Results 1-64 of 64 (Search time: 0.005 seconds).

Issue DateTitleAuthor(s)TypescopusWOSFulltext/Archive link
12019Calebin-A induced death of malignant peripheral nerve sheath tumor cells by activation of histone acetyltransferaseMING-JEN LEE ; Tsai Y.-J.; Lin M.-Y.; You H.-L.; Kalyanam N.; Ho C.-T.; Pan M.-H.journal article66
22019Anomalous enhancement of resurgent Na+ currents at high temperatures by SCN9A mutations underlies the episodic heat-enhanced pain in inherited erythromelalgiaHuang C.-W.; Lai H.-J.; Huang P.-Y.; MING-JEN LEE ; Kuo C.-C.journal article11
32019Detrimental effects of intracerebral haemorrhage on patients with CADASIL harbouring NOTCH3 R544C mutationChen 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.letter23
42019Cardiac manifestations and prognostic implications of hereditary transthyretin amyloidosis associated with transthyretin Ala97SerLai H.-J.; Huang K.-C.; Liang Y.-C.; Chien K.-L.; MING-JEN LEE ; Hsieh S.-T.; Chao C.-C.; Yang C.-C.journal article22
52017Antagonism of proteasome inhibitor-induced heme oxygenase-1 expression by PINK1 mutationSheng X.-J.; Tu H.-J.; Chien W.-L.; Kang K.-H.; Lu D.-H.; Liou H.-H.; MING-JEN LEE ; Fu W.-M.journal article710
62017Doxycycline potentiates antitumor effect of 5-aminolevulinic acid-mediated photodynamic therapy in malignant peripheral nerve sheath tumor cellsMING-JEN LEE ; Hung S.-H.; Huang M.-C.; Tsai T.; Chen C.-T.journal article87
72017Burning pain: Axonal dysfunction in erythromelalgiaFarrar M.A.; MING-JEN LEE ; Howells J.; Andrews P.I.; Lin C.S.-Y.journal article55
82016Microglia-derived cytokines/chemokines are involved in the enhancement of LPS-induced loss of nigrostriatal dopaminergic neurons in DJ-1 knockout miceChien C.-H.; MING-JEN LEE ; Liou H.-C.; Liou H.-H.; Fu W.-M.journal article1511
92016A single nucleotide TDP-43 mutation within a Taiwanese family: A multifaceted demonCheng Y.-W.; MING-JEN LEE ; Chen T.-F.; Cheng T.-W.; Lai Y.-M.; Hua M.-S.; Chiu M.-J.journal article11
102016The Biophysical Basis Underlying Gating Changes in the p.V1316A Mutant Nav1.7 Channel and the Molecular Pathogenesis of Inherited ErythromelalgiaHuang C.-W.; Lai H.-J.; Huang P.-Y.; MING-JEN LEE ; Kuo C.-C.journal article52
112016Growth hormone is increased in the lungs and enhances experimental lung metastasis of melanoma in DJ-1 KO miceChien C.-H.; MING-JEN LEE ; Liou H.-C.; Liou H.-H.; Fu W.-M.journal article99
122015Mutation genotypes of RNF213 gene from moyamoya patients in TaiwanMING-JEN LEE ; Chen Y.-F.; Fan P.-C.; Wang K.-C.; Wang K.; Wang J.; Kuo M.-F.journal article1517
132015Local immunosuppressive microenvironment enhances migration of melanoma cells to lungs in DJ-1 knockout miceChien C.-H.; MING-JEN LEE ; Liou H.-C.; Liou H.-H.; Fu W.-M.journal article1210
142015Sudomotor innervation in transthyretin amyloid neuropathy: Pathology and functional correlatesChao 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.journal article3327
152015Increased histone deacetylase activity involved in the suppressed invasion of cancer cells survived from ALA-mediated photodynamic treatmentLi P.-T.; Tsai Y.-J.; MING-JEN LEE ; Chen C.-T.journal article65
162015Motor and Sensory Axon Excitability Properties from the Median and Ulnar Nerves and the Effects of Age on These PropertiesLai H.-J.; Chiang Y.-W.; MING-JEN LEE journal article44
172015The temporal profiles of changes in nerve excitability indices in familial amyloid polyneuropathyLai H.-J.; Chiang Y.-W.; Yang C.-C.; Hsieh S.-T.; Chao C.-C.; MING-JEN LEE ; Kuo C.-C.journal article87
182014BST1 rs11724635 interacts with environmental factors to increase the risk of Parkinson's disease in a Taiwanese populationChen M.-L.; Lin C.-H.; MING-JEN LEE ; Wu R.-M.journal article1612
192014Soluble AXL: a possible circulating biomarker for neurofibromatosis type 1 related tumor burdenJohansson G.; Peng P.-C.; Huang P.-Y.; Chien H.-F.; Hua K.-T.; Kuo M.-L.; Chen C.-T.; MING-JEN LEE journal article1414
