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Journal Abstract Search

454 related items for PubMed ID: 15477393

  • 1. Mitochondrial tRNA 3' end metabolism and human disease.
    Levinger L, Mörl M, Florentz C.
    Nucleic Acids Res; 2004; 32(18):5430-41. PubMed ID: 15477393
    [Abstract] [Full Text] [Related]

  • 2. In vitro 3'-end endonucleolytic processing defect in a human mitochondrial tRNA(Ser(UCN)) precursor with the U7445C substitution, which causes non-syndromic deafness.
    Levinger L, Jacobs O, James M.
    Nucleic Acids Res; 2001 Nov 01; 29(21):4334-40. PubMed ID: 11691920
    [Abstract] [Full Text] [Related]

  • 3. A pathogenesis-associated mutation in human mitochondrial tRNALeu(UUR) leads to reduced 3'-end processing and CCA addition.
    Levinger L, Oestreich I, Florentz C, Mörl M.
    J Mol Biol; 2004 Mar 26; 337(3):535-44. PubMed ID: 15019775
    [Abstract] [Full Text] [Related]

  • 4. Pathogenesis-related mutations in the T-loops of human mitochondrial tRNAs affect 3' end processing and tRNA structure.
    Levinger L, Serjanov D.
    RNA Biol; 2012 Mar 26; 9(3):283-91. PubMed ID: 22336717
    [Abstract] [Full Text] [Related]

  • 5. Human mitochondrial tRNAs: biogenesis, function, structural aspects, and diseases.
    Suzuki T, Nagao A, Suzuki T.
    Annu Rev Genet; 2011 Mar 26; 45():299-329. PubMed ID: 21910628
    [Abstract] [Full Text] [Related]

  • 6. Drosophila RNase Z processes mitochondrial and nuclear pre-tRNA 3' ends in vivo.
    Dubrovsky EB, Dubrovskaya VA, Levinger L, Schiffer S, Marchfelder A.
    Nucleic Acids Res; 2004 Mar 26; 32(1):255-62. PubMed ID: 14715923
    [Abstract] [Full Text] [Related]

  • 7. Human mitochondrial tRNA quality control in health and disease: a channelling mechanism?
    Belostotsky R, Frishberg Y, Entelis N.
    RNA Biol; 2012 Jan 26; 9(1):33-9. PubMed ID: 22258151
    [Abstract] [Full Text] [Related]

  • 8. Human mitochondrial diseases caused by lack of taurine modification in mitochondrial tRNAs.
    Suzuki T, Nagao A, Suzuki T.
    Wiley Interdiscip Rev RNA; 2011 Jan 26; 2(3):376-86. PubMed ID: 21957023
    [Abstract] [Full Text] [Related]

  • 9. Involvement of human ELAC2 gene product in 3' end processing of mitochondrial tRNAs.
    Brzezniak LK, Bijata M, Szczesny RJ, Stepien PP.
    RNA Biol; 2011 Jan 26; 8(4):616-26. PubMed ID: 21593607
    [Abstract] [Full Text] [Related]

  • 10. A tRNA's fate is decided at its 3' end: Collaborative actions of CCA-adding enzyme and RNases involved in tRNA processing and degradation.
    Wellner K, Betat H, Mörl M.
    Biochim Biophys Acta Gene Regul Mech; 2018 Apr 26; 1861(4):433-441. PubMed ID: 29374586
    [Abstract] [Full Text] [Related]

  • 11. tRNAs marked with CCACCA are targeted for degradation.
    Wilusz JE, Whipple JM, Phizicky EM, Sharp PA.
    Science; 2011 Nov 11; 334(6057):817-21. PubMed ID: 22076379
    [Abstract] [Full Text] [Related]

  • 12. The identity of the discriminator base has an impact on CCA addition.
    Wende S, Bonin S, Götze O, Betat H, Mörl M.
    Nucleic Acids Res; 2015 Jun 23; 43(11):5617-29. PubMed ID: 25958396
    [Abstract] [Full Text] [Related]

  • 13. Does the evolutionary history of aminoacyl-tRNA synthetases explain the loss of mitochondrial tRNA genes?
    Schneider A.
    Trends Genet; 2001 Oct 23; 17(10):557-9. PubMed ID: 11585646
    [Abstract] [Full Text] [Related]

  • 14. Import of tRNAs and aminoacyl-tRNA synthetases into mitochondria.
    Duchêne AM, Pujol C, Maréchal-Drouard L.
    Curr Genet; 2009 Feb 23; 55(1):1-18. PubMed ID: 19083240
    [Abstract] [Full Text] [Related]

  • 15. Handling mammalian mitochondrial tRNAs and aminoacyl-tRNA synthetases for functional and structural characterization.
    Sissler M, Lorber B, Messmer M, Schaller A, Pütz J, Florentz C.
    Methods; 2008 Feb 23; 44(2):176-89. PubMed ID: 18241799
    [Abstract] [Full Text] [Related]

  • 16. Mitochondrial aminoacyl-tRNA synthetases in human disease.
    Konovalova S, Tyynismaa H.
    Mol Genet Metab; 2013 Apr 23; 108(4):206-11. PubMed ID: 23433712
    [Abstract] [Full Text] [Related]

  • 17. A new mechanism for mtDNA pathogenesis: impairment of post-transcriptional maturation leads to severe depletion of mitochondrial tRNASer(UCN) caused by T7512C and G7497A point mutations.
    Möllers M, Maniura-Weber K, Kiseljakovic E, Bust M, Hayrapetyan A, Jaksch M, Helm M, Wiesner RJ, von Kleist-Retzow JC.
    Nucleic Acids Res; 2005 Apr 23; 33(17):5647-58. PubMed ID: 16199753
    [Abstract] [Full Text] [Related]

  • 18. The CCA-adding enzyme: A central scrutinizer in tRNA quality control.
    Betat H, Mörl M.
    Bioessays; 2015 Sep 23; 37(9):975-82. PubMed ID: 26172425
    [Abstract] [Full Text] [Related]

  • 19. Mitochondrial Aminoacyl-tRNA Synthetase and Disease: The Yeast Contribution for Functional Analysis of Novel Variants.
    Figuccia S, Degiorgi A, Ceccatelli Berti C, Baruffini E, Dallabona C, Goffrini P.
    Int J Mol Sci; 2021 Apr 26; 22(9):. PubMed ID: 33926074
    [Abstract] [Full Text] [Related]

  • 20. Mitochondrial tRNA import and its consequences for mitochondrial translation.
    Schneider A.
    Annu Rev Biochem; 2011 Apr 26; 80():1033-53. PubMed ID: 21417719
    [Abstract] [Full Text] [Related]

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