Min-Xin Guan (Minxin Guan)

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2016-2023
Publications (10 Years): 19

Top Venues

Nucleic acids research

Human molecular genetics

The Journal of biological chemistry

Journal of biomedical science

University of California San Diego

Australian National University (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

University of California San Diego Jun 01 2018

United States

Adjunct Professor :: Surgery

University of Toronto May 24 2016

Canada

Professor status only :: Molecular Genetics

Zhejiang University Apr 10 2015

China

Associate Dean of Medicine and Pharmacy, Professor of Genetics :: Genetics

Zhejiang University Jan 20 2011

China

Director/Professor of Genetics :: Institute of Genetics

Zhejiang University Jan 20 2011 - Nov 10 2013

China

Dean, College of Life Science :: College of Life Sciences

Wenzhou Medical University Apr 01 2004 - Dec 31 2011

China

Professor, Dean of Life Sciences :: Life Science

Cincinnati Children's Hospital Medical Center Aug 06 1999 - Oct 01 2011

United States

Assistant, Associate and Full Professor of Pediatrics and Genetics :: Human Genetics

Education History

Australian National University Oct 20 1989 - Jul 06 1993

Australia

PHD :: Research School of Biological Sciences

Zhejiang University Sep 01 1979 - Jul 10 1983

China

BSC :: Biology

Publications

Jing Wang, Yanchun Ji, Cheng Ai, Jia-Rong Chen, Dingyi Gan, Juanjuan Zhang, Jun Q Mo, Min-Xin Guan
Optimized allotopic expression of mitochondrial ND6 transgene restored complex I and apoptosis deficiencies caused by LHON-linked ND6 14484T > C mutation. Journal of biomedical science 30 (1) (2023)
Chao Chen, Min-Xin Guan
Induced pluripotent stem cells: ex vivo models for human diseases due to mitochondrial DNA mutations. Journal of biomedical science 30 (1) (2023)
Jia-Rong Chen, Chao Chen, Jie Chen, Yanchun Ji, Yanna Lian, Juanjuan Zhang, Jialing Yu, Xiang-Yao Li, Jia Qu, Min-Xin Guan
Nuclear modifier YARS2 allele correction restored retinal ganglion cells-specific deficiencies in Leber's hereditary optic neuropathy. Human molecular genetics (2023)
Liang Chen, Yucong Wang, Jiamei Lin, Zhenxing Song, Qinwei Wang, Wenfang Zhao, Yan Wang, Xiaoyu Xiu, Yuqi Deng, Xiuzhi Li, Qiqi Li, Xiaolin Wang, Jingxin Li, Xu Liu, Kunpeng Liu, Jincong Zhou, Kuan Li, Yuchan Liu, Shanhui Liao, Qin Deng, Chao Xu, Qianwen Sun, Shengzhou Wu, Kaiming Zhang, Min-Xin Guan, Tianhua Zhou, Fei Sun, Xiujun Cai, Chuan Huang, Ge Shan
Exportin 4 depletion leads to nuclear accumulation of a subset of circular RNAs. Nature communications 13 (1) (2022)
Zhipeng Nie, Chenhui Wang, Jiarong Chen, Yanchun Ji, Hongxing Zhang, Fuxin Zhao, Xiangtian Zhou, Min-Xin Guan
Abnormal morphology and function in retinal ganglion cells derived from patients-specific iPSCs generated from individuals with Leber's hereditary optic neuropathy. Human molecular genetics (2022)
Shihao Yao, Boyuan Ma, Qiuzi Yi, Min-Xin Guan, Xiaohui Cang
Investigating the Broad Matrix-Gate Network in the Mitochondrial ADP/ATP Carrier through Molecular Dynamics Simulations. Molecules (Basel, Switzerland) 27 (3) (2022)
Chao Chen, Min-Xin Guan
Genetic correction of TRMU allele restored the mitochondrial dysfunction-induced deficiencies in iPSCs-derived hair cells of hearing-impaired patients. Human molecular genetics 31 (18) (2022)
Zidong Jia, Feilong Meng, Hui Chen, Gao Zhu, Xincheng Li, Yunfan He, Liyao Zhang, Xiao He, Huisen Zhan, Mengquan Chen, Yanchun Ji, Meng Wang, Min-Xin Guan
