A citation-based method for searching scientific literature

Genki Hayashi, Gino Cortopassi. Free Radic Biol Med 2015
Times Cited: 95



Joanna Szczepanowska, Dominika Malinska, Mariusz R Wieckowski, Jerzy Duszynski. Biochim Biophys Acta 2012
Times Cited: 38




List of shared articles



Times cited

Mitochondriopathies as a Clue to Systemic Disorders-Analytical Tools and Mitigating Measures in Context of Predictive, Preventive, and Personalized (3P) Medicine.
Alena Liskova, Marek Samec, Lenka Koklesova, Erik Kudela, Peter Kubatka, Olga Golubnitschaja. Int J Mol Sci 2021
18

A hypertension-associated mitochondrial DNA mutation alters the tertiary interaction and function of tRNALeu(UUR).
Mi Zhou, Meng Wang, Ling Xue, Zhi Lin, Qiufen He, Wenwen Shi, Yaru Chen, Xiaofen Jin, Haiying Li, Pingping Jiang,[...]. J Biol Chem 2017
19

Biochemical evidence for a mitochondrial genetic modifier in the phenotypic manifestation of Leber's hereditary optic neuropathy-associated mitochondrial DNA mutation.
Pingping Jiang, Min Liang, Chaofan Zhang, Xiaoxu Zhao, Qiufen He, Limei Cui, Xiaoling Liu, Yan-Hong Sun, Qun Fu, Yanchun Ji,[...]. Hum Mol Genet 2016
27

Complex I mutations synergize to worsen the phenotypic expression of Leber's hereditary optic neuropathy.
Yanchun Ji, Juanjuan Zhang, Yuanyuan Lu, Qiuzi Yi, Mengquan Chen, Shipeng Xie, Xiaoting Mao, Yun Xiao, Feilong Meng, Minglian Zhang,[...]. J Biol Chem 2020
14

Leber's hereditary optic neuropathy (LHON)-associated ND5 12338T > C mutation altered the assembly and function of complex I, apoptosis and mitophagy.
Juanjuan Zhang, Yanchun Ji, Yuanyuan Lu, Runing Fu, Man Xu, Xiaoling Liu, Min-Xin Guan. Hum Mol Genet 2018
42

A Deafness- and Diabetes-associated tRNA Mutation Causes Deficient Pseudouridinylation at Position 55 in tRNAGlu and Mitochondrial Dysfunction.
Meng Wang, Hao Liu, Jing Zheng, Bobei Chen, Mi Zhou, Wenlu Fan, Hen Wang, Xiaoyang Liang, Xiaolong Zhou, Gilbert Eriani,[...]. J Biol Chem 2016
45

Contribution of mitochondrial ND1 3394T>C mutation to the phenotypic manifestation of Leber's hereditary optic neuropathy.
Yanchun Ji, Juanjuan Zhang, Jialing Yu, Ying Wang, Yuanyuan Lu, Min Liang, Qiang Li, Xiaofen Jin, Yinsheng Wei, Feilong Meng,[...]. Hum Mol Genet 2019
16

A novel ADOA-associated OPA1 mutation alters the mitochondrial function, membrane potential, ROS production and apoptosis.
Juanjuan Zhang, Xiaoling Liu, Xiaoyang Liang, Yuanyuan Lu, Ling Zhu, Runing Fu, Yanchun Ji, Wenlu Fan, Jie Chen, Bing Lin,[...]. Sci Rep 2017
30