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116 related items for PubMed ID: 38552739

  • 1. Deafness-associated tRNAPhe mutation impaired mitochondrial and cellular integrity.
    Chen X, Meng F, Chen C, Li S, Chou Z, Xu B, Mo JQ, Guo Y, Guan MX.
    J Biol Chem; 2024 May; 300(5):107235. PubMed ID: 38552739
    [Abstract] [Full Text] [Related]

  • 2. Late onset nonsyndromic hearing loss in a Dongxiang Chinese family is associated with the 593T>C variant in the mitochondrial tRNAPhe gene.
    Chen X, Nie Z, Wang F, Wang J, Liu XW, Zheng J, Guo YF, Guan MX.
    Mitochondrion; 2017 Jul; 35():111-118. PubMed ID: 28579530
    [Abstract] [Full Text] [Related]

  • 3. Defective post-transcriptional modification of tRNA disrupts mitochondrial homeostasis in Leber's hereditary optic neuropathy.
    Zhang J, Li W, Liu Z, Chen Y, Wei X, Peng L, Xu M, Ji Y.
    J Biol Chem; 2024 Sep; 300(9):107728. PubMed ID: 39214298
    [Abstract] [Full Text] [Related]

  • 4. Overexpression of mitochondrial histidyl-tRNA synthetase restores mitochondrial dysfunction caused by a deafness-associated tRNAHis mutation.
    Gong S, Wang X, Meng F, Cui L, Yi Q, Zhao Q, Cang X, Cai Z, Mo JQ, Liang Y, Guan MX.
    J Biol Chem; 2020 Jan 24; 295(4):940-954. PubMed ID: 31819004
    [Abstract] [Full Text] [Related]

  • 5. Contribution of the tRNAIle 4317A→G mutation to the phenotypic manifestation of the deafness-associated mitochondrial 12S rRNA 1555A→G mutation.
    Meng F, He Z, Tang X, Zheng J, Jin X, Zhu Y, Ren X, Zhou M, Wang M, Gong S, Mo JQ, Shu Q, Guan MX.
    J Biol Chem; 2018 Mar 02; 293(9):3321-3334. PubMed ID: 29348176
    [Abstract] [Full Text] [Related]

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  • 7. Mechanistic insights into mitochondrial tRNAAla 3'-end metabolism deficiency.
    Ji Y, Nie Z, Meng F, Hu C, Chen H, Jin L, Chen M, Zhang M, Zhang J, Liang M, Wang M, Guan MX.
    J Biol Chem; 2021 Jul 02; 297(1):100816. PubMed ID: 34023389
    [Abstract] [Full Text] [Related]

  • 8. A Deafness- and Diabetes-associated tRNA Mutation Causes Deficient Pseudouridinylation at Position 55 in tRNAGlu and Mitochondrial Dysfunction.
    Wang M, Liu H, Zheng J, Chen B, Zhou M, Fan W, Wang H, Liang X, Zhou X, Eriani G, Jiang P, Guan MX.
    J Biol Chem; 2016 Sep 30; 291(40):21029-21041. PubMed ID: 27519417
    [Abstract] [Full Text] [Related]

  • 9. A deafness-associated mitochondrial DNA mutation caused pleiotropic effects on DNA replication and tRNA metabolism.
    Meng F, Jia Z, Zheng J, Ji Y, Wang J, Xiao Y, Fu Y, Wang M, Ling F, Guan MX.
    Nucleic Acids Res; 2022 Sep 09; 50(16):9453-9469. PubMed ID: 36039763
    [Abstract] [Full Text] [Related]

  • 10. A deafness-associated tRNA mutation caused pleiotropic effects on the m1G37 modification, processing, stability and aminoacylation of tRNAIle and mitochondrial translation.
    Meng F, Zhou M, Xiao Y, Mao X, Zheng J, Lin J, Lin T, Ye Z, Cang X, Fu Y, Wang M, Guan MX.
    Nucleic Acids Res; 2021 Jan 25; 49(2):1075-1093. PubMed ID: 33398350
    [Abstract] [Full Text] [Related]

