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Nucleic Acids Research|June 13, 2014
A deafness-associated tRNAHis mutation alters the mitochondrial function, ROS production and membrane potentialShasha Gong, Yanyan Peng, Pingping Jiang, et al.
Drug Design, Development and Therapy|October 7, 2021
Transcriptome-Based Analysis Reveals Therapeutic Effects of Resveratrol on Endometriosis in aRat ModelChunyan Wang, Zhengyun Chen, Xianlei Zhao, et al.
The Journal of Biological Chemistry|February 21, 2021
An animal model for mitochondrial tyrosyl-tRNA synthetase deficiency reveals links between oxidative phosphorylation and retinal functionXiaofen Jin, Zengming Zhang, Zhipeng Nie, et al.
Nucleic Acids Research|February 22, 2005
Functional characterization of the mitochondrial 12S rRNA C1494T mutation associated with aminoglycoside-induced and non-syndromic hearing lossHui Zhao, Wie-Yen Young, Qingfeng Yan, et al.
Biochemical and Biophysical Research Communications|April 25, 2007
The coexistence of mitochondrial ND6 T14484C and 12S rRNA A1555G mutations in a Chinese family with Leber's hereditary optic neuropathy and hearing lossQi-Ping Wei, Xiangtian Zhou, Li Yang, et al.
The Journal of Biological Chemistry|July 7, 2017
A hypertension-associated mitochondrial DNA mutation alters the tertiary interaction and function of tRNALeu(UUR)Mi Zhou, Meng Wang, Ling Xue, et al.
Communications Biology|November 26, 2020
Photosensitive tyrosine analogues unravel site-dependent phosphorylation in TrkA initiated MAPK/ERK signalingShu Zhao, Jia Shi, Guohua Yu, et al.
European Journal of Ophthalmology|April 21, 2025
Are blood platelet parameters associated with retinal nerve fiber layer thickness Among healthy young adults? a university-based studyDan-Lin Li, Min-Xin Liu, Zhi-Jian Yin, et al.
Human Mutation|May 3, 2012
Mitochondrial tRNA mutations are associated with maternally inherited hypertension in two Han Chinese pedigreesQiaomeng Qiu, Ronghua Li, Pingping Jiang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|October 11, 2011
[The mitochondrial tRNA(Thr) A15951G mutation may be associated with Leber's hereditary optic neuropathy in two Chinese families]Yu Zhang, Juan-juan Zhang, Yan-chun Ji, et al.
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