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Journal Abstract Search

381 related items for PubMed ID: 19199257

  • 1. [Analysis of mitochondrial DNA gene tRNALeu(UUR) A3243G mutation in diabetic pedigrees].
    Wang CL, Li F, Hou QZ, Li HZ, Zhang Y, Ning G.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Feb; 26(1):74-7. PubMed ID: 19199257
    [Abstract] [Full Text] [Related]

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

  • 3. Maternally transmitted diabetes mellitus associated with the mitochondrial tRNA(Leu(UUR)) A3243G mutation in a four-generation Han Chinese family.
    Lu J, Wang D, Li R, Li W, Ji J