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 *

137 related articles for article (PubMed ID: 2322247)

  • 1. Marked decrease of mitochondrial DNA with multiple deletions in a patient with familial mitochondrial myopathy.
    Otsuka M; Niijima K; Mizuno Y; Yoshida M; Kagawa Y; Ohta S
    Biochem Biophys Res Commun; 1990 Mar; 167(2):680-5. PubMed ID: 2322247
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Multiple deletions in mitochondrial DNA at direct repeats of non-D-loop regions in cases of familial mitochondrial myopathy.
    Yuzaki M; Ohkoshi N; Kanazawa I; Kagawa Y; Ohta S
    Biochem Biophys Res Commun; 1989 Nov; 164(3):1352-7. PubMed ID: 2590206
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Nucleus-driven multiple large-scale deletions of the human mitochondrial genome: a new autosomal dominant disease.
    Zeviani M; Bresolin N; Gellera C; Bordoni A; Pannacci M; Amati P; Moggio M; Servidei S; Scarlato G; DiDonato S
    Am J Hum Genet; 1990 Dec; 47(6):904-14. PubMed ID: 1978558
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. Detection of mitochondrial DNA deletions in blood using the polymerase chain reaction: non-invasive diagnosis of mitochondrial myopathy.
    Poulton J; Deadman ME; Turnbull DM; Lake B; Gardiner RM
    Clin Genet; 1991 Jan; 39(1):33-8. PubMed ID: 1997213
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. Mitochondrial myopathy of childhood associated with depletion of mitochondrial DNA.
    Tritschler HJ; Andreetta F; Moraes CT; Bonilla E; Arnaudo E; Danon MJ; Glass S; Zelaya BM; Vamos E; Telerman-Toppet N
    Neurology; 1992 Jan; 42(1):209-17. PubMed ID: 1734306
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A molecular genetic study of focal histochemical defects in mitochondrial encephalomyopathies.
    Hammans SR; Sweeney MG; Wicks DA; Morgan-Hughes JA; Harding AE
    Brain; 1992 Apr; 115 ( Pt 2)():343-65. PubMed ID: 1606473
    [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. Double-strand breaks of mouse muscle mtDNA promote large deletions similar to multiple mtDNA deletions in humans.
    Srivastava S; Moraes CT
    Hum Mol Genet; 2005 Apr; 14(7):893-902. PubMed ID: 15703189
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Duplications of mitochondrial DNA in mitochondrial myopathy.
    Poulton J; Deadman ME; Gardiner RM
    Lancet; 1989 Feb; 1(8632):236-40. PubMed ID: 2563411
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. 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]  

  • 18. 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]  

  • 19. Maternally inherited mitochondrial myopathy and myoclonic epilepsy.
    Rosing HS; Hopkins LC; Wallace DC; Epstein CM; Weidenheim K
    Ann Neurol; 1985 Mar; 17(3):228-37. PubMed ID: 3922281
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Disorders associated with multiple deletions of mitochondrial DNA.
    Haltia M; Suomalainen A; Majander A; Somer H
    Brain Pathol; 1992 Apr; 2(2):133-9. PubMed ID: 1341954
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.