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Journal Abstract Search

147 related items for PubMed ID: 15079803

  • 1. [Study on mitochondrial DNA gene tRNA(Leu(UUR)) A3243G mutation in type 2 diabetes mellitus].
    Zhang XY, Zhang SL, Ke BS, Jiang ZS, Sun R.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Apr; 21(2):168-70. PubMed ID: 15079803
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  • 3. Search for mitochondrial A3243G tRNA(Leu) mutation in Polish patients with type 2 diabetes mellitus.
    Małecki M, Klupa T, Wanic K, Frey J, Cyganek K, Sieradzki J.
    Med Sci Monit; 2001 Apr; 7(2):246-50. PubMed ID: 11257730
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  • 4. [Mitochondrial DNA 3243, 3316 point mutations and type 2 diabetes mellitus].
    Tang J, Li J, Tian X, Kong Q, Zhang Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Apr; 22(2):198-200. PubMed ID: 15793785
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  • 10. [Diabetes mellitus associated with the A3243G mutation of mitochondrial DNA. Apropos a case].
    Biarnés J, Barrientos A, Ricart W, Nunes V, Fernández-Castañer M, Soler J.
    Med Clin (Barc); 1999 Jan 30; 112(3):99-101. PubMed ID: 10074618
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  • 11. Phenotypic heterogeneity in a Chinese family with mitochondrial disease and A3243G mutation of mitochondrial DNA.
    Thajeb P, Lee HC, Pang CY, Jeng CM, Huang SF, Wei YH.
    Zhonghua Yi Xue Za Zhi (Taipei); 2000 Jan 30; 63(1):71-6. PubMed ID: 10645055
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  • 16. Functional and morphological abnormalities of mitochondria harbouring the tRNA(Leu)(UUR) mutation in mitochondrial DNA derived from patients with maternally inherited diabetes and deafness (MIDD) and progressive kidney disease.
    van den Ouweland JM, Maechler P, Wollheim CB, Attardi G, Maassen JA.
    Diabetologia; 1999 Apr 30; 42(4):485-92. PubMed ID: 10230654
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  • 17. Mutational analysis of the mitochondrial tRNALeu(UUR) gene in Tunisian patients with mitochondrial diseases.
    Mkaouar-Rebai E, Tlili A, Masmoudi S, Belguith N, Charfeddine I, Mnif M, Triki C, Fakhfakh F.
    Biochem Biophys Res Commun; 2007 Apr 20; 355(4):1031-7. PubMed ID: 17336924
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  • 18. [Development of a DNA chip screening mitochondrial DNA mutations in patients with diabetes mellitus].
    Liu SM, Zhou X, Zheng F, Li X, Qin H, Zhang HM, Li D.
    Zhonghua Yi Xue Za Zhi; 2006 Oct 31; 86(40):2853-7. PubMed ID: 17200023
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  • 19. A novel mitochondrial DNA missense mutation at G3421A in a family with maternally inherited diabetes and deafness.
    Chen FL, Liu Y, Song XY, Hu HY, Xu HB, Zhang XM, Shi JH, Hu J, Shen Y, Lu B, Wang XC, Hu RM.
    Mutat Res; 2006 Dec 01; 602(1-2):26-33. PubMed ID: 16949108
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  • 20. Screening of patients with maternally transmitted diabetes for mitochondrial gene mutations in the tRNA[Leu(UUR)] region.
    Tsukuda K, Suzuki Y, Kameoka K, Osawa N, Goto Y, Katagiri H, Asano T, Yazaki Y, Oka Y.
    Diabet Med; 1997 Dec 01; 14(12):1032-7. PubMed ID: 9455930
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