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 *

174 related articles for article (PubMed ID: 9636647)

  • 1. Tissue-specific involvement of multiple mitochondrial DNA deletions in familial mitochondrial myopathy.
    Nishizuka S; Tamura G; Goto Y; Murayama K; Konno T; Hakozaki M; Nonaka I; Tohgi H; Satodate R
    Biochem Biophys Res Commun; 1998 Jun; 247(1):24-7. PubMed ID: 9636647
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Mitochondrial DNA deletion mutations in patients with neuropsychiatric symptoms.
    Kato M; Nakamura M; Ichiba M; Tomiyasu A; Shimo H; Higuchi I; Ueno S; Sano A
    Neurosci Res; 2011 Apr; 69(4):331-6. PubMed ID: 21185889
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. Fine mapping of randomly distributed multiple deletions of mitochondrial DNA in a case of chronic progressive external ophthalmoplegia.
    Ville-Ferlin T; Dumoulin R; Stepien G; Matha V; Bady B; Flocard F; Carrier H; Mathieu M; Mousson B
    Mol Cell Probes; 1995 Jun; 9(3):207-14. PubMed ID: 7477015
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. Multiple mitochondrial DNA deletions in a patient with mitochondrial myopathy and cardiomyopathy but no ophthalmoplegia.
    Takei Y; Ikeda S; Yanagisawa N; Takahashi W; Sekiguchi M; Hayashi T
    Muscle Nerve; 1995 Nov; 18(11):1321-5. PubMed ID: 7565930
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Myopathy and Ophthalmologic Abnormalities in Association With Multiple Skeletal Muscle Mitochondrial DNA Deletions.
    Carey AR; Miller NR; Cui H; Allis K; Balog A; Bai R; Vernon HJ
    J Neuroophthalmol; 2024 Jun; 44(2):247-252. PubMed ID: 37665646
    [TBL] [Abstract][Full Text] [Related]  

  • 12. POLG mutations in sporadic mitochondrial disorders with multiple mtDNA deletions.
    Di Fonzo A; Bordoni A; Crimi M; Sara G; Del Bo R; Bresolin N; Comi GP
    Hum Mutat; 2003 Dec; 22(6):498-9. PubMed ID: 14635118
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Multiple mtDNA deletions features in autosomal dominant and recessive diseases suggest distinct pathogeneses.
    Carrozzo R; Hirano M; Fromenty B; Casali C; Santorelli FM; Bonilla E; DiMauro S; Schon EA; Miranda AF
    Neurology; 1998 Jan; 50(1):99-106. PubMed ID: 9443465
    [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. 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]  

  • 16. 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]  

  • 17. Autosomal dominant progressive external ophthalmoplegia: distribution of multiple mitochondrial DNA deletions.
    Moslemi AR; Melberg A; Holme E; Oldfors A
    Neurology; 1999 Jul; 53(1):79-84. PubMed ID: 10408540
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Partial depletion and multiple deletions of muscle mtDNA in familial MNGIE syndrome.
    Papadimitriou A; Comi GP; Hadjigeorgiou GM; Bordoni A; Sciacco M; Napoli L; Prelle A; Moggio M; Fagiolari G; Bresolin N; Salani S; Anastasopoulos I; Giassakis G; Divari R; Scarlato G
    Neurology; 1998 Oct; 51(4):1086-92. PubMed ID: 9781534
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Multiple mitochondrial DNA deletions in chronic progressive external ophthalmoplegia (CPEO)].
    Kawashima S; Nishizawa M
    Nihon Rinsho; 1993 Sep; 51(9):2391-5. PubMed ID: 8411718
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Multiple deletions of mitochondrial DNA in a patient with periodic attacks of paralysis.
    Prelle A; Moggio M; Checcarelli N; Comi G; Bresolin N; Battistel A; Bordoni A; Scarlato G
    J Neurol Sci; 1993 Jul; 117(1-2):24-7. PubMed ID: 8410061
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.