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Journal Abstract Search

755 related items for PubMed ID: 7910800

  • 21. Mitochondrial gene variation in type 2 diabetes mellitus: detection of a novel mutation associated with maternally inherited diabetes in a Chinese family.
    Ma L, Wang H, Chen J, Jin W, Liu L, Ban B, Shen J, Hua Z, Chai J.
    Chin Med J (Engl); 2000 Feb; 113(2):111-6. PubMed ID: 11775531
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  • 32. Nephropathy and growth hormone deficiency in a patient with mitochondrial tRNA(Leu(UUR)) mutation.
    Yorifuji T, Kawai M, Momoi T, Sasaki H, Furusho K, Muroi J, Shimizu K, Takahashi Y, Matsumura M, Nambu M, Okuno T.
    J Med Genet; 1996 Jul; 33(7):621-2. PubMed ID: 8818955
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  • 33. Progressive sensorineural hearing impairment in maternally inherited diabetes mellitus and deafness (MIDD).
    Hendrickx JJ, Mudde AH, 't Hart LM, Huygen PL, Cremers CW.
    Otol Neurotol; 2006 Sep; 27(6):802-8. PubMed ID: 16788417
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  • 34. Pancreatic beta-cell secretory defect associated with mitochondrial point mutation of the tRNA(LEU(UUR)) gene: a study in seven families with mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS).
    Suzuki S, Hinokio Y, Hirai S, Onoda M, Matsumoto M, Ohtomo M, Kawasaki H, Satoh Y, Akai H, Abe K.
    Diabetologia; 1994 Aug; 37(8):818-25. PubMed ID: 7988784
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  • 36. 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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  • 37. The mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episode syndrome-associated human mitochondrial tRNALeu(UUR) mutation causes aminoacylation deficiency and concomitant reduced association of mRNA with ribosomes.
    Chomyn A, Enriquez JA, Micol V, Fernandez-Silva P, Attardi G.
    J Biol Chem; 2000 Jun 23; 275(25):19198-209. PubMed ID: 10858457
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  • 38. The mitochondrial DNA transfer RNALeu(UUR) A-->G(3243) mutation. A clinical and genetic study.
    Hammans SR, Sweeney MG, Hanna MG, Brockington M, Morgan-Hughes JA, Harding AE.
    Brain; 1995 Jun 23; 118 ( Pt 3)():721-34. PubMed ID: 7600089
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  • 40. Extra-pancreatic manifestations in diabetes secondary to mitochondrial DNA point mutation within the tRNALeu(UUR) gene.
    Vialettes B, Paquis-Fluckinger V, Silvestre-Aillaud P, Ben Dahan D, Pelissier JF, Etchary-Bouyx F, Raccah D, Gin H, Guillausseau PJ, Vanuxen D.
    Diabetes Care; 1995 Jul 23; 18(7):1023-8. PubMed ID: 7555536
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