BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

163 related articles for article (PubMed ID: 2143377)

  • 1. 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]  

  • 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. [Multiple mitochondrial DNA deletions in cardiomyopathy].
    Hattori K
    Nihon Rinsho; 1993 Jun; 51(6):1429-34. PubMed ID: 8320825
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Molecular basis of hypertrophic and dilated cardiomyopathy.
    Marian AJ; Roberts R
    Tex Heart Inst J; 1994; 21(1):6-15. PubMed ID: 8180512
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Specific mitochondrial DNA deletions in idiopathic dilated cardiomyopathy.
    Marin-Garcia J; Goldenthal MJ; Ananthakrishnan R; Pierpont ME; Fricker FJ; Lipshultz SE; Perez-Atayde A
    Cardiovasc Res; 1996 Feb; 31(2):306-13. PubMed ID: 8730408
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mitochondrial DNA deletions in dilated cardiomyopathy: a clinical study employing endomyocardial sampling.
    Remes AM; Hassinen IE; Ikäheimo MJ; Herva R; Hirvonen J; Peuhkurinen KJ
    J Am Coll Cardiol; 1994 Mar; 23(4):935-42. PubMed ID: 8106699
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Inherited idiopathic dilated cardiomyopathy with multiple deletions of mitochondrial DNA.
    Suomalainen A; Paetau A; Leinonen H; Majander A; Peltonen L; Somer H
    Lancet; 1992 Nov; 340(8831):1319-20. PubMed ID: 1360038
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Mitochondrial DNA deletions in cardiomyopathies.
    Ruppert V; Maisch B
    Herz; 2000 May; 25(3):161-7. PubMed ID: 10904834
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Significant existence of deleted mitochondrial DNA in cirrhotic liver surrounding hepatic tumor.
    Yamamoto H; Tanaka M; Katayama M; Obayashi T; Nimura Y; Ozawa T
    Biochem Biophys Res Commun; 1992 Jan; 182(2):913-20. PubMed ID: 1310403
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Both hypertrophic and dilated cardiomyopathies are caused by mutation of the same gene, delta-sarcoglycan, in hamster: an animal model of disrupted dystrophin-associated glycoprotein complex.
    Sakamoto A; Ono K; Abe M; Jasmin G; Eki T; Murakami Y; Masaki T; Toyo-oka T; Hanaoka F
    Proc Natl Acad Sci U S A; 1997 Dec; 94(25):13873-8. PubMed ID: 9391120
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Mitochondrial DNA mutations in patients with myocardial diseases].
    Li YY; Xu J; Zhang JN
    Zhonghua Yi Xue Za Zhi; 1994 Jun; 74(6):345-8, 350. PubMed ID: 7994642
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Novel locus for an inherited cardiomyopathy maps to chromosome 7.
    Song L; DePalma SR; Kharlap M; Zenovich AG; Cirino A; Mitchell R; McDonough B; Maron BJ; Seidman CE; Seidman JG; Ho CY
    Circulation; 2006 May; 113(18):2186-92. PubMed ID: 16651466
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mitochondrial DNA mutations and disturbances of energy metabolism in myocardium.
    Ozawa T; Sugiyama S; Tanaka M; Hattori K
    Jpn Circ J; 1991 Nov; 55(11):1158-64. PubMed ID: 1749073
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genotype phenotype correlations of cardiac beta-myosin heavy chain mutations in Indian patients with hypertrophic and dilated cardiomyopathy.
    Rai TS; Ahmad S; Bahl A; Ahuja M; Ahluwalia TS; Singh B; Talwar KK; Khullar M
    Mol Cell Biochem; 2009 Jan; 321(1-2):189-96. PubMed ID: 18953637
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Cardiomyopathy: molecular and immunological aspects (review).
    Takeda N
    Int J Mol Med; 2003 Jan; 11(1):13-6. PubMed ID: 12469210
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 9.