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Bei Sha

Showing results (151-160 of 236) with videos related to

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Neuroscience Letters|July 7, 2010
FBXO7 gene mutations may be rare in Chinese early-onset Parkinsonism patientsLin-zi Luo, Qian Xu, Ji-feng Guo, et al.
Neuroscience Letters|April 17, 2012
Mutation analysis of LRRK2, SCNA, UCHL1, HtrA2 and GIGYF2 genes in Chinese patients with autosomal dorminant Parkinson's diseaseJin-yong Tian, Ji-feng Guo, Lei Wang, et al.
Neurobiology of Aging|January 4, 2016
Relationship between Alzheimer's disease GWAS-linked top hits and risk of Parkinson's disease with or without cognitive decline: a Chinese population-based studyYa-qin Wang, Bei-sha Tang, Yang Yang, et al.
Zhonghua Yi Xue Za Zhi|September 24, 2005
[Mutation analysis of PINK1 gene in Chinese patients with autosomal recessive early-onset parkinsonism type 6]Yu-hu Zhang, Bei-sha Tang, Ji-feng Guo, et al.
The International Journal of Neuroscience|July 10, 2014
The BAG2 and BAG5 proteins inhibit the ubiquitination of pathogenic ataxin3-80QXiang-Qian Che, Bei-Sha Tang, Hong-Feng Wang, et al.
Chinese Medical Journal|January 17, 2018
Screening for <i>SH3TC2, PMP2</i>, and <i>BSCL2</i> Variants in a Cohort of Chinese Patients with Charcot-Marie-ToothXin Zhao, Ming-Ming Jiang, Yi-Zhou Yan, et al.
Journal of Thrombosis and Thrombolysis|November 28, 2012
TNFSF4 gene polymorphism rs3861950 but not rs3850641 is associated with the risk of cerebral infarction in a Chinese populationJie Feng, Yun-Hai Liu, Qi-Dong Yang, et al.
Parkinsonism & Related Disorders|August 19, 2018
Prevalence of pre-diagnostic symptoms did not differ between LRRK2-related, GBA-related and idiopathic patients with Parkinson's diseaseShu-Ying Liu, Zheng Zheng, Zhu-Qin Gu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|October 11, 2011
[Cellular expression of (R127W)HSPB1 and its co-localization with neurofilament light chain]Ru-xu Zhang, Xi Yang, Xiao-hong Zi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 12, 2008
Mutation analysis of Parkin, PINK1, DJ-1 and ATP13A2 genes in Chinese patients with autosomal recessive early-onset ParkinsonismJi-Feng Guo, Bin Xiao, Bing Liao, et al.
Pageof 24

Showing results (151-160 of 236) with videos related to

Sort By:
Pageof 24
Neuroscience Letters|July 7, 2010
FBXO7 gene mutations may be rare in Chinese early-onset Parkinsonism patientsLin-zi Luo, Qian Xu, Ji-feng Guo, et al.
Neuroscience Letters|April 17, 2012
Mutation analysis of LRRK2, SCNA, UCHL1, HtrA2 and GIGYF2 genes in Chinese patients with autosomal dorminant Parkinson's diseaseJin-yong Tian, Ji-feng Guo, Lei Wang, et al.
Neurobiology of Aging|January 4, 2016
Relationship between Alzheimer's disease GWAS-linked top hits and risk of Parkinson's disease with or without cognitive decline: a Chinese population-based studyYa-qin Wang, Bei-sha Tang, Yang Yang, et al.
Zhonghua Yi Xue Za Zhi|September 24, 2005
[Mutation analysis of PINK1 gene in Chinese patients with autosomal recessive early-onset parkinsonism type 6]Yu-hu Zhang, Bei-sha Tang, Ji-feng Guo, et al.
The International Journal of Neuroscience|July 10, 2014
The BAG2 and BAG5 proteins inhibit the ubiquitination of pathogenic ataxin3-80QXiang-Qian Che, Bei-Sha Tang, Hong-Feng Wang, et al.
Chinese Medical Journal|January 17, 2018
Screening for <i>SH3TC2, PMP2</i>, and <i>BSCL2</i> Variants in a Cohort of Chinese Patients with Charcot-Marie-ToothXin Zhao, Ming-Ming Jiang, Yi-Zhou Yan, et al.
Journal of Thrombosis and Thrombolysis|November 28, 2012
TNFSF4 gene polymorphism rs3861950 but not rs3850641 is associated with the risk of cerebral infarction in a Chinese populationJie Feng, Yun-Hai Liu, Qi-Dong Yang, et al.
Parkinsonism & Related Disorders|August 19, 2018
Prevalence of pre-diagnostic symptoms did not differ between LRRK2-related, GBA-related and idiopathic patients with Parkinson's diseaseShu-Ying Liu, Zheng Zheng, Zhu-Qin Gu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|October 11, 2011
[Cellular expression of (R127W)HSPB1 and its co-localization with neurofilament light chain]Ru-xu Zhang, Xi Yang, Xiao-hong Zi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 12, 2008
Mutation analysis of Parkin, PINK1, DJ-1 and ATP13A2 genes in Chinese patients with autosomal recessive early-onset ParkinsonismJi-Feng Guo, Bin Xiao, Bing Liao, et al.
Pageof 24