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Yanchun Ji

Showing results (11-20 of 48) with videos related to

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Human Molecular Genetics|August 10, 2022
Abnormal morphology and function in retinal ganglion cells derived from patients-specific iPSCs generated from individuals with Leber's hereditary optic neuropathyZhipeng Nie, Chenghui Wang, Jiarong Chen, et al.
JCI Insight|March 4, 2025
Vitamin A treatment restores vision failures arising from Leber's hereditary optic neuropathy-linked mtDNA mutationCheng Ai, Huiying Li, Chunyan Wang, et al.
Mitochondrion|May 27, 2022
Mitochondrial tRNA variants in 811 Chinese probands with Leber's hereditary optic neuropathyYanchun Ji, Juanjuan Zhang, Min Liang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|February 11, 2017
[Progress in research on pathogenic genes and gene therapy for inherited retinal diseases]Ling Zhu, Cong Cao, Jiji Sun, et al.
Journal of Translational Medicine|February 18, 2024
Autoinducer-2 promotes the colonization of Lactobacillus rhamnosus GG to improve the intestinal barrier function in a neonatal mouse model of antibiotic-induced intestinal dysbiosisRiqiang Hu, Ting Yang, Qing Ai, et al.
Journal of Biomedical Science|August 3, 2023
Optimized allotopic expression of mitochondrial ND6 transgene restored complex I and apoptosis deficiencies caused by LHON-linked ND6 14484T > C mutationJing Wang, Yanchun Ji, Cheng Ai, et al.
Biomedical Reports|February 2, 2018
Mutation analysis of Leber's hereditary optic neuropathy using a multi-gene panelYu Dai, Chenghui Wang, Zhipeng Nie, et al.
International Immunopharmacology|March 21, 2025
Low levels of CD39+ Tregs may predict poor outcome in children with sepsisYanchun Ji, Chenhao Wang, Bo Wang, et al.
Brazilian Journal of Cardiovascular Surgery|February 12, 2025
Identification of TGFBR1 Gene Variants in Two Chinese Pedigrees with Loeys-Dietz SyndromeJiehua Qiu, Wei Chen, Xixi Min, et al.
Human Molecular Genetics|May 14, 2022
Leber's hereditary optic neuropathy-associated ND6 14484T > C mutation caused pleiotropic effects on the complex I, RNA homeostasis, apoptosis and mitophagyMin Liang, Yanchun Ji, Liyao Zhang, et al.
Pageof 5

Showing results (11-20 of 48) with videos related to

Sort By:
Pageof 5
Human Molecular Genetics|August 10, 2022
Abnormal morphology and function in retinal ganglion cells derived from patients-specific iPSCs generated from individuals with Leber's hereditary optic neuropathyZhipeng Nie, Chenghui Wang, Jiarong Chen, et al.
JCI Insight|March 4, 2025
Vitamin A treatment restores vision failures arising from Leber's hereditary optic neuropathy-linked mtDNA mutationCheng Ai, Huiying Li, Chunyan Wang, et al.
Mitochondrion|May 27, 2022
Mitochondrial tRNA variants in 811 Chinese probands with Leber's hereditary optic neuropathyYanchun Ji, Juanjuan Zhang, Min Liang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|February 11, 2017
[Progress in research on pathogenic genes and gene therapy for inherited retinal diseases]Ling Zhu, Cong Cao, Jiji Sun, et al.
Journal of Translational Medicine|February 18, 2024
Autoinducer-2 promotes the colonization of Lactobacillus rhamnosus GG to improve the intestinal barrier function in a neonatal mouse model of antibiotic-induced intestinal dysbiosisRiqiang Hu, Ting Yang, Qing Ai, et al.
Journal of Biomedical Science|August 3, 2023
Optimized allotopic expression of mitochondrial ND6 transgene restored complex I and apoptosis deficiencies caused by LHON-linked ND6 14484T > C mutationJing Wang, Yanchun Ji, Cheng Ai, et al.
Biomedical Reports|February 2, 2018
Mutation analysis of Leber's hereditary optic neuropathy using a multi-gene panelYu Dai, Chenghui Wang, Zhipeng Nie, et al.
International Immunopharmacology|March 21, 2025
Low levels of CD39+ Tregs may predict poor outcome in children with sepsisYanchun Ji, Chenhao Wang, Bo Wang, et al.
Brazilian Journal of Cardiovascular Surgery|February 12, 2025
Identification of TGFBR1 Gene Variants in Two Chinese Pedigrees with Loeys-Dietz SyndromeJiehua Qiu, Wei Chen, Xixi Min, et al.
Human Molecular Genetics|May 14, 2022
Leber's hereditary optic neuropathy-associated ND6 14484T > C mutation caused pleiotropic effects on the complex I, RNA homeostasis, apoptosis and mitophagyMin Liang, Yanchun Ji, Liyao Zhang, et al.
Pageof 5