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Yanchun Ji

Showing results (1-10 of 48) with videos related to

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Mitochondrion|April 28, 2012
Mitochondrial tRNA mutations associated with deafnessJing Zheng, Yanchun Ji, Min-Xin Guan
Gene|August 15, 2024
Dysregulation of mitochondria, apoptosis and mitophagy in Leber's hereditary optic neuropathy with MT-ND1 3635G>A mutationYingqi Chen, Xiaoyang Wei, Xiaorui Ci, et al.
Mitochondrial DNA. Part B, Resources|December 28, 2020
Frequency and spectrum of <i>MT-TT</i> variants associated with Leber's hereditary optic neuropathy in a Chinese cohort of subjectsYuanyuan Lyu, Man Xu, Jie Chen, et al.
BMC Cardiovascular Disorders|May 31, 2025
Mechanism of adenosine monophosphate-activated protein kinase promoting lower extremity varicose veins development via cytoskeletal dynamicsYongmei Zhang, Zhinan Ju, Kanghui Dai, et al.
Mitochondrion|December 12, 2017
Leber's hereditary optic neuropathy caused by a mutation in mitochondrial tRNA<sup>Thr</sup> in eight Chinese pedigreesJuanjuan Zhang, Yanchun Ji, Xiaoling Liu, et al.
Human Molecular Genetics|March 27, 2018
Leber's hereditary optic neuropathy (LHON)-associated ND5 12338T > C mutation altered the assembly and function of complex I, apoptosis and mitophagyJuanjuan Zhang, Yanchun Ji, Yuanyuan Lu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|December 17, 2016
[The role of MT-ND1 m.3635G>A mutation in Leber's hereditary optic neuropathy]Juanjuan Zhang, Zengjun Zhang, Runing Fu, et al.
The Journal of Biological Chemistry|August 30, 2024
Defective post-transcriptional modification of tRNA disrupts mitochondrial homeostasis in Leber's hereditary optic neuropathyJuanjuan Zhang, Wenxu Li, Zhen Liu, et al.
Bioscience Reports|December 8, 2020
Mitochondrial tRNA mutations in Chinese Children with Tic DisordersPeifang Jiang, Yinjie Ling, Tao Zhu, et al.
Bioscience Reports|December 24, 2019
Obesity associated with a novel mitochondrial tRNACys 5802A>G mutation in a Chinese familyJinling Wang, Ningning Zhao, Xiaoting Mao, et al.
Pageof 5

Showing results (1-10 of 48) with videos related to

Sort By:
Pageof 5
Mitochondrion|April 28, 2012
Mitochondrial tRNA mutations associated with deafnessJing Zheng, Yanchun Ji, Min-Xin Guan
Gene|August 15, 2024
Dysregulation of mitochondria, apoptosis and mitophagy in Leber's hereditary optic neuropathy with MT-ND1 3635G>A mutationYingqi Chen, Xiaoyang Wei, Xiaorui Ci, et al.
Mitochondrial DNA. Part B, Resources|December 28, 2020
Frequency and spectrum of <i>MT-TT</i> variants associated with Leber's hereditary optic neuropathy in a Chinese cohort of subjectsYuanyuan Lyu, Man Xu, Jie Chen, et al.
BMC Cardiovascular Disorders|May 31, 2025
Mechanism of adenosine monophosphate-activated protein kinase promoting lower extremity varicose veins development via cytoskeletal dynamicsYongmei Zhang, Zhinan Ju, Kanghui Dai, et al.
Mitochondrion|December 12, 2017
Leber's hereditary optic neuropathy caused by a mutation in mitochondrial tRNA<sup>Thr</sup> in eight Chinese pedigreesJuanjuan Zhang, Yanchun Ji, Xiaoling Liu, et al.
Human Molecular Genetics|March 27, 2018
Leber's hereditary optic neuropathy (LHON)-associated ND5 12338T > C mutation altered the assembly and function of complex I, apoptosis and mitophagyJuanjuan Zhang, Yanchun Ji, Yuanyuan Lu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|December 17, 2016
[The role of MT-ND1 m.3635G>A mutation in Leber's hereditary optic neuropathy]Juanjuan Zhang, Zengjun Zhang, Runing Fu, et al.
The Journal of Biological Chemistry|August 30, 2024
Defective post-transcriptional modification of tRNA disrupts mitochondrial homeostasis in Leber's hereditary optic neuropathyJuanjuan Zhang, Wenxu Li, Zhen Liu, et al.
Bioscience Reports|December 8, 2020
Mitochondrial tRNA mutations in Chinese Children with Tic DisordersPeifang Jiang, Yinjie Ling, Tao Zhu, et al.
Bioscience Reports|December 24, 2019
Obesity associated with a novel mitochondrial tRNACys 5802A>G mutation in a Chinese familyJinling Wang, Ningning Zhao, Xiaoting Mao, et al.
Pageof 5