1. A coronary artery disease-associated tRNAThr mutation altered mitochondrial function, apoptosis and angiogenesis. Issue 4 (12th December 2018) Authors: Jia, Zidong; Zhang, Ye; Li, Qiang; Ye, Zhenzhen; Liu, Yuqi; Fu, Changzhu; Cang, Xiaohui; Wang, Meng; Guan, Min-Xin Journal: Nucleic acids research Issue: Volume 47:Issue 4(2019) Page Start: 2056 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A deafness-associated mitochondrial DNA mutation caused pleiotropic effects on DNA replication and tRNA metabolism. Issue 16 (30th August 2022) Authors: Meng, Feilong; Jia, Zidong; Zheng, Jing; Ji, Yanchun; Wang, Jing; Xiao, Yun; Fu, Yong; Wang, Meng; Ling, Feng; Guan, Min-Xin Journal: Nucleic acids research Issue: Volume 50:Issue 16(2022) Page Start: 9453 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A deafness-associated tRNA mutation caused pleiotropic effects on the m1G37 modification, processing, stability and aminoacylation of tRNAIle and mitochondrial translation. Issue 2 (4th January 2021) Authors: Meng, Feilong; Zhou, Mi; Xiao, Yun; Mao, Xiaoting; Zheng, Jing; Lin, Jiaxi; Lin, Tianxiang; Ye, Zhenzhen; Cang, Xiaohui; Fu, Yong; Wang, Meng; Guan, Min-Xin Journal: Nucleic acids research Issue: Volume 49:Issue 2(2021) Page Start: 1075 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. A deafness-associated tRNAAsp mutation alters the m1G37 modification, aminoacylation and stability of tRNAAsp and mitochondrial function. Issue 22 (17th August 2016) Authors: Wang, Meng; Peng, Yanyan; Zheng, Jing; Zheng, Binjiao; Jin, Xiaofen; Liu, Hao; Wang, Yong; Tang, Xiaowen; Huang, Taosheng; Jiang, Pingping; Guan, Min-Xin Journal: Nucleic acids research Issue: Volume 44:Issue 22(2016) Page Start: 10974 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. A peep into mitochondrial disorder: multifaceted from mitochondrial DNA mutations to nuclear gene modulation. Issue 12 (18th June 2015) Authors: Chen, Chao; Chen, Ye; Guan, Min-Xin Journal: Protein & cell Issue: Volume 6:Issue 12(2015) Page Start: 862 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Ablation of Mto1 in zebrafish exhibited hypertrophic cardiomyopathy manifested by mitochondrion RNA maturation deficiency. Issue 8 (9th April 2021) Authors: Zhang, Qinghai; He, Xiao; Yao, Shihao; Lin, Tianxiang; Zhang, Luwen; Chen, Danni; Chen, Chao; Yang, Qingxian; Li, Feng; Zhu, Yi-Min; Guan, Min-Xin Journal: Nucleic acids research Issue: Volume 49:Issue 8(2021) Page Start: 4689 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Abnormal morphology and function in retinal ganglion cells derived from patients-specific iPSCs generated from individuals with Leber's hereditary optic neuropathy. Issue 2 (10th August 2022) Authors: Nie, Zhipeng; Wang, Chenghui; Chen, Jiarong; Ji, Yanchun; Zhang, Hongxing; Zhao, Fuxin; Zhou, Xiangtian; Guan, Min-Xin Journal: Human molecular genetics Issue: Volume 32:Issue 2(2023) Page Start: 231 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Asymmetrical effects of deafness-associated mitochondrial DNA 7516delA mutation on the processing of RNAs in the H-strand and L-strand polycistronic transcripts. Issue 19 (12th October 2020) Authors: Xiao, Yun; Wang, Meng; He, Qiufen; Xu, Lei; Zhang, Qinghai; Meng, Feilong; Jia, Zidong; Zhang, Fengguo; Wang, Haibo; Guan, Min-Xin Journal: Nucleic acids research Issue: Volume 48:Issue 19(2020) Page Start: 11113 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Biallelic mutations in the ferredoxin reductase gene cause novel mitochondriopathy with optic atrophy. (5th October 2017) Authors: Peng, Yanyan; Shinde, Deepali N; Valencia, C Alexander; Mo, Jun-Song; Rosenfeld, Jill; Truitt Cho, Megan; Chamberlin, Adam; Li, Zhuo; Liu, Jie; Gui, Baoheng; Brockhage, Rachel; Basinger, Alice; Alvarez-Leon, Brenda; Heydemann, Peter; Magoulas, Pilar L; Lewis, Andrea M; Scaglia, Fernando; Gril, So... Journal: Human molecular genetics Issue: Volume 26:Number 24(2017:Dec. 15) Page Start: 4937 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Contribution of mitochondrial ND1 3394T>C mutation to the phenotypic manifestation of Leber's hereditary optic neuropathy. (31st December 2018) 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 Journal: Human molecular genetics Issue: Volume 28:Number 9(2019) Page Start: 1515 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