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Journal Abstract Search

278 related items for PubMed ID: 8773598

  • 1. Mitochondrial DNA and RNA processing in MELAS.
    Kaufmann P, Koga Y, Shanske S, Hirano M, DiMauro S, King MP, Schon EA.
    Ann Neurol; 1996 Aug; 40(2):172-80. PubMed ID: 8773598
    [Abstract] [Full Text] [Related]

  • 2. Increased mitochondrial DNA in blood vessels and ragged-red fibers in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).
    Tokunaga M, Mita S, Sakuta R, Nonaka I, Araki S.
    Ann Neurol; 1993 Mar; 33(3):275-80. PubMed ID: 7684581
    [Abstract] [Full Text] [Related]

  • 3. Mitochondrial DNA 3243A>G mutation and increased expression of LARS2 gene in the brains of patients with bipolar disorder and schizophrenia.
    Munakata K, Iwamoto K, Bundo M, Kato T.
    Biol Psychiatry; 2005 Mar 01; 57(5):525-32. PubMed ID: 15737668
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  • 4. Impairment of mitochondrial transcription termination by a point mutation associated with the MELAS subgroup of mitochondrial encephalomyopathies.
    Hess JF, Parisi MA, Bennett JL, Clayton DA.
    Nature; 1991 May 16; 351(6323):236-9. PubMed ID: 1755869
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  • 5. Phenotypic heterogeneity in a Chinese family with mitochondrial disease and A3243G mutation of mitochondrial DNA.
    Thajeb P, Lee HC, Pang CY, Jeng CM, Huang SF, Wei YH.
    Zhonghua Yi Xue Za Zhi (Taipei); 2000 Jan 16; 63(1):71-6. PubMed ID: 10645055
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  • 6. A mitochondrial tRNA(Leu)(UUR) mutation at 3,256 associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).
    Sato W, Hayasaka K, Shoji Y, Takahashi T, Takada G, Saito M, Fukawa O, Wachi E.
    Biochem Mol Biol Int; 1994 Aug 16; 33(6):1055-61. PubMed ID: 7804130
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  • 7. Quantification of OXPHOS gene transcripts during muscle cell differentiation in patients with mitochondrial myopathies.
    Bonod-Bidaud C, Giraud S, Mandon G, Mousson B, Stepien G.
    Exp Cell Res; 1999 Jan 10; 246(1):91-7. PubMed ID: 9882518
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  • 8. ["MELAS" (A3243G) mutation of mitochondrial DNA: a study of the relationships between the clinical phenotype in 19 patients and morphological and molecular data].
    Laforêt P, Ziegler F, Sternberg D, Rouche A, Frachon P, Fardeau M, Eymard B, Lombès A.
    Rev Neurol (Paris); 2000 Dec 10; 156(12):1136-47. PubMed ID: 11139730
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  • 9. Clinical, pathologic and genetic studies on mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes.
    Guo Y, Guo Z, Chen L, Zhang J, Wang W, Liu X, Ren H, Gao S.
    Chin Med J (Engl); 1997 Nov 10; 110(11):851-5. PubMed ID: 9772417
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  • 14. [MELAS (mitochondrial myopathy, encephalopathy lactic acidosis, and stroke-like episodes): clinical features and mitochondrial DNA mutations].
    Goto Y.
    Nihon Rinsho; 1993 Sep 10; 51(9):2373-8. PubMed ID: 8411715
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  • 15. Diagnosis and management of MELAS.
    Thambisetty M, Newman NJ.
    Expert Rev Mol Diagn; 2004 Sep 10; 4(5):631-44. PubMed ID: 15347257
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  • 17. Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS) syndrome: an autopsy report.
    Prayson RA, Wang N.
    Arch Pathol Lab Med; 1998 Nov 10; 122(11):978-81. PubMed ID: 9822126
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  • 18. Reduction of mitochondrial tRNALeu(UUR) aminoacylation by some MELAS-associated mutations.
    Hao R, Yao YN, Zheng YG, Xu MG, Wang ED.
    FEBS Lett; 2004 Dec 03; 578(1-2):135-9. PubMed ID: 15581630
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  • 19. Mitochondrial tRNA gene mutations in patients having mitochondrial disease with lactic acidosis.
    Ueki I, Koga Y, Povalko N, Akita Y, Nishioka J, Yatsuga S, Fukiyama R, Matsuishi T.
    Mitochondrion; 2006 Feb 03; 6(1):29-36. PubMed ID: 16337222
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