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Journal Abstract Search

591 related items for PubMed ID: 11532943

  • 1. Wobble modification defect in tRNA disturbs codon-anticodon interaction in a mitochondrial disease.
    Yasukawa T, Suzuki T, Ishii N, Ohta S, Watanabe K.
    EMBO J; 2001 Sep 03; 20(17):4794-802. PubMed ID: 11532943
    [Abstract] [Full Text] [Related]

  • 2. Defect in modification at the anticodon wobble nucleotide of mitochondrial tRNA(Lys) with the MERRF encephalomyopathy pathogenic mutation.
    Yasukawa T, Suzuki T, Ishii N, Ueda T, Ohta S, Watanabe K.
    FEBS Lett; 2000 Feb 11; 467(2-3):175-8. PubMed ID: 10675533
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  • 4. Nuclear DNA-encoded tRNAs targeted into mitochondria can rescue a mitochondrial DNA mutation associated with the MERRF syndrome in cultured human cells.
    Kolesnikova OA, Entelis NS, Jacquin-Becker C, Goltzene F, Chrzanowska-Lightowlers ZM, Lightowlers RN, Martin RP, Tarassov I.
    Hum Mol Genet; 2004 Oct 15; 13(20):2519-34. PubMed ID: 15317755
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  • 6. Identity elements for specific aminoacylation of a tRNA by mammalian lysyl-tRNA synthetase bearing a nonspecific tRNA-interacting factor.
    Francin M, Mirande M.
    Biochemistry; 2006 Aug 22; 45(33):10153-60. PubMed ID: 16906773
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  • 7. The role of modifications in codon discrimination by tRNA(Lys)UUU.
    Murphy FV, Ramakrishnan V, Malkiewicz A, Agris PF.
    Nat Struct Mol Biol; 2004 Dec 22; 11(12):1186-91. PubMed ID: 15558052
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  • 10. Structural effects of hypermodified nucleosides in the Escherichia coli and human tRNALys anticodon loop: the effect of nucleosides s2U, mcm5U, mcm5s2U, mnm5s2U, t6A, and ms2t6A.
    Durant PC, Bajji AC, Sundaram M, Kumar RK, Davis DR.
    Biochemistry; 2005 Jun 07; 44(22):8078-89. PubMed ID: 15924427
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  • 11. [Molecular genetic analysis for myoclonus epilepsy associated with ragged-red fibers (MERRF)].
    Tanno Y, Yoneda M, Tanaka K, Tsuji S.
    Nihon Rinsho; 1993 Sep 07; 51(9):2379-85. PubMed ID: 8411716
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  • 12. [Wobble modification defect suppresses translational activity of tRNAs with MERRF and MELAS mutations].
    Yasukawa T, Suzuki T, Watanabe K, Yasukawa T, Ohta S.
    Nihon Rinsho; 2002 Apr 07; 60 Suppl 4():197-201. PubMed ID: 12013848
    [No Abstract] [Full Text] [Related]

  • 13. MERRF/MELAS overlap syndrome: a double pathogenic mutation in mitochondrial tRNA genes.
    Nakamura M, Yabe I, Sudo A, Hosoki K, Yaguchi H, Saitoh S, Sasaki H.
    J Med Genet; 2010 Oct 07; 47(10):659-64. PubMed ID: 20610441
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  • 14. The A3243G tRNALeu(UUR) MELAS mutation causes amino acid misincorporation and a combined respiratory chain assembly defect partially suppressed by overexpression of EFTu and EFG2.
    Sasarman F, Antonicka H, Shoubridge EA.
    Hum Mol Genet; 2008 Dec 01; 17(23):3697-707. PubMed ID: 18753147
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  • 15. The expanding mutational spectrum of MERRF substitution G8361A in the mitochondrial tRNALys gene.
    Rossmanith W, Raffelsberger T, Roka J, Kornek B, Feucht M, Bittner RE.
    Ann Neurol; 2003 Dec 01; 54(6):820-3. PubMed ID: 14681892
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  • 16. Human mitochondrial diseases caused by lack of taurine modification in mitochondrial tRNAs.
    Suzuki T, Nagao A, Suzuki T.
    Wiley Interdiscip Rev RNA; 2011 Dec 01; 2(3):376-86. PubMed ID: 21957023
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  • 17. Detection of known base substitution mutations in human mitochondrial DNA of MERRF and MELAS by biochip technology.
    Du W, Li W, Chen G, Cao H, Tang H, Tang X, Jin Q, Sun Z, Zhao H, Zhou W, He S, Lv Y, Zhao J, Zhang X.
    Biosens Bioelectron; 2009 Apr 15; 24(8):2371-6. PubMed ID: 19155171
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  • 18. Modulation of the suppression efficiency and amino acid identity of an artificial yeast amber isoleucine transfer RNA in Escherichia coli by a G-U pair in the anticodon stem.
    Büttcher V, Senger B, Schumacher S, Reinbolt J, Fasiolo F.
    Biochem Biophys Res Commun; 1994 Apr 15; 200(1):370-7. PubMed ID: 8166708
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  • 19. Specific correlation between the wobble modification deficiency in mutant tRNAs and the clinical features of a human mitochondrial disease.
    Kirino Y, Goto Y, Campos Y, Arenas J, Suzuki T.
    Proc Natl Acad Sci U S A; 2005 May 17; 102(20):7127-32. PubMed ID: 15870203
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  • 20. Preferences of AAA/AAG codon recognition by modified nucleosides, τm5s2U34 and t6A37 present in tRNALys.
    Sonawane KD, Kamble AS, Fandilolu PM.
    J Biomol Struct Dyn; 2018 Dec 17; 36(16):4182-4196. PubMed ID: 29243556
    [Abstract] [Full Text] [Related]

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