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

Jingmin Wang

Showing results (21-30 of 175) with videos related to

Pageof 18
Sort By:
Journal of Child Neurology|December 15, 2007
Clinical and genetic study in Chinese patients with Alexander diseaseYe Wu, Qiang Gu, Jingmin Wang, et al.
Neuropediatrics|July 17, 2017
Different Mutations of Gap Junction Connexin 47 Lead to Discrepant Activation of Unfolded Protein Response Pathway in Pelizaeus-Merzbacher-Like DiseaseNa Chen, Jingmin Wang, Yuwu Jiang, et al.
Brain : a Journal of Neurology|February 15, 2018
The recurrent mutation in TMEM106B also causes hypomyelinating leukodystrophy in China and is a CpG hotspotHuifang Yan, Thomas Kubisiak, Haoran Ji, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|July 6, 2010
Characterization of developing rat cortical neurons after epileptiform dischargesQian Jiang, Ye Wu, Jingmin Wang, et al.
ACS Applied Bio Materials|January 24, 2026
Taraxacum-Based Carbon Dots Mitigate Hyperuricemia by Alleviating Oxidative Stress and Reinstating Intestinal Microbiota HomeostasisXinyu Cheng, Zifan Chen, Shuyang Zhang, et al.
Plos One|April 15, 2022
Silencing LncRNA CASC9 inhibits proliferation and invasion of colorectal cancer cells by MiR-542-3p/ILKHeping Zhang, Jingfang Wang, Taoyuan Yu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|July 10, 2022
[Clinical and genetic analysis of three children with 22q13 deletion syndrome]Junyu Wang, Ruoyu Duan, Huifang Yan, et al.
Neuroscience Letters|August 19, 2008
Early-life epileptiform discharges exert both rapid and long-lasting effects on AMPAR subunit composition and distribution in developing neuronsQian Jiang, Jingmin Wang, Ye Wu, et al.
Orphanet Journal of Rare Diseases|November 12, 2020
Clinical and genetic characteristics and prenatal diagnosis of patients presented GDD/ID with rare monogenic causesLiling Lin, Ying Zhang, Hong Pan, et al.
Orphanet Journal of Rare Diseases|September 15, 2020
Pilot trial on the efficacy and safety of pantethine in children with pantothenate kinase-associated neurodegeneration: a single-arm, open-label studyXuting Chang, Jie Zhang, Yuwu Jiang, et al.
Pageof 18

Showing results (21-30 of 175) with videos related to

Sort By:
Pageof 18
Journal of Child Neurology|December 15, 2007
Clinical and genetic study in Chinese patients with Alexander diseaseYe Wu, Qiang Gu, Jingmin Wang, et al.
Neuropediatrics|July 17, 2017
Different Mutations of Gap Junction Connexin 47 Lead to Discrepant Activation of Unfolded Protein Response Pathway in Pelizaeus-Merzbacher-Like DiseaseNa Chen, Jingmin Wang, Yuwu Jiang, et al.
Brain : a Journal of Neurology|February 15, 2018
The recurrent mutation in TMEM106B also causes hypomyelinating leukodystrophy in China and is a CpG hotspotHuifang Yan, Thomas Kubisiak, Haoran Ji, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|July 6, 2010
Characterization of developing rat cortical neurons after epileptiform dischargesQian Jiang, Ye Wu, Jingmin Wang, et al.
ACS Applied Bio Materials|January 24, 2026
Taraxacum-Based Carbon Dots Mitigate Hyperuricemia by Alleviating Oxidative Stress and Reinstating Intestinal Microbiota HomeostasisXinyu Cheng, Zifan Chen, Shuyang Zhang, et al.
Plos One|April 15, 2022
Silencing LncRNA CASC9 inhibits proliferation and invasion of colorectal cancer cells by MiR-542-3p/ILKHeping Zhang, Jingfang Wang, Taoyuan Yu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|July 10, 2022
[Clinical and genetic analysis of three children with 22q13 deletion syndrome]Junyu Wang, Ruoyu Duan, Huifang Yan, et al.
Neuroscience Letters|August 19, 2008
Early-life epileptiform discharges exert both rapid and long-lasting effects on AMPAR subunit composition and distribution in developing neuronsQian Jiang, Jingmin Wang, Ye Wu, et al.
Orphanet Journal of Rare Diseases|November 12, 2020
Clinical and genetic characteristics and prenatal diagnosis of patients presented GDD/ID with rare monogenic causesLiling Lin, Ying Zhang, Hong Pan, et al.
Orphanet Journal of Rare Diseases|September 15, 2020
Pilot trial on the efficacy and safety of pantethine in children with pantothenate kinase-associated neurodegeneration: a single-arm, open-label studyXuting Chang, Jie Zhang, Yuwu Jiang, et al.
Pageof 18