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Journal Abstract Search

344 related items for PubMed ID: 1732728

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  • 3. Respiration-deficient cells are caused by a single point mutation in the mitochondrial tRNA-Leu (UUR) gene in mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS).
    Kobayashi Y, Momoi MY, Tominaga K, Shimoizumi H, Nihei K, Yanagisawa M, Kagawa Y, Ohta S.
    Am J Hum Genet; 1991 Sep; 49(3):590-9. PubMed ID: 1715668
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  • 6. A point mutation in the mitochondrial tRNA(Leu)(UUR) gene in MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes).
    Kobayashi Y, Momoi MY, Tominaga K, Momoi T, Nihei K, Yanagisawa M, Kagawa Y, Ohta S.
    Biochem Biophys Res Commun; 1990 Dec 31; 173(3):816-22. PubMed ID: 2268345
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  • 8. Respiratory chain activity in tissues from patients (MELAS) with a point mutation of the mitochondrial genome [tRNA(Leu(UUR))].
    Obermaier-Kusser B, Paetzke-Brunner I, Enter C, Müller-Höcker J, Zierz S, Ruitenbeek W, Gerbitz KD.
    FEBS Lett; 1991 Jul 29; 286(1-2):67-70. PubMed ID: 1713858
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  • 10. 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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  • 12. Mitochondrial encephalomyopathies with the mutation of the mitochondrial tRNA(Leu(UUR)) gene.
    Inui K, Fukushima H, Tsukamoto H, Taniike M, Midorikawa M, Tanaka J, Nishigaki T, Okada S.
    J Pediatr; 1992 Jan 11; 120(1):62-6. PubMed ID: 1370535
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  • 13. A new mtDNA mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS).
    Goto Y, Nonaka I, Horai S.
    Biochim Biophys Acta; 1991 Oct 21; 1097(3):238-40. PubMed ID: 1932147
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  • 17. A specific point mutation in the mitochondrial genome of Caucasians with MELAS.
    Enter C, Müller-Höcker J, Zierz S, Kurlemann G, Pongratz D, Förster C, Obermaier-Kusser B, Gerbitz KD.
    Hum Genet; 1991 Dec 21; 88(2):233-6. PubMed ID: 1684568
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  • 19. Human mitochondrial leucyl-tRNA synthetase corrects mitochondrial dysfunctions due to the tRNALeu(UUR) A3243G mutation, associated with mitochondrial encephalomyopathy, lactic acidosis, and stroke-like symptoms and diabetes.
    Li R, Guan MX.
    Mol Cell Biol; 2010 May 21; 30(9):2147-54. PubMed ID: 20194621
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  • 20. Organ distribution of mutant mitochondrial tRNA(leu(UUR)) gene in a MELAS patient.
    Hamazaki S, Koshiba M, Sugiyama T.
    Acta Pathol Jpn; 1993 Apr 21; 43(4):187-91. PubMed ID: 8493868
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