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Journal Abstract Search

339 related items for PubMed ID: 9571188

  • 21. Presence of a major WFS1 mutation in Spanish Wolfram syndrome pedigrees.
    Gómez-Zaera M, Strom TM, Rodríguez B, Estivill X, Meitinger T, Nunes V.
    Mol Genet Metab; 2001 Jan; 72(1):72-81. PubMed ID: 11161832
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  • 22. Prevalence and clinical characteristics of maternally inherited diabetes and deafness caused by the mt3243A > G mutation in young adult diabetic subjects in Sri Lanka.
    Katulanda P, Groves CJ, Barrett A, Sheriff R, Matthews DR, McCarthy MI, Gloyn AL.
    Diabet Med; 2008 Mar; 25(3):370-4. PubMed ID: 18279408
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  • 23. 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 Mar; 7(2):246-50. PubMed ID: 11257730
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  • 24. 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; 14(12):1032-7. PubMed ID: 9455930
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  • 27. 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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  • 28. A pilot study of mitochondrial DNA point mutation A3243G in a sample of Croatian patients having type 2 diabetes mellitus associated with maternal inheritance.
    Martin-Kleiner I, Pape-Medvidović E, Pavlić-Renar I, Metelko Z, Kusec R, Gabrilovac J, Boranić M.
    Acta Diabetol; 2004 Dec; 41(4):179-84. PubMed ID: 15660201
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  • 29. The effects of coenzyme Q10 treatment on maternally inherited diabetes mellitus and deafness, and mitochondrial DNA 3243 (A to G) mutation.
    Suzuki S, Hinokio Y, Ohtomo M, Hirai M, Hirai A, Chiba M, Kasuga S, Satoh Y, Akai H, Toyota T.
    Diabetologia; 1998 May; 41(5):584-8. PubMed ID: 9628277
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  • 30. Accumulation of somatic mutation in mitochondrial DNA extracted from peripheral blood cells in diabetic patients.
    Nomiyama T, Tanaka Y, Hattori N, Nishimaki K, Nagasaka K, Kawamori R, Ohta S.
    Diabetologia; 2002 Nov; 45(11):1577-83. PubMed ID: 12436342
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  • 33. Mitochondrial DNA variations in patients with maternally inherited diabetes and deafness syndrome.
    Perucca-Lostanlen D, Narbonne H, Hernandez JB, Staccini P, Saunieres A, Paquis-Flucklinger V, Vialettes B, Desnuelle C.
    Biochem Biophys Res Commun; 2000 Nov 02; 277(3):771-5. PubMed ID: 11062027
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  • 34. [Association of mitochondrial DNA variation with type 2 diabetes mellitus].
    Tang DL, Zhou X, Zhou KY, Li X, Zhao L, Liu F, Zheng F, Liu SM.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Dec 02; 22(6):636-40. PubMed ID: 16331560
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  • 35. A novel mitochondrial point mutation in a maternal pedigree with sensorineural deafness.
    Reid FM, Vernham GA, Jacobs HT.
    Hum Mutat; 1994 Dec 02; 3(3):243-7. PubMed ID: 8019558
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  • 36. Novel mitochondrial DNA length variants and genetic instability in a family with diabetes and deafness.
    Janssen GM, Neu A, 't Hart LM, van de Sande CM, Antonie Maassen J.
    Exp Clin Endocrinol Diabetes; 2006 Apr 02; 114(4):168-74. PubMed ID: 16705548
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  • 39. Level of heteroplasmy for the mitochondrial mutation A3243G correlates with age at onset of diabetes and deafness.
    Olsson C, Zethelius B, Lagerström-Fermér M, Asplund J, Berne C, Landegren U.
    Hum Mutat; 1998 Apr 02; 12(1):52-8. PubMed ID: 9633820
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  • 40. New insights in the molecular pathogenesis of the maternally inherited diabetes and deafness syndrome.
    Maassen JA, Jahangir Tafrechi RS, Janssen GM, Raap AK, Lemkes HH, 't Hart LM.
    Endocrinol Metab Clin North Am; 2006 Jun 02; 35(2):385-96, x-xi. PubMed ID: 16632100
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