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Hong-Fu Li

Showing results (61-70 of 70) with videos related to

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Journal of Ethnopharmacology|May 13, 2024
Evaluation of hemostatic, anti-inflammatory, wound healing, skin irritation and allergy, and antimicrobial properties of active fraction from the ethanol extract of Chromolaena odorata (L.) R.M. King & H. RobHong-Fu Li, Han Feng, Yong Wang, et al.
Gene|August 14, 2013
Novel SLC20A2 mutations identified in southern Chinese patients with idiopathic basal ganglia calcificationWan-Jin Chen, Xiang-Ping Yao, Qi-Jie Zhang, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|January 15, 2025
Biallelic variants in SREBF2 cause autosomal recessive spastic paraplegiaQiao Wei, Wenlu Fan, Hong-Fu Li, et al.
Aging and Disease|December 3, 2019
Genetic Spectrum and Variability in Chinese Patients with Amyotrophic Lateral SclerosisZhi-Jun Liu, Hui-Xia Lin, Qiao Wei, et al.
Research (Washington, D.C.)|December 12, 2024
Single-Nucleus RNA Sequencing Reveals the Spatiotemporal Dynamics of Disease-Associated Microglia in Amyotrophic Lateral SclerosisLu-Xi Chen, Mei-Di Zhang, Hai-Feng Xu, et al.
CNS Neuroscience & Therapeutics|July 16, 2017
Clinical features and mutation spectrum in Chinese patients with CADASIL: A multicenter retrospective studySheng Chen, Wang Ni, Xin-Zhen Yin, et al.
Journal of Agricultural and Food Chemistry|December 14, 2020
Global Profiling and Structural Characterization of Metabolites of Ononin Using HPLC-ESI-IT-TOF-MS<sup></sup> After Oral Administration to RatsHong-Fu Li, Teng Li, Ping Yang, et al.
Nature Genetics|November 22, 2011
Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesiaWan-Jin Chen, Yu Lin, Zhi-Qi Xiong, et al.
Journal of Inherited Metabolic Disease|January 13, 2021
CHIP control degradation of mutant ETF:QO through ubiquitylation in late-onset multiple acyl-CoA dehydrogenase deficiencyXin-Yi Liu, Xue-Jiao Chen, Miao Zhao, et al.
Cell Research|October 24, 2017
PRRT2 deficiency induces paroxysmal kinesigenic dyskinesia by regulating synaptic transmission in cerebellumGuo-He Tan, Yuan-Yuan Liu, Lu Wang, et al.
Pageof 7

Showing results (61-70 of 70) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 70 results.
Journal of Ethnopharmacology|May 13, 2024
Evaluation of hemostatic, anti-inflammatory, wound healing, skin irritation and allergy, and antimicrobial properties of active fraction from the ethanol extract of Chromolaena odorata (L.) R.M. King & H. RobHong-Fu Li, Han Feng, Yong Wang, et al.
Gene|August 14, 2013
Novel SLC20A2 mutations identified in southern Chinese patients with idiopathic basal ganglia calcificationWan-Jin Chen, Xiang-Ping Yao, Qi-Jie Zhang, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|January 15, 2025
Biallelic variants in SREBF2 cause autosomal recessive spastic paraplegiaQiao Wei, Wenlu Fan, Hong-Fu Li, et al.
Aging and Disease|December 3, 2019
Genetic Spectrum and Variability in Chinese Patients with Amyotrophic Lateral SclerosisZhi-Jun Liu, Hui-Xia Lin, Qiao Wei, et al.
Research (Washington, D.C.)|December 12, 2024
Single-Nucleus RNA Sequencing Reveals the Spatiotemporal Dynamics of Disease-Associated Microglia in Amyotrophic Lateral SclerosisLu-Xi Chen, Mei-Di Zhang, Hai-Feng Xu, et al.
CNS Neuroscience & Therapeutics|July 16, 2017
Clinical features and mutation spectrum in Chinese patients with CADASIL: A multicenter retrospective studySheng Chen, Wang Ni, Xin-Zhen Yin, et al.
Journal of Agricultural and Food Chemistry|December 14, 2020
Global Profiling and Structural Characterization of Metabolites of Ononin Using HPLC-ESI-IT-TOF-MS<sup></sup> After Oral Administration to RatsHong-Fu Li, Teng Li, Ping Yang, et al.
Nature Genetics|November 22, 2011
Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesiaWan-Jin Chen, Yu Lin, Zhi-Qi Xiong, et al.
Journal of Inherited Metabolic Disease|January 13, 2021
CHIP control degradation of mutant ETF:QO through ubiquitylation in late-onset multiple acyl-CoA dehydrogenase deficiencyXin-Yi Liu, Xue-Jiao Chen, Miao Zhao, et al.
Cell Research|October 24, 2017
PRRT2 deficiency induces paroxysmal kinesigenic dyskinesia by regulating synaptic transmission in cerebellumGuo-He Tan, Yuan-Yuan Liu, Lu Wang, et al.
Pageof 7