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Journal Abstract Search

221 related items for PubMed ID: 30262995

  • 1. Overexpression of human mitochondrial alanyl-tRNA synthetase suppresses biochemical defects of the mt-tRNAAla mutation in cybrids.
    Zhao X, Han J, Zhu L, Xiao Y, Wang C, Hong F, Jiang P, Guan MX.
    Int J Biol Sci; 2018; 14(11):1437-1444. PubMed ID: 30262995
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. Novel alanyl-tRNA synthetase 2 (AARS2) homozygous mutation in a consanguineous Chinese family with premature ovarian insufficiency.
    Zhou Y, Chen B, Li L, Pan H, Liu B, Li T, Wang R, Ma X, Wang B, Cao Y.
    Fertil Steril; 2019 Sep 24; 112(3):569-576.e2. PubMed ID: 31280959
    [Abstract] [Full Text] [Related]

  • 4. Instability of the mitochondrial alanyl-tRNA synthetase underlies fatal infantile-onset cardiomyopathy.
    Sommerville EW, Zhou XL, Oláhová M, Jenkins J, Euro L, Konovalova S, Hilander T, Pyle A, He L, Habeebu S, Saunders C, Kelsey A, Morris AAM, McFarland R, Suomalainen A, Gorman GS, Wang ED, Thiffault I, Tyynismaa H, Taylor RW.
    Hum Mol Genet; 2019 Jan 15; 28(2):258-268. PubMed ID: 30285085
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  • 5. Human mitochondrial leucyl tRNA synthetase can suppress non cognate pathogenic mt-tRNA mutations.
    Hornig-Do HT, Montanari A, Rozanska A, Tuppen HA, Almalki AA, Abg-Kamaludin DP, Frontali L, Francisci S, Lightowlers RN, Chrzanowska-Lightowlers ZM.
    EMBO Mol Med; 2014 Feb 15; 6(2):183-93. PubMed ID: 24413189
    [Abstract] [Full Text] [Related]

  • 6. Expression of Arabidopsis thaliana mitochondrial alanyl-tRNA synthetase is not sufficient to trigger mitochondrial import of tRNAAla in yeast.
    Mireau H, Cosset A, Marechal-Drouard L, Fox TD, Small ID, Dietrich A.
    J Biol Chem; 2000 May 05; 275(18):13291-6. PubMed ID: 10788435
    [Abstract] [Full Text] [Related]

  • 7. Mitochondrial aminoacyl-tRNA synthetase disorders: an emerging group of developmental disorders of myelination.
    Fine AS, Nemeth CL, Kaufman ML, Fatemi A.
    J Neurodev Disord; 2019 Dec 16; 11(1):29. PubMed ID: 31839000
    [Abstract] [Full Text] [Related]

  • 8. 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]

  • 9. 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]

  • 10. Allosteric interaction of nucleotides and tRNA(ala) with E. coli alanyl-tRNA synthetase.
    Dignam JD, Guo J, Griffith WP, Garbett NC, Holloway A, Mueser T.
    Biochemistry; 2011 Nov 15; 50(45):9886-900. PubMed ID: 21985608
    [Abstract] [Full Text] [Related]

  • 11. 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 15; 297(1):100816. PubMed ID: 34023389
    [Abstract] [Full Text] [Related]

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  • 14. Suppression of temperature-sensitive aminoacyl-tRNA synthetase mutations by ribosomal mutations: a possible mechanism.
    Buckel P, Piepersberg W, Böck A.
    Mol Gen Genet; 1976 Nov 24; 149(1):51-61. PubMed ID: 796671
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  • 18. Isoleucyl-tRNA synthetase levels modulate the penetrance of a homoplasmic m.4277T>C mitochondrial tRNA(Ile) mutation causing hypertrophic cardiomyopathy.
    Perli E, Giordano C, Tuppen HA, Montopoli M, Montanari A, Orlandi M, Pisano A, Catanzaro D, Caparrotta L, Musumeci B, Autore C, Morea V, Di Micco P, Campese AF, Leopizzi M, Gallo P, Francisci S, Frontali L, Taylor RW, d'Amati G.
    Hum Mol Genet; 2012 Jan 01; 21(1):85-100. PubMed ID: 21945886
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