21. Hypertension-associated mitochondrial DNA 4401A>G mutation caused the aberrant processing of tRNAMet, all 8 tRNAs and ND6 mRNA in the light-strand transcript. Issue 19 (28th August 2019) Authors: Zhao, Xiaoxu; Cui, Limei; Xiao, Yun; Mao, Qin; Aishanjiang, Maerhaba; Kong, Wanzhong; Liu, Yuqi; Chen, Hong; Hong, Fang; Jia, Zidong; Wang, Meng; Jiang, Pingping; Guan, Min-Xin Journal: Nucleic acids research Issue: Volume 47:Issue 19(2019) Page Start: 10340 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
22. Leber's hereditary optic neuropathy (LHON)-associated ND5 12338T > C mutation altered the assembly and function of complex I, apoptosis and mitophagy. (22nd March 2018) Authors: Zhang, Juanjuan; Ji, Yanchun; Lu, Yuanyuan; Fu, Runing; Xu, Man; Liu, Xiaoling; Guan, Min-Xin Journal: Human molecular genetics Issue: Volume 27:Number 11(2018:Jun. 01) Page Start: 1999 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
23. Leber's hereditary optic neuropathy-associated ND6 14484T > C mutation caused pleiotropic effects on the complex I, RNA homeostasis, apoptosis and mitophagy. Issue 19 (14th May 2022) Authors: Liang, Min; Ji, Yanchun; Zhang, Liyao; Wang, Xuan; Hu, Cuifang; Zhang, Juanjuan; Zhu, Yiwei; Mo, Jun Q; Guan, Min-Xin Journal: Human molecular genetics Issue: Volume 31:Issue 19(2022) Page Start: 3299 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
24. Maternally transmitted late-onset non-syndromic deafness is associated with the novel heteroplasmic T12201C mutation in the mitochondrial tRNAHis gene. Issue 10 (19th September 2011) Authors: Yan, Xukun; Wang, Xinjian; Wang, Zhengmin; Sun, Shan; Chen, Guoling; He, Yingzi; Mo, Jun Qin; Li, Ronghua; Jiang, Pingping; Lin, Qin; Sun, Mingzhi; Li, Wen; Bai, Yan; Zhang, Jianning; Zhu, Yi; Lu, Jianxin; Yan, Qingfeng; Li, Huawei; Guan, Min-Xin Journal: Journal of medical genetics Issue: Volume 48:Issue 10(2011) Page Start: 682 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
25. Mitochondrial haplogroup B increases the risk for hearing loss among the Eastern Asian pedigrees carrying 12S rRNA 1555A>G mutation. Issue 11 (11th September 2015) Authors: Ying, Zhengbiao; Zheng, Jing; Cai, Zhaoyang; Liu, Li; Dai, Yu; Yao, Juan; Wang, Hui; Gao, Yinglong; Zheng, Binjiao; Tang, Xiaowen; Zhu, Yi; Guan, Min-Xin; Chen, Ye Journal: Protein & cell Issue: Volume 6:Issue 11(2015) Page Start: 844 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
26. Mitochondrial haplogroup D4j specific variant m.11696G > a(MT-ND4) may increase the penetrance and expressivity of the LHON-associated m.11778G > a mutation in Chinese pedigrees. (4th May 2017) Authors: Xie, Shipeng; Zhang, Juanjuan; Sun, Jiji; Zhang, Minglian; Zhao, Fuxin; Wei, Qi-Ping; Tong, Yi; Liu, Xiaoling; Zhou, Xiangtian; Jiang, Pingping; Ji, Yanchun; Guan, Min-Xin Journal: Mitochondrial DNA Issue: Volume 28:Number 3(2017) Page Start: 434 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
27. Modeling autosomal dominant optic atrophy using induced pluripotent stem cells and identifying potential therapeutic targets. Issue 1 (December 2016) Authors: Chen, Jing; Riazifar, Hamidreza; Guan, Min-Xin; Huang, Taosheng Journal: Stem cell research & therapy Issue: Volume 7:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
28. Nuclear modifier YARS2 allele correction restored retinal ganglion cells-specific deficiencies in Leber's hereditary optic neuropathy. Issue 9 (5th January 2023) Authors: Chen, Jia-Rong; Chen, Chao; Chen, Jie; Ji, Yanchun; Lian, Yanna; Zhang, Juanjuan; Yu, Jialing; Li, Xiang-Yao; Qu, Jia; Guan, Min-Xin Journal: Human molecular genetics Issue: Volume 32:Issue 9(2023) Page Start: 1539 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
29. The defective expression of gtpbp3 related to tRNA modification alters the mitochondrial function and development of zebrafish. (August 2016) Authors: Chen, Danni; Li, Feng; Yang, Qingxian; Tian, Miao; Zhang, Zengming; Zhang, Qinghai; Chen, Ye; Guan, Min-Xin Journal: International journal of biochemistry & cell biology Issue: Volume 77:Part A(2016:Aug.) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
30. The role of mitochondria in osteogenic, adipogenic and chondrogenic differentiation of mesenchymal stem cells. Issue 6 (7th March 2017) Authors: Li, Qianqian; Gao, Zewen; Chen, Ye; Guan, Min-Xin Journal: Protein & cell Issue: Volume 8:Issue 6(2017) Page Start: 439 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