BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

164 related articles for article (PubMed ID: 11446509)

  • 1. A case of cardiomyopathy showing progression from the hypertrophic to the dilated form: association of Mt8348A-->G mutation in the mitochondrial tRNA(Lys) gene with severe ultrastructural alterations of mitochondria in cardiomyocytes.
    Terasaki F; Tanaka M; Kawamura K; Kanzaki Y; Okabe M; Hayashi T; Shimomura H; Ito T; Suwa M; Gong JS; Zhang J; Kitaura Y
    Jpn Circ J; 2001 Jul; 65(7):691-4. PubMed ID: 11446509
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mitochondrial DNA mutations in cardiomyopathy.
    Ito T; Hattori K; Obayashi T; Tanaka M; Sugiyama S; Ozawa T
    Jpn Circ J; 1992 Oct; 56(10):1045-53. PubMed ID: 1433821
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Rapid progression of cardiomyopathy in mitochondrial diabetes.
    Momiyama Y; Atsumi Y; Ohsuzu F; Ui S; Morinaga S; Matsuoka K; Kimura M
    Jpn Circ J; 1999 Feb; 63(2):130-2. PubMed ID: 10084376
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Multiple mitochondrial DNA deletions exist in cardiomyocytes of patients with hypertrophic or dilated cardiomyopathy.
    Ozawa T; Tanaka M; Sugiyama S; Hattori K; Ito T; Ohno K; Takahashi A; Sato W; Takada G; Mayumi B
    Biochem Biophys Res Commun; 1990 Jul; 170(2):830-6. PubMed ID: 2143377
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mitochondrial diseases and the heart: an overview of molecular basis, diagnosis, treatment and clinical course.
    Limongelli G; Masarone D; D'Alessandro R; Elliott PM
    Future Cardiol; 2012 Jan; 8(1):71-88. PubMed ID: 22185447
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Morphometric comparison of mitochondria and myofibrils of cardiomyocytes between hypertrophic and dilated cardiomyopathies.
    Tashiro A; Masuda T; Segawa I
    Virchows Arch A Pathol Anat Histopathol; 1990; 416(6):473-8. PubMed ID: 2110695
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mitochondrial cardiomyopathy: molecular and biochemical analysis.
    Marin-Garcia J; Goldenthal MJ
    Pediatr Cardiol; 1997; 18(4):251-60. PubMed ID: 9175519
    [TBL] [Abstract][Full Text] [Related]  

  • 8. First description of a novel mitochondrial mutation in the MT-TI gene associated with multiple mitochondrial DNA deletion and depletion in family with severe dilated mitochondrial cardiomyopathy.
    Alila-Fersi O; Tabebi M; Maalej M; Belguith N; Keskes L; Mkaouar-Rebai E; Fakhfakh F
    Biochem Biophys Res Commun; 2018 Mar; 497(4):1049-1054. PubMed ID: 29481798
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Genetics of neonatal cardiomyopathy.
    Towbin JA; Lipshultz SE
    Curr Opin Cardiol; 1999 May; 14(3):250-62. PubMed ID: 10358797
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mitochondrial DNA mutations and mitochondrial abnormalities in dilated cardiomyopathy.
    Arbustini E; Diegoli M; Fasani R; Grasso M; Morbini P; Banchieri N; Bellini O; Dal Bello B; Pilotto A; Magrini G; Campana C; Fortina P; Gavazzi A; Narula J; ViganĂ² M
    Am J Pathol; 1998 Nov; 153(5):1501-10. PubMed ID: 9811342
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Aspects of molecular mechanisms in myocardial hypertrophy, particular morphological changes and cell bioenergetic characteristics in patients with dilated cardiomyopathy.
    Branishte T; Minciuna V; Braniste A
    Rev Med Chir Soc Med Nat Iasi; 2013; 117(4):851-6. PubMed ID: 24502060
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Novel mutation in the alpha-tropomyosin gene and transition from hypertrophic to hypocontractile dilated cardiomyopathy.
    Regitz-Zagrosek V; Erdmann J; Wellnhofer E; Raible J; Fleck E
    Circulation; 2000 Oct; 102(17):E112-6. PubMed ID: 11044437
    [No Abstract]   [Full Text] [Related]  

  • 14. A homoplasmic mitochondrial transfer ribonucleic acid mutation as a cause of maternally inherited hypertrophic cardiomyopathy.
    Taylor RW; Giordano C; Davidson MM; d'Amati G; Bain H; Hayes CM; Leonard H; Barron MJ; Casali C; Santorelli FM; Hirano M; Lightowlers RN; DiMauro S; Turnbull DM
    J Am Coll Cardiol; 2003 May; 41(10):1786-96. PubMed ID: 12767666
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mitochondrial dysfunction caused by m.2336T>C mutation with hypertrophic cardiomyopathy in cybrid cell lines.
    Li D; Sun Y; Zhuang Q; Song Y; Wu B; Jia Z; Pan H; Zhou H; Hu S; Zhang B; Qiu Y; Dai Y; Chen S; Xu X; Zhu X; Lin A; Huang W; Liu Z; Yan Q
    Mitochondrion; 2019 May; 46():313-320. PubMed ID: 30196098
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Point mutations in mitochondrial DNA in patients with hypertrophic cardiomyopathy.
    Obayashi T; Hattori K; Sugiyama S; Tanaka M; Tanaka T; Itoyama S; Deguchi H; Kawamura K; Koga Y; Toshima H
    Am Heart J; 1992 Nov; 124(5):1263-9. PubMed ID: 1442494
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clinical presentations of mitochondrial cardiomyopathies.
    Lev D; Nissenkorn A; Leshinsky-Silver E; Sadeh M; Zeharia A; Garty BZ; Blieden L; Barash V; Lerman-Sagie T
    Pediatr Cardiol; 2004; 25(5):443-50. PubMed ID: 15185043
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mitochondrial encephalomyopathy with A to G transition of mitochondrial transfer RNA(Leu(UUR)) 3,243 presenting hypertrophic cardiomyopathy.
    Hiruta Y; Chin K; Shitomi K; Ichihara T; Mochizuki M; Adachi K; Obayashi T; Tanaka M; Ozawa T
    Intern Med; 1995 Jul; 34(7):670-3. PubMed ID: 7496082
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Fatal hypertrophic cardiomyopathy associated with an A8296G mutation in the mitochondrial tRNA(Lys) gene.
    Akita Y; Koga Y; Iwanaga R; Wada N; Tsubone J; Fukuda S; Nakamura Y; Kato H
    Hum Mutat; 2000 Apr; 15(4):382. PubMed ID: 10737988
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [The research progress of the association of mitochondrial DNA mutation with cardiomyopathy].
    Lu JJ; Lu HL
    Fa Yi Xue Za Zhi; 2001 Nov; 17(4):242-4, 248. PubMed ID: 12533876
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.