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Journal Abstract Search

125 related items for PubMed ID: 8591702

  • 1. Clinical and laboratory characteristics in the families with diabetes and a mitochondrial tRNA(LEU(UUR)) gene mutation.
    Iwanishi M, Obata T, Yamada S, Maegawa H, Tachikawa-Ide R, Ugi S, Hasegawa M, Kojima H, Oguni T, Toudo R.
    Diabetes Res Clin Pract; 1995 Aug; 29(2):75-82. PubMed ID: 8591702
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  • 3. Clinical manifestations due to a point mutation of the mitochondrial tRNAleu(UUR) gene in five families with diabetes mellitus.
    Shigemoto M, Yoshimasa Y, Yamamoto Y, Hayashi T, Suga J, Inoue G, Okamoto M, Jingami H, Tsuda K, Yamamoto T, Yagura T, Oishi M, Tsujii S, Kuzuya H, Nakao K.
    Intern Med; 1998 Mar; 37(3):265-72. PubMed ID: 9617861
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  • 5. 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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  • 6. Diminished insulin secretory response to glucose but normal insulin and glucagon secretory responses to arginine in a family with maternally inherited diabetes and deafness caused by mitochondrial tRNA(LEU(UUR)) gene mutation.
    Brändle M, Lehmann R, Maly FE, Schmid C, Spinas GA.
    Diabetes Care; 2001 Jul; 24(7):1253-8. PubMed ID: 11423511
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  • 8. Prevalence and clinical characterization of Japanese diabetes mellitus with an A-to-G mutation at nucleotide 3243 of the mitochondrial tRNA(Leu(UUR)) gene.
    Odawara M, Sasaki K, Yamashita K.
    J Clin Endocrinol Metab; 1995 Apr; 80(4):1290-4. PubMed ID: 7714102
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  • 10. Mutation in mitochondrial tRNA(Leu)(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness.
    van den Ouweland JM, Lemkes HH, Ruitenbeek W, Sandkuijl LA, de Vijlder MF, Struyvenberg PA, van de Kamp JJ, Maassen JA.
    Nat Genet; 1992 Aug; 1(5):368-71. PubMed ID: 1284550
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  • 14. Diabetes associated with a novel 3264 mitochondrial tRNA(Leu)(UUR) mutation.
    Suzuki Y, Suzuki S, Hinokio Y, Chiba M, Atsumi Y, Hosokawa K, Shimada A, Asahina T, Matsuoka K.
    Diabetes Care; 1997 Jul; 20(7):1138-40. PubMed ID: 9203451
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  • 15. Mitochondrial tRNA(Leu(UUR)) gene mutation diabetes mellitus in Chinese.
    Xiang K, Wang Y, Wu S, Lu H, Zheng T, Sun D, Weng Q, Jia W, Shen W, Pu L, He J.
    Chin Med J (Engl); 1997 May; 110(5):372-8. PubMed ID: 9594306
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  • 16. Characterization of Japanese families with early-onset type 2 (non-insulin dependent) diabetes mellitus and screening for mutations in the glucokinase and mitochondrial tRNA(Leu(UUR)) genes.
    Iwasaki N, Ohgawara H, Nagahara H, Kawamura M, Bell GI, Omori Y.
    Acta Diabetol; 1995 Mar; 32(1):17-22. PubMed ID: 7542040
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  • 17. Mitochondrial gene mutations that affect the binding of the termination factor and their prevalence among Japanese diabetes mellitus.
    Odawara M, Asano M, Yamashita K.
    Nucleic Acids Symp Ser; 1995 Mar; (34):237-8. PubMed ID: 8841639
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  • 18. Beta-cell function in individuals carrying the mitochondrial tRNA leu (UUR) mutation.
    Salles JE, Kasamatsu TS, Dib SA, Moisés RS.
    Pancreas; 2007 Jan; 34(1):133-7. PubMed ID: 17198195
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