臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)

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機構	日期	題名	作者
臺大學術典藏	2020-03-03T02:33:35Z	Complex haplotypic effects of the ABCB1 gene on epilepsy treatment response	Hung C.-C.; Tai J.J.; Lin C.-J.; MING-JEN LEE; Liou H.-H.
臺大學術典藏	2020-03-03T02:33:35Z	Six novel NPC1 mutations in Chinese patients with Niemann-Pick disease type C	Yang C.-C.; Su Y.-N.; Chiou P.-C.; Fietz M.J.; Yu C.-L.; Hwu W.-L.; MING-JEN LEE
臺大學術典藏	2020-03-03T02:33:35Z	Arg332Cys mutation of NOTCH3 gene in the first known Taiwanese family with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy	Tang S.-C.; MING-JEN LEE; Jeng J.-S.; Yip P.-K.
臺大學術典藏	2020-03-03T02:33:34Z	Mutations of the SPG11 gene in patients with autosomal recessive spastic paraparesis and thin corpus callosum	MING-JEN LEE; Cheng T.-W.; Hua M.-S.; Pan M.-K.; Wang J.; Stephenson D.A.; Yang C.-C.
臺大學術典藏	2020-03-03T02:33:34Z	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.; Hsieh S.-T.; MING-JEN LEE; Yang C.-C.; Liu C.-S.; Huang C.-C.; Lyu R.-K.; Ro L.-S.
臺大學術典藏	2020-03-03T02:33:34Z	Nerve function and dysfunction in acute intermittent porphyria	Lin C.S.-Y.; Krishnan A.V.; MING-JEN LEE; Zagami A.S.; You H.-L.; Yang C.-C.; Bostock H.; Kiernan M.C.
臺大學術典藏	2020-03-03T02:33:34Z	Acute intermittent porphyria with peripheral neuropathy: A follow-up study after hematin treatment	Kuo H.-C.; MING-JEN LEE; Chuang W.-L.; Huang C.-C.
臺大學術典藏	2020-03-03T02:33:34Z	Recent developments in neurofibromatosis type 1	MING-JEN LEE; Stephenson D.A.
臺大學術典藏	2020-03-03T02:33:33Z	Leptin induces migration and invasion of glioma cells through MMP-13 production	Yeh W.-L.; Lu D.-Y.; MING-JEN LEE; Fu W.-M.
臺大學術典藏	2020-03-03T02:33:33Z	Notch signaling and CADASIL	Tang S.-C.; Jeng J.-S.; MING-JEN LEE; Yip P.-K.
臺大學術典藏	2020-03-03T02:33:33Z	Genotype-phenotype correlates in Taiwanese patients with early-onset recessive Parkinsonism	MING-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.
臺大學術典藏	2020-03-03T02:33:33Z	Rapid prenatal confirmation of LIT1 hypomethylation using a novel quantitative method (E-Q-PCR) in fetuses with Beckwith-Wiedemann syndrome impressed with ultrasonography	Ma G.-C.; Chang S.-D.; Chang Y.; Chang S.-P.; Yang C.-W.; MING-JEN LEE; Lee T.-H.; Chen M.
臺大學術典藏	2020-03-03T02:33:33Z	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
臺大學術典藏	2020-03-03T02:33:32Z	Focal brain glucose hypermetabolism in myoclonus-dystonia syndrome caused by an epsilon-sarcoglycan gene mutation	Tai C.-H.; Yen R.-F.; Lin C.-H.; Yen K.-Y.; Yip P.-K.; Wu R.-M.; MING-JEN LEE
臺大學術典藏	2020-03-03T02:33:32Z	Cerebral amyloid angiopathy in East and West	Chen Y.-W.; MING-JEN LEE; Smith E.E.
臺大學術典藏	2020-03-03T02:33:32Z	Clinical presentations and skin denervation in amyloid neuropathy due to transthyretin Ala97Ser	Yang 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.
臺大學術典藏	2020-03-03T02:33:32Z	Longitudinal evaluation of an N-Ethyl-N-nitrosourea-created murine model with normal pressure hydrocephalus	MING-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.
臺大學術典藏	2020-03-03T02:33:31Z	Clinical phenotype of G206D mutation in the presenilin 1 gene in pathologically confirmed familial Alzheimer's disease	Wu Y.-Y.; Cheng I.H.-J.; Lee C.-C.; Chiu M.-J.; MING-JEN LEE; Chen T.-F.; Hsu J.-L.
臺大學術典藏	2020-03-03T02:33:31Z	Neurological complications of acute intermittent porphyria	Kuo 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.
臺大學術典藏	2020-03-03T02:33:31Z	rs5848 variant of progranulin gene is a risk of Alzheimer's disease in the Taiwanese population	MING-JEN LEE; Chen T.-F.; Cheng T.-W.; Chiu M.-J.
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.

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