| 臺大學術典藏 |
2020-03-03T02:33:31Z |
Impairment of oxidative stress-induced heme oxygenase-1 expression by the defect of Parkinson-related gene of PINK1
|
MING-JEN LEE; Chien W.-L.; Lee T.-R.; Hung S.-Y.; Kang K.-H.; Fu W.-M. |
| 臺大學術典藏 |
2020-03-03T02:33:31Z |
The microRNA spectrum in 12 body fluids
|
Weber J.A.; Baxter D.H.; Zhang S.; Huang D.Y.; Huang K.H.; MING-JEN LEE; Galas D.J.; Wang K. |
| 臺大學術典藏 |
2020-03-03T02:33:30Z |
The influences of reserpine and imipramine on the 5-HT2 receptor binding site and its coupled second messenger in rat cerebral cortex
|
MING-JEN LEE; Wei J.-W. |
| 臺大學術典藏 |
2020-03-03T02:33:30Z |
PRRT2 mutations in paroxysmal kinesigenic dyskinesia with infantile convulsions in a Taiwanese cohort
|
Lee Y.-C.; MING-JEN LEE; Yu H.-Y.; Chen C.; Hsu C.-H.; Lin K.-P.; Liao K.-K.; Chang M.-H.; Liao Y.-C.; Soong B.-W. |
| 臺大學術典藏 |
2020-03-03T02:33:30Z |
The systems biology of neurofibromatosis type 1 - Critical roles for microRNA
|
MING-JEN LEE; Cho J.-H.; Galas D.J.; Wang K. |
| 臺大學術典藏 |
2020-03-03T02:33:30Z |
Purple pigments: The pathophysiology of acute porphyric neuropathy
|
Lin C.S.-Y.; MING-JEN LEE; Park S.B.; Kiernan M.C. |
| 臺大學術典藏 |
2020-03-03T02:33:30Z |
Valosin-containing protein and neurofibromin interact to regulate dendritic spine density
|
Wang H.-F.; Shih Y.-T.; Chen C.-Y.; Chao H.-W.; MING-JEN LEE; Hsueh Y.-P. |
| 臺大學術典藏 |
2020-03-03T02:33:29Z |
Soluble AXL: a possible circulating biomarker for neurofibromatosis type 1 related tumor burden
|
Johansson G.; Peng P.-C.; Huang P.-Y.; Chien H.-F.; Hua K.-T.; Kuo M.-L.; Chen C.-T.; MING-JEN LEE |
| 臺大學術典藏 |
2020-03-03T02:33:29Z |
Molecular pathogenesis of neurofibromatosis type 1
|
MING-JEN LEE; Etheridge A.; Galas D.J.; Wang K. |
| 臺大學術典藏 |
2020-03-03T02:33:29Z |
Increase of oxidative stress by a novel PINK1 mutation, P209A
|
Chien W.-L.; Lee T.-R.; Hung S.-Y.; Kang K.-H.; Wu R.-M.; MING-JEN LEE; Fu W.-M. |
| 臺大學術典藏 |
2020-03-03T02:33:29Z |
Microstructural integrity of cerebral fiber tracts in hereditary spastic paraparesis with SPG11 mutation
|
Pan M.-K.; Huang S.-C.; Lo Y.-C.; Yang C.-C.; Cheng T.-W.; Hua M.-S.; MING-JEN LEE; Tseng W.-Y.I. |
| 臺大學術典藏 |
2020-03-03T02:33:29Z |
Overweight modulates APOE and APOA5 alleles on the risk of severe hypertriglyceridemia
|
MING-JEN LEE; Chien K.-L.; Chen M.-F.; Stephenson D.A.; Su T.-C. |
| 臺大學術典藏 |
2020-03-03T02:33:29Z |
A Novel SCN9A Mutation Responsible for Primary Erythromelalgia and Is Resistant to the Treatment of Sodium Channel Blockers
|
Wu M.-T.; Huang P.-Y.; Yen C.-T.; Chen C.-C.; MING-JEN LEE |
| 臺大學術典藏 |
2020-03-03T02:33:28Z |
Motor and Sensory Axon Excitability Properties from the Median and Ulnar Nerves and the Effects of Age on These Properties
|
Lai H.-J.; Chiang Y.-W.; MING-JEN LEE |
| 臺大學術典藏 |
2020-03-03T02:33:28Z |
Sudomotor innervation in transthyretin amyloid neuropathy: Pathology and functional correlates
|
Chao C.-C.; Huang C.-M.; Chiang H.-H.; Luo K.-R.; Kan H.-W.; Yang N.C.-C.; Chiang H.; Lin W.-M.; Lai S.-M.; MING-JEN LEE; Shun C.-T.; Hsieh S.-T. |
| 臺大學術典藏 |
2020-03-03T02:33:28Z |
A novel XK gene mutation in a Taiwanese family with McLeod syndrome
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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.
|
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
|
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
|
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
|
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
|
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
|
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
|
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. |
