A citation-based method for searching scientific literature

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







List of co-cited articles
770 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


A deafness-associated tRNAHis mutation alters the mitochondrial function, ROS production and membrane potential.
Shasha Gong, Yanyan Peng, Pingping Jiang, Meng Wang, Mingjie Fan, Xinjian Wang, Hong Zhou, Huawei Li, Qingfeng Yan, Taosheng Huang,[...]. Nucleic Acids Res 2014
80
26

Assessing bioenergetic function in response to oxidative stress by metabolic profiling.
Brian P Dranka, Gloria A Benavides, Anne R Diers, Samantha Giordano, Blake R Zelickson, Colin Reily, Luyun Zou, John C Chatham, Bradford G Hill, Jianhua Zhang,[...]. Free Radic Biol Med 2011
313
18

Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA.
R M Andrews, I Kubacka, P F Chinnery, R N Lightowlers, D M Turnbull, N Howell. Nat Genet 1999
18





A Hypertension-Associated tRNAAla Mutation Alters tRNA Metabolism and Mitochondrial Function.
Pingping Jiang, Meng Wang, Ling Xue, Yun Xiao, Jialing Yu, Hui Wang, Juan Yao, Hao Liu, Yanyan Peng, Hanqing Liu,[...]. Mol Cell Biol 2016
41
39


Human mitochondrial tRNAs: biogenesis, function, structural aspects, and diseases.
Tsutomu Suzuki, Asuteka Nagao, Takeo Suzuki. Annu Rev Genet 2011
348
15


An enhanced MITOMAP with a global mtDNA mutational phylogeny.
Eduardo Ruiz-Pesini, Marie T Lott, Vincent Procaccio, Jason C Poole, Marty C Brandon, Dan Mishmar, Christina Yi, James Kreuziger, Pierre Baldi, Douglas C Wallace. Nucleic Acids Res 2007
424
13



An assembled complex IV maintains the stability and activity of complex I in mammalian mitochondria.
Youfen Li, Marilena D'Aurelio, Jian-Hong Deng, Jeong-Soon Park, Giovanni Manfredi, Peiqing Hu, Jianxin Lu, Yidong Bai. J Biol Chem 2007
87
13


Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy.
D C Wallace, G Singh, M T Lott, J A Hodge, T G Schurr, A M Lezza, L J Elsas, E K Nikoskelainen. Science 1988
11

Leber's hereditary optic neuropathy caused by the homoplasmic ND1 m.3635G>A mutation in nine Han Chinese families.
Juanjuan Zhang, Pingping Jiang, Xiaofen Jin, Xiaoling Liu, Minglian Zhang, Shipeng Xie, Min Gao, Sai Zhang, Yan-Hong Sun, Jinping Zhu,[...]. Mitochondrion 2014
28
35

Leber's hereditary optic neuropathy is associated with the T3866C mutation in mitochondrial ND1 gene in three Han Chinese Families.
Xiangtian Zhou, Yaping Qian, Juanjuan Zhang, Yi Tong, Pingping Jiang, Min Liang, Xianning Dai, Huihui Zhou, Fuxin Zhao, Yanchun Ji,[...]. Invest Ophthalmol Vis Sci 2012
30
33

Mutation in TRMU related to transfer RNA modification modulates the phenotypic expression of the deafness-associated mitochondrial 12S ribosomal RNA mutations.
Min-Xin Guan, Qingfeng Yan, Xiaoming Li, Yelena Bykhovskaya, Jaime Gallo-Teran, Petr Hajek, Noriko Umeda, Hui Zhao, Gema Garrido, Emebet Mengesha,[...]. Am J Hum Genet 2006
177
10

Mitochondria-mediated transformation of human rho(0) cells.
M P King, G Attadi. Methods Enzymol 1996
67
14

The novel A4435G mutation in the mitochondrial tRNAMet may modulate the phenotypic expression of the LHON-associated ND4 G11778A mutation.
Jia Qu, Ronghua Li, Xiangtian Zhou, Yi Tong, Fan Lu, Yaping Qian, Yongwu Hu, Jun Qin Mo, Constance E West, Min-Xin Guan. Invest Ophthalmol Vis Sci 2006
105
9

Analysis of aminoacylation of human mitochondrial tRNAs.
J A Enríquez, G Attardi. Methods Enzymol 1996
53
16


Biochemical characterization of the mitochondrial tRNASer(UCN) T7511C mutation associated with nonsyndromic deafness.
Xiaoming Li, Nathan Fischel-Ghodsian, Faina Schwartz, Qingfeng Yan, Rick A Friedman, Min-Xin Guan. Nucleic Acids Res 2004
108
9


