| Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder AJ Abrams, RB Hufnagel, A Rebelo, C Zanna, N Patel, MA Gonzalez, ... Nature genetics 47 (8), 926-932, 2015 | 210 | 2015 |
| A deafness-associated tRNAHis mutation alters the mitochondrial function, ROS production and membrane potential S Gong, Y Peng, P Jiang, M Wang, M Fan, X Wang, H Zhou, H Li, Q Yan, ... Nucleic acids research 42 (12), 8039-8048, 2014 | 121 | 2014 |
| The exome sequencing identified the mutation in YARS2 encoding the mitochondrial tyrosyl-tRNA synthetase as a nuclear modifier for the phenotypic manifestation of Leber's … P Jiang, X Jin, Y Peng, M Wang, H Liu, X Liu, Z Zhang, Y Ji, J Zhang, ... Human Molecular Genetics 25 (3), 584-596, 2016 | 108 | 2016 |
| Physical model test study on shear strength characteristics of slope sliding surface in Nanfen open-pit mine Z Tao, Y Shu, X Yang, Y Peng, Q Chen, H Zhang International Journal of Mining Science and Technology 30 (3), 421-429, 2020 | 90 | 2020 |
| A Hypertension-Associated tRNAAla Mutation Alters tRNA Metabolism and Mitochondrial Function P Jiang, M Wang, L Xue, Y Xiao, J Yu, H Wang, J Yao, H Liu, Y Peng, ... Molecular and cellular biology 36 (14), 1920-1930, 2016 | 56 | 2016 |
| Characterization of Osterix protein stability and physiological role in osteoblast differentiation Y Peng, K Shi, L Wang, J Lu, H Li, S Pan, C Ma PLoS One 8 (2), e56451, 2013 | 55 | 2013 |
| Neuronopathic Gaucher disease: dysregulated mRNAs and miRNAs in brain pathogenesis and effects of pharmacologic chaperone treatment in a mouse model N Dasgupta, Y Xu, R Li, Y Peng, MK Pandey, SL Tinch, B Liou, V Inskeep, ... Human molecular genetics 24 (24), 7031-7048, 2015 | 53 | 2015 |
| Osthole inhibits proliferation of human breast cancer cells by inducing cell cycle arrest and apoptosis L Wang, Y Peng, K Shi, H Wang, J Lu, Y Li, C Ma Journal of Biomedical Research 29 (2), 132, 2015 | 53 | 2015 |
| Loss of SLC25A46 causes neurodegeneration by affecting mitochondrial dynamics and energy production in mice Z Li, Y Peng, RB Hufnagel, YC Hu, C Zhao, LF Queme, Z Khuchua, ... Human molecular genetics 26 (19), 3776-3791, 2017 | 49 | 2017 |
| Biochemical evidence for a nuclear modifier allele (A10S) in TRMU (Methylaminomethyl-2-thiouridylate-methyltransferase) related to mitochondrial tRNA modification in the … F Meng, X Cang, Y Peng, R Li, Z Zhang, F Li, Q Fan, AS Guan, ... Journal of Biological Chemistry 292 (7), 2881-2892, 2017 | 49 | 2017 |
| Pathobiological pseudohypoxia as a putative mechanism underlying myelodysplastic syndromes Y Hayashi, Y Zhang, A Yokota, X Yan, J Liu, K Choi, B Li, G Sashida, ... Cancer discovery 8 (11), 1438-1457, 2018 | 46 | 2018 |
| Biallelic mutations in the ferredoxin reductase gene cause novel mitochondriopathy with optic atrophy Y Peng, DN Shinde, CA Valencia, JS Mo, J Rosenfeld, M Truitt Cho, ... Human molecular genetics 26 (24), 4937-4950, 2017 | 45 | 2017 |
| Whole-exome sequencing uncovers oxidoreductases DHTKD1 and OGDHL as linkers between mitochondrial dysfunction and eosinophilic esophagitis JD Sherrill, KC Kiran, X Wang, T Wen, A Chamberlin, EM Stucke, ... JCI insight 3 (8), 2018 | 42 | 2018 |
| A deafness-associated tRNAAsp mutation alters the m1G37 modification, aminoacylation and stability of tRNAAsp and mitochondrial function M Wang, Y Peng, J Zheng, B Zheng, X Jin, H Liu, Y Wang, X Tang, ... Nucleic acids research 44 (22), 10974-10985, 2016 | 42 | 2016 |
| Modulating ryanodine receptors with dantrolene attenuates neuronopathic phenotype in Gaucher disease mice B Liou, Y Peng, R Li, V Inskeep, W Zhang, B Quinn, N Dasgupta, ... Human molecular genetics 25 (23), 5126-5141, 2016 | 42 | 2016 |
| miRNAs in mtDNA-less cell mitochondria N Dasgupta, Y Peng, Z Tan, G Ciraolo, D Wang, R Li Cell death discovery 1 (1), 1-6, 2015 | 42 | 2015 |
| Mitochondrial tRNA mutations in 2070 Chinese Han subjects with hypertension L Xue, M Wang, H Li, H Wang, F Jiang, L Hou, J Geng, Z Lin, Y Peng, ... Mitochondrion 30, 208-221, 2016 | 39 | 2016 |
| Neonatal multiorgan failure due to ACAD9 mutation and complex I deficiency with mitochondrial hyperplasia in liver, cardiac myocytes, skeletal muscle, and renal tubules N Leslie, X Wang, Y Peng, CA Valencia, Z Khuchua, J Hata, D Witte, ... Human Pathology 49, 27-32, 2016 | 36 | 2016 |
| Biallelic mutations in FDXR cause neurodegeneration associated with inflammation J Slone, Y Peng, A Chamberlin, B Harris, J Kaylor, MT McDonald, ... Journal of human genetics 63 (12), 1211-1222, 2018 | 27 | 2018 |
| Systemic enzyme delivery by blood-brain barrier-penetrating SapC-DOPS nanovesicles for treatment of neuronopathic Gaucher disease Y Sun, B Liou, Z Chu, V Fannin, R Blackwood, Y Peng, GA Grabowski, ... EBioMedicine 55, 2020 | 26 | 2020 |
Min-Xin GuanZhejiang UniversityVerified email at zju.edu.cn
