BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

255 related articles for article (PubMed ID: 10885662)

  • 1. Mutations in mtDNA: are we scraping the bottom of the barrel?
    DiMauro S; Andreu AL
    Brain Pathol; 2000 Jul; 10(3):431-41. PubMed ID: 10885662
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mitochondrial DNA mutations in human disease.
    DiMauro S; Schon EA
    Am J Med Genet; 2001; 106(1):18-26. PubMed ID: 11579421
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Lessons from mitochondrial DNA mutations.
    DiMauro S
    Semin Cell Dev Biol; 2001 Dec; 12(6):397-405. PubMed ID: 11735374
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mitochondrial DNA medicine.
    DiMauro S
    Biosci Rep; 2007 Jun; 27(1-3):5-9. PubMed ID: 17484047
    [TBL] [Abstract][Full Text] [Related]  

  • 5. New genetics of mitochondrial DNA diseases.
    Poulton J
    Br J Hosp Med; 1996 Jun 5-18; 55(11):712-6. PubMed ID: 8793140
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Diseases of oxidative phosphorylation due to mtDNA mutations.
    DiMauro S; Andreu AL; Musumeci O; Bonilla E
    Semin Neurol; 2001 Sep; 21(3):251-60. PubMed ID: 11641815
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mitochondrial diseases.
    Vu TH; Hirano M; DiMauro S
    Neurol Clin; 2002 Aug; 20(3):809-39, vii-viii. PubMed ID: 12432831
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mitochondrial DNA and disease.
    Dimauro S; Davidzon G
    Ann Med; 2005; 37(3):222-32. PubMed ID: 16019721
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mitochondrial genetics and human disease.
    Grossman LI; Shoubridge EA
    Bioessays; 1996 Dec; 18(12):983-91. PubMed ID: 8976155
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Revolution in mitochondrial medicine.
    Larsson NG; Luft R
    FEBS Lett; 1999 Jul; 455(3):199-202. PubMed ID: 10437772
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mitochondrial DNA mutations in human degenerative diseases and aging.
    Wallace DC; Shoffner JM; Trounce I; Brown MD; Ballinger SW; Corral-Debrinski M; Horton T; Jun AS; Lott MT
    Biochim Biophys Acta; 1995 May; 1271(1):141-51. PubMed ID: 7599200
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Two pathogenic point mutations exist in the authentic mitochondrial genome, not in the nuclear pseudogene.
    Akanuma J; Muraki K; Komaki H; Nonaka I; Goto Y
    J Hum Genet; 2000; 45(6):337-41. PubMed ID: 11185741
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mitochondrial DNA mutations in diseases of energy metabolism.
    Wallace DC
    J Bioenerg Biomembr; 1994 Jun; 26(3):241-50. PubMed ID: 8077179
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mitochondrial DNA mutations and oxidative damage in aging and diseases: an emerging paradigm of gerontology and medicine.
    Wei YH
    Proc Natl Sci Counc Repub China B; 1998 Apr; 22(2):55-67. PubMed ID: 9615468
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mitochondria in neuromuscular disorders.
    DiMauro S; Bonilla E; Davidson M; Hirano M; Schon EA
    Biochim Biophys Acta; 1998 Aug; 1366(1-2):199-210. PubMed ID: 9714805
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Pathogenesis and treatment of mitochondrial myopathies: recent advances.
    DiMauro S
    Acta Myol; 2010 Oct; 29(2):333-8. PubMed ID: 21314015
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Progress in genetic counselling and prenatal diagnosis of maternally inherited mtDNA diseases.
    Poulton J; Marchington DR
    Neuromuscul Disord; 2000 Oct; 10(7):484-7. PubMed ID: 10996778
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular basis for treatment of mitochondrial myopathies.
    Taylor RW; Wardell TM; Lightowlers RN; Turnbull DM
    Neurol Sci; 2000; 21(5 Suppl):S909-12. PubMed ID: 11382188
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mitochondrial DNA and disease.
    Suomalainen A
    Ann Med; 1997 Jun; 29(3):235-46. PubMed ID: 9240629
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Towards reliable prenatal diagnosis of mtDNA point mutations: studies of nt8993 mutations in oocytes, fetal tissues, children and adults.
    Dahl HH; Thorburn DR; White SL
    Hum Reprod; 2000 Jul; 15 Suppl 2():246-55. PubMed ID: 11041530
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.