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JiaoYang Chen

Showing results (21-30 of 32) with videos related to

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Seizure|May 22, 2019
Infantile epilepsy with multifocal myoclonus caused by TBC1D24 mutationsJing Zhang, Jiaoyang Chen, Qi Zeng, et al.
Developmental Medicine and Child Neurology|July 21, 2020
Phenotypic spectrum of patients with GABRB2 variants: from mild febrile seizures to severe epileptic encephalopathyYing Yang, Wenshu Xiangwei, Xiaoli Zhang, et al.
International Journal of Biological Macromolecules|April 10, 2025
Supramolecular interaction-enhanced green active packaging films: Design and performance of Ca<sup>2+</sup>-crosslinked carboxymethyl chitosan composite filmsCheng Wang, Hao Yu, QiHang Bu, et al.
Nano Letters|May 30, 2023
Cationic Oxidative Leaching Engineering Modulated <i>In Situ</i> Self-Reconstruction of Nickel Sulfide for Superior Water OxidationXuanzhi Liu, Jianchuan Wang, Hanxiao Liao, et al.
Toxics|November 24, 2023
Effects of Ambient O<sub>3</sub> on Respiratory Mortality, Especially the Combined Effects of PM<sub>2.5</sub> and O<sub>3</sub>Ye Deng, Junlong Wang, Li Sun, et al.
Advanced Materials (Deerfield Beach, Fla.)|March 25, 2023
Room-Temperature Self-Healing Soft Composite Network with Unprecedented Crack Propagation Resistance Enabled by a Supramolecular Assembled Lamellar StructureJianHua Xu, YuKun Li, Tong Liu, et al.
Brain Communications|June 7, 2021
Dravet syndrome-associated mutations in <i>GABRA1</i>, <i>GABRB2</i> and <i>GABRG2</i> define the genetic landscape of defects of GABA<sub>A</sub> receptorsCiria C Hernandez, XiaoJuan Tian, Ningning Hu, et al.
Frontiers in Neurology|November 21, 2022
<i>PCDH19</i>-related epilepsy in mosaic males: The phenotypic implication of genotype and variant allele frequencyYi Chen, Xiaoxu Yang, Jiaoyang Chen, et al.
Journal of Human Genetics|December 9, 2022
Detecting genomic mosaicism in "de novo" genetic epilepsy by amplicon-based deep sequencingJiaoyang Chen, Yi Chen, Ying Yang, et al.
Frontiers in Molecular Neuroscience|April 18, 2022
<i>SCN2A</i>-Related Epilepsy: The Phenotypic Spectrum, Treatment and PrognosisQi Zeng, Ying Yang, Jing Duan, et al.
Pageof 4

Showing results (21-30 of 32) with videos related to

Sort By:
Pageof 4
Seizure|May 22, 2019
Infantile epilepsy with multifocal myoclonus caused by TBC1D24 mutationsJing Zhang, Jiaoyang Chen, Qi Zeng, et al.
Developmental Medicine and Child Neurology|July 21, 2020
Phenotypic spectrum of patients with GABRB2 variants: from mild febrile seizures to severe epileptic encephalopathyYing Yang, Wenshu Xiangwei, Xiaoli Zhang, et al.
International Journal of Biological Macromolecules|April 10, 2025
Supramolecular interaction-enhanced green active packaging films: Design and performance of Ca<sup>2+</sup>-crosslinked carboxymethyl chitosan composite filmsCheng Wang, Hao Yu, QiHang Bu, et al.
Nano Letters|May 30, 2023
Cationic Oxidative Leaching Engineering Modulated <i>In Situ</i> Self-Reconstruction of Nickel Sulfide for Superior Water OxidationXuanzhi Liu, Jianchuan Wang, Hanxiao Liao, et al.
Toxics|November 24, 2023
Effects of Ambient O<sub>3</sub> on Respiratory Mortality, Especially the Combined Effects of PM<sub>2.5</sub> and O<sub>3</sub>Ye Deng, Junlong Wang, Li Sun, et al.
Advanced Materials (Deerfield Beach, Fla.)|March 25, 2023
Room-Temperature Self-Healing Soft Composite Network with Unprecedented Crack Propagation Resistance Enabled by a Supramolecular Assembled Lamellar StructureJianHua Xu, YuKun Li, Tong Liu, et al.
Brain Communications|June 7, 2021
Dravet syndrome-associated mutations in <i>GABRA1</i>, <i>GABRB2</i> and <i>GABRG2</i> define the genetic landscape of defects of GABA<sub>A</sub> receptorsCiria C Hernandez, XiaoJuan Tian, Ningning Hu, et al.
Frontiers in Neurology|November 21, 2022
<i>PCDH19</i>-related epilepsy in mosaic males: The phenotypic implication of genotype and variant allele frequencyYi Chen, Xiaoxu Yang, Jiaoyang Chen, et al.
Journal of Human Genetics|December 9, 2022
Detecting genomic mosaicism in "de novo" genetic epilepsy by amplicon-based deep sequencingJiaoyang Chen, Yi Chen, Ying Yang, et al.
Frontiers in Molecular Neuroscience|April 18, 2022
<i>SCN2A</i>-Related Epilepsy: The Phenotypic Spectrum, Treatment and PrognosisQi Zeng, Ying Yang, Jing Duan, et al.
Pageof 4