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Xiaona Luo

Showing results (1-10 of 23) with videos related to

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Frontiers in Neurology|April 20, 2026
Study on Leigh syndrome caused by <i>SURF1</i> gene mutations and its mechanismsChunmei Wang, Longlong Lin, Yuanfeng Zhang, et al.
Scientific Reports|December 19, 2025
Optimization of ultrasound-assisted enzymatic extraction of saponins from Panax zingiberensis stems and leavesXiaojing Shen, Yunmei Wang, Huicui Deng, et al.
Nanoscale Research Letters|February 10, 2017
Graphene Oxide-Polymer Composite Langmuir Films Constructed by Interfacial Thiol-Ene PhotopolymerizationXiaona Luo, Kai Ma, Tifeng Jiao, et al.
Pharmacogenomics and Personalized Medicine|June 3, 2024
Preliminary Study on Clinical Characteristics and Pathogenesis of <i>IQSEC2</i> Mutations PatientsYun Ren, Xiaona Luo, Haiyan Tong, et al.
BMC Pediatrics|November 19, 2022
Clinical characteristics and prognosis of pediatric myelin oligodendrocyte glycoprotein antibody-associated diseases in ChinaXiaoang Sun, Meiyan Liu, Xiaona Luo, et al.
Molecular Genetics & Genomic Medicine|June 8, 2023
Clinical features and underlying mechanisms of KAT6B disease in a Chinese boyXiaoang Sun, Xiaona Luo, Longlong Lin, et al.
ACS Applied Materials & Interfaces|January 11, 2018
Potassium Tethered Carbons with Unparalleled Adsorption Capacity and Selectivity for Low-Cost Carbon Dioxide Capture from Flue GasHongyu Zhao, Lei Shi, Zhongzheng Zhang, et al.
Frontiers in Pediatrics|December 5, 2022
Clinical characteristics and genetics of ten Chinese children with PRRT2-associated neurological diseasesMeiyan Liu, Xiaoang Sun, Longlong Lin, et al.
Frontiers in Pediatrics|May 26, 2022
Correlation Between Tic Disorders and Serum 25-Hydroxyvitamin D Levels in Chinese ChildrenSimei Wang, Quanmei Xu, Anqi Wang, et al.
Cell Death and Differentiation|August 11, 2023
FBXL4 mutations cause excessive mitophagy via BNIP3/BNIP3L accumulation leading to mitochondrial DNA depletion syndromeYingji Chen, Dongyue Jiao, Yang Liu, et al.
Pageof 3

Showing results (1-10 of 23) with videos related to

Sort By:
Pageof 3
Frontiers in Neurology|April 20, 2026
Study on Leigh syndrome caused by <i>SURF1</i> gene mutations and its mechanismsChunmei Wang, Longlong Lin, Yuanfeng Zhang, et al.
Scientific Reports|December 19, 2025
Optimization of ultrasound-assisted enzymatic extraction of saponins from Panax zingiberensis stems and leavesXiaojing Shen, Yunmei Wang, Huicui Deng, et al.
Nanoscale Research Letters|February 10, 2017
Graphene Oxide-Polymer Composite Langmuir Films Constructed by Interfacial Thiol-Ene PhotopolymerizationXiaona Luo, Kai Ma, Tifeng Jiao, et al.
Pharmacogenomics and Personalized Medicine|June 3, 2024
Preliminary Study on Clinical Characteristics and Pathogenesis of <i>IQSEC2</i> Mutations PatientsYun Ren, Xiaona Luo, Haiyan Tong, et al.
BMC Pediatrics|November 19, 2022
Clinical characteristics and prognosis of pediatric myelin oligodendrocyte glycoprotein antibody-associated diseases in ChinaXiaoang Sun, Meiyan Liu, Xiaona Luo, et al.
Molecular Genetics & Genomic Medicine|June 8, 2023
Clinical features and underlying mechanisms of KAT6B disease in a Chinese boyXiaoang Sun, Xiaona Luo, Longlong Lin, et al.
ACS Applied Materials & Interfaces|January 11, 2018
Potassium Tethered Carbons with Unparalleled Adsorption Capacity and Selectivity for Low-Cost Carbon Dioxide Capture from Flue GasHongyu Zhao, Lei Shi, Zhongzheng Zhang, et al.
Frontiers in Pediatrics|December 5, 2022
Clinical characteristics and genetics of ten Chinese children with PRRT2-associated neurological diseasesMeiyan Liu, Xiaoang Sun, Longlong Lin, et al.
Frontiers in Pediatrics|May 26, 2022
Correlation Between Tic Disorders and Serum 25-Hydroxyvitamin D Levels in Chinese ChildrenSimei Wang, Quanmei Xu, Anqi Wang, et al.
Cell Death and Differentiation|August 11, 2023
FBXL4 mutations cause excessive mitophagy via BNIP3/BNIP3L accumulation leading to mitochondrial DNA depletion syndromeYingji Chen, Dongyue Jiao, Yang Liu, et al.
Pageof 3