Overexpression of mitochondrial histidyl-tRNA synthetase restores mitochondrial dysfunction caused by a deafness-associated tRNAHis mutation

Authors: Gong, Shasha, Wang, Xiaoqiong, Meng, Feilong ^**, Cui, Limei, Yi, Qiuzi, Zhao, Qiong, Cang, Xiaohui, Cai, Zhiyi, Mo, Jun Qin, Liang, Yong, Guan, Min-Xin ^**

Source: In Journal of Biological Chemistry 24 January 2020 295(4):940-954

Contribution of a mitochondrial tyrosyl-tRNA synthetase mutation to the phenotypic expression of the deafness-associated tRNASer(UCN) 7511A>G mutation

Authors: Fan, Wenlu, Zheng, Jing, Kong, Wanzhong, Cui, Limei, Aishanjiang, Maerhaba, Yi, Qiuzi, Wang, Min, Cang, Xiaohui, Tang, Xiaowen, Chen, Ye, Mo, Jun Qin, Sondheimer, Neal ^**, Ge, Wanzhong, Guan, Min-Xin

Source: In Journal of Biological Chemistry 13 December 2019 294(50):19292-19305

Concurrent ependymal and ganglionic differentiation in a subset of supratentorial neuroepithelial tumors with EWSR1-PLAGL1 rearrangement.

Authors: Lee, Julieann C., Koo, Selene C., Furtado, Larissa V., Breuer, Alex, Eldomery, Mohammad K., Bag, Asim K., Stow, Pat, Rose, Gary, Larkin, Trisha, Sances, Rick, Kleinschmidt-DeMasters, Bette K., Bodmer, Jenna L., Willard, Nicholas, Gokden, Murat, Dahiya, Sonika, Roberts, Kaleigh, Bertrand, Kelsey C., Moreira, Daniel C., Robinson, Giles W., Mo, Jun Qin

Source: Acta Neuropathologica Communications; 9/3/2024, Vol. 12 Issue 1, p1-14, 14p

Subject Terms: RNA methylation, RNA sequencing, DISEASE progression, CELL anatomy, HISTOLOGY

Contribution of the tRNAIle 4317A→G mutation to the phenotypic manifestation of the deafness-associated mitochondrial 12S rRNA 1555A→G mutation

Authors: Meng, Feilong, He, Zheyun, Tang, Xiaowen, Zheng, Jing, Jin, Xiaofen, Zhu, Yi ^**, Ren, Xiaoyan, Zhou, Mi, Wang, Meng, Gong, Shasha, Mo, Jun Qin, Shu, Qiang, Guan, Min-Xin

Source: In Journal of Biological Chemistry 2 March 2018 293(9):3321-3334

Mitochondrial tRNA mutations in 2070 Chinese Han subjects with hypertension

Authors: Xue, Ling, Wang, Meng, Li, Haiying, Wang, Heng, Jiang, Feng, Hou, Lingling, Geng, Junwei, Lin, Zhi, Peng, Yanyan, Zhou, Hong, Yu, Han, Jiang, Pingping, Mo, Jun Qin, Guan, Min-Xin

Source: In Mitochondrion September 2016 30:208-221

Maternally inherited diabetes is associated with a homoplasmic T10003C mutation in the mitochondrial tRNAGly gene

Authors: Liu, Hao, Li, Ronghua, Li, Weixing, Wang, Meng, Ji, Jingzhang, Zheng, Jing, Mao, Zhuochao, Mo, Jun Qin, Jiang, Pingping, Lu, Jianxin, Guan, Min-Xin

Source: In Mitochondrion March 2015 21:49-57

Mitochondrial haplotypes may modulate the phenotypic manifestation of the LHON-associated m.14484T>C (MT-ND6) mutation in Chinese families

Authors: Zhang, Juanjuan, Zhao, Fuxin, Fu, Qun, Liang, Min, Tong, Yi, Liu, Xiaoling, Lin, Bei, Mi, Hui, Zhang, Minglian, Wei, Qi-Ping, Xue, Ling, Jiang, Pingping, Zhou, Xiangtian, Mo, Jun Qin, Huang, Taosheng, Qu, Jia, Guan, Min-Xin

Source: In Mitochondrion November 2013 13(6):772-781

Clinical evaluation and mitochondrial DNA sequence analysis in three Chinese families with Leber’s hereditary optic neuropathy

Authors: Qian, Yaping, Zhou, Xiangtian, Hu, Yongwu, Tong, Yi, Li, Ronghua, Lu, Fan, Yang, Huanming, Mo, Jun Qin, Qu, Jia, Guan, Min-Xin

Source: In Biochemical and Biophysical Research Communications 2005 332(2):614-621

Genetic or Pharmacological Iron Chelation Prevents MPTP-Induced Neurotoxicity In Vivo: A Novel Therapy for Parkinson's Disease

Authors: Kaur, Deepinder, Yantiri, Ferda, Rajagopalan, Subramanian, Kumar, Jyothi, Mo, Jun Qin, Boonplueang, Rapee, Viswanath, Veena, Jacobs, Russell, Yang, Lichuan, Beal, M.Flint, DiMonte, Dino, Volitaskis, Irene, Ellerby, Lisa, Cherny, Robert A, Bush, Ashley I, Andersen, Julie K ^*

Source: In Neuron 2003 37(6):899-909

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Contribution of mitochondrial ND1 3394T>C mutation to the phenotypic manifestation of Leber's hereditary optic neuropathy.

Authors: Ji, Yanchun, Zhang, Juanjuan, Yu, Jialing, Wang, Ying, Lu, Yuanyuan, Liang, Min, Li, Qiang, Jin, Xiaofen, Wei, Yinsheng, Meng, Feilong, Gao, Yinglong, Cang, Xiaohui, Tong, Yi, Liu, Xiaoling, Zhang, Minglian, Jiang, Peifang, Zhu, Tao, Mo, Jun Qin, Huang, Taosheng, Jiang, Pingping

Source: Human Molecular Genetics; May2019, Vol. 28 Issue 9, p1515-1529, 15p

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