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 *

170 related articles for article (PubMed ID: 8170566)

  • 21. 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]  

  • 22. Parkinson syndrome, neuropathy, and myopathy caused by the mutation A8344G (MERRF) in tRNALys.
    Horvath R; Kley RA; Lochmüller H; Vorgerd M
    Neurology; 2007 Jan; 68(1):56-8. PubMed ID: 17200493
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Rapid detection of the A----G(8344) mutation of mtDNA in Italian families with myoclonus epilepsy and ragged-red fibers (MERRF).
    Zeviani M; Amati P; Bresolin N; Antozzi C; Piccolo G; Toscano A; DiDonato S
    Am J Hum Genet; 1991 Feb; 48(2):203-11. PubMed ID: 1899320
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. A new mtDNA mutation in the tRNA(Lys) gene associated with myoclonic epilepsy and ragged-red fibers (MERRF).
    Silvestri G; Moraes CT; Shanske S; Oh SJ; DiMauro S
    Am J Hum Genet; 1992 Dec; 51(6):1213-7. PubMed ID: 1361099
    [TBL] [Abstract][Full Text] [Related]  

  • 26. High prevalence of the COII/tRNA(Lys) intergenic 9-bp deletion in mitochondrial DNA of Taiwanese patients with MELAS or MERRF syndrome.
    Liu CS; Cheng WL; Chen YY; Ma YS; Pang CY; Wei YH
    Ann N Y Acad Sci; 2005 May; 1042():82-7. PubMed ID: 15965049
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A tRNA(Lys) mutation in the mtDNA is the causal genetic lesion underlying myoclonic epilepsy and ragged-red fiber (MERRF) syndrome.
    Noer AS; Sudoyo H; Lertrit P; Thyagarajan D; Utthanaphol P; Kapsa R; Byrne E; Marzuki S
    Am J Hum Genet; 1991 Oct; 49(4):715-22. PubMed ID: 1910259
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Simple detection of tRNA(Lys) mutation in myoclonus epilepsy associated with ragged-red fibers (MERRF) by polymerase chain reaction with a mismatched primer.
    Yoneda M; Tanno Y; Nonaka I; Miyatake T; Tsuji S
    Neurology; 1991 Nov; 41(11):1838-40. PubMed ID: 1682854
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Rapamycin rescues mitochondrial dysfunction in cells carrying the m.8344A > G mutation in the mitochondrial tRNA
    Capristo M; Del Dotto V; Tropeano CV; Fiorini C; Caporali L; La Morgia C; Valentino ML; Montopoli M; Carelli V; Maresca A
    Mol Med; 2022 Aug; 28(1):90. PubMed ID: 35922766
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Expanding the phenotype of the 8344 transfer RNAlysine mitochondrial DNA mutation.
    Austin SA; Vriesendorp FJ; Thandroyen FT; Hecht JT; Jones OT; Johns DR
    Neurology; 1998 Nov; 51(5):1447-50. PubMed ID: 9818878
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. Generation of an induced pluripotent stem cell (iPSC) line from a 40-year-old patient with the A8344G mutation of mitochondrial DNA and MERRF (myoclonic epilepsy with ragged red fibers) syndrome.
    Wu YT; Hsu YH; Huang CY; Ho MC; Cheng YC; Wen CH; Ko HW; Lu HE; Chen YC; Tsai CL; Hsu YC; Wei YH; Hsieh PCH
    Stem Cell Res; 2018 Mar; 27():10-14. PubMed ID: 29288969
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Distribution and threshold expression of the tRNA(Lys) mutation in skeletal muscle of patients with myoclonic epilepsy and ragged-red fibers (MERRF).
    Boulet L; Karpati G; Shoubridge EA
    Am J Hum Genet; 1992 Dec; 51(6):1187-200. PubMed ID: 1334369
    [TBL] [Abstract][Full Text] [Related]  

  • 34. MERRF syndrome with overwhelming lactic acidosis.
    Sanger TD; Jain KD
    Pediatr Neurol; 1996 Jan; 14(1):57-61. PubMed ID: 8652018
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Automatic sequencing of mitochondrial tRNA genes in patients with mitochondrial encephalomyopathy.
    Houshmand M; Larsson NG; Holme E; Oldfors A; Tulinius MH; Andersen O
    Biochim Biophys Acta; 1994 Apr; 1226(1):49-55. PubMed ID: 8155739
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Myoclonus epilepsy associated with ragged-red fibers: a G-to-A mutation at nucleotide pair 8363 in mitochondrial tRNA(Lys) in two families.
    Ozawa M; Nishino I; Horai S; Nonaka I; Goto YI
    Muscle Nerve; 1997 Mar; 20(3):271-8. PubMed ID: 9052804
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Analysis of mtDNA copy number and composition of single mitochondrial particles using flow cytometry and PCR.
    Cavelier L; Johannisson A; Gyllensten U
    Exp Cell Res; 2000 Aug; 259(1):79-85. PubMed ID: 10942580
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Altered mitochondrial function in fibroblasts containing MELAS or MERRF mitochondrial DNA mutations.
    James AM; Wei YH; Pang CY; Murphy MP
    Biochem J; 1996 Sep; 318 ( Pt 2)(Pt 2):401-7. PubMed ID: 8809026
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. A common mitochondrial DNA mutation in the t-RNA(Lys) of patients with myoclonus epilepsy associated with ragged-red fibers.
    Yoneda M; Tanno Y; Horai S; Ozawa T; Miyatake T; Tsuji S
    Biochem Int; 1990 Aug; 21(5):789-96. PubMed ID: 2124116
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.