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Yanchun Ji

Showing results (21-30 of 48) with videos related to

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Plant Physiology|November 20, 2024
Histone modification H3K27me3 is essential during chilling-induced flowering in Litchi chinensisXifen Pan, Xingyu Lu, Lijie Huang, et al.
Mitochondrion|March 15, 2020
Mitochondrial tRNA mutations in 887 Chinese subjects with hearing lossJing Zheng, Xiaohui Bai, Yun Xiao, et al.
Mitochondrion|December 26, 2013
Loss of MED1 triggers mitochondrial biogenesis in C2C12 cellsJialing Yu, Yun Xiao, Junxia Liu, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|September 12, 2024
Mitochondrial tRNA<sup>Glu</sup> 14693A > G Mutation, an "Enhancer" to the Phenotypic Expression of Leber's Hereditary Optic NeuropathyLihao Jin, Dingyi Gan, Wentao He, et al.
Nucleic Acids Research|August 30, 2022
A deafness-associated mitochondrial DNA mutation caused pleiotropic effects on DNA replication and tRNA metabolismFeilong Meng, Zidong Jia, Jing Zheng, et al.
Investigative Ophthalmology & Visual Science|June 22, 2021
Leber's Hereditary Optic Neuropathy Arising From the Synergy Between ND1 3635G>A Mutation and Mitochondrial YARS2 MutationsXiaofen Jin, Juanjuan Zhang, Qiuzi Yi, et al.
Investigative Ophthalmology & Visual Science|July 26, 2021
Assocation Between Leber's Hereditary Optic Neuropathy and MT-ND1 3460G>A Mutation-Induced Alterations in Mitochondrial Function, Apoptosis, and MitophagyJuanjuan Zhang, Yanchun Ji, Jie Chen, et al.
Human Molecular Genetics|January 7, 2023
Nuclear modifier YARS2 allele correction restored retinal ganglion cells-specific deficiencies in Leber's hereditary optic neuropathyJia-Rong Chen, Chao Chen, Jie Chen, et al.
Molecular Medicine Reports|October 10, 2017
Leber's hereditary optic neuropathy is potentially associated with a novel m.5587T>C mutation in two pedigreesYanchun Ji, Lihua Qiao, Xiaoyang Liang, et al.
Molecular Genetics and Metabolism|July 15, 2010
Very high penetrance and occurrence of Leber's hereditary optic neuropathy in a large Han Chinese pedigree carrying the ND4 G11778A mutationXiangtian Zhou, Hongxing Zhang, Fuxin Zhao, et al.
Pageof 5

Showing results (21-30 of 48) with videos related to

Sort By:
Pageof 5
Plant Physiology|November 20, 2024
Histone modification H3K27me3 is essential during chilling-induced flowering in Litchi chinensisXifen Pan, Xingyu Lu, Lijie Huang, et al.
Mitochondrion|March 15, 2020
Mitochondrial tRNA mutations in 887 Chinese subjects with hearing lossJing Zheng, Xiaohui Bai, Yun Xiao, et al.
Mitochondrion|December 26, 2013
Loss of MED1 triggers mitochondrial biogenesis in C2C12 cellsJialing Yu, Yun Xiao, Junxia Liu, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|September 12, 2024
Mitochondrial tRNA<sup>Glu</sup> 14693A > G Mutation, an "Enhancer" to the Phenotypic Expression of Leber's Hereditary Optic NeuropathyLihao Jin, Dingyi Gan, Wentao He, et al.
Nucleic Acids Research|August 30, 2022
A deafness-associated mitochondrial DNA mutation caused pleiotropic effects on DNA replication and tRNA metabolismFeilong Meng, Zidong Jia, Jing Zheng, et al.
Investigative Ophthalmology & Visual Science|June 22, 2021
Leber's Hereditary Optic Neuropathy Arising From the Synergy Between ND1 3635G>A Mutation and Mitochondrial YARS2 MutationsXiaofen Jin, Juanjuan Zhang, Qiuzi Yi, et al.
Investigative Ophthalmology & Visual Science|July 26, 2021
Assocation Between Leber's Hereditary Optic Neuropathy and MT-ND1 3460G>A Mutation-Induced Alterations in Mitochondrial Function, Apoptosis, and MitophagyJuanjuan Zhang, Yanchun Ji, Jie Chen, et al.
Human Molecular Genetics|January 7, 2023
Nuclear modifier YARS2 allele correction restored retinal ganglion cells-specific deficiencies in Leber's hereditary optic neuropathyJia-Rong Chen, Chao Chen, Jie Chen, et al.
Molecular Medicine Reports|October 10, 2017
Leber's hereditary optic neuropathy is potentially associated with a novel m.5587T>C mutation in two pedigreesYanchun Ji, Lihua Qiao, Xiaoyang Liang, et al.
Molecular Genetics and Metabolism|July 15, 2010
Very high penetrance and occurrence of Leber's hereditary optic neuropathy in a large Han Chinese pedigree carrying the ND4 G11778A mutationXiangtian Zhou, Hongxing Zhang, Fuxin Zhao, et al.
Pageof 5