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Journal Abstract Search

120 related items for PubMed ID: 9344764

  • 1. Point mutations in mitochondrial DNA of patients with dilated cardiomyopathy.
    Li YY, Maisch B, Rose ML, Hengstenberg C.
    J Mol Cell Cardiol; 1997 Oct; 29(10):2699-709. PubMed ID: 9344764
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  • 3. 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
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  • 4. 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, Viganò M.
    Am J Pathol; 1998 Nov; 153(5):1501-10. PubMed ID: 9811342
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  • 5. [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
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  • 6. Concerted action of two novel tRNA mtDNA point mutations in chronic progressive external ophthalmoplegia.
    Kornblum C, Zsurka G, Wiesner RJ, Schröder R, Kunz WS.
    Biosci Rep; 2008 Apr; 28(2):89-96. PubMed ID: 18384291
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  • 9. The mitochondrial DNA mutation T12297C affects a highly conserved nucleotide of tRNA(Leu(CUN)) and is associated with dilated cardiomyopathy.
    Grasso M, Diegoli M, Brega A, Campana C, Tavazzi L, Arbustini E.
    Eur J Hum Genet; 2001 Apr; 9(4):311-5. PubMed ID: 11313776
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  • 10. 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
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  • 13. A novel mitochondrial DNA tRNAIle (m.4322dupC) mutation associated with idiopathic dilated cardiomyopathy.
    Mahjoub S, Sternberg D, Boussaada R, Filaut S, Gmira F, Mechmech R, Jardel C, Arab SB.
    Diagn Mol Pathol; 2007 Dec; 16(4):238-42. PubMed ID: 18043288
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  • 15. Dilated cardiomyopathy and atrioventricular conduction blocks induced by heart-specific inactivation of mitochondrial DNA gene expression.
    Wang J, Wilhelmsson H, Graff C, Li H, Oldfors A, Rustin P, Brüning JC, Kahn CR, Clayton DA, Barsh GS, Thorén P, Larsson NG.
    Nat Genet; 1999 Jan; 21(1):133-7. PubMed ID: 9916807
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  • 16. [Multiple sclerosis and Leber's hereditary optic neuropathy mitochondrial DNA mutations].
    Pénisson-Besnier I, Moreau C, Jacques C, Roger JC, Dubas F, Reynier P.
    Rev Neurol (Paris); 2001 May; 157(5):537-41. PubMed ID: 11438773
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  • 18. Novel mitochondrial 16S rRNA mutation, 3200T-->C, associated with adult-onset type 2 diabetes.
    Yang T, Lam CW, Tsang MW, Tong SF, Kam GY, Chan LY, Poon PM, Wu X, Pang CP.
    Chin Med J (Engl); 2002 May; 115(5):753-8. PubMed ID: 12133550
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  • 19. Age-related mitochondrial DNA point mutations in patients with mitochondrial myopathy.
    da Costa CK, Kiyomoto BH, Schmidt B, Oliveira AS, Gabbai AA, Tengan CH.
    J Neurol Sci; 2007 Dec 15; 263(1-2):139-44. PubMed ID: 17698085
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  • 20. Detection of mitochondrial DNA mutations using temporal temperature gradient gel electrophoresis.
    Wong LJ, Chen TJ, Tan DJ.
    Electrophoresis; 2004 Aug 15; 25(15):2602-10. PubMed ID: 15300781
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