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Sha Tang

Showing results (221-230 of 448) with videos related to

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Neurobiology of Aging|August 4, 2015
LRRK2 A419V variant is a risk factor for Parkinson's disease in Asian populationKai Li, Bei-sha Tang, Zhen-hua Liu, et al.
International Journal of Clinical and Experimental Medicine|January 16, 2016
Involvement of Bcl-2-associated athanogene (BAG)-family proteins in the neuroprotection by rasagilineJi-Feng Guo, Shuang He, Ji-Feng Kang, et al.
Chinese Medical Journal|February 9, 2010
A new variant of the ATP13A2 gene in Chinese patients with early-onset parkinsonismLei Wang, Ji-Feng Guo, Li-Luo Nie, et al.
BMC Genetics|August 1, 2014
Single-base-resolution methylomes of Populus trichocarpa reveal the association between DNA methylation and drought stressDan Liang, Zhoujia Zhang, Honglong Wu, et al.
International Journal of Clinical and Experimental Medicine|November 10, 2015
Association study between SMPD1 p.L302P and sporadic Parkinson's disease in ethnic Chinese populationKai Li, Bei-Sha Tang, Nan-Nan Yang, et al.
Clinical Neurology and Neurosurgery|March 23, 2011
Expansion of the phenotypic spectrum of SPG6 caused by mutation in NIPA1Juan Du, Ya-Cen Hu, Bei-Sha Tang, et al.
Journal of the Neurological Sciences|August 31, 2011
CCG polymorphisms in the huntingtin gene have no effect on the pathogenesis of patients with Huntington's disease in mainland Chinese familiesBao-rong Zhang, Jun Tian, Ya-ping Yan, et al.
Traffic (Copenhagen, Denmark)|October 8, 2016
Characterization of a caveolin-1 mutation associated with both pulmonary arterial hypertension and congenital generalized lipodystrophyBing Han, Courtney A Copeland, Yumeko Kawano, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|March 31, 2015
The single nucleotide polymorphism Rs12817488 is associated with Parkinson's disease in the Chinese populationRi-li Yu, Ji-feng Guo, Ya-qin Wang, et al.
Neuroscience Letters|March 18, 2014
Association analysis of STK39, MCCC1/LAMP3 and sporadic PD in the Chinese Han populationYa-qin Wang, Bei-sha Tang, Ri-li Yu, et al.
Pageof 45

Showing results (221-230 of 448) with videos related to

Sort By:
Pageof 45
Neurobiology of Aging|August 4, 2015
LRRK2 A419V variant is a risk factor for Parkinson's disease in Asian populationKai Li, Bei-sha Tang, Zhen-hua Liu, et al.
International Journal of Clinical and Experimental Medicine|January 16, 2016
Involvement of Bcl-2-associated athanogene (BAG)-family proteins in the neuroprotection by rasagilineJi-Feng Guo, Shuang He, Ji-Feng Kang, et al.
Chinese Medical Journal|February 9, 2010
A new variant of the ATP13A2 gene in Chinese patients with early-onset parkinsonismLei Wang, Ji-Feng Guo, Li-Luo Nie, et al.
BMC Genetics|August 1, 2014
Single-base-resolution methylomes of Populus trichocarpa reveal the association between DNA methylation and drought stressDan Liang, Zhoujia Zhang, Honglong Wu, et al.
International Journal of Clinical and Experimental Medicine|November 10, 2015
Association study between SMPD1 p.L302P and sporadic Parkinson's disease in ethnic Chinese populationKai Li, Bei-Sha Tang, Nan-Nan Yang, et al.
Clinical Neurology and Neurosurgery|March 23, 2011
Expansion of the phenotypic spectrum of SPG6 caused by mutation in NIPA1Juan Du, Ya-Cen Hu, Bei-Sha Tang, et al.
Journal of the Neurological Sciences|August 31, 2011
CCG polymorphisms in the huntingtin gene have no effect on the pathogenesis of patients with Huntington's disease in mainland Chinese familiesBao-rong Zhang, Jun Tian, Ya-ping Yan, et al.
Traffic (Copenhagen, Denmark)|October 8, 2016
Characterization of a caveolin-1 mutation associated with both pulmonary arterial hypertension and congenital generalized lipodystrophyBing Han, Courtney A Copeland, Yumeko Kawano, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|March 31, 2015
The single nucleotide polymorphism Rs12817488 is associated with Parkinson's disease in the Chinese populationRi-li Yu, Ji-feng Guo, Ya-qin Wang, et al.
Neuroscience Letters|March 18, 2014
Association analysis of STK39, MCCC1/LAMP3 and sporadic PD in the Chinese Han populationYa-qin Wang, Bei-sha Tang, Ri-li Yu, et al.
Pageof 45