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Journal Abstract Search

475 related items for PubMed ID: 31819004

  • 21. Recognition of human mitochondrial tRNALeu(UUR) by its cognate leucyl-tRNA synthetase.
    Sohm B, Sissler M, Park H, King MP, Florentz C.
    J Mol Biol; 2004 May 21; 339(1):17-29. PubMed ID: 15123417
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  • 22. 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 21; 300(5):107235. PubMed ID: 38552739
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  • 23. Mutations in mitochondrial histidyl tRNA synthetase HARS2 cause ovarian dysgenesis and sensorineural hearing loss of Perrault syndrome.
    Pierce SB, Chisholm KM, Lynch ED, Lee MK, Walsh T, Opitz JM, Li W, Klevit RE, King MC.
    Proc Natl Acad Sci U S A; 2011 Apr 19; 108(16):6543-8. PubMed ID: 21464306
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  • 24. 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
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  • 25. Structural analyses of a human lysyl-tRNA synthetase mutant associated with autosomal recessive nonsyndromic hearing impairment.
    Wu S, Hei Z, Zheng L, Zhou J, Liu Z, Wang J, Fang P.
    Biochem Biophys Res Commun; 2021 May 21; 554():83-88. PubMed ID: 33784510
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  • 26. Biochemical characterization of the mitochondrial tRNASer(UCN) T7511C mutation associated with nonsyndromic deafness.
    Li X, Fischel-Ghodsian N, Schwartz F, Yan Q, Friedman RA, Guan MX.
    Nucleic Acids Res; 2004 May 21; 32(3):867-77. PubMed ID: 14960712
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  • 30. Correction of the consequences of mitochondrial 3243A>G mutation in the MT-TL1 gene causing the MELAS syndrome by tRNA import into mitochondria.
    Karicheva OZ, Kolesnikova OA, Schirtz T, Vysokikh MY, Mager-Heckel AM, Lombès A, Boucheham A, Krasheninnikov IA, Martin RP, Entelis N, Tarassov I.
    Nucleic Acids Res; 2011 Oct 21; 39(18):8173-86. PubMed ID: 21724600
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  • 31. Mutation in MTO1 involved in tRNA modification impairs mitochondrial RNA metabolism in the yeast Saccharomyces cerevisiae.
    Wang X, Yan Q, Guan MX.
    Mitochondrion; 2009 Jun 21; 9(3):180-5. PubMed ID: 19460296
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  • 32. 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
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  • 33. Overexpressed mitochondrial leucyl-tRNA synthetase suppresses the A3243G mutation in the mitochondrial tRNA(Leu(UUR)) gene.
    Park H, Davidson E, King MP.
    RNA; 2008 Nov 28; 14(11):2407-16. PubMed ID: 18796578
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  • 34. Kinetic discrimination of tRNA identity by the conserved motif 2 loop of a class II aminoacyl-tRNA synthetase.
    Guth EC, Francklyn CS.
    Mol Cell; 2007 Feb 23; 25(4):531-42. PubMed ID: 17317626
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  • 37. Maternally transmitted late-onset non-syndromic deafness is associated with the novel heteroplasmic T12201C mutation in the mitochondrial tRNAHis gene.
    Yan X, Wang X, Wang Z, Sun S, Chen G, He Y, Mo JQ, Li R, Jiang P, Lin Q, Sun M, Li W, Bai Y, Zhang J, Zhu Y, Lu J, Yan Q, Li H, Guan MX.
    J Med Genet; 2011 Oct 23; 48(10):682-90. PubMed ID: 21931169
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  • 38. Maternally transmitted nonsyndromic hearing impairment may be associated with mitochondrial tRNAAla 5601C>T and tRNALeu(CUN) 12311T>C mutations.
    Yu X, Li S, Ding Y.
    J Clin Lab Anal; 2022 Apr 23; 36(4):e24298. PubMed ID: 35218233
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