  • 11. A deafness-associated tRNAAsp mutation alters the m1G37 modification, aminoacylation and stability of tRNAAsp and mitochondrial function.
    Wang M, Peng Y, Zheng J, Zheng B, Jin X, Liu H, Wang Y, Tang X, Huang T, Jiang P, Guan MX.
    Nucleic Acids Res; 2016 Dec 15; 44(22):10974-10985. PubMed ID: 27536005
    [Abstract] [Full Text] [Related]

  • 12. Contribution of a mitochondrial tyrosyl-tRNA synthetase mutation to the phenotypic expression of the deafness-associated tRNASer(UCN) 7511A>G mutation.
    Fan W, Zheng J, Kong W, Cui L, Aishanjiang M, Yi Q, Wang M, Cang X, Tang X, Chen Y, Mo JQ, Sondheimer N, Ge W, Guan MX.
    J Biol Chem; 2019 Dec 13; 294(50):19292-19305. PubMed ID: 31685661
    [Abstract] [Full Text] [Related]

  • 13. Biochemical Evidence for a Nuclear Modifier Allele (A10S) in TRMU (Methylaminomethyl-2-thiouridylate-methyltransferase) Related to Mitochondrial tRNA Modification in the Phenotypic Manifestation of Deafness-associated 12S rRNA Mutation.
    Meng F, Cang X, Peng Y, Li R, Zhang Z, Li F, Fan Q, Guan AS, Fischel-Ghosian N, Zhao X, Guan MX.
    J Biol Chem; 2017 Feb 17; 292(7):2881-2892. PubMed ID: 28049726
    [Abstract] [Full Text] [Related]

  • 14. Asymmetrical effects of deafness-associated mitochondrial DNA 7516delA mutation on the processing of RNAs in the H-strand and L-strand polycistronic transcripts.
    Xiao Y, Wang M, He Q, Xu L, Zhang Q, Meng F, Jia Z, Zhang F, Wang H, Guan MX.
    Nucleic Acids Res; 2020 Nov 04; 48(19):11113-11129. PubMed ID: 33045734
    [Abstract] [Full Text] [Related]

  • 15. Deficient tRNA posttranscription modification dysregulated the mitochondrial quality controls and apoptosis.
    He Y, Zhu G, Li X, Zhou M, Guan MX.
    iScience; 2024 Feb 16; 27(2):108883. PubMed ID: 38318358
    [Abstract] [Full Text] [Related]

  • 16. A deafness-associated tRNAHis mutation alters the mitochondrial function, ROS production and membrane potential.
    Gong S, Peng Y, Jiang P, Wang M, Fan M, Wang X, Zhou H, Li H, Yan Q, Huang T, Guan MX.
    Nucleic Acids Res; 2014 Jul 16; 42(12):8039-48. PubMed ID: 24920829
    [Abstract] [Full Text] [Related]

  • 17. Loss of MIEF1/MiD51 confers susceptibility to BAX-mediated cell death and PINK1-PRKN-dependent mitophagy.
    Xian H, Liou YC.
    Autophagy; 2019 Dec 16; 15(12):2107-2125. PubMed ID: 30894073
    [Abstract] [Full Text] [Related]

  • 18. Is mitochondrial tRNA(phe) variant m.593T>C a synergistically pathogenic mutation in Chinese LHON families with m.11778G>A?
    Zhang AM, Bandelt HJ, Jia X, Zhang W, Li S, Yu D, Wang D, Zhuang XY, Zhang Q, Yao YG.
    PLoS One; 2011 Dec 16; 6(10):e26511. PubMed ID: 22039503
    [Abstract] [Full Text] [Related]

  • 19. Assocation Between Leber's Hereditary Optic Neuropathy and MT-ND1 3460G>A Mutation-Induced Alterations in Mitochondrial Function, Apoptosis, and Mitophagy.
    Zhang J, Ji Y, Chen J, Xu M, Wang G, Ci X, Lin B, Mo JQ, Zhou X, Guan MX.
    Invest Ophthalmol Vis Sci; 2021 Jul 01; 62(9):38. PubMed ID: 34311469
    [Abstract] [Full Text] [Related]

  • 20. Leber's hereditary optic neuropathy caused by a mutation in mitochondrial tRNAThr in eight Chinese pedigrees.
    Zhang J, Ji Y, Liu X, Chen J, Wang B, Zhang M, Guan MX.
    Mitochondrion; 2018 Sep 01; 42():84-91. PubMed ID: 29225014
    [Abstract] [Full Text] [Related]

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