BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

388 related articles for article (PubMed ID: 10888364)

  • 1. 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]  

  • 2. Muscle fibres: applications for the study of the metabolic consequences of enzyme deficiencies in skeletal muscle.
    Vielhaber S; Kudin A; Schröder R; Elger CE; Kunz WS
    Biochem Soc Trans; 2000 Feb; 28(2):159-64. PubMed ID: 10816119
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Mitochondrial respiratory rates and activities of respiratory chain complexes correlate linearly with heteroplasmy of deleted mtDNA without threshold and independently of deletion size.
    Gellerich FN; Deschauer M; Chen Y; Müller T; Neudecker S; Zierz S
    Biochim Biophys Acta; 2002 Oct; 1556(1):41-52. PubMed ID: 12351217
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The clinical, myopathological, and genetic analysis of 155 Chinese mitochondrial ophthalmoplegia patients with mitochondrial DNA single large deletions.
    Zhao Y; Hou Y; Zhao X; Liufu T; Yu M; Zhang W; Xie Z; Zhang VW; Yuan Y; Wang Z
    Mol Genet Genomic Med; 2024 Jan; 12(1):e2328. PubMed ID: 38018320
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Chronic progressive external ophthalmoplegia with ragged-red fibers: clinical, morphological and genetic investigations in 43 patients.
    Laforêt P; Lombès A; Eymard B; Danan C; Chevallay M; Rouche A; Frachon P; Fardeau M
    Neuromuscul Disord; 1995 Sep; 5(5):399-413. PubMed ID: 7496174
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Chronic progressive external ophthalmoplegia: a correlative study of quantitative molecular data and histochemical and biochemical profile.
    Fassati A; Bordoni A; Amboni P; Fortunato F; Fagiolari G; Bresolin N; Prelle A; Comi G; Scarlato G
    J Neurol Sci; 1994 May; 123(1-2):140-6. PubMed ID: 8064307
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Flux control of cytochrome c oxidase in human skeletal muscle.
    Kunz WS; Kudin A; Vielhaber S; Elger CE; Attardi G; Villani G
    J Biol Chem; 2000 Sep; 275(36):27741-5. PubMed ID: 10869362
    [TBL] [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; 42(2):180-8. PubMed ID: 9266727
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clonal expansion of mitochondrial DNA with multiple deletions in autosomal dominant progressive external ophthalmoplegia.
    Moslemi AR; Melberg A; Holme E; Oldfors A
    Ann Neurol; 1996 Nov; 40(5):707-13. PubMed ID: 8957011
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mitochondrial DNA defects and selective extraocular muscle involvement in CPEO.
    Greaves LC; Yu-Wai-Man P; Blakely EL; Krishnan KJ; Beadle NE; Kerin J; Barron MJ; Griffiths PG; Dickinson AJ; Turnbull DM; Taylor RW
    Invest Ophthalmol Vis Sci; 2010 Jul; 51(7):3340-6. PubMed ID: 20164463
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Multi-Omics Approach to Mitochondrial DNA Damage in Human Muscle Fibers.
    Elstner M; Olszewski K; Prokisch H; Klopstock T; Murgia M
    Int J Mol Sci; 2021 Oct; 22(20):. PubMed ID: 34681740
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Molecular analysis of the muscle pathology associated with mitochondrial DNA deletions.
    Moraes CT; Ricci E; Petruzzella V; Shanske S; DiMauro S; Schon EA; Bonilla E
    Nat Genet; 1992 Aug; 1(5):359-67. PubMed ID: 1284549
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Progressive external ophthalmoplegia and the Kearns-Sayre syndrome: a clinical and molecular study of 6 cases].
    Barrientos A; Casademont J; Grau JM; Cardellach F; Montoya J; Estivill X; Urbano-Márquez A; Nunes V
    Med Clin (Barc); 1995 Jul; 105(5):180-4. PubMed ID: 7630231
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Oxidative damage to skeletal muscle DNA from patients with mitochondrial encephalomyopathies.
    Mitsui T; Kawai H; Nagasawa M; Kunishige M; Akaike M; Kimura Y; Saito S
    J Neurol Sci; 1996 Jul; 139(1):111-6. PubMed ID: 8836981
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Mitochondrial DNA deletions in Kearns-Sayre syndrome].
    Carod-Artal FJ; Lopez Gallardo E; Solano A; Dahmani Y; Herrero MD; Montoya J
    Neurologia; 2006 Sep; 21(7):357-64. PubMed ID: 16977556
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Accumulation of mitochondrial DNA deletions in myotubes cultured from muscles of patients with mitochondrial myopathies.
    Collombet JM; Mandon G; Dumoulin R; Mousson B; Stepien G
    Mol Gen Genet; 1996 Nov; 253(1-2):182-8. PubMed ID: 9003302
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 20.