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Journal Abstract Search

230 related items for PubMed ID: 8603770

  • 1. Clinical phenotypes, insulin secretion, and insulin sensitivity in kindreds with maternally inherited diabetes and deafness due to mitochondrial tRNALeu(UUR) gene mutation.
    Velho G, Byrne MM, Clément K, Sturis J, Pueyo ME, Blanché H, Vionnet N, Fiet J, Passa P, Robert JJ, Polonsky KS, Froguel P.
    Diabetes; 1996 Apr; 45(4):478-87. PubMed ID: 8603770
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  • 2. 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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  • 3. Insulin sensitivity in patients with NIDDM and the A-to-G mutation at nucleotide 3,243 of the mitochondrial tRNALeu(UUR) gene.
    Iwasaki N, Wasada T, Takahashi Y, Babazono T, Ohgawara H, Omori Y.
    Diabetes Care; 1995 Jun; 18(6):886-8. PubMed ID: 7555525
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  • 4. Beta-cell loss and glucose induced signalling defects in diabetes mellitus caused by mitochondrial tRNALeu(UUR) gene mutation.
    Oka Y, Katagiri H, Ishihara H, Asano T, Kobayashi T, Kikuchi M.
    Diabet Med; 1996 Sep; 13(9 Suppl 6):S98-102. PubMed ID: 8894492
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  • 5. Insulin secretion and insulin sensitivity are normal in non-diabetic subjects from maternal inheritance diabetes and deafness families.
    Holmes-Walker DJ, Ward GM, Boyages SC.
    Diabet Med; 2001 May; 18(5):381-7. PubMed ID: 11472449
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  • 7. Maternally inherited diabetes and deafness is a distinct subtype of diabetes and associates with a single point mutation in the mitochondrial tRNA(Leu(UUR)) gene.
    van den Ouweland JM, Lemkes HH, Trembath RC, Ross R, Velho G, Cohen D, Froguel P, Maassen JA.
    Diabetes; 1994 Jun; 43(6):746-51. PubMed ID: 7910800
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  • 10. Does mitochondrial genome mutation in subjects with maternally inherited diabetes and deafness decrease severity of diabetic retinopathy?
    Holmes-Walker DJ, Mitchell P, Boyages SC.
    Diabet Med; 1998 Nov; 15(11):946-52. PubMed ID: 9827849
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  • 11. Lack of control by glucose of ultradian insulin secretory oscillations in impaired glucose tolerance and in non-insulin-dependent diabetes mellitus.
    O'Meara NM, Sturis J, Van Cauter E, Polonsky KS.
    J Clin Invest; 1993 Jul; 92(1):262-71. PubMed ID: 8325993
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  • 13. Altered insulin secretory responses to glucose in diabetic and nondiabetic subjects with mutations in the diabetes susceptibility gene MODY3 on chromosome 12.
    Byrne MM, Sturis J, Menzel S, Yamagata K, Fajans SS, Dronsfield MJ, Bain SC, Hattersley AT, Velho G, Froguel P, Bell GI, Polonsky KS.
    Diabetes; 1996 Nov; 45(11):1503-10. PubMed ID: 8866553
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  • 14. Disruption of circadian insulin secretion is associated with reduced glucose uptake in first-degree relatives of patients with type 2 diabetes.
    Boden G, Chen X, Polansky M.
    Diabetes; 1999 Nov; 48(11):2182-8. PubMed ID: 10535452
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  • 16. 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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  • 17. 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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  • 18. Insulin resistance associated with maternally inherited diabetes and deafness.
    Gebhart SS, Shoffner JM, Koontz D, Kaufman A, Wallace D.
    Metabolism; 1996 Apr; 45(4):526-31. PubMed ID: 8609843
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