These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

183 related articles for article (PubMed ID: 15100439)

  • 1. Aminoacylation properties of pathology-related human mitochondrial tRNA(Lys) variants.
    Sissler M; Helm M; Frugier M; Giege R; Florentz C
    RNA; 2004 May; 10(5):841-53. PubMed ID: 15100439
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Comparative analysis of the pathogenic mechanisms associated with the G8363A and A8296G mutations in the mitochondrial tRNA(Lys) gene.
    Bornstein B; Mas JA; Patrono C; Fernández-Moreno MA; González-Vioque E; Campos Y; Carrozzo R; Martín MA; del Hoyo P; Santorelli FM; Arenas J; Garesse R
    Biochem J; 2005 May; 387(Pt 3):773-8. PubMed ID: 15554876
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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; 20(17):4794-802. PubMed ID: 11532943
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A double mutation (A8296G and G8363A) in the mitochondrial DNA tRNA (Lys) gene associated with myoclonus epilepsy with ragged-red fibers.
    Arenas J; Campos Y; Bornstein B; Ribacoba R; Martín MA; Rubio JC; Santorelli FM; Zeviani M; DiMauro S; Garesse R
    Neurology; 1999 Jan; 52(2):377-82. PubMed ID: 9932960
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Towards understanding human mitochondrial leucine aminoacylation identity.
    Sohm B; Frugier M; Brulé H; Olszak K; Przykorska A; Florentz C
    J Mol Biol; 2003 May; 328(5):995-1010. PubMed ID: 12729737
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A Watson-Crick base-pair-disrupting methyl group (m1A9) is sufficient for cloverleaf folding of human mitochondrial tRNALys.
    Helm M; Giegé R; Florentz C
    Biochemistry; 1999 Oct; 38(40):13338-46. PubMed ID: 10529209
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Hearing impairment-associated KARS mutations lead to defects in aminoacylation of both cytoplasmic and mitochondrial tRNA
    Wang Y; Zhou JB; Zeng QY; Wu S; Xue MQ; Fang P; Wang ED; Zhou XL
    Sci China Life Sci; 2020 Aug; 63(8):1227-1239. PubMed ID: 32189241
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Nuclear control of cloverleaf structure of human mitochondrial tRNA(Lys).
    Helm M; Attardi G
    J Mol Biol; 2004 Mar; 337(3):545-60. PubMed ID: 15019776
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mitochondrial DNA G8363A mutation in the tRNA Lys gene: clinical, biochemical and pathological study.
    Virgilio R; Ronchi D; Bordoni A; Fassone E; Bonato S; Donadoni C; Torgano G; Moggio M; Corti S; Bresolin N; Comi GP
    J Neurol Sci; 2009 Jun; 281(1-2):85-92. PubMed ID: 19278689
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Decreased mitochondrial tRNALys steady-state levels and aminoacylation are associated with the pathogenic G8313A mitochondrial DNA mutation.
    Bacman SR; Atencio DP; Moraes CT
    Biochem J; 2003 Aug; 374(Pt 1):131-6. PubMed ID: 12737626
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Decreased aminoacylation in pathology-related mutants of mitochondrial tRNATyr is associated with structural perturbations in tRNA architecture.
    Bonnefond L; Florentz C; Giegé R; Rudinger-Thirion J
    RNA; 2008 Apr; 14(4):641-8. PubMed ID: 18268021
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Pathogenic mechanism of a human mitochondrial tRNAPhe mutation associated with myoclonic epilepsy with ragged red fibers syndrome.
    Ling J; Roy H; Qin D; Rubio MA; Alfonzo JD; Fredrick K; Ibba M
    Proc Natl Acad Sci U S A; 2007 Sep; 104(39):15299-304. PubMed ID: 17878308
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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; 339(1):17-29. PubMed ID: 15123417
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Human mitochondrial diseases associated with tRNA wobble modification deficiency.
    Kirino Y; Suzuki T
    RNA Biol; 2005 Apr; 2(2):41-4. PubMed ID: 17132941
    [TBL] [Abstract][Full Text] [Related]  

  • 15. MtDNA mutation in MERRF syndrome causes defective aminoacylation of tRNA(Lys) and premature translation termination.
    Enriquez JA; Chomyn A; Attardi G
    Nat Genet; 1995 May; 10(1):47-55. PubMed ID: 7647790
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Functional defects of pathogenic human mitochondrial tRNAs related to structural fragility.
    Kelley SO; Steinberg SV; Schimmel P
    Nat Struct Biol; 2000 Oct; 7(10):862-5. PubMed ID: 11017193
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Transfer RNA recognition by class I lysyl-tRNA synthetase from the Lyme disease pathogen Borrelia burgdorferi.
    Ambrogelly A; Frugier M; Ibba M; Söll D; Giegé R
    FEBS Lett; 2005 May; 579(12):2629-34. PubMed ID: 15862301
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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; 45(33):10153-60. PubMed ID: 16906773
    [TBL] [Abstract][Full Text] [Related]  

  • 19. RNA modification landscape of the human mitochondrial tRNA
    Richter U; Evans ME; Clark WC; Marttinen P; Shoubridge EA; Suomalainen A; Wredenberg A; Wedell A; Pan T; Battersby BJ
    Nat Commun; 2018 Sep; 9(1):3966. PubMed ID: 30262910
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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; 13(20):2519-34. PubMed ID: 15317755
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.