| 臺大學術典藏 |
2018-09-10T05:12:07Z |
Complex haplotypic effects of the ABCB1 gene on epilepsy treatment response
|
Hung, C.-C.;Tai, J.J.;Lin, C.-J.;Lee, M.-J.;Liou, H.-H.; Horng-Huei Liou; CHUN-JUNG LIN; MING-JEN LEE |
| 臺大學術典藏 |
2018-09-10T05:01:23Z |
Cutaneous and sympathetic denervation in neonatal rats with a mutation in the delta subunit of the cytosolic chaperonin-containing t-complex peptide-1 gene
|
Hsu, S.-H. and Lee, M.-J. and Hsieh, S.-C. and Scaravilli, F. and Hsieh, S.-T.; SHU-HAO HSU; SUNG-TSANG HSIEH; MING-JEN LEE |
| 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 |
2018-09-10T04:05:42Z |
Mutation of the sterol 27-hydroxylase gene (CYP27A1) in a Taiwanese family with cerebrotendinous xanthomatosis [4]
|
Lee, M.-J. and Huang, Y.-C. and Sweeney, M.G. and Wood, N.W. and Reilly, M.M. and Yip, P.-K.; MING-JEN LEE |
| 臺大學術典藏 |
2018-09-10T04:05:42Z |
Six novel connexin32 (GJB1) mutations in X-linked Charcot-Marie-Tooth disease
|
Lee, M.-J. and Nelson, I. and Houlden, H. and Sweeney, M.G. and Hilton-Jones, D. and Blake, J. and Wood, N.W. and Reilly, M.M.; MING-JEN LEE |
| 臺大學術典藏 |
2018-09-10T03:41:56Z |
Biochemical events coupled to the activation of serotonin receptors in brain regions of the rat
|
Wei, J.-W. and Lee, M.-J. and Yeh, S.-R.; MING-JEN LEE |
| 臺大學術典藏 |
2018-09-10T03:24:14Z |
Genetic aspects of hereditary motor and sensory neuropathy
|
Lee, M.-J. and Reilly, M.M.; MING-JEN LEE |
| 中國醫藥大學 |
2013-05 |
Increase of oxidative stress by a novel PINK1 mutation, P209A.
|
(Wei-Lin Chien);(Tzeng-Ruei Lee);洪詩雅(Shih-Ya Hung);(Kai-Hsiang Kang);(Ruey-Meei Wu);(Ming-Jen Lee);(Wen-Mei Fu)* |
| 中國醫藥大學 |
2009-09 |
Focal brain glucose hypermetabolism in myoclonus-dystonia syndrome caused by an epsilon-sarcoglycan gene mutation
|
(Chun-Hwei Tai);顏若芳(Ruoh-Fan Yen);(Chin-Hsien Lin);顏國揚(Kuo-Yang Yen);(Ping-Keung Yip);(Ruey-Meei Wu);(Ming-Jen Lee)* |
| 臺大學術典藏 |
2006 |
Novel mutation of neurofibromatosis type 1 in a patient with cerebral vasculopathy and fatal ischemic stroke
|
Yip P.-K.; Jeng J.-S.; MING-JEN LEE; Tang S.-C. |
| 臺大學術典藏 |
2005 |
Six novel NPC1 mutations in Chinese patients with Niemann-Pick disease type C
|
Yang, C.-C. and Su, Y.-N. and Chiou, P.-C. and Fietz, M.J. and Yu, C.-L. and Hwu, W.-L. and Lee, M.-J.; MING-JEN LEE; WUH-LIANG HWU; Chih-Chao Yang |
| 臺大學術典藏 |
2005 |
Complex haplotypic effects of the ABCB1 gene on epilepsy treatment response
|
Liou H.-H.; MING-JEN LEE; Lin C.-J.; Tai J.J.; Hung C.-C. |
| 臺大學術典藏 |
2002 |
Mutation of the sterol 27-hydroxylase gene (CYP27A1) in a Taiwanese family with cerebrotendinous xanthomatosis [4]
|
Yip P.-K.; Reilly M.M.; Wood N.W.; Sweeney M.G.; Huang Y.-C.; MING-JEN LEE |