Human mitochondrial tRNAs in health and disease.
C Florentz, B Sohm, P Tryoen-Tóth, J Pütz, M Sissler. Cell Mol Life Sci 2003
192
9

A deafness-associated tRNAAsp mutation alters the m1G37 modification, aminoacylation and stability of tRNAAsp and mitochondrial function.
Meng Wang, Yanyan Peng, Jing Zheng, Binjiao Zheng, Xiaofen Jin, Hao Liu, Yong Wang, Xiaowen Tang, Taosheng Huang, Pingping Jiang,[...]. Nucleic Acids Res 2016
26
34

Respiratory chain enzyme analysis in muscle and liver.
D R Thorburn, C W Chow, D M Kirby. Mitochondrion 2004
69
13


Prevalence of Mitochondrial ND4 Mutations in 1281 Han Chinese Subjects With Leber's Hereditary Optic Neuropathy.
Pingping Jiang, Min Liang, Juanjuan Zhang, Yinglong Gao, Zheyun He, Han Yu, Fuxin Zhao, Yanchun Ji, Xiaoling Liu, Minglian Zhang,[...]. Invest Ophthalmol Vis Sci 2015
36
22

Retinal ganglion cell neurodegeneration in mitochondrial inherited disorders.
Valerio Carelli, Chiara La Morgia, Maria Lucia Valentino, Piero Barboni, Fred N Ross-Cisneros, Alfredo A Sadun. Biochim Biophys Acta 2009
157
8

Inherited mitochondrial optic neuropathies.
P Yu-Wai-Man, P G Griffiths, G Hudson, P F Chinnery. J Med Genet 2009
263
8


Coronary heart disease is associated with a mutation in mitochondrial tRNA.
Zidong Jia, Xinjian Wang, Yanwen Qin, Ling Xue, Pingping Jiang, Yanzi Meng, Suxue Shi, Yan Wang, Jun Qin Mo, Min-Xin Guan. Hum Mol Genet 2013
46
17

Frequency and spectrum of mitochondrial ND6 mutations in 1218 Han Chinese subjects with Leber's hereditary optic neuropathy.
Min Liang, Pingping Jiang, Feng Li, Juanjuan Zhang, Yanchun Ji, Yiqun He, Meifen Xu, Jinping Zhu, Xiangjuan Meng, Fuxin Zhao,[...]. Invest Ophthalmol Vis Sci 2014
36
22



Maternally inherited aminoglycoside-induced and nonsyndromic deafness is associated with the novel C1494T mutation in the mitochondrial 12S rRNA gene in a large Chinese family.
Hui Zhao, Ronghua Li, Qiuju Wang, Qingfeng Yan, Jian-Hong Deng, Dongyi Han, Yidong Bai, Wie-Yen Young, Min-Xin Guan. Am J Hum Genet 2004
254
8


Effect of mtDNA point mutations on cellular bioenergetics.
Joanna Szczepanowska, Dominika Malinska, Mariusz R Wieckowski, Jerzy Duszynski. Biochim Biophys Acta 2012
38
21


Tissue-specific differences in human transfer RNA expression.
Kimberly A Dittmar, Jeffrey M Goodenbour, Tao Pan. PLoS Genet 2006
404
8

Maternally inherited essential hypertension is associated with the novel 4263A>G mutation in the mitochondrial tRNAIle gene in a large Han Chinese family.
Shiwen Wang, Ronghua Li, Andrea Fettermann, Zongbin Li, Yaping Qian, Yuqi Liu, Xinjian Wang, Anna Zhou, Jun Qin Mo, Li Yang,[...]. Circ Res 2011
99
8

ROS function in redox signaling and oxidative stress.
Michael Schieber, Navdeep S Chandel. Curr Biol 2014
8

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
44
18

Mitochondrial membrane potential monitored by JC-1 dye.
M Reers, S T Smiley, C Mottola-Hartshorn, A Chen, M Lin, L B Chen. Methods Enzymol 1995
520
8

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
26

A hypertension-associated mitochondrial DNA mutation introduces an m1G37 modification into tRNAMet, altering its structure and function.
Mi Zhou, Ling Xue, Yaru Chen, Haiying Li, Qiufen He, Bibin Wang, Feilong Meng, Meng Wang, Min-Xin Guan. J Biol Chem 2018
42
19

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
39
20


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.