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Showing items 81-105 of 155 (7 Page(s) Totally)
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Institution	Date	Title	Author
臺大學術典藏	2020-03-05T01:18:02Z	Lack of RAB39B mutations in early-onset and familial Parkinson's disease in a Taiwanese cohort	Lin H.-H.; Wu R.-M.; Lin H.-I.; Chen M.-L.; CHUN-HWEI TAI; Lin C.-H.
臺大學術典藏	2020-03-04T07:45:31Z	Generation of induced pluripotent stem cells from a patient with Parkinson's disease carrying LRRK2 p.I2012T mutation	CHIN-HSIEN LIN; Cheng Y.-C.; Lin H.-I.; Ho M.-C.; Hsu Y.-H.; Wen C.-H.; Ko H.-W.; Lu H.-E.; Huang C.-Y.; Hsieh P.C.H.
臺大學術典藏	2020-03-04T07:45:30Z	Depression and Catechol-O-methyltransferase (COMT) genetic variants are associated with pain in Parkinson's disease	Chaudhuri K.R.; Fan J.-Y.; Ko C.-I.; Rizos A.; Chang C.-W.; Lin H.-I.; Wu Y.-R.; CHIN-HSIEN LIN
臺大學術典藏	2020-03-04T07:45:30Z	Generation of induced pluripotent stem cells (IBMSi011-A) from a patient with Parkinson's disease carrying LRRK2 p.I1371V mutation	Lin H.-I.; Cheng Y.-C.; Ko H.-W.; Wen C.-H.; Lu H.-E.; Huang C.-Y.; Hsieh P.C.H.; CHIN-HSIEN LIN
臺大學術典藏	2020-03-04T07:45:30Z	Reprogramming of a human induced pluripotent stem cell (iPSC) line (IBMSi012-A) from an early-onset Parkinson's disease patient harboring a homozygous p.D331Y mutation in the PLA2G6 gene	Cheng Y.-C.; Lin H.-I.; Syu S.-H.; Lu H.-E.; Huang C.-Y.; CHIN-HSIEN LIN; Hsieh P.C.H.
臺大學術典藏	2020-03-04T07:45:30Z	Generation of 2 induced pluripotent stem cell lines derived from patients with Parkinson's disease carrying LRRK2 G2385R variant	Hsu Y.-H.; Syu S.-H.; Lu H.-E.; Lin H.-I.; CHIN-HSIEN LIN; Hsieh P.C.H.; Huang C.-Y.; Ho M.-C.; Cheng Y.-C.
臺大學術典藏	2020-03-04T07:45:25Z	Craniocervical dystonia with levodopa-responsive parkinsonism co-segregating with a pathogenic ANO3 mutation in a Taiwanese family	Kuo M.-C.; Lin H.-I.; CHIN-HSIEN LIN
臺大學術典藏	2020-03-04T07:45:25Z	Catechol-O-methyltransferase (COMT) genetic variants are associated with cognitive decline in patients with Parkinson's disease	CHIN-HSIEN LIN; Fan J.-Y.; Lin H.-I.; Chang C.-W.; Wu Y.-R.
臺大學術典藏	2020-03-04T07:45:25Z	Clinical heterogeneity of LRRK2 p.I2012T mutation	Fan T.-S.; Wu R.-M.; Chen P.-L.; Chen T.-F.; Li H.-Y.; Lin Y.-H.; Chen C.-Y.; Chen M.-L.; Tai C.-H.; Lin H.-I.; CHIN-HSIEN LIN
臺大學術典藏	2020-03-04T07:45:24Z	The p.L302P mutation in the lysosomal enzyme gene SMPD1 is a risk factor for Parkinson disease.	Wu R.M.; CHIN-HSIEN LIN; Lin H.I.
臺大學術典藏	2020-03-04T07:45:23Z	Lack of CHCHD2 mutations in Parkinson's disease in a Taiwanese population	Fan T.-S.; Lin H.-I.; CHIN-HSIEN LIN; Wu R.-M.
