Biblio

Author Title Type [ Year(Asc)]
Filters: Author is Guan, Min-Xin  [Clear All Filters]
2023
Chen C, Guan M-X. Induced pluripotent stem cells: ex vivo models for human diseases due to mitochondrial DNA mutations. J Biomed Sci. 2023;30(1):82.
Chen J-R, Chen C, Chen J, Ji Y, Lian Y, Zhang J, Yu J, Li X-Y, Qu J, Guan M-X. Nuclear modifier YARS2 allele correction restored retinal ganglion cells-specific deficiencies in Leber's hereditary optic neuropathy. Hum Mol Genet. 2023.
2022
Nie Z, Wang C, Chen J, Ji Y, Zhang H, Zhao F, Zhou X, Guan M-X. Abnormal morphology and function in retinal ganglion cells derived from patients-specific iPSCs generated from individuals with Leber's hereditary optic neuropathy. Hum Mol Genet. 2022.
Chen C, Guan M-X. Genetic correction of TRMU allele restored the mitochondrial dysfunction-induced deficiencies in iPSCs-derived hair cells of hearing-impaired patients. Hum Mol Genet. 2022.
2018
Jia Z, Zhang Y, Li Q, Ye Z, Liu Y, Fu C, Cang X, Wang M, Guan M-X. A coronary artery disease-associated tRNAThr mutation altered mitochondrial function, apoptosis and angiogenesis. Nucleic Acids Res. 2018.
2015
Liu H, Li R, Li W, Wang M, Ji J, Zheng J, Mao Z, Mo JQin, Jiang P, Lu J, et al. Maternally Inherited diabetes is associated with a homoplasmic T10003C mutation in the mitochondrial tRNA(Gly) gene. Mitochondrion. 2015.
Simon M, Richard EM, Wang X, Shahzad M, Huang VH, Qaiser TA, Potluri P, Mahl SE, Davila A, Nazli S, et al. Mutations of Human NARS2, Encoding the Mitochondrial Asparaginyl-tRNA Synthetase, Cause Nonsyndromic Deafness and Leigh Syndrome. PLoS Genet. 2015;11(3):e1005097.
Riazifar H, Sun G, Wang X, Rupp A, Vemaraju S, Ross-Cisneros FN, Lang RA, Sadun AA, Hattar S, Guan M-X, et al. Phenotypic and functional characterization of Bst+/- mouse retina. Dis Model Mech. 2015.