Human TRUB1 is a highly conserved pseudouridine synthase responsible for the formation of Ψ55 in mitochondrial tRNAAsn, tRNAGln, tRNAGlu and tRNAPro. Nucleic acids research 50 (16) (2022)
Feilong Meng, Zidong Jia, Jing Zheng, Yanchun Ji, Jing Wang, Yun Xiao, Yong Fu, Meng Wang, Feng Ling, Min-Xin Guan
A deafness-associated mitochondrial DNA mutation caused pleiotropic effects on DNA replication and tRNA metabolism. Nucleic acids research 50 (16) (2022)
Min Liang, Yanchun Ji, Liyao Zhang, Xuan Wang, Cuifang Hu, Juanjuan Zhang, Yiwei Zhu, Jun Q Mo, Min-Xin Guan
Leber's hereditary optic neuropathy-associated ND6 14484T > C mutation caused pleiotropic effects on the complex I, RNA homeostasis, apoptosis and mitophagy. Human molecular genetics 31 (19) (2022)
Qinghai Zhang, Xiao He, Shihao Yao, Tianxiang Lin, Luwen Zhang, Danni Chen, Chao Chen, Qingxian Yang, Feng Li, Yi-Min Zhu, Min-Xin Guan
Ablation of Mto1 in zebrafish exhibited hypertrophic cardiomyopathy manifested by mitochondrion RNA maturation deficiency. Nucleic acids research 49 (8) (2021)
Wenlu Fan, Xiaoye Jin, Man Xu, Yongmei Xi, Weiguo Lu, Xiaohang Yang, Min-Xin Guan, Wanzhong Ge
FARS2 deficiency in Drosophila reveals the developmental delay and seizure manifested by aberrant mitochondrial tRNA metabolism. Nucleic acids research (2021)
Zhengyun Chen, Chunyan Wang, Cuicui Lin, Lifeng Zhang, Huimei Zheng, Yong Zhou, Xiaoyong Li, Chen Li, Xinmei Zhang, Xiaohang Yang, Min-Xin Guan, Yongmei Xi
Lipidomic Alterations and PPARα Activation Induced by Resveratrol Lead to Reduction in Lesion Size in Endometriosis Models. Oxidative medicine and cellular longevity 2021 (2021)
Shu Zhao, Jia Shi, Guohua Yu, Dali Li, Meng Wang, Chonggang Yuan, Huihui Zhou, Amirabbas Parizadeh, Zhenlin Li, Min-Xin Guan, Shixin Ye
Photosensitive tyrosine analogues unravel site-dependent phosphorylation in TrkA initiated MAPK/ERK signaling. Communications biology 3 (1) (2020)
Kun Hou, Hui Jiang, Md Rezaul Karim, Chao Zhong, Zhouwen Xu, Lin Liu, Min-Xin Guan, Jianzhong Shao, Xiao Huang
A Critical E-box in Barhl1 3' Enhancer Is Essential for Auditory Hair Cell Differentiation. Cells 8 (5) (2019)
Wenlu Fan, Jing Zheng, Wanzhong Kong, Limei Cui, Maerhaba Aishanjiang, Qiuzi Yi, Min Wang, Xiaohui Cang, Xiaowen Tang, Ye Chen, Jun Qin Mo, Neal Sondheimer, Wanzhong Ge, Min-Xin Guan
Contribution of a mitochondrial tyrosyl-tRNA synthetase mutation to the phenotypic expression of the deafness-associated tRNASer(UCN) 7511A>G mutation. The Journal of biological chemistry 294 (50) (2019)
Shasha Gong, Xiaoqiong Wang, Feilong Meng, Limei Cui, Qiuzi Yi, Qiong Zhao, Xiaohui Cang, Zhiyi Cai, Jun Qin Mo, Yong Liang, Min-Xin Guan
Overexpression of mitochondrial histidyl-tRNA synthetase restores mitochondrial dysfunction caused by a deafness-associated tRNAHis mutation. The Journal of biological chemistry 295 (4) (2019)
Meng Wang, Yanyan Peng, Jing Zheng, Binjiao Zheng, Xiaofen Jin, Hao Liu, Yong Wang, Xiaowen Tang, Taosheng Huang, Pingping Jiang, Min-Xin Guan
A deafness-associated tRNAAsp mutation alters the m1G37 modification, aminoacylation and stability of tRNAAsp and mitochondrial function. Nucleic acids research 44 (22) (2016)
Pingping Jiang, Meng Wang, Ling Xue, Yun Xiao, Jialing Yu, Hui Wang, Juan Yao, Hao Liu, Yanyan Peng, Hanqing Liu, Haiying Li, Ye Chen, Min-Xin Guan
A Hypertension-Associated tRNAAla Mutation Alters tRNA Metabolism and Mitochondrial Function. Molecular and cellular biology 36 (14) (2016)

Min-Xin Guan.css-eqlu8i{font-size:small;padding-left:4px;} (Minxin Guan)

Publication Activity (10 Years)

Top Topics

Top Venues

Min-Xin Guan (Minxin Guan)