202014A novel XK gene mutation in a Taiwanese family with McLeod syndromeChen P.-Y.; Lai S.-C.; Yang C.-C.; MING-JEN LEE ; Chiu Y.-H.; Yan S.-H.; Lu C.-S.; Yeh T.-H.journal article33
212014A case of familial amyloidotic polyneuropathy with a rare Phe33Leu mutation in the TTR geneChen C.-H.; Huang C.-W.; MING-JEN LEE journal article20
222013A Novel SCN9A Mutation Responsible for Primary Erythromelalgia and Is Resistant to the Treatment of Sodium Channel BlockersWu M.-T.; Huang P.-Y.; Yen C.-T.; Chen C.-C.; MING-JEN LEE journal article3631
232013Molecular pathogenesis of neurofibromatosis type 1MING-JEN LEE ; Etheridge A.; Galas D.J.; Wang K.book chapter0
242013Increase of oxidative stress by a novel PINK1 mutation, P209AChien W.-L.; Lee T.-R.; Hung S.-Y.; Kang K.-H.; Wu R.-M.; MING-JEN LEE ; Fu W.-M.journal article1212
252013The influences of reserpine and imipramine on the 5-HT2 receptor binding site and its coupled second messenger in rat cerebral cortexMING-JEN LEE ; Wei J.-W.journal article22
262013Microstructural integrity of cerebral fiber tracts in hereditary spastic paraparesis with SPG11 mutationPan M.-K.; Huang S.-C.; Lo Y.-C.; Yang C.-C.; Cheng T.-W.; Yang C.-C.; Hua M.-S.; MING-JEN LEE ; Tseng W.-Y.I.journal article44
272013Overweight modulates APOE and APOA5 alleles on the risk of severe hypertriglyceridemiaMING-JEN LEE ; Chien K.-L.; Chen M.-F.; Stephenson D.A.; Su T.-C.journal article1613
282012PRRT2 mutations in paroxysmal kinesigenic dyskinesia with infantile convulsions in a Taiwanese cohortLee 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.journal article4135
292012The systems biology of neurofibromatosis type 1 - Critical roles for microRNAMING-JEN LEE ; Cho J.-H.; Galas D.J.; Wang K.Review53
302011Neurological complications of acute intermittent porphyriaKuo H.-C.; Huang C.-C.; Chu C.-C.; MING-JEN LEE ; Chuang W.-L.; Wu C.-L.; Wu T.; Ning H.-C.; Liu C.-Y.journal article1614
312011Valosin-containing protein and neurofibromin interact to regulate dendritic spine densityWang H.-F.; Shih Y.-T.; Chen C.-Y.; Chao H.-W.; MING-JEN LEE ; Hsueh Y.-P.journal article4237
322011rs5848 variant of progranulin gene is a risk of Alzheimer's disease in the Taiwanese populationMING-JEN LEE ; Chen T.-F.; Cheng T.-W.; Chiu M.-J.journal article3128
332011Impairment of oxidative stress-induced heme oxygenase-1 expression by the defect of Parkinson-related gene of PINK1MING-JEN LEE ; Chien W.-L.; Lee T.-R.; Hung S.-Y.; Kang K.-H.; Fu W.-M.journal article3030
342011Purple pigments: The pathophysiology of acute porphyric neuropathyLin C.S.-Y.; MING-JEN LEE ; Park S.B.; Kiernan M.C.Review3222
352011Clinical phenotype of G206D mutation in the presenilin 1 gene in pathologically confirmed familial Alzheimer's diseaseWu Y.-Y.; Cheng I.H.-J.; Lee C.-C.; Chiu M.-J.; MING-JEN LEE ; Chen T.-F.; Hsu J.-L.journal article54
362010Clinical presentations and skin denervation in amyloid neuropathy due to transthyretin Ala97SerYang N.C.-C.; MING-JEN LEE ; Chao C.-C.; Chuang Y.-T.; Lin W.-M.; Chang M.-F.; Hsieh P.-C.; Kan H.-W.; Lin Y.-H.; Yang C.-C.; Chiu M.-J.; Liou H.-H.; Hsieh S.-T.journal article5346
372010Cerebral amyloid angiopathy in East and WestChen Y.-W.; MING-JEN LEE ; Smith E.E.Review2222
382010The microRNA spectrum in 12 body fluidsWeber J.A.; Baxter D.H.; Zhang S.; Huang D.Y.; Huang K.H.; MING-JEN LEE ; Galas D.J.; Wang K.journal article14181330
392009Genotype-phenotype correlates in Taiwanese patients with early-onset recessive ParkinsonismMING-JEN LEE ; Mata I.F.; Lin C.-H.; Tzen K.-Y.; Lincoln S.J.; Bounds R.; Lockhart P.J.; Hulihan M.M.; Farrer M.J.; Wu R.-M.journal article2319
402009Focal brain glucose hypermetabolism in myoclonus-dystonia syndrome caused by an epsilon-sarcoglycan gene mutationTai C.-H.; Yen R.-F.; Lin C.-H.; Yen K.-Y.; Yip P.-K.; Wu R.-M.; MING-JEN LEE letter32
412009Leptin induces migration and invasion of glioma cells through MMP-13 productionYeh W.-L.; Lu D.-Y.; MING-JEN LEE ; Fu W.-M.journal article6964
422009Notch signaling and CADASILTang S.-C.; Jeng J.-S.; MING-JEN LEE ; Yip P.-K.Review130
