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1334 related items for PubMed ID: 16537564

  • 1. Apoptosis in mitochondrial myopathies is linked to mitochondrial proliferation.
    Auré K, Fayet G, Leroy JP, Lacène E, Romero NB, Lombès A.
    Brain; 2006 May; 129(Pt 5):1249-59. PubMed ID: 16537564
    [Abstract] [Full Text] [Related]

  • 2. Spectrum of myopathic findings in 50 patients with the 3243A>G mutation in mitochondrial DNA.
    Kärppä M, Herva R, Moslemi AR, Oldfors A, Kakko S, Majamaa K.
    Brain; 2005 Aug; 128(Pt 8):1861-9. PubMed ID: 15857931
    [Abstract] [Full Text] [Related]

  • 3. Apoptosis is suspended in muscle of mitochondrial encephalomyopathies.
    Ikezoe K, Nakagawa M, Yan C, Kira J, Goto Y, Nonaka I.
    Acta Neuropathol; 2002 Jun; 103(6):531-40. PubMed ID: 12012084
    [Abstract] [Full Text] [Related]

  • 4. Immunohistochemical analysis of the oxidative phosphorylation complexes in skeletal muscle from patients with mitochondrial DNA encoded tRNA gene defects.
    De Paepe B, Smet J, Lammens M, Seneca S, Martin JJ, De Bleecker J, De Meirleir L, Lissens W, Van Coster R.
    J Clin Pathol; 2009 Feb; 62(2):172-6. PubMed ID: 19181635
    [Abstract] [Full Text] [Related]

  • 5. [Expressions of PDCD5 and other apoptosis-related proteins in muscle of patients with mitochondrial cytopathy].
    Li YF, Wang ZX, Gao XG, Hong DJ, Yuan Y.
    Zhonghua Yi Xue Za Zhi; 2009 Jun 16; 89(23):1593-6. PubMed ID: 19957502
    [Abstract] [Full Text] [Related]

  • 6. Aerobic training is safe and improves exercise capacity in patients with mitochondrial myopathy.
    Jeppesen TD, Schwartz M, Olsen DB, Wibrand F, Krag T, Dunø M, Hauerslev S, Vissing J.
    Brain; 2006 Dec 16; 129(Pt 12):3402-12. PubMed ID: 16815877
    [Abstract] [Full Text] [Related]

  • 7. Single muscle fiber analysis of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).
    Tokunaga M, Mita S, Murakami T, Kumamoto T, Uchino M, Nonaka I, Ando M.
    Ann Neurol; 1994 Apr 16; 35(4):413-9. PubMed ID: 8154867
    [Abstract] [Full Text] [Related]

  • 8. 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 16; 33(3):275-80. PubMed ID: 7684581
    [Abstract] [Full Text] [Related]

  • 9. Evidence of apoptosis via TUNEL staining in muscle biopsy from patients with mitochondrial encephaloneuromyopathies.
    Formichi P, Battisti C, Bianchi S, Cardaioli E, Federico A.
    J Submicrosc Cytol Pathol; 2003 Jan 16; 35(1):29-34. PubMed ID: 12762649
    [Abstract] [Full Text] [Related]

  • 10. Association of myopathy with large-scale mitochondrial DNA duplications and deletions: which is pathogenic?
    Manfredi G, Vu T, Bonilla E, Schon EA, DiMauro S, Arnaudo E, Zhang L, Rowland LP, Hirano M.
    Ann Neurol; 1997 Aug 16; 42(2):180-8. PubMed ID: 9266727
    [Abstract] [Full Text] [Related]

  • 11. Apoptosis-related changes in skeletal muscles of patients with mitochondrial diseases.
    Umaki Y, Mitsui T, Endo I, Akaike M, Matsumoto T.
    Acta Neuropathol; 2002 Feb 16; 103(2):163-70. PubMed ID: 11810183
    [Abstract] [Full Text] [Related]

  • 12. Mitochondrial DNA copy number threshold in mtDNA depletion myopathy.
    Durham SE, Bonilla E, Samuels DC, DiMauro S, Chinnery PF.
    Neurology; 2005 Aug 09; 65(3):453-5. PubMed ID: 16087914
    [Abstract] [Full Text] [Related]

  • 13. Mitochondrial (mt)DNA changes in tissue may not be reflected by depletion of mtDNA in peripheral blood mononuclear cells in HIV-infected patients.
    Maagaard A, Holberg-Petersen M, Kollberg G, Oldfors A, Sandvik L, Bruun JN.
    Antivir Ther; 2006 Aug 09; 11(5):601-8. PubMed ID: 16964828
    [Abstract] [Full Text] [Related]

  • 14. Mitochondrial diseases.
    Nonaka I.
    Curr Opin Neurol Neurosurg; 1992 Oct 09; 5(5):622-32. PubMed ID: 1392136
    [Abstract] [Full Text] [Related]

  • 15. Mitochondrial abnormalities in inclusion-body myositis.
    Oldfors A, Moslemi AR, Jonasson L, Ohlsson M, Kollberg G, Lindberg C.
    Neurology; 2006 Jan 24; 66(2 Suppl 1):S49-55. PubMed ID: 16432145
    [Abstract] [Full Text] [Related]

  • 16. Functional mitochondrial heterogeneity in heteroplasmic cells carrying the mitochondrial DNA mutation associated with the MELAS syndrome (mitochondrial encephalopathy, lactic acidosis, and strokelike episodes).
    Bakker A, Barthélémy C, Frachon P, Chateau D, Sternberg D, Mazat JP, Lombès A.
    Pediatr Res; 2000 Aug 24; 48(2):143-50. PubMed ID: 10926287
    [Abstract] [Full Text] [Related]

  • 17. [Mitochondrial myopathy, deafness and type 2 diabetes mellitus with tRNALeu(UUR) point mutation in mitochondrial DNA].
    Stratilová L, Zeman J, Hansíková H, Houstĕk J, Hermanská J, Dudková Z, Konrádová V, Hůlková H, Elleder M.
    Cas Lek Cesk; 1998 Jul 13; 137(14):430-3. PubMed ID: 9748738
    [Abstract] [Full Text] [Related]

  • 18. A defect in the thymidine kinase 2 gene causing isolated mitochondrial myopathy without mtDNA depletion.
    Leshinsky-Silver E, Michelson M, Cohen S, Ginsberg M, Sadeh M, Barash V, Lerman-Sagie T, Lev D.
    Eur J Paediatr Neurol; 2008 Jul 13; 12(4):309-13. PubMed ID: 17951082
    [Abstract] [Full Text] [Related]

  • 19. Two novel pathogenic mitochondrial DNA mutations affecting organelle number and protein synthesis. Is the tRNA(Leu(UUR)) gene an etiologic hot spot?
    Moraes CT, Ciacci F, Bonilla E, Jansen C, Hirano M, Rao N, Lovelace RE, Rowland LP, Schon EA, DiMauro S.
    J Clin Invest; 1993 Dec 13; 92(6):2906-15. PubMed ID: 8254046
    [Abstract] [Full Text] [Related]

  • 20. Age-dependent respiratory function decline and DNA deletions in human muscle mitochondria.
    Hsieh RH, Hou JH, Hsu HS, Wei YH.
    Biochem Mol Biol Int; 1994 Apr 13; 32(6):1009-22. PubMed ID: 8061617
    [Abstract] [Full Text] [Related]

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