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756 related items for PubMed ID: 7910800

  • 1. 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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  • 2. 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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  • 3. Maternally inherited diabetes and deafness (MIDD): a distinct subtype of diabetes associated with a mitochondrial tRNA(Leu)(UUR) gene point mutation.
    van den Ouweland JM, Lemkes HH, Gerbitz KD, Maassen JA.
    Muscle Nerve Suppl; 1995 Aug; 3():S124-30. PubMed ID: 7603513
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  • 4. 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; 42(4):485-92. PubMed ID: 10230654
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  • 5. Diabetes mellitus carrying a mutation in the mitochondrial tRNA(Leu(UUR)) gene.
    Kishimoto M, Hashiramoto M, Araki S, Ishida Y, Kazumi T, Kanda E, Kasuga M.
    Diabetologia; 1995 Feb; 38(2):193-200. PubMed ID: 7713314
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  • 6. Adult-onset diabetes mellitus and neurosensory hearing loss in maternal relatives of MELAS patients in a family with the tRNA(Leu(UUR)) mutation.
    Remes AM, Majamaa K, Herva R, Hassinen IE.
    Neurology; 1993 May; 43(5):1015-20. PubMed ID: 8492919
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  • 7. A mitochondrial tRNA(Leu)(UUR) mutation at 3,256 associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).
    Sato W, Hayasaka K, Shoji Y, Takahashi T, Takada G, Saito M, Fukawa O, Wachi E.
    Biochem Mol Biol Int; 1994 Aug; 33(6):1055-61. PubMed ID: 7804130
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  • 8. [Pedigree analysis and sequence analysis of mtDNA 12srRNA, tRNA(Leu(UUR)), tRNA(Ser(UCN)) gene in nonsyndromic inherited deafness pedigrees].
    Li W, Han D, Yuan H, Cao J.
    Lin Chuang Er Bi Yan Hou Ke Za Zhi; 2004 Oct; 18(10):582-5, 589. PubMed ID: 15620132
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  • 9. Mitochondrial diabetes mellitus: prevalence and clinical characterization of diabetes due to mitochondrial tRNA(Leu(UUR)) gene mutation in Japanese patients.
    Katagiri H, Asano T, Ishihara H, Inukai K, Anai M, Yamanouchi T, Tsukuda K, Kikuchi M, Kitaoka H, Ohsawa N.
    Diabetologia; 1994 May; 37(5):504-10. PubMed ID: 8056189
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  • 10. Modification defect at anticodon wobble nucleotide of mitochondrial tRNAs(Leu)(UUR) with pathogenic mutations of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes.
    Yasukawa T, Suzuki T, Ueda T, Ohta S, Watanabe K.
    J Biol Chem; 2000 Feb 11; 275(6):4251-7. PubMed ID: 10660592
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  • 11. 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 11; 14(12):1032-7. PubMed ID: 9455930
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  • 12. Mutation in mitochondrial tRNA(Leu(UUR)) gene associated with progressive kidney disease.
    Jansen JJ, Maassen JA, van der Woude FJ, Lemmink HA, van den Ouweland JM, t' Hart LM, Smeets HJ, Bruijn JA, Lemkes HH.
    J Am Soc Nephrol; 1997 Jul 11; 8(7):1118-24. PubMed ID: 9219161
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  • 13. [Detection of a mutation in mitochondrial DNA in a family with sensorineural deafness and diabetes mellitus as the predominant clinical features].
    Tamagawa Y, Tanaka H, Hagiwara H, Ishida T, Kitamura K, Nishizawa M.
    Nihon Jibiinkoka Gakkai Kaiho; 1995 Jul 11; 98(7):1104-10. PubMed ID: 7562231
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  • 18. Detection of low levels of the mitochondrial tRNALeu(UUR) 3243A>G mutation in blood derived from patients with diabetes.
    Procaccio V, Neckelmann N, Paquis-Flucklinger V, Bannwarth S, Jimenez R, Davila A, Poole JC, Wallace DC.
    Mol Diagn Ther; 2006 Jul 11; 10(6):381-9. PubMed ID: 17154655
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