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 *

164 related articles for article (PubMed ID: 2841928)

  • 1. Maternal inheritance of deleted mitochondrial DNA in a family with mitochondrial myopathy.
    Ozawa T; Yoneda M; Tanaka M; Ohno K; Sato W; Suzuki H; Nishikimi M; Yamamoto M; Nonaka I; Horai S
    Biochem Biophys Res Commun; 1988 Aug; 154(3):1240-7. PubMed ID: 2841928
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mutations of the mitochondrial DNA: the contribution of DNA techniques to the diagnosis of mitochondrial encephalomyopathies.
    Gerbitz KD; Obermaier-Kusser B; Lestienne P; Zierz S; Müller-Höcker J; Pongratz D; Paetzke-Brunner I; Deufel T
    J Clin Chem Clin Biochem; 1990 Apr; 28(4):241-50. PubMed ID: 2162908
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome.
    Moraes CT; DiMauro S; Zeviani M; Lombes A; Shanske S; Miranda AF; Nakase H; Bonilla E; Werneck LC; Servidei S
    N Engl J Med; 1989 May; 320(20):1293-9. PubMed ID: 2541333
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Deletion mutants are functionally dominant over wild-type mitochondrial genomes in skeletal muscle fiber segments in mitochondrial disease.
    Shoubridge EA; Karpati G; Hastings KE
    Cell; 1990 Jul; 62(1):43-9. PubMed ID: 2163769
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Myoclonus epilepsy with ragged red fibers and multiple mtDNA deletions.
    Blumenthal DT; Shanske S; Schochet SS; Santorelli FM; DiMauro S; Jaynesm M; Bodensteiner J
    Neurology; 1998 Feb; 50(2):524-5. PubMed ID: 9484389
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies.
    Holt IJ; Harding AE; Morgan-Hughes JA
    Nature; 1988 Feb; 331(6158):717-9. PubMed ID: 2830540
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Dominantly inherited mitochondrial myopathy with multiple deletions of mitochondrial DNA: clinical, morphologic, and biochemical studies.
    Servidei S; Zeviani M; Manfredi G; Ricci E; Silvestri G; Bertini E; Gellera C; Di Mauro S; Di Donato S; Tonali P
    Neurology; 1991 Jul; 41(7):1053-9. PubMed ID: 2067633
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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; 32(6):1009-22. PubMed ID: 8061617
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mitochondrial myopathies: clinical and biochemical features of 30 patients with major deletions of muscle mitochondrial DNA.
    Holt IJ; Harding AE; Cooper JM; Schapira AH; Toscano A; Clark JB; Morgan-Hughes JA
    Ann Neurol; 1989 Dec; 26(6):699-708. PubMed ID: 2604380
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Spontaneous Kearns-Sayre/chronic external ophthalmoplegia plus syndrome associated with a mitochondrial DNA deletion: a slip-replication model and metabolic therapy.
    Shoffner JM; Lott MT; Voljavec AS; Soueidan SA; Costigan DA; Wallace DC
    Proc Natl Acad Sci U S A; 1989 Oct; 86(20):7952-6. PubMed ID: 2554297
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetic biochemical and pathophysiological characterization of a familial mitochondrial encephalomyopathy (MERRF).
    Seibel P; Degoul F; Bonne G; Romero N; François D; Paturneau-Jouas M; Ziegler F; Eymard B; Fardeau M; Marsac C
    J Neurol Sci; 1991 Oct; 105(2):217-24. PubMed ID: 1661776
    [TBL] [Abstract][Full Text] [Related]  

  • 12. An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region.
    Zeviani M; Servidei S; Gellera C; Bertini E; DiMauro S; DiDonato S
    Nature; 1989 May; 339(6222):309-11. PubMed ID: 2725645
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Phenotype-genotype correlations in skeletal muscle of patients with mtDNA deletions.
    Moraes CT; Sciacco M; Ricci E; Tengan CH; Hao H; Bonilla E; Schon EA; DiMauro S
    Muscle Nerve Suppl; 1995; 3():S150-3. PubMed ID: 7603517
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Increased mitochondrial DNA deletions in the skeletal muscle of myotonic dystrophy.
    Sahashi K; Tanaka M; Tashiro M; Ohno K; Ibi T; Takahashi A; Ozawa T
    Gerontology; 1992; 38(1-2):18-29. PubMed ID: 1319380
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Single-fiber PCR in MELAS(3243) patients: correlations between intratissue distribution and phenotypic expression of the mtDNA(A3243G) genotype.
    Silvestri G; Rana M; Odoardi F; Modoni A; Paris E; Papacci M; Tonali P; Servidei S
    Am J Med Genet; 2000 Sep; 94(3):201-6. PubMed ID: 10995506
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Specific amplification of deleted mitochondrial DNA from a myopathic patient and analysis of deleted region with S1 nuclease.
    Tanaka-Yamamoto T; Tanaka M; Ohno K; Sato W; Horai S; Ozawa T
    Biochim Biophys Acta; 1989 Nov; 1009(2):151-5. PubMed ID: 2804078
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Direct sequencing of deleted mitochondrial DNA in myopathic patients.
    Tanaka M; Sato W; Ohno K; Yamamoto T; Ozawa T
    Biochem Biophys Res Commun; 1989 Oct; 164(1):156-63. PubMed ID: 2803291
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mitochondrial encephalomyopathies: biochemical approach.
    Dimauro S; Moraes CT; Shanske S; Lombes A; Nakase H; Mita S; Tritschler HJ; Bonilla E; Miranda AF; Schon EA
    Rev Neurol (Paris); 1991; 147(6-7):443-9. PubMed ID: 1660180
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 9.