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JingMin Wang

Showing results (161-170 of 175) with videos related to

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Neuroscience|September 10, 2021
Novel Insight into the Potential Pathogenicity of Mitochondrial Dysfunction Resulting from PLP1 Duplication Mutations in Patients with Pelizaeus-Merzbacher DiseaseRuoyu Duan, Liuju Li, Huifang Yan, et al.
Advanced Materials (Deerfield Beach, Fla.)|March 18, 2025
Giant Non-Saturating Exchange Striction in a Noncollinear AntiferromagnetXiaoning Wang, Wen-Han Dong, Peixin Qin, et al.
American Journal of Human Genetics|August 21, 2018
De Novo Mutations of CCNK Cause a Syndromic Neurodevelopmental Disorder with Distinctive Facial DysmorphismYanjie Fan, Wu Yin, Bing Hu, et al.
Metabolic Brain Disease|April 12, 2017
Identification of novel ATP7A mutations and prenatal diagnosis in Chinese patients with Menkes diseaseBinbin Cao, Xiaoping Yang, Yinyin Chen, et al.
Nature Communications|January 28, 2026
Ultralong-range exciton transport in submillimeter-scale spherulite film of π-conjugated polymersLili Sun, Yong Yuan, Yang Xu, et al.
Nature Communications|January 16, 2026
Efficient solution-processed light-emitting diodes based on organic-inorganic hybrid antimony halidesZhuangzhuang Ma, Weihong Chu, Qiming Peng, et al.
American Journal of Human Genetics|October 8, 2019
Heterozygous Variants in the Mechanosensitive Ion Channel TMEM63A Result in Transient Hypomyelination during InfancyHuifang Yan, Guy Helman, Swetha E Murthy, et al.
Plos One|February 17, 2018
Hypomyelinating disorders in China: The clinical and genetic heterogeneity in 119 patientsHaoran Ji, Dongxiao Li, Ye Wu, et al.
Human Mutation|February 10, 2022
Genome sequencing demonstrates high diagnostic yield in children with undiagnosed global developmental delay/intellectual disability: A prospective studyYu Sun, Jing Peng, Desheng Liang, et al.
EMBO Molecular Medicine|August 2, 2022
FIBCD1 is an endocytic GAG receptor associated with a novel neurodevelopmental disorderChristopher W Fell, Astrid Hagelkruys, Ana Cicvaric, et al.
Pageof 18

Showing results (161-170 of 175) with videos related to

Sort By:
Pageof 18
Neuroscience|September 10, 2021
Novel Insight into the Potential Pathogenicity of Mitochondrial Dysfunction Resulting from PLP1 Duplication Mutations in Patients with Pelizaeus-Merzbacher DiseaseRuoyu Duan, Liuju Li, Huifang Yan, et al.
Advanced Materials (Deerfield Beach, Fla.)|March 18, 2025
Giant Non-Saturating Exchange Striction in a Noncollinear AntiferromagnetXiaoning Wang, Wen-Han Dong, Peixin Qin, et al.
American Journal of Human Genetics|August 21, 2018
De Novo Mutations of CCNK Cause a Syndromic Neurodevelopmental Disorder with Distinctive Facial DysmorphismYanjie Fan, Wu Yin, Bing Hu, et al.
Metabolic Brain Disease|April 12, 2017
Identification of novel ATP7A mutations and prenatal diagnosis in Chinese patients with Menkes diseaseBinbin Cao, Xiaoping Yang, Yinyin Chen, et al.
Nature Communications|January 28, 2026
Ultralong-range exciton transport in submillimeter-scale spherulite film of π-conjugated polymersLili Sun, Yong Yuan, Yang Xu, et al.
Nature Communications|January 16, 2026
Efficient solution-processed light-emitting diodes based on organic-inorganic hybrid antimony halidesZhuangzhuang Ma, Weihong Chu, Qiming Peng, et al.
American Journal of Human Genetics|October 8, 2019
Heterozygous Variants in the Mechanosensitive Ion Channel TMEM63A Result in Transient Hypomyelination during InfancyHuifang Yan, Guy Helman, Swetha E Murthy, et al.
Plos One|February 17, 2018
Hypomyelinating disorders in China: The clinical and genetic heterogeneity in 119 patientsHaoran Ji, Dongxiao Li, Ye Wu, et al.
Human Mutation|February 10, 2022
Genome sequencing demonstrates high diagnostic yield in children with undiagnosed global developmental delay/intellectual disability: A prospective studyYu Sun, Jing Peng, Desheng Liang, et al.
EMBO Molecular Medicine|August 2, 2022
FIBCD1 is an endocytic GAG receptor associated with a novel neurodevelopmental disorderChristopher W Fell, Astrid Hagelkruys, Ana Cicvaric, et al.
Pageof 18