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

关于TAIR
	计画说明

浏览
	典藏机构
	作者
	题名
	日期
	统计图表
	机构即时统计
	学术趋势

消息
	2019臺灣學術機構典藏研討會
	機構典藏系統RC7版本已發佈

著作权
	出版社及期刊政策查询
	TAIR著作权会议记录

相关连结
	機構典藏計畫網站
	ROAR
	OpenDOAR
	SHERPA
	OAIster
	JAIRO
	Ira
	DSPACE
	RWWR
	臺大學術典藏NTU Scholars

"ming jen lee"的相关文件

回到依作者浏览
依题名排序	依日期排序

显示项目 21-45 / 123 (共5页)
1 2 3 4 5 > >>
每页显示[10|25|50]项目

机构	日期	题名	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.

显示项目 21-45 / 123 (共5页)
1 2 3 4 5 > >>
每页显示[10|25|50]项目

	English \| 正體中文 \| 简体中文 \| 总笔数 :0
	造访人次 : 51170708 在线人数 : 696 教育部委托研究计画计画执行:国立台湾大学图书馆