臺大學術典藏	2020-03-04T07:45:23Z	COQ2 p.V393A variant, rs148156462, is not associated with Parkinson's disease in a Taiwanese population	CHIN-HSIEN LIN; Lin H.-I.; Chen M.-L.; Wu R.-M.
臺大學術典藏	2020-03-04T07:45:23Z	Vitamin D receptor genetic variants and Parkinson's disease in a Taiwanese population	CHIN-HSIEN LIN; Chen K.-H.; Chen M.-L.; Lin H.-I.; Wu R.-M.
臺大學術典藏	2020-03-04T07:45:22Z	PDE8B mutation is not associated with Parkinson's disease in a Taiwanese population	Fan T.-S.; Wu R.-M.; Lin H.-I.; Cheng C.; CHIN-HSIEN LIN
臺大學術典藏	2020-03-04T07:45:22Z	Lack of RAB39B mutations in early-onset and familial Parkinson's disease in a Taiwanese cohort	Lin H.-H.; Wu R.-M.; Lin H.-I.; Chen M.-L.; Tai C.-H.; CHIN-HSIEN LIN
臺大學術典藏	2020-03-04T07:45:22Z	Mutational analysis of SYNJ1 gene (PARK20) in Parkinson's disease in a Taiwanese population	Chen K.-H.; Wu R.-M.; Lin H.-I.; Tai C.-H.; CHIN-HSIEN LIN
臺大學術典藏	2020-03-04T07:45:20Z	A clinical and genetic study of early-onset and familial parkinsonism in taiwan: An integrated approach combining gene dosage analysis and next-generation sequencing	CHIN-HSIEN LIN; Chen P.-L.; Tai C.-H.; Lin H.-I.; Chen C.-S.; Chen M.-L.; Wu R.-M.
臺大學術典藏	2020-03-04T07:45:15Z	Lovastatin protects neurite degeneration in LRRK2-G2019S parkinsonism through activating the Akt/Nrf pathway and inhibiting GSK3�] activity	CHIN-HSIEN LIN; Lin H.-I.; Chen M.-L.; Lai T.-T.; Cao L.-P.; Farrer M.J.; Wu R.-M.; Chien C.-T.
臺大學術典藏	2020-03-04T07:45:14Z	Lack of C9orf72 repeat expansion in Taiwanese patients with mixed neurodegenerative disorders	CHIN-HSIEN LIN; Chen T.-F.; Chiu M.-J.; Lin H.-I.; Wu R.-M.
臺大學術典藏	2020-03-04T07:45:12Z	A limb-girdle myopathy phenotype of RUNX2 mutation in a patient with cleidocranial dysplasia: A case study and literature review	Hsueh S.-J.; Lee N.-C.; Yang S.-H.; Lin H.-I.; CHIN-HSIEN LIN
臺大學術典藏	2020-03-04T07:45:10Z	Lack of TMEM230 mutations in patients with familial and sporadic Parkinson's disease in a Taiwanese population	Fan T.-S.; CHIN-HSIEN LIN; Lin H.-I.; Chen M.-L.; Wu R.-M.
臺大學術典藏	2020-03-04T05:35:00Z	Lack of C9orf72 repeat expansion in Taiwanese patients with mixed neurodegenerative disorders	Lin C.-H.; Chen T.-F.; MING-JANG CHIU; Lin H.-I.; Wu R.-M.
臺大學術典藏	2020-03-03T01:14:45Z	Lack of C9orf72 repeat expansion in Taiwanese patients with mixed neurodegenerative disorders	Lin C.-H; TA-FU CHEN; Chiu M.-J; Lin H.-I; Wu R.-M.
臺大學術典藏	2020-03-03T01:14:42Z	Clinical heterogeneity of LRRK2 p.I2012T mutation	Fan T.-S; Wu R.-M; Chen P.-L; TA-FU CHEN; Li H.-Y; Lin Y.-H; Chen C.-Y; Chen M.-L; Tai C.-H; Lin H.-I; Lin C.-H.
臺大學術典藏	2020-02-25T08:01:25Z	The p.L302P mutation in the lysosomal enzyme gene SMPD1 is a risk factor for Parkinson disease.	RUEY-MEEI WU; Lin C.H; Lin H.I.

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