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 *

140 related articles for article (PubMed ID: 1707573)

  • 1. In situ hybridization of muscle mitochondrial mRNA in mitochondrial myopathies.
    Nakamura S; Sato T; Hirawake H; Kobayashi R; Fukuda Y; Kawamura J; Ujike H; Horai S
    Acta Neuropathol; 1990; 81(1):1-6. PubMed ID: 1707573
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Localization of mitochondrial DNA in normal and pathological muscle using immunological probes: a new approach to the study of mitochondrial myopathies.
    Andreetta F; Tritschler HJ; Schon EA; DiMauro S; Bonilla E
    J Neurol Sci; 1991 Sep; 105(1):88-92. PubMed ID: 1665507
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Vascular pathology in chronic progressive external ophthalmoplegia with ragged-red fibers].
    Hasegawa H; Matsuoka T; Goto Y; Nonaka I
    Rinsho Shinkeigaku; 1992 Feb; 32(2):155-60. PubMed ID: 1611773
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [A case of mitochondrial encephalomyopathy with myoclonic attacks, hyper-lactic-pyruvic acidemia, and decreased activities of complex II and cytochrome c oxidase].
    Harigaya Y; Shoji M; Okamoto K; Hirai S; Sato T
    Rinsho Shinkeigaku; 1988 Jan; 28(1):24-31. PubMed ID: 2838211
    [No Abstract]   [Full Text] [Related]  

  • 5. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The mitochondrial tRNA(Leu(UUR)) mutation in mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes (MELAS): genetic, biochemical, and morphological correlations in skeletal muscle.
    Moraes CT; Ricci E; Bonilla E; DiMauro S; Schon EA
    Am J Hum Genet; 1992 May; 50(5):934-49. PubMed ID: 1315123
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Quantitative evaluation of electron transport system proteins in mitochondrial encephalomyopathy.
    Haginoya K; Miyabayashi S; Iinuma K; Tada K
    Acta Neuropathol; 1993; 85(4):370-7. PubMed ID: 8386896
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Depletion of mitochondrial DNA in the liver of an infant with neonatal giant cell hepatitis.
    Müller-Höcker J; Muntau A; Schäfer S; Jaksch M; Staudt F; Pongratz D; Taanman JW
    Hum Pathol; 2002 Feb; 33(2):247-53. PubMed ID: 11957153
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Chronic progressive external ophthalmoplegia: a correlative study of mitochondrial DNA deletions and their phenotypic expression in muscle biopsies.
    Goto Y; Koga Y; Horai S; Nonaka I
    J Neurol Sci; 1990 Dec; 100(1-2):63-9. PubMed ID: 1965208
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Detection and analysis of mitochondrial DNA and RNA in muscle by in situ hybridization and single-fiber PCR.
    Moraes CT; Schon EA
    Methods Enzymol; 1996; 264():522-40. PubMed ID: 8965724
    [No Abstract]   [Full Text] [Related]  

  • 11. Cytochemistry and immunocytochemistry of mitochondria in tissue sections.
    Sciacco M; Bonilla E
    Methods Enzymol; 1996; 264():509-21. PubMed ID: 8965723
    [No Abstract]   [Full Text] [Related]  

  • 12. Deletions of mitochondrial DNA in Kearns-Sayre syndrome and ocular myopathies: genetic, biochemical and morphological studies.
    Degoul F; Nelson I; Lestienne P; Francois D; Romero N; Duboc D; Eymard B; Fardeau M; Ponsot G; Paturneau-Jouas M
    J Neurol Sci; 1991 Feb; 101(2):168-77. PubMed ID: 1851820
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mitochondrial DNA deletions and cytochrome c oxidase deficiency in muscle fibres.
    Oldfors A; Larsson NG; Holme E; Tulinius M; Kadenbach B; Droste M
    J Neurol Sci; 1992 Jul; 110(1-2):169-77. PubMed ID: 1324295
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Atypical clinical presentations associated with the MELAS mutation at position 3243 of human mitochondrial DNA.
    Moraes CT; Ciacci F; Silvestri G; Shanske S; Sciacco M; Hirano M; Schon EA; Bonilla E; DiMauro S
    Neuromuscul Disord; 1993 Jan; 3(1):43-50. PubMed ID: 8392410
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Impaired mitochondrial beta-oxidation in a patient with an abnormality of the respiratory chain. Studies in skeletal muscle mitochondria.
    Watmough NJ; Bindoff LA; Birch-Machin MA; Jackson S; Bartlett K; Ragan CI; Poulton J; Gardiner RM; Sherratt HS; Turnbull DM
    J Clin Invest; 1990 Jan; 85(1):177-84. PubMed ID: 2153151
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Strongly succinate dehydrogenase-reactive blood vessels (SSV) in various neuromuscular diseases].
    Matsuoka T; Hasegawa H; Nonaka I
    Rinsho Shinkeigaku; 1992 Jun; 32(6):645-7. PubMed ID: 1424348
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mitochondrial genome distribution in histochemically cytochrome c oxidase-negative muscle fibres in patients with a mixture of deleted and wild type mitochondrial DNA.
    Collins S; Rudduck C; Marzuki S; Dennett X; Byrne E
    Biochim Biophys Acta; 1991 Nov; 1097(4):309-17. PubMed ID: 1660306
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Focal cytochrome c oxidase deficiency in various neuromuscular diseases.
    Yamamoto M; Koga Y; Ohtaki E; Nonaka I
    J Neurol Sci; 1989 Jun; 91(1-2):207-13. PubMed ID: 2545831
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cytoplasmic body and mitochondrial DNA deletion.
    Sahashi K; Ohno K; Tanaka M; Ibi T; Yamamoto T; Tashiro M; Sato W; Takahashi A; Ozawa T
    J Neurol Sci; 1990 Nov; 99(2-3):291-300. PubMed ID: 1964959
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mitochondrial oculoskeletal myopathy: case report.
    Colombo A; Merelli E; Sola P; Panzetti P; Quaglino D; Fornieri C
    Ital J Neurol Sci; 1988 Aug; 9(4):385-9. PubMed ID: 2851565
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.