公開日期 | 標題 | 作者 | 來源出版物 | scopus | WOS | 全文 |
2008 | Comparison of two PCR-based molecular methods in the diagnosis of CMT 1A and HNPP diseases in Chinese | Chen S.-R.; Lin K.-P.; Kuo H.-C.; Chen C.-M.; SUNG-TSANG HSIEH ; MING-JEN LEE ; Yang C.-C.; Liu C.-S.; Huang C.-C.; Lyu R.-K.; Ro L.-S. | Clinical Neurology and Neurosurgery | 7 | 5 | |
2005 | Complex haplotypic effects of the ABCB1 gene on epilepsy treatment response | Hung, Chin-Chuan; Tai J.J.; CHUN-JUNG LIN ; MING-JEN LEE ; HORNG-HUEI LIOU | Pharmacogenomics | 118 | 102 | |
2004 | Cutaneous and sympathetic denervation in neonatal rats with a mutation in the delta subunit of the cytosolic chaperonin-containing t-complex peptide-1 gene | SHU-HAO HSU ; MING-JEN LEE ; SONG-CHOU HSIEH ; Scaravilli F.; SUNG-TSANG HSIEH | Neurobiology of Disease | 4 | 4 | |
2019 | Detrimental effects of intracerebral haemorrhage on patients with CADASIL harbouring NOTCH3 R544C mutation | Chen C.-H.; SUNG-CHUN TANG ; 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.; JIANN-SHING JENG | | 16 | 14 | |
2021 | DNA hypermethylation involves in the down-regulation of chloride intracellular channel 4 (CLIC4) induced by photodynamic therapy | Chiang, Pei Chi; Li, Pei Tzu; MING-JEN LEE ; CHIN-TIN CHEN | Biomedicines | 1 | 1 | |
2017 | 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.; CHIN-TIN CHEN | PLoS ONE | 24 | 16 | |
2020 | Electrophysiological parameters that contribute to the pathogenesis of familial amyloid polyneuropathy caused by transthyretin mutations | Lai H.-J.; Lai W.-T.; Jin L.; KUAN-TING KUO ; MING-JEN LEE | Journal of the Neurological Sciences | 2 | 2 | |
2022 | EXPLORE B: A prospective, long-term natural history study of patients with acute hepatic porphyria with chronic symptoms | Cassiman, David; Kauppinen, Raili; Monroy, Susana; MING-JEN LEE ; Bonkovsky, Herbert L; Thapar, Manish; Guillén-Navarro, Encarna; Minder, Anna-Elisabeth; Hale, Cecilia; Sweetser, Marianne T; Ivanova, Aneta | Journal of inherited metabolic disease | 4 | 1 | |
2009 | Focal brain glucose hypermetabolism in myoclonus-dystonia syndrome caused by an epsilon-sarcoglycan gene mutation | CHUN-HWEI TAI ; RUOH-FANG YEN ; CHIN-HSIEN LIN ; Yen K.-Y.; Yip P.-K.; RUEY-MEEI WU ; MING-JEN LEE | Parkinsonism and Related Disorders | 3 | 2 | |
2000 | Genetic aspects of hereditary motor and sensory neuropathy | MING-JEN LEE ; Reilly M.M. | Acta Neurologica Taiwanica | 0 | | |
2009 | Genotype-phenotype correlates in Taiwanese patients with early-onset recessive Parkinsonism | MING-JEN LEE ; Mata I.F.; CHIN-HSIEN LIN ; KAI-YUAN TZEN ; Lincoln S.J.; Bounds R.; Lockhart P.J.; Hulihan M.M.; Farrer M.J.; RUEY-MEEI WU | Movement Disorders | 29 | 23 | |
2016 | 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.; HORNG-HUEI LIOU ; WEN-MEI FU | BMC Cancer | 17 | 14 | |
2003 | 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. | Human Molecular Genetics | 46 | 45 | |
2008 | HMBS mutations in chinese patients with acute intermittent porphyria | Yang C.-C.; Kuo H.-C.; You H.-L.; Wang J.; Huang C.-C.; Liu C.-Y.; Lan M.-Y.; Stephenson D.A.; MING-JEN LEE | Annals of Human Genetics | 20 | 17 | |
2006 | Identification of forty-five novel and twenty-three known NF1 mutations in Chinese patients with neurofibromatosis type 1. | MING-JEN LEE ; Su Y.N.; You H.L.; Chiou S.C.; Lin L.C.; Yang C.C.; Lee W.C.; WUH-LIANG HWU ; FON-JOU HSIEH ; Stephenson D.A.; CHIA-LI YU | Human mutation | 32 | 27 | |
2019 | The Impact of Moyamoya Disease and RNF213 Mutations on the Spectrum of Plasma Protein and MicroRNA | MING-JEN LEE ; Fallen, Shannon; Zhou, Yong; Baxter, David; Scherler, Kelsey; MENG-FAI KUO ; Wang, Kai | Journal of clinical medicine | 9 | 7 | |
2023 | Impact of Vutrisiran on Quality of Life and Physical Function in Patients with Hereditary Transthyretin-Mediated Amyloidosis with Polyneuropathy | Obici, Laura; Ajroud-Driss, Senda; Lin, Kon-Ping; Berk, John L; Gillmore, Julian D; Kale, Parag; Koike, Haruki; Danese, David; Aldinc, Emre; Chen, Chongshu; Vest, John; Adams, David; MING-JEN LEE ; HSUEH-WEN HSUEH ; LI-KAI TSAI ; JEN-JEN SU ; Chou, Hsi-Chieh; CHI-CHAO CHAO ; SUNG-TSANG HSIEH | Neurology and therapy | 3 | 1 | |
2011 | 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.; WEN-MEI FU | Journal of Neurochemistry | 36 | 35 | |
2013 | Increase of oxidative stress by a novel PINK1 mutation, P209A | Chien W.-L.; Lee T.-R.; Hung S.-Y.; Kang K.-H.; RUEY-MEEI WU ; MING-JEN LEE ; WEN-MEI FU | Free Radical Biology and Medicine | 17 | 15 | |
2015 | 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. | International Journal of Molecular Sciences | 12 | 11 | |