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  1. NTU Scholars
  2. Research Outputs

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0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
Showing results 1 to 20 of 68  next >
Issue DateTitleAuthor(s)SourcescopusWOSFulltext/Archive link
2007Acute intermittent porphyria with peripheral neuropathy: A follow-up study after hematin treatmentKuo H.-C.; MING-JEN LEE ; Chuang W.-L.; Huang C.-C.Journal of the Neurological Sciences
2019Anomalous 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.Scientific Reports
2017Antagonism 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.PLoS ONE
2005Arg332Cys 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 of the Neurological Sciences
1991Biochemical events coupled to the activation of serotonin receptors in brain regions of the ratWei J.-W.; MING-JEN LEE ; Yeh S.-R.Chinese Journal of Physiology
2016The 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.PLoS Biology
2014BST1 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.Parkinsonism and Related Disorders
2017Burning pain: Axonal dysfunction in erythromelalgiaFarrar M.A.; MING-JEN LEE ; Howells J.; Andrews P.I.; Lin C.S.-Y.Pain
2019Calebin-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.Phytomedicine
2020Cardiac 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 of the Formosan Medical Association
2014A case of familial amyloidotic polyneuropathy with a rare Phe33Leu mutation in the TTR geneChen C.-H.; Huang C.-W.; MING-JEN LEE Journal of the Formosan Medical Association
2010Cerebral amyloid angiopathy in East and WestChen Y.-W.; MING-JEN LEE ; Smith E.E.International Journal of Stroke
2020Changes of resurgent Na+ currents in the Nav1.4 channel resulting from an SCN4A mutation contributing to sodium channel myotoniaHuang C.-W.; Lai H.-J.; Lin P.-C.; MING-JEN LEE International Journal of Molecular Sciences
2007Characterization 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 of Neurology
1997Clinical and electrophysiological characteristics of inflammatory demyelinating neuropathiesMING-JEN LEE ; Chang Y.-C.; Chen R.-C.; Hsieh S.-T.Acta Neurologica Taiwanica
2011Clinical 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 of Alzheimer's Disease
2010Clinical 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.Neurology
2008Comparison 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.Clinical Neurology and Neurosurgery
2005Complex haplotypic effects of the ABCB1 gene on epilepsy treatment responseHung C.-C.; Tai J.J.; Lin C.-J.; MING-JEN LEE ; Liou H.-H.Pharmacogenomics
2004Cutaneous 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.Neurobiology of Disease
Showing results 1 to 20 of 68  next >

臺大位居世界頂尖大學之列,為永久珍藏及向國際展現本校豐碩的研究成果及學術能量,圖書館整合機構典藏(NTUR)與學術庫(AH)不同功能平台,成為臺大學術典藏NTU scholars。期能整合研究能量、促進交流合作、保存學術產出、推廣研究成果。

To permanently archive and promote researcher profiles and scholarly works, Library integrates the services of “NTU Repository” with “Academic Hub” to form NTU Scholars.

總館學科館員 (Main Library)
醫學圖書館學科館員 (Medical Library)
社會科學院辜振甫紀念圖書館學科館員 (Social Sciences Library)

開放取用是從使用者角度提升資訊取用性的社會運動,應用在學術研究上是透過將研究著作公開供使用者自由取閱,以促進學術傳播及因應期刊訂購費用逐年攀升。同時可加速研究發展、提升研究影響力,NTU Scholars即為本校的開放取用典藏(OA Archive)平台。(點選深入了解OA)

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    Please represent that the submission is your original work, and that you have the right to grant the rights to upload.
  • 若欲上傳已出版的全文電子檔,可使用Sherpa Romeo網站查詢,以確認出版單位之版權政策。
    Please use Sherpa Romeo to find a summary of permissions that are normally given as part of each publisher's copyright transfer agreement.
  • 網站簡介 (Quickstart Guide)
  • 使用手冊 (Instruction Manual)
  • 線上預約服務 (Booking Service)
  • 方案一:臺灣大學計算機中心帳號登入
    (With C&INC Email Account)
  • 方案二:ORCID帳號登入 (With ORCID)
  • 方案一:定期更新ORCID者,以ID匯入 (Search for identifier (ORCID))
  • 方案二:自行建檔 (Default mode Submission)
  • 方案三:學科館員協助匯入 (Email worklist to subject librarians)
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