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Journal Abstract Search

307 related items for PubMed ID: 8280119

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  • 2. Altered mitochondrial function in fibroblasts containing MELAS or MERRF mitochondrial DNA mutations.
    James AM, Wei YH, Pang CY, Murphy MP.
    Biochem J; 1996 Sep 01; 318 ( Pt 2)(Pt 2):401-7. PubMed ID: 8809026
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  • 3. Analysis of cybrids harboring MELAS mutations in the mitochondrial tRNA(Leu(UUR)) gene.
    Koga Y, Davidson M, Schon EA, King MP.
    Muscle Nerve Suppl; 1995 Sep 01; 3():S119-23. PubMed ID: 7603512
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  • 6. Fine mapping of mitochondrial RNAs derived from the mtDNA region containing a point mutation associated with MELAS.
    Koga Y, Davidson M, Schon EA, King MP.
    Nucleic Acids Res; 1993 Feb 11; 21(3):657-62. PubMed ID: 7680123
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  • 8. Acquisition of the wobble modification in mitochondrial tRNALeu(CUN) bearing the G12300A mutation suppresses the MELAS molecular defect.
    Kirino Y, Yasukawa T, Marjavaara SK, Jacobs HT, Holt IJ, Watanabe K, Suzuki T.
    Hum Mol Genet; 2006 Mar 15; 15(6):897-904. PubMed ID: 16446307
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  • 10. Tissue distribution of mutant mitochondrial DNA in mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS).
    Shoji Y, Sato W, Hayasaka K, Takada G.
    J Inherit Metab Dis; 1993 Mar 15; 16(1):27-30. PubMed ID: 8487499
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  • 11. Organ distribution of mutant mitochondrial tRNA(leu(UUR)) gene in a MELAS patient.
    Hamazaki S, Koshiba M, Sugiyama T.
    Acta Pathol Jpn; 1993 Apr 15; 43(4):187-91. PubMed ID: 8493868
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  • 13. Functional and morphological abnormalities of mitochondria in human cells containing mitochondrial DNA with pathogenic point mutations in tRNA genes.
    Hayashi J, Ohta S, Kagawa Y, Takai D, Miyabayashi S, Tada K, Fukushima H, Inui K, Okada S, Goto Y.
    J Biol Chem; 1994 Jul 22; 269(29):19060-6. PubMed ID: 7518448
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  • 16. Secondary coenzyme Q10 deficiency triggers mitochondria degradation by mitophagy in MELAS fibroblasts.
    Cotán D, Cordero MD, Garrido-Maraver J, Oropesa-Ávila M, Rodríguez-Hernández A, Gómez Izquierdo L, De la Mata M, De Miguel M, Lorite JB, Infante ER, Jackson S, Navas P, Sánchez-Alcázar JA.
    FASEB J; 2011 Aug 22; 25(8):2669-87. PubMed ID: 21551238
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  • 18. A new point mutation at nucleotide pair 3291 of the mitochondrial tRNA(Leu(UUR)) gene in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).
    Goto Y, Tsugane K, Tanabe Y, Nonaka I, Horai S.
    Biochem Biophys Res Commun; 1994 Aug 15; 202(3):1624-30. PubMed ID: 7520241
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  • 19. Mitochondrial DNA (mtDNA) diseases: correlation of genotype to phenotype.
    Morgan-Hughes JA, Sweeney MG, Cooper JM, Hammans SR, Brockington M, Schapira AH, Harding AE, Clark JB.
    Biochim Biophys Acta; 1995 May 24; 1271(1):135-40. PubMed ID: 7599199
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