學術典藏 |
2018-09-10T07:22:27Z |
Notch signaling and CADASIL
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Tang, S.-C. and Jeng, J.-S. and Lee, M.-J. and Yip, P.-K.; MING-JEN LEE |
| 臺大學術典藏 |
2018-09-10T07:11:38Z |
Comparison of two PCR-based molecular methods in the diagnosis of CMT 1A and HNPP diseases in Chinese
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Chen, S.-R. and Lin, K.-P. and Kuo, H.-C. and Chen, C.-M. and Hsieh, S.-T. and Lee, M.-J. and Yang, C.-C. and Liu, C.-S. and Huang, C.-C. and Lyu, R.-K. and Ro, L.-S.; SUNG-TSANG HSIEH; MING-JEN LEE; Chih-Chao Yang |
| 臺大學術典藏 |
2018-09-10T06:50:20Z |
HMBS mutations in chinese patients with acute intermittent porphyria
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Yang, C.-C.;Kuo, H.-C.;You, H.-L.;Wang, J.;Huang, C.-C.;Liu, C.-Y.;Lan, M.-Y.;Stephenson, D.A.;Lee, M.-J.; MING-JEN LEE; Chih-Chao Yang |
| 臺大學術典藏 |
2018-09-10T06:50:20Z |
Mutations of the SPG11 gene in patients with autosomal recessive spastic paraparesis and thin corpus callosum
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李銘仁;鄭婷文;花茂棽;潘明楷;楊智超; Lee, M-J; Cheng, T-W; Hua, M-S; Pan, M-K; Wang, J; Stephenson, D A; Yang, C-C; Lee, M.-J. and Cheng, T.-W. and Hua, M.-S. and Pan, M.-K. and Wang, J. and Stephenson, D.A. and Yang, C.-C.; LEE, MING-JEN;CHENG, TING-WEN;HUA, MAU- SUN;PAN, MING-KAI;YANG, CHIH-CHAO; Lee, M-J; Ming-Kai Pan; MING-JEN LEE; Cheng, T-W; Chih-Chao Yang; Hua, M-S; Pan, M-K; Wang, J; LEE, MING-JEN; Stephenson, D A; Yang, C-C; CHENG, TING-WEN; HUA, MAU- SUN; PAN, MING-KAI; YANG, CHIH-CHAO |
| 臺大學術典藏 |
2018-09-10T06:50:20Z |
Nerve function and dysfunction in acute intermittent porphyria
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Lin, C.S.-Y. and Krishnan, A.V. and Lee, M.-J. and Zagami, A.S. and You, H.-L. and Yang, C.-C. and Bostock, H. and Kiernan, M.C.; 李銘仁;楊智超; Lin, C. S.-Y.; Krishnan, A. V.; Lee, M.-J.; Zagami, A. S.; You, H.-L.; Yang, C.-C.; Bostock, H.; Kiernan, M. C.; MING-JEN LEE; Chih-Chao Yang; Lin, C. S.-Y.; Krishnan, A. V.; Lee, M.-J.; Zagami, A. S.; You, H.-L.; Yang, C.-C.; Bostock, H.; Kiernan, M. C. |
| 臺大學術典藏 |
2018-09-10T06:40:07Z |
Characterization of a familial case with primary erythromelalgia from Taiwan
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Lee, M.-J.;Yu, H.-S.;Hsieh, S.-T.;Stephenson, D.A.;Lu, C.-J.;Yang, C.-C.; SUNG-TSANG HSIEH; MING-JEN LEE; Chih-Chao Yang |
| 臺大學術典藏 |
2018-09-10T06:15:01Z |
Acute intermittent porphyria with peripheral neuropathy: A follow-up study after hematin treatment
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Kuo, H.-C. and Lee, M.-J. and Chuang, W.-L. and Huang, C.-C.; MING-JEN LEE |
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