432009Longitudinal evaluation of an N-Ethyl-N-nitrosourea-created murine model with normal pressure hydrocephalusMING-JEN LEE ; Chang C.-P.; Lee Y.-H.; Wu Y.-C.; Tseng H.-W.; Tung Y.-Y.; Wu M.-T.; Chen Y.-H.; Kuo L.-T.; Stephenson D.; Hung S.-L.; Wu J.-Y.; Chang C.; Chen Y.-T.; Chern Y.journal article88
442008HMBS mutations in chinese patients with acute intermittent porphyriaYang 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 journal article1112
452008Mutations of the SPG11 gene in patients with autosomal recessive spastic paraparesis and thin corpus callosumMING-JEN LEE ; Cheng T.-W.; Hua M.-S.; Pan M.-K.; Wang J.; Stephenson D.A.; Yang C.-C.letter1715
462008Comparison of two PCR-based molecular methods in the diagnosis of CMT 1A and HNPP diseases in ChineseChen S.-R.; Lin K.-P.; Kuo H.-C.; Chen C.-M.; Hsieh S.-T.; MING-JEN LEE ; Yang C.-C.; Liu C.-S.; Huang C.-C.; Lyu R.-K.; Ro L.-S.journal article75
472008Rapid prenatal confirmation of LIT1 hypomethylation using a novel quantitative method (E-Q-PCR) in fetuses with Beckwith-Wiedemann syndrome impressed with ultrasonographyMa G.-C.; Chang S.-D.; Chang Y.; Chang S.-P.; Yang C.-W.; MING-JEN LEE ; Lee T.-H.; Chen M.journal article21
482008Nerve function and dysfunction in acute intermittent porphyriaLin C.S.-Y.; Krishnan A.V.; MING-JEN LEE ; Zagami A.S.; You H.-L.; Yang C.-C.; Bostock H.; Kiernan M.C.journal article5648
492007Recent developments in neurofibromatosis type 1MING-JEN LEE ; Stephenson D.A.Review7668
502007Acute intermittent porphyria with peripheral neuropathy: A follow-up study after hematin treatmentKuo H.-C.; MING-JEN LEE ; Chuang W.-L.; Huang C.-C.journal article1413
512007Characterization of a familial case with primary erythromelalgia from TaiwanMING-JEN LEE ; Yu H.-S.; Hsieh S.-T.; Stephenson D.A.; Lu C.-J.; Yang C.-C.journal article4238
522006Identification 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.; Hwu W.L.; Hsieh F.J.; Stephenson D.A.; Yu C.L.journal article2421
532006Novel mutation of neurofibromatosis type 1 in a patient with cerebral vasculopathy and fatal ischemic strokeTang S.-C.; MING-JEN LEE ; Jeng J.-S.; Yip P.-K.journal article108
542005Six novel NPC1 mutations in Chinese patients with Niemann-Pick disease type CYang C.-C.; Su Y.-N.; Chiou P.-C.; Fietz M.J.; Yu C.-L.; Hwu W.-L.; MING-JEN LEE journal article2019
552005Arg332Cys mutation of NOTCH3 gene in the first known Taiwanese family with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathyTang S.-C.; MING-JEN LEE ; Jeng J.-S.; Yip P.-K.journal article2014
562005Complex haplotypic effects of the ABCB1 gene on epilepsy treatment responseHung C.-C.; Tai J.J.; Lin C.-J.; MING-JEN LEE ; Liou H.-H.journal article10693
572004Cutaneous and sympathetic denervation in neonatal rats with a mutation in the delta subunit of the cytosolic chaperonin-containing t-complex peptide-1 geneHsu S.-H.; MING-JEN LEE ; Hsieh S.-C.; Scaravilli F.; Hsieh S.-T.journal article44
582003Hereditary sensory neuropathy is caused by a mutation in the delta subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct4) geneMING-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.journal article4040
592002Mutation of the sterol 27-hydroxylase gene (CYP27A1) in a Taiwanese family with cerebrotendinous xanthomatosis [4]MING-JEN LEE ; Huang Y.-C.; Sweeney M.G.; Wood N.W.; Reilly M.M.; Yip P.-K.letter63
602002Six novel connexin32 (GJB1) mutations in X-linked Charcot-Marie-Tooth diseaseMING-JEN LEE ; Nelson I.; Houlden H.; Sweeney M.G.; Hilton-Jones D.; Blake J.; Wood N.W.; Reilly M.M.journal article5242
612001The spinocerebellar ataxias-genotype-phenotype correlationWood N.W.; MING-JEN LEE Review0
622000Genetic aspects of hereditary motor and sensory neuropathyMING-JEN LEE ; Reilly M.M.Review0
631997Clinical and electrophysiological characteristics of inflammatory demyelinating neuropathiesMING-JEN LEE ; Chang Y.-C.; Chen R.-C.; Hsieh S.-T.journal article1
641991Biochemical events coupled to the activation of serotonin receptors in brain regions of the ratWei J.-W.; MING-JEN LEE ; Yeh S.-R.journal article10