BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

91 related articles for article (PubMed ID: 7864851)

  • 1. Genotype and phenotype of severe mitochondrial cardiomyopathy: a recipient of heart transplantation and the genetic control.
    Ozawa T; Katsumata K; Hayakawa M; Tanaka M; Sugiyama S; Tanaka T; Itoyama S; Nunoda S; Sekiguchi M
    Biochem Biophys Res Commun; 1995 Feb; 207(2):613-20. PubMed ID: 7864851
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Fragmentation of human heart mitochondrial DNA associated with premature aging.
    Katsumata K; Hayakawa M; Tanaka M; Sugiyama S; Ozawa T
    Biochem Biophys Res Commun; 1994 Jul; 202(1):102-10. PubMed ID: 8037701
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mechanism of somatic mitochondrial DNA mutations associated with age and diseases.
    Ozawa T
    Biochim Biophys Acta; 1995 May; 1271(1):177-89. PubMed ID: 7599206
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mitochondrial cardiomyopathy.
    Ozawa T
    Herz; 1994 Apr; 19(2):105-18, 125. PubMed ID: 8194831
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The complete sequence of mtDNA genes in idiopathic dilated cardiomyopathy shows novel missense and tRNA mutations.
    Marin-Garcia J; Goldenthal MJ; Ananthakrishnan R; Pierpont ME
    J Card Fail; 2000 Dec; 6(4):321-9. PubMed ID: 11145757
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. A new mtDNA mutation in the tRNA(Leu(UUR)) gene associated with maternally inherited cardiomyopathy.
    Silvestri G; Santorelli FM; Shanske S; Whitley CB; Schimmenti LA; Smith SA; DiMauro S
    Hum Mutat; 1994; 3(1):37-43. PubMed ID: 7906985
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A novel gly290asp mitochondrial cytochrome b mutation linked to a complex III deficiency in progressive exercise intolerance.
    Dumoulin R; Sagnol I; Ferlin T; Bozon D; Stepien G; Mousson B
    Mol Cell Probes; 1996 Oct; 10(5):389-91. PubMed ID: 8910895
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Apoptosis in mitochondrial myopathies is linked to mitochondrial proliferation.
    Auré K; Fayet G; Leroy JP; Lacène E; Romero NB; Lombès A
    Brain; 2006 May; 129(Pt 5):1249-59. PubMed ID: 16537564
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A novel mitochondrial tRNA(Phe) mutation inhibiting anticodon stem formation associated with a muscle disease.
    Kleinle S; Schneider V; Moosmann P; Brandner S; Krähenbühl S; Liechti-Gallati S
    Biochem Biophys Res Commun; 1998 Jun; 247(1):112-5. PubMed ID: 9636664
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Two novel pathogenic mitochondrial DNA mutations affecting organelle number and protein synthesis. Is the tRNA(Leu(UUR)) gene an etiologic hot spot?
    Moraes CT; Ciacci F; Bonilla E; Jansen C; Hirano M; Rao N; Lovelace RE; Rowland LP; Schon EA; DiMauro S
    J Clin Invest; 1993 Dec; 92(6):2906-15. PubMed ID: 8254046
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Wolfram (DIDMOAD) syndrome and Leber hereditary optic neuropathy (LHON) are associated with distinct mitochondrial DNA haplotypes.
    Hofmann S; Bezold R; Jaksch M; Obermaier-Kusser B; Mertens S; Kaufhold P; Rabl W; Hecker W; Gerbitz KD
    Genomics; 1997 Jan; 39(1):8-18. PubMed ID: 9027481
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Novel point mutations in the mitochondrial DNA detected in patients with dilated cardiomyopathy by screening the whole mitochondrial genome.
    Ruppert V; Nolte D; Aschenbrenner T; Pankuweit S; Funck R; Maisch B
    Biochem Biophys Res Commun; 2004 May; 318(2):535-43. PubMed ID: 15120634
    [TBL] [Abstract][Full Text] [Related]  

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

  • 15. Adult onset limb-girdle type mitochondrial myopathy with a mitochondrial DNA np8291 A-to-G substitution.
    Hirata K; Nakagawa M; Higuchi I; Hashimoto K; Hanada K; Takahashi K; Niiyama T; Izumi K; Sakoda S; Yamada H; Osame M
    J Hum Genet; 1999; 44(3):210-4. PubMed ID: 10319590
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The ribosomal RNA gene region in Acanthamoeba castellanii mitochondrial DNA. A case of evolutionary transfer of introns between mitochondria and plastids?
    Lonergan KM; Gray MW
    J Mol Biol; 1994 Jun; 239(4):476-99. PubMed ID: 8006963
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mitochondrial DNA mutations associated with the 11778 mutation in Leber's disease.
    Sawano T; Tanaka M; Ohno K; Yoneda M; Ota Y; Terasaki H; Awaya S; Ozawa T
    Biochem Mol Biol Int; 1996 Apr; 38(4):693-700. PubMed ID: 8728098
    [TBL] [Abstract][Full Text] [Related]  

  • 18. DNA deletions and clonal mutations drive premature aging in mitochondrial mutator mice.
    Vermulst M; Wanagat J; Kujoth GC; Bielas JH; Rabinovitch PS; Prolla TA; Loeb LA
    Nat Genet; 2008 Apr; 40(4):392-4. PubMed ID: 18311139
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Maternally inherited deafness associated with a T1095C mutation in the mDNA.
    Tessa A; Giannotti A; Tieri L; Vilarinho L; Marotta G; Santorelli FM
    Eur J Hum Genet; 2001 Feb; 9(2):147-9. PubMed ID: 11313749
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Mitochondrial cardiomyopathy].
    Tanaka M
    Nihon Rinsho; 2002 Apr; 60 Suppl 4():306-11. PubMed ID: 12013873
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 5.