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He Shi

Showing results (141-150 of 197) with videos related to

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Frontiers in Neurology|November 22, 2019
Carboxyl Terminus of Hsp70-Interacting Protein Is Increased in Serum and Cerebrospinal Fluid of Patients With Spinocerebellar Ataxia Type 3Zheng-Wei Hu, Zhi-Hua Yang, Shuo Zhang, et al.
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|April 17, 2016
MC1R variants in Chinese Han patients with sporadic Parkinson's diseaseChang-He Shi, Hui Wang, Cheng-Yuan Mao, et al.
Hepatology Research : the Official Journal of the Japan Society of Hepatology|July 22, 2016
High promoter methylation levels of glutathione-S-transferase M3 predict poor prognosis of acute-on-chronic hepatitis B liver failureFeng-Kai Sun, Shuai Gao, Yu-Chen Fan, et al.
Journal of the Neurological Sciences|March 26, 2014
Genotype-phenotype correlation in a cohort of paroxysmal kinesigenic dyskinesia casesCheng-Yuan Mao, Chang-He Shi, Bo Song, et al.
Frontiers in Molecular Neuroscience|July 19, 2019
Metabolic Profiling Reveals Biochemical Pathways and Potential Biomarkers of Spinocerebellar Ataxia 3Zhi-Hua Yang, Chang-He Shi, Li-Na Zhou, et al.
Neurobiology of Aging|May 27, 2018
DNAJC12 mutation is rare in Chinese Han population with Parkinson's diseaseYu Fan, Zhi-Hua Yang, Fang Li, et al.
Fa Yi Xue Za Zhi|October 20, 2023
Research Progress on Microbial Community Succession in the Postmortem Interval EstimationQing-Qing Xiang, Li-Fang Chen, Qin Su, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 13, 2016
A novel RAB39B gene mutation in X-linked juvenile parkinsonism with basal ganglia calcificationChang-He Shi, Shu-Yu Zhang, Zhi-Hua Yang, et al.
Pageof 20

Showing results (141-150 of 197) with videos related to

Sort By:
Pageof 20
Frontiers in Neurology|November 22, 2019
Carboxyl Terminus of Hsp70-Interacting Protein Is Increased in Serum and Cerebrospinal Fluid of Patients With Spinocerebellar Ataxia Type 3Zheng-Wei Hu, Zhi-Hua Yang, Shuo Zhang, et al.
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|April 17, 2016
MC1R variants in Chinese Han patients with sporadic Parkinson's diseaseChang-He Shi, Hui Wang, Cheng-Yuan Mao, et al.
Hepatology Research : the Official Journal of the Japan Society of Hepatology|July 22, 2016
High promoter methylation levels of glutathione-S-transferase M3 predict poor prognosis of acute-on-chronic hepatitis B liver failureFeng-Kai Sun, Shuai Gao, Yu-Chen Fan, et al.
Journal of the Neurological Sciences|March 26, 2014
Genotype-phenotype correlation in a cohort of paroxysmal kinesigenic dyskinesia casesCheng-Yuan Mao, Chang-He Shi, Bo Song, et al.
Frontiers in Molecular Neuroscience|July 19, 2019
Metabolic Profiling Reveals Biochemical Pathways and Potential Biomarkers of Spinocerebellar Ataxia 3Zhi-Hua Yang, Chang-He Shi, Li-Na Zhou, et al.
Neurobiology of Aging|May 27, 2018
DNAJC12 mutation is rare in Chinese Han population with Parkinson's diseaseYu Fan, Zhi-Hua Yang, Fang Li, et al.
Fa Yi Xue Za Zhi|October 20, 2023
Research Progress on Microbial Community Succession in the Postmortem Interval EstimationQing-Qing Xiang, Li-Fang Chen, Qin Su, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 13, 2016
A novel RAB39B gene mutation in X-linked juvenile parkinsonism with basal ganglia calcificationChang-He Shi, Shu-Yu Zhang, Zhi-Hua Yang, et al.
Pageof 20