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Journal Abstract Search

222 related items for PubMed ID: 13679382

  • 1.
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  • 2. Limited dCTP availability accounts for mitochondrial DNA depletion in mitochondrial neurogastrointestinal encephalomyopathy (MNGIE).
    González-Vioque E, Torres-Torronteras J, Andreu AL, Martí R.
    PLoS Genet; 2011 Mar; 7(3):e1002035. PubMed ID: 21483760
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  • 5. Molecular analysis of mutations in the hprt gene of V79 hamster fibroblasts: effects of imbalances in the dCTP, dGTP and dTTP pools.
    Darè E, Zhang LH, Jenssen D, Bianchi V.
    J Mol Biol; 1995 Oct 06; 252(5):514-21. PubMed ID: 7563070
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  • 6. ND5 is a hot-spot for multiple atypical mitochondrial DNA deletions in mitochondrial neurogastrointestinal encephalomyopathy.
    Nishigaki Y, Marti R, Hirano M.
    Hum Mol Genet; 2004 Jan 01; 13(1):91-101. PubMed ID: 14613972
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  • 7. Selective expansion of mitochondrial nucleoside triphosphate pools in antimetabolite-treated HeLa cells.
    Bestwick RK, Moffett GL, Mathews CK.
    J Biol Chem; 1982 Aug 25; 257(16):9300-4. PubMed ID: 6213605
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  • 8. Site-specific somatic mitochondrial DNA point mutations in patients with thymidine phosphorylase deficiency.
    Nishigaki Y, Martí R, Copeland WC, Hirano M.
    J Clin Invest; 2003 Jun 25; 111(12):1913-21. PubMed ID: 12813027
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  • 9. Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): a disease of two genomes.
    Hirano M, Nishigaki Y, Martí R.
    Neurologist; 2004 Jan 25; 10(1):8-17. PubMed ID: 14720311
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  • 10. Mitochondrial deoxynucleotide pools in quiescent fibroblasts: a possible model for mitochondrial neurogastrointestinal encephalomyopathy (MNGIE).
    Ferraro P, Pontarin G, Crocco L, Fabris S, Reichard P, Bianchi V.
    J Biol Chem; 2005 Jul 01; 280(26):24472-80. PubMed ID: 15878850
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  • 11. Thymidine phosphorylase mutations cause instability of mitochondrial DNA.
    Hirano M, Lagier-Tourenne C, Valentino ML, Martí R, Nishigaki Y.
    Gene; 2005 Jul 18; 354():152-6. PubMed ID: 15975738
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  • 14. Mitochondrial neurogastrointestinal encephalomyopathy: evidence of mitochondrial DNA depletion in the small intestine.
    Giordano C, Sebastiani M, Plazzi G, Travaglini C, Sale P, Pinti M, Tancredi A, Liguori R, Montagna P, Bellan M, Valentino ML, Cossarizza A, Hirano M, d'Amati G, Carelli V.
    Gastroenterology; 2006 Mar 18; 130(3):893-901. PubMed ID: 16530527
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  • 15. Mitochondrial neurogastrointestinal encephalomyopathy: an autosomal recessive disorder due to thymidine phosphorylase mutations.
    Nishino I, Spinazzola A, Papadimitriou A, Hammans S, Steiner I, Hahn CD, Connolly AM, Verloes A, Guimarães J, Maillard I, Hamano H, Donati MA, Semrad CE, Russell JA, Andreu AL, Hadjigeorgiou GM, Vu TH, Tadesse S, Nygaard TG, Nonaka I, Hirano I, Bonilla E, Rowland LP, DiMauro S, Hirano M.
    Ann Neurol; 2000 Jun 18; 47(6):792-800. PubMed ID: 10852545
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  • 16. Quantitation of cellular deoxynucleoside triphosphates.
    Ferraro P, Franzolin E, Pontarin G, Reichard P, Bianchi V.
    Nucleic Acids Res; 2010 Apr 18; 38(6):e85. PubMed ID: 20008099
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  • 17. Changes in deoxyribonucleoside triphosphate pools in the starfish oocyte during maturation and early embryogenesis.
    Nagano H, Okano K, Ikegami S.
    Exp Cell Res; 1983 Apr 15; 145(1):219-22. PubMed ID: 6406250
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  • 18. Deoxyribonucleoside triphosphate pools in mutagen sensitive mutants of Neurospora crassa.
    Srivastava VK, Schroeder AL.
    Biochem Biophys Res Commun; 1989 Jul 31; 162(2):583-90. PubMed ID: 2527032
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  • 19. Deoxyribonucleoside triphosphate metabolism and the mammalian cell cycle. Effects of hydroxyurea on mutant and wild-type mouse S49 T-lymphoma cells.
    Eriksson S, Skog S, Tribukait B, Wallström B.
    Exp Cell Res; 1987 Jan 31; 168(1):79-88. PubMed ID: 3096753
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