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Journal Abstract Search

141 related items for PubMed ID: 7882812

  • 1. Diabetes with mitochondrial gene tRNALYS mutation.
    Suzuki S, Hinokio Y, Hirai S, Onoda M, Matsumoto M, Ohtomo M, Kawasaki H, Satoh Y, Akai H, Abe K.
    Diabetes Care; 1994 Dec; 17(12):1428-32. PubMed ID: 7882812
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. 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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  • 4. 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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  • 5. [Clinical characterization of diabetes mellitus in the families with mitochondrial encephalomyopathies].
    Suzuki S.
    Nihon Rinsho; 1994 Oct; 52(10):2606-10. PubMed ID: 7527090
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  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. Novel mitochondrial DNA mutation in tRNA(Lys) (8296A-->G) associated with diabetes.
    Kameoka K, Isotani H, Tanaka K, Azukari K, Fujimura Y, Shiota Y, Sasaki E, Majima M, Furukawa K, Haginomori S, Kitaoka H, Ohsawa N.
    Biochem Biophys Res Commun; 1998 Apr 17; 245(2):523-7. PubMed ID: 9571188
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  • 9. Impaired insulin secretion in Japanese diabetic subjects with an A-to-G mutation at nucleotide 8296 of the mitochondrial DNA in tRNA(Lys).
    Kameoka K, Isotani H, Tanaka K, Kitaoka H, Ohsawa N.
    Diabetes Care; 1998 Nov 17; 21(11):2034-5. PubMed ID: 9802769
    [No Abstract] [Full Text] [Related]

  • 10. Quantification of mitochondrial DNA carrying the tRNA(8344Lys) point mutation in myoclonus epilepsy and ragged-red-fiber disease.
    Suomalainen A, Kollmann P, Octave JN, Söderlund H, Syvänen AC.
    Eur J Hum Genet; 1993 Nov 17; 1(1):88-95. PubMed ID: 8069655
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  • 11. 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 17; 37(3):265-72. PubMed ID: 9617861
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  • 13. A double mutation (A8296G and G8363A) in the mitochondrial DNA tRNA (Lys) gene associated with myoclonus epilepsy with ragged-red fibers.
    Arenas J, Campos Y, Bornstein B, Ribacoba R, Martín MA, Rubio JC, Santorelli FM, Zeviani M, DiMauro S, Garesse R.
    Neurology; 1999 Jan 15; 52(2):377-82. PubMed ID: 9932960
    [Abstract] [Full Text] [Related]

  • 14. The mitochondrial DNA transfer RNA(Lys)A-->G(8344) mutation and the syndrome of myoclonic epilepsy with ragged red fibres (MERRF). Relationship of clinical phenotype to proportion of mutant mitochondrial DNA.
    Hammans SR, Sweeney MG, Brockington M, Lennox GG, Lawton NF, Kennedy CR, Morgan-Hughes JA, Harding AE.
    Brain; 1993 Jun 15; 116 ( Pt 3)():617-32. PubMed ID: 8513395
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  • 16. Phenotypic heterogeneity in families with the myoclonic epilepsy and ragged-red fiber disease point mutation in mitochondrial DNA.
    Graf WD, Sumi SM, Copass MK, Ojemann LM, Longstreth WT, Shanske S, Lombes A, DiMauro S.
    Ann Neurol; 1993 Jun 15; 33(6):640-5. PubMed ID: 8388680
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  • 17. Mitochondrial DNA mutations are associated with both decreased insulin secretion and advanced microvascular complications in Japanese diabetic subjects.
    Fukuda M, Nakano S, Imaizumi N, Kitazawa M, Nishizawa M, Kigoshi T, Uchida K.
    J Diabetes Complications; 1999 Jun 15; 13(5-6):277-83. PubMed ID: 10765002
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  • 18. MtDNA mutation in MERRF syndrome causes defective aminoacylation of tRNA(Lys) and premature translation termination.
    Enriquez JA, Chomyn A, Attardi G.
    Nat Genet; 1995 May 15; 10(1):47-55. PubMed ID: 7647790
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  • 19. 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 15; 20(7):1138-40. PubMed ID: 9203451
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