BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

136 related articles for article (PubMed ID: 11118331)

  • 1. Multiple deletions of mtDNA remove the light strand origin of replication.
    Bank C; Soulimane T; Schröder JM; Buse G; Zanssen S
    Biochem Biophys Res Commun; 2000 Dec; 279(2):595-601. PubMed ID: 11118331
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Analysis of multiple mitochondrial DNA deletions in inclusion body myositis.
    Moslemi AR; Lindberg C; Oldfors A
    Hum Mutat; 1997; 10(5):381-6. PubMed ID: 9375854
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Age-associated mitochondrial DNA deletions in mouse skeletal muscle: comparison of different regions of the mitochondrial genome.
    Eimon PM; Chung SS; Lee CM; Weindruch R; Aiken JM
    Dev Genet; 1996; 18(2):107-13. PubMed ID: 8934872
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Whole mitochondrial genome amplification reveals basal level multiple deletions in mtDNA of patients with dilated cardiomyopathy.
    Li YY; Hengstenberg C; Maisch B
    Biochem Biophys Res Commun; 1995 May; 210(1):211-8. PubMed ID: 7741744
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Deleted mitochondrial DNA in the skeletal muscle of aged individuals.
    Katayama M; Tanaka M; Yamamoto H; Ohbayashi T; Nimura Y; Ozawa T
    Biochem Int; 1991 Sep; 25(1):47-56. PubMed ID: 1772448
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mitochondrial DNA minicircles, lacking replication origins, exist in the cardiac muscle of a young normal subject.
    Hayakawa M; Katsumata K; Yoneda M; Tanaka M; Sugiyama S; Ozawa T
    Biochem Biophys Res Commun; 1995 Oct; 215(3):952-60. PubMed ID: 7488066
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molecular analyses of mtDNA deletion mutations in microdissected skeletal muscle fibers from aged rhesus monkeys.
    Gokey NG; Cao Z; Pak JW; Lee D; McKiernan SH; McKenzie D; Weindruch R; Aiken JM
    Aging Cell; 2004 Oct; 3(5):319-26. PubMed ID: 15379855
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Myoglobinuria caused by multiple deletions of mitochondrial DNA].
    Tanaka M; Ohno K; Sahashi K; Ibi T; Tashiro M; Ino H; Takahashi A; Ozawa T
    Rinsho Byori; 1991 Feb; 39(2):133-9. PubMed ID: 2041210
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Accumulation of deletions in MtDNA during tissue aging: analysis by long PCR.
    Reynier P; Malthiery Y
    Biochem Biophys Res Commun; 1995 Dec; 217(1):59-67. PubMed ID: 8526940
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A tandem duplication in the D-loop of human mitochondrial DNA is associated with deletions in mitochondrial myopathies.
    Brockington M; Sweeney MG; Hammans SR; Morgan-Hughes JA; Harding AE
    Nat Genet; 1993 May; 4(1):67-71. PubMed ID: 8513327
    [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. D-loop mutations in mitochondrial DNA: link with mitochondrial DNA depletion?
    Barthélémy C; de Baulny HO; Lombès A
    Hum Genet; 2002 May; 110(5):479-87. PubMed ID: 12073019
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Multiple deletions of the mitochondrial DNA in polymyalgia rheumatica.
    Reynier P; Pellissier JF; Harle JR; Malthiéry Y
    Biochem Biophys Res Commun; 1994 Nov; 205(1):375-80. PubMed ID: 7999051
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Multiple skeletal muscle mitochondrial DNA deletions in patients with unilateral peripheral arterial disease.
    Brass EP; Wang H; Hiatt WR
    Vasc Med; 2000; 5(4):225-30. PubMed ID: 11213234
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Three divergent mitochondrial genomes from California populations of the copepod Tigriopus californicus.
    Burton RS; Byrne RJ; Rawson PD
    Gene; 2007 Nov; 403(1-2):53-9. PubMed ID: 17855023
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Novel heteroplasmic frameshift and missense somatic mitochondrial DNA mutations in oral cancer of betel quid chewers.
    Tan DJ; Chang J; Chen WL; Agress LJ; Yeh KT; Wang B; Wong LJ
    Genes Chromosomes Cancer; 2003 Jun; 37(2):186-94. PubMed ID: 12696067
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mitochondrial abnormalities in inclusion-body myositis.
    Oldfors A; Moslemi AR; Jonasson L; Ohlsson M; Kollberg G; Lindberg C
    Neurology; 2006 Jan; 66(2 Suppl 1):S49-55. PubMed ID: 16432145
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Mitochondrial DNA mutations in patients with chronic progressive external ophthalmoplegia and Kearns-Sayre syndrome].
    Wang ZX; Yuan Y; Gao F; Qi Y; Shen DG; Chen QT
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Aug; 20(4):273-8. PubMed ID: 12903032
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.