Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Hong-Fu Li

Showing results (51-60 of 70) with videos related to

Pageof 7
Sort By:
International Journal of Biological Macromolecules|November 2, 2023
Green synthesis of silver nanoparticles using Phlebopus portentosus polysaccharide and their antioxidant, antidiabetic, anticancer, and antimicrobial activitiesHong-Fu Li, Zhang-Chao Pan, Jiao-Man Chen, et al.
Chinese Medical Journal|March 10, 2018
Variant of <i>EOMES</i> Associated with Increasing Risk in Chinese Patients with Relapsing-remitting Multiple SclerosisSheng Chen, Juan Zhang, Qi-Bing Liu, et al.
Parkinsonism & Related Disorders|January 13, 2019
Associations between neuroanatomical abnormality and motor symptoms in paroxysmal kinesigenic dyskinesiaHong-Fu Li, Liqin Yang, Dazhi Yin, et al.
Phytochemical Analysis : PCA|April 19, 2024
20 potentially new compounds and 11 new bioactive constituents found in Smilacis Glabrae Rhizoma utilizing HPLC-DAD-ESI-IT-TOF-MS<sup>n</sup>Gegentana, Feng Xu, Yan-Fei Huang, et al.
Molecules (Basel, Switzerland)|December 1, 2020
Exploring the In Vivo Existence Forms (23 Original Constituents and 147 Metabolites) of Astragali Radix Total Flavonoids and Their Distributions in Rats Using HPLC-DAD-ESI-IT-TOF-MS<sup>n</sup>Li-Jia Liu, Hong-Fu Li, Feng Xu, et al.
Clinical Genetics|February 20, 2019
Clinical and genetic characterization of a cohort of Chinese patients with hereditary spastic paraplegiaYang-Tian Yan, Qiao Wei, Yicen Zheng, et al.
CNS Neuroscience & Therapeutics|May 25, 2019
Functional study and pathogenicity classification of PRRT2 missense variants in PRRT2-related disordersShao-Yun Zhao, Li-Xi Li, Yu-Lan Chen, et al.
Brain : a Journal of Neurology|March 22, 2021
Bi-allelic loss of function variants in COX20 gene cause autosomal recessive sensory neuronopathyHai-Lin Dong, Yin Ma, Hao Yu, et al.
Translational Neurodegeneration|July 11, 2019
Clinical features and genetic spectrum in Chinese patients with recessive hereditary spastic paraplegiaQiao Wei, Hai-Lin Dong, Li-Ying Pan, et al.
Clinical Genetics|August 3, 2019
Genetic spectrum and clinical profiles in a southeast Chinese cohort of Charcot-Marie-Tooth diseaseCong-Xin Chen, Hai-Lin Dong, Qiao Wei, et al.
Pageof 7

Showing results (51-60 of 70) with videos related to

Sort By:
Pageof 7
International Journal of Biological Macromolecules|November 2, 2023
Green synthesis of silver nanoparticles using Phlebopus portentosus polysaccharide and their antioxidant, antidiabetic, anticancer, and antimicrobial activitiesHong-Fu Li, Zhang-Chao Pan, Jiao-Man Chen, et al.
Chinese Medical Journal|March 10, 2018
Variant of <i>EOMES</i> Associated with Increasing Risk in Chinese Patients with Relapsing-remitting Multiple SclerosisSheng Chen, Juan Zhang, Qi-Bing Liu, et al.
Parkinsonism & Related Disorders|January 13, 2019
Associations between neuroanatomical abnormality and motor symptoms in paroxysmal kinesigenic dyskinesiaHong-Fu Li, Liqin Yang, Dazhi Yin, et al.
Phytochemical Analysis : PCA|April 19, 2024
20 potentially new compounds and 11 new bioactive constituents found in Smilacis Glabrae Rhizoma utilizing HPLC-DAD-ESI-IT-TOF-MS<sup>n</sup>Gegentana, Feng Xu, Yan-Fei Huang, et al.
Molecules (Basel, Switzerland)|December 1, 2020
Exploring the In Vivo Existence Forms (23 Original Constituents and 147 Metabolites) of Astragali Radix Total Flavonoids and Their Distributions in Rats Using HPLC-DAD-ESI-IT-TOF-MS<sup>n</sup>Li-Jia Liu, Hong-Fu Li, Feng Xu, et al.
Clinical Genetics|February 20, 2019
Clinical and genetic characterization of a cohort of Chinese patients with hereditary spastic paraplegiaYang-Tian Yan, Qiao Wei, Yicen Zheng, et al.
CNS Neuroscience & Therapeutics|May 25, 2019
Functional study and pathogenicity classification of PRRT2 missense variants in PRRT2-related disordersShao-Yun Zhao, Li-Xi Li, Yu-Lan Chen, et al.
Brain : a Journal of Neurology|March 22, 2021
Bi-allelic loss of function variants in COX20 gene cause autosomal recessive sensory neuronopathyHai-Lin Dong, Yin Ma, Hao Yu, et al.
Translational Neurodegeneration|July 11, 2019
Clinical features and genetic spectrum in Chinese patients with recessive hereditary spastic paraplegiaQiao Wei, Hai-Lin Dong, Li-Ying Pan, et al.
Clinical Genetics|August 3, 2019
Genetic spectrum and clinical profiles in a southeast Chinese cohort of Charcot-Marie-Tooth diseaseCong-Xin Chen, Hai-Lin Dong, Qiao Wei, et al.
Pageof 7