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Hong-Fu Li

Showing results (41-50 of 70) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|March 3, 2026
Heterozygous Loss-of-Function Variants of KCNJ10 Cause Paroxysmal Kinesigenic DyskinesiaWan-Bing Sun, Jiao-Jiao Xu, Yu-Lan Chen, et al.
Stem Cells International|January 16, 2016
Modeling Neurological Disease by Rapid Conversion of Human Urine Cells into Functional NeuronsShu-Zhen Zhang, Li-Xiang Ma, Wen-Jing Qian, et al.
Neurobiology of Aging|December 3, 2014
Intermediate-length polyglutamine in ATXN2 is a possible risk factor among Eastern Chinese patients with amyotrophic lateral sclerosisHai-Peng Lu, Shi-Rui Gan, Sheng Chen, et al.
Neurobiology of Aging|March 26, 2017
Clinical features of Chinese patients with Gerstmann-Sträussler-Scheinker identified by targeted next-generation sequencingHong-Fu Li, Zhi-Jun Liu, Hai-Lin Dong, et al.
Frontiers in Genetics|August 29, 2022
Identified novel heterozygous <i>HTRA1</i> pathogenic variants in Chinese patients with <i>HTRA1</i>-associated dominant cerebral small vessel diseaseMei-Jiao Chen, Yi Zhang, Wen-Jiao Luo, et al.
Molecules (Basel, Switzerland)|September 21, 2016
Detection of 191 Taxifolin Metabolites and Their Distribution in Rats Using HPLC-ESI-IT-TOF-MS(n)Ping Yang, Feng Xu, Hong-Fu Li, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|March 20, 2019
Identification and functional analysis of novel mutations in the <i>SOD1</i> gene in Chinese patients with amyotrophic lateral sclerosisHui-Xia Lin, Qing-Qing Tao, Qiao Wei, et al.
Neurobiology of Aging|August 12, 2014
Identify mutation in amyotrophic lateral sclerosis cases using HaloPlex target enrichment systemZhi-Jun Liu, Hong-Fu Li, Guo-He Tan, et al.
Journal of Neurology|August 31, 2020
Common genetic variants in PRRC2A are associated with both neuromyelitis optica spectrum disorder and multiple sclerosis in Han Chinese populationJuan Zhang, Mei-Jiao Chen, Gui-Xian Zhao, et al.
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research|January 13, 2018
Evaluation of Multislice Spiral Computed Tomography Perfusion Imaging for the Efficacy of Preoperative Concurrent Chemoradiotherapy in Middle-aged and Elderly Patients with Locally Advanced Gastric CancerJian-Xiao Liang, Xiu-Juan Bi, Xiao-Mei Li, et al.
Pageof 7

Showing results (41-50 of 70) with videos related to

Sort By:
Pageof 7
Movement Disorders : Official Journal of the Movement Disorder Society|March 3, 2026
Heterozygous Loss-of-Function Variants of KCNJ10 Cause Paroxysmal Kinesigenic DyskinesiaWan-Bing Sun, Jiao-Jiao Xu, Yu-Lan Chen, et al.
Stem Cells International|January 16, 2016
Modeling Neurological Disease by Rapid Conversion of Human Urine Cells into Functional NeuronsShu-Zhen Zhang, Li-Xiang Ma, Wen-Jing Qian, et al.
Neurobiology of Aging|December 3, 2014
Intermediate-length polyglutamine in ATXN2 is a possible risk factor among Eastern Chinese patients with amyotrophic lateral sclerosisHai-Peng Lu, Shi-Rui Gan, Sheng Chen, et al.
Neurobiology of Aging|March 26, 2017
Clinical features of Chinese patients with Gerstmann-Sträussler-Scheinker identified by targeted next-generation sequencingHong-Fu Li, Zhi-Jun Liu, Hai-Lin Dong, et al.
Frontiers in Genetics|August 29, 2022
Identified novel heterozygous <i>HTRA1</i> pathogenic variants in Chinese patients with <i>HTRA1</i>-associated dominant cerebral small vessel diseaseMei-Jiao Chen, Yi Zhang, Wen-Jiao Luo, et al.
Molecules (Basel, Switzerland)|September 21, 2016
Detection of 191 Taxifolin Metabolites and Their Distribution in Rats Using HPLC-ESI-IT-TOF-MS(n)Ping Yang, Feng Xu, Hong-Fu Li, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|March 20, 2019
Identification and functional analysis of novel mutations in the <i>SOD1</i> gene in Chinese patients with amyotrophic lateral sclerosisHui-Xia Lin, Qing-Qing Tao, Qiao Wei, et al.
Neurobiology of Aging|August 12, 2014
Identify mutation in amyotrophic lateral sclerosis cases using HaloPlex target enrichment systemZhi-Jun Liu, Hong-Fu Li, Guo-He Tan, et al.
Journal of Neurology|August 31, 2020
Common genetic variants in PRRC2A are associated with both neuromyelitis optica spectrum disorder and multiple sclerosis in Han Chinese populationJuan Zhang, Mei-Jiao Chen, Gui-Xian Zhao, et al.
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research|January 13, 2018
Evaluation of Multislice Spiral Computed Tomography Perfusion Imaging for the Efficacy of Preoperative Concurrent Chemoradiotherapy in Middle-aged and Elderly Patients with Locally Advanced Gastric CancerJian-Xiao Liang, Xiu-Juan Bi, Xiao-Mei Li, et al.
Pageof 7