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Journal Abstract Search

219 related items for PubMed ID: 30541130

  • 1. A coronary artery disease-associated tRNAThr mutation altered mitochondrial function, apoptosis and angiogenesis.
    Jia Z, Zhang Y, Li Q, Ye Z, Liu Y, Fu C, Cang X, Wang M, Guan MX.
    Nucleic Acids Res; 2019 Feb 28; 47(4):2056-2074. PubMed ID: 30541130
    [Abstract] [Full Text] [Related]

  • 2. Coronary heart disease is associated with a mutation in mitochondrial tRNA.
    Jia Z, Wang X, Qin Y, Xue L, Jiang P, Meng Y, Shi S, Wang Y, Qin Mo J, Guan MX.
    Hum Mol Genet; 2013 Oct 15; 22(20):4064-73. PubMed ID: 23736300
    [Abstract] [Full Text] [Related]

  • 3. 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 15; 42():84-91. PubMed ID: 29225014
    [Abstract] [Full Text] [Related]

  • 4. 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 15; 300(9):107728. PubMed ID: 39214298
    [Abstract] [Full Text] [Related]

  • 5. A deafness-associated mitochondrial DNA mutation altered the tRNASer(UCN) metabolism and mitochondrial function.
    Xue L, Chen Y, Tang X, Yao J, Huang H, Wang M, Ye S, Wang M, Guan MX.
    Mitochondrion; 2019 May 15; 46():370-379. PubMed ID: 30336267
    [Abstract] [Full Text] [Related]

  • 6. Mitochondrial tRNAThr G15927A mutation may modulate the phenotypic manifestation of ototoxic 12S rRNA A1555G mutation in four Chinese families.
    Wang X, Lu J, Zhu Y, Yang A, Yang L, Li R, Chen B, Qian Y, Tang X, Wang J, Zhang X, Guan MX.
    Pharmacogenet Genomics; 2008 Dec 15; 18(12):1059-70. PubMed ID: 18820594
    [Abstract] [Full Text] [Related]

  • 7. 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]

  • 8. A hypertension-associated mitochondrial DNA mutation introduces an m1G37 modification into tRNAMet, altering its structure and function.
    Zhou M, Xue L, Chen Y, Li H, He Q, Wang B, Meng F, Wang M, Guan MX.
    J Biol Chem; 2018 Jan 26; 293(4):1425-1438. PubMed ID: 29222331
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. A Hypertension-Associated tRNAAla Mutation Alters tRNA Metabolism and Mitochondrial Function.
    Jiang P, Wang M, Xue L, Xiao Y, Yu J, Wang H, Yao J, Liu H, Peng Y, Liu H, Li H, Chen Y, Guan MX.
    Mol Cell Biol; 2016 Jul 15; 36(14):1920-30. PubMed ID: 27161322
    [Abstract] [Full Text] [Related]

  • 11. The Mitochondrial tRNAHis G12192A Mutation May Modulate the Clinical Expression of Deafness-Associated tRNAThr G15927A Mutation in a Chinese Pedigree.
    Ding Y, Teng YS, Zhuo GC, Xia BH, Leng JH.
    Curr Mol Med; 2019 Jul 15; 19(2):136-146. PubMed ID: 30854964
    [Abstract] [Full Text] [Related]

  • 12. A hypertension-associated mitochondrial DNA mutation alters the tertiary interaction and function of tRNALeu(UUR).
    Zhou M, Wang M, Xue L, Lin Z, He Q, Shi W, Chen Y, Jin X, Li H, Jiang P, Guan MX.
    J Biol Chem; 2017 Aug 25; 292(34):13934-13946. PubMed ID: 28679533
    [Abstract] [Full Text] [Related]

  • 13. 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 25; 297(1):100816. PubMed ID: 34023389
    [Abstract] [Full Text] [Related]

  • 14. Variations in mitochondrial tRNA(Thr) gene may not be associated with coronary heart disease.
    Pei H, Peng Q, Lan C, Liu BC.
    Mitochondrial DNA A DNA Mapp Seq Anal; 2016 Jul 25; 27(1):565-8. PubMed ID: 24708135
    [Abstract] [Full Text] [Related]

  • 15. A natural non-Watson-Crick base pair in human mitochondrial tRNAThr causes structural and functional susceptibility to local mutations.
    Wang Y, Zeng QY, Zheng WQ, Ji QQ, Zhou XL, Wang ED.
    Nucleic Acids Res; 2018 May 18; 46(9):4662-4676. PubMed ID: 29648639
    [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 18; 42(12):8039-48. PubMed ID: 24920829
    [Abstract] [Full Text] [Related]

  • 17. 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]

  • 18. Mitochondrial tRNAThr 15891C>G mutation was not associated with Leber's hereditary optic neuropathy in Han Chinese patients.
    Jiang Z, Yu J, Xia B, Zhuo G.
    Mitochondrial DNA A DNA Mapp Seq Anal; 2016 Jan 25; 27(2):1564-6. PubMed ID: 25186221
    [Abstract] [Full Text] [Related]

  • 19. Mitochondrial tRNA mutations associated with deafness.
    Zheng J, Ji Y, Guan MX.
    Mitochondrion; 2012 May 25; 12(3):406-13. PubMed ID: 22538251
    [Abstract] [Full Text] [Related]

  • 20. Heteroplasmic and homoplasmic m.616T>C in mitochondria tRNAPhe promote isolated chronic kidney disease and hyperuricemia.
    Xu C, Tong L, Rao J, Ye Q, Chen Y, Zhang Y, Xu J, Mao X, Meng F, Shen H, Lu Z, Cang X, Fu H, Wang S, Gu W, Lai EY, Guan MX, Jiang P, Mao J.
    JCI Insight; 2022 Jun 08; 7(11):. PubMed ID: 35472031
    [Abstract] [Full Text] [Related]

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