Jump to the main content block

Professor Ming-Jen Lee publication

李銘仁教授(Ming-Jen Lee)

  • Tai CH, Yen RF, Lin CH, Yen KY, Yip PK, Wu RM, Lee MJ. Focal brain glucose hypermetabolism in myoclonus-dystonia syndrome caused by an epsilon-sarcoglycan gene mutation. Parkinsonism Relat Disord. 2009

 

  • Yeh WL, Lu DY, Lee MJ, Fu WM. Leptin induces migration and invasion of glioma cells through mmp-13 production. Glia. 2009;57:454-464

 

  • Lee MJ, Ignacio F. Mata, Lin CH, Tzen KY, Sarah J. Lincoln, Rebecca Bounds, Paul J. Lockhart, Mary M. Hulihan, Matthew J. Farrer, Wu RM. Genotype-Phenotype correlates in    Taiwanese patients with early-onset  recessive Parkinsonism. Movement Disorder 2009 Jan  15;24(1):104-8

 

  • Yeh WL, Lu DY, Lee MJ, Fu WM. Leptin induces migration and invasion  of glioma cells     through MMP-13 production. Glia. 2009 Mar; 57(4):454-64.

 

  • Tai CH, Yen RF, Liu CH, Yen KY, Yip PK, Wu RM, Lee MJ. Focal brainglucose    hypermetabolism in myoclonus-dystonia syndrome caused by an  epsilon-sacroglycan gene     mutation. Parkinsonism Relat Disord. 2009  Sep;15(8):614-6

 

  • Lee MJ, Chang CP, Lee YH, Wu YC, Tseng HW, Tung YY,Chen YH,, We MZ,  Kuo LT, Stephenson DA, Hung SI, Wu JY, Chang C, Chen YT, Chern Y.Longitudinal evaluation of an N-ethyl-N-nitrosourea-created murine model with normal pressure hydrocephalus. PLoS One 2009 Nov17;4(11):e7868.

 

  • Yang Naomi CC*, Lee MJ*, Chao CC*, Chuang YT, Lin WM, Chang MF, Hsieh PC, Kan     HW, Lin YH, Yang CC, Chiu MJ, Liou HH, Hsieh ST. Clinical presentations and skin     denervation in amyloid neuropathy due to transthyretin Ala97Ser. NEUROLOGY 2010 Aug 10;75(6):532-8  (*  Co-the first)

 

  • Chen YW, Lee MJ, Smith EE. Cerebral amyloid angiopathy in east and west. International Journal of Stroke 2010 Oct;5:403-411

 

  • Weber J A, Baxter DH, Zhang Shile, Huang DY., Huang KH, Lee MJ, Galas DJ, Wang K. The MicroRNA Spectrum in 12 Body Fluids. Clinical Chemistry 2010 (in press)

 

  • Chien,WL; Lee,TR; Hung,SY; Kang,KH; Lee,MJ; Fu,WM. Impairment Of  Oxidative   Stress-Induced Heme Oxygenase-1 Expression By The Defect Of Parkinson-Related Gene Of PINK1. Journal Of Neurochemistry 2011MAY;117(4) :643-653

 

  • Kuo,HC; Huang,CC; Chu,CC; Lee,MJ; Chuang,WL; Wu,CL; Wu,T; Ning,HC; Liu,CY.     Neurological Complications of Acute Intermittent Porphyria. European neurology 2011;66    (5) :247-252

 

  • Lee,MJ; Chen,TF; Cheng,TW; Chiu,MJ . rs5848 Variant of Progranulin Gene Is a Risk of      Alzheimer's Disease in   the Taiwanese Population. Neurodegenerative Diseases 2011;8      (4) :216-220

 

  • Lin,CSY; Lee,MJ; Park,SB; Kiernan,MC . Purple pigments: The pathophysiology of acute      porphyric neuropathy. Clinical Neurophysiology 2011 Dec;122 (12) :2336-2344

 

  • Wang,HF; Shih,YT; Chen,CY; Chao,HW; Lee,MJ; Hsueh,YP. Valosin-containing protein and neurofibromin interact to regulate dendritic spine density. Journal Of Clinical  Investigation 2011 Dec;121 (12) :4820-4837

 

  • Wu,YY; Cheng,IHJ; Lee,CC; Chiu,MJ; Lee,MJ; Chen,TF; Hsu,JL.Clinical Phenotype of      G206D Mutation in the Presenilin 1 Gene in   Pathologically Confirmed Familial      Alzheimer's Disease. Journal Of Alzheimers Disease 2011;25 (1) :145-150

 

  • Lee MJ, Cho JH, Galas DJ, Wang K.. The systems biology of neurofibromatosis type 1 - Critical roles for microRNA.. Exp Neurol. 2012 Jun;235(2):464-8.

 

  • Lee YC, Lee MJ, Yu HY, Chen C, Hsu CH, Lin KP, Liao KK, Chang MH, Liao YC, Soong BW. PRRT2 mutations in paroxysmal kinesigenic dyskinesia with infantile convulsions in a Taiwanese cohort. PLoS One.2012;7(8):e38543.

 

  • Wu, MT Huang, PY Yen, CT Chen, CC Lee, MJ A Novel SCN9A Mutation Responsible for Primary Erythromelalgia and Is Resistant to the Treatment of Sodium Channel Blockers PLoS One 2013

 

  • Chien, WL Lee, TR Hung, SY Kang, KH Wu, RM Lee, MJ(corresponding author)* Fu, WM* Increase of oxidative stress by a novel PINK1 mutation, P209A Free Radic. Biol. Med. 2013

 

  • Chien, WL Kang, KH Lee, MJ Fu, WM Impairment of inflammatory cytokine-induced manganese superoxide dismutase expression by the PINK1 G309D mutation Acta Pharmacol.Sin 2013

 

  • Ming-Jen Lee,  Ming-Kai Pan Microstructural integrity of cerebral fiber tracts in hereditary spastic paraparesis with SPG11 mutation American Journal of Neuroradiology , vol. 34, no. 5 , page 990-996 , 2013

 

  • Ming-Jen Lee Molecular pathogenesis of neurofibromatosis type 1 Neurofibromatosis Type 1: Symptoms, Treatment and Prognosis , page 1-22 , 2013

 

  • KUO-LIONG CHIEN, Ming-Jen Lee Overweight modulates APOE and APOA5 alleles on the risk of severe hypertriglyceridemia Clinica Chimica Acta , vol. 416 , page 31-35 , 2013

 

  • Ming-Jen Lee The influences of reserpine and imipramine on the 5-HT2 receptor binding site and its coupled second messenger in rat cerebral cortex. The Chinese journal of physiology , vol. 56, no. 4 , page 199-208 , 2013

 

  • Chih-Chao Yang,  Ming-Jen Lee A novel XK gene mutation in a Taiwanese family with McLeod syndrome Journal of the Neurological Sciences , vol. 340, no. 1-2 , page 221-224 , 2014

 

  • Ruey-Meei Wu,  Ming-Jen Lee BST1 rs11724635 interacts with environmental factors to increase the risk of Parkinson's disease in a Taiwanese population Parkinsonism and Related Disorders , vol. 20, no. 3 , page 280-283 , 2014

 

  • Ming-Jen Lee A case of familial amyloidotic polyneuropathy with a rare Phe33Leu mutation in the TTR gene Journal of the Formosan Medical Association , vol. 113, no. 8 , page 575-576 , 2014