These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

146 related articles for article (PubMed ID: 8593534)

  • 1. mtDNA deletion in a patient with symptoms of mitochondrial cytopathy but without ragged red fibers.
    Blok RB; Thorburn DR; Danks DM; Dahl HH
    Biochem Mol Med; 1995 Oct; 56(1):26-30. PubMed ID: 8593534
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Specific detection of deleted mitochondrial DNA by in situ hybridization using a chimera probe.
    Nakamura N; Hattori N; Tanaka M; Mizuno Y
    Biochim Biophys Acta; 1996 Sep; 1308(3):215-21. PubMed ID: 8809113
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mitochondrial DNA deletions in muscle fibers in inclusion body myositis.
    Oldfors A; Moslemi AR; Fyhr IM; Holme E; Larsson NG; Lindberg C
    J Neuropathol Exp Neurol; 1995 Jul; 54(4):581-7. PubMed ID: 7602331
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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; 42(2):180-8. PubMed ID: 9266727
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Frequencies of myohistological mitochondrial changes in patients with mitochondrial DNA deletions and the common m.3243A>G point mutation.
    Zierz CM; Joshi PR; Zierz S
    Neuropathology; 2015 Apr; 35(2):130-6. PubMed ID: 25378026
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mitochondrial DNA defects in Brazilian patients with chronic progressive external ophthalmoplegia.
    Kiyomoto BH; Tengan CH; Moraes CT; Oliveira AS; Gabbai AA
    J Neurol Sci; 1997 Nov; 152(2):160-5. PubMed ID: 9415537
    [TBL] [Abstract][Full Text] [Related]  

  • 8. False-positive diagnosis of a single, large-scale mitochondrial DNA deletion by Southern blot analysis: the role of neutral polymorphisms.
    Deschauer M; Krasnianski A; Zierz S; Taylor RW
    Genet Test; 2004; 8(4):395-9. PubMed ID: 15684869
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mitochondrial myopathy associated with a novel mutation in mtDNA.
    Pancrudo J; Shanske S; Coku J; Lu J; Mardach R; Akman O; Krishna S; Bonilla E; DiMauro S
    Neuromuscul Disord; 2007 Aug; 17(8):651-4. PubMed ID: 17588757
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Widespread tissue distribution of multiple mitochondrial DNA deletions in familial mitochondrial myopathy.
    Kawashima S; Ohta S; Kagawa Y; Yoshida M; Nishizawa M
    Muscle Nerve; 1994 Jul; 17(7):741-6. PubMed ID: 8008000
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A MERRF/MELAS overlap syndrome associated with a new point mutation in the mitochondrial DNA tRNA(Lys) gene.
    Zeviani M; Muntoni F; Savarese N; Serra G; Tiranti V; Carrara F; Mariotti C; DiDonato S
    Eur J Hum Genet; 1993; 1(1):80-7. PubMed ID: 8069654
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Juvenile form of Alexander disease with GFAP mutation and mitochondrial abnormality.
    Nobuhara Y; Nakahara K; Higuchi I; Yoshida T; Fushiki S; Osame M; Arimura K; Nakagawa M
    Neurology; 2004 Oct; 63(7):1302-4. PubMed ID: 15477559
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Inter- and/or intra-organ distribution of mitochondrial C3303T or A3243G mutation in mitochondrial cytopathy.
    Iwanaga R; Koga Y; Aramaki S; Kato S; Kato H
    Acta Neuropathol; 2001 Feb; 101(2):179-84. PubMed ID: 11271374
    [TBL] [Abstract][Full Text] [Related]  

  • 14. New insights into the metabolic consequences of large-scale mtDNA deletions: a quantitative analysis of biochemical, morphological, and genetic findings in human skeletal muscle.
    Schröder R; Vielhaber S; Wiedemann FR; Kornblum C; Papassotiropoulos A; Broich P; Zierz S; Elger CE; Reichmann H; Seibel P; Klockgether T; Kunz WS
    J Neuropathol Exp Neurol; 2000 May; 59(5):353-60. PubMed ID: 10888364
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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; 12(4):309-13. PubMed ID: 17951082
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Multiple deletions of mtDNA in two brothers with sideroblastic anemia and mitochondrial myopathy and in their asymptomatic mother.
    Casademont J; Barrientos A; Cardellach F; Rötig A; Grau JM; Montoya J; Beltrán B; Cervantes F; Rozman C; Estivill X
    Hum Mol Genet; 1994 Nov; 3(11):1945-9. PubMed ID: 7874110
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Developmental genetics of deleted mtDNA in mitochondrial oculomyopathy.
    Marzuki S; Berkovic SF; Saifuddin Noer A; Kapsa RM; Kalnins RM; Byrne E; Sasmono T; Sudoyo H
    J Neurol Sci; 1997 Feb; 145(2):155-62. PubMed ID: 9094043
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mitochondrial DNA depletion in single fibers in a patient with novel TK2 mutations.
    Roos S; Lindgren U; Ehrstedt C; Moslemi AR; Oldfors A
    Neuromuscul Disord; 2014 Aug; 24(8):713-20. PubMed ID: 24953930
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A new mtDNA mutation showing accumulation with time and restriction to skeletal muscle.
    Weber K; Wilson JN; Taylor L; Brierley E; Johnson MA; Turnbull DM; Bindoff LA
    Am J Hum Genet; 1997 Feb; 60(2):373-80. PubMed ID: 9012410
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Mitochondrial DNA mutation analysis in patients with mitochondrial myopathy].
    Zhang XA; Wu HC; Zhang BF; Yu W; Fan QS
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Feb; 22(1):18-21. PubMed ID: 15696472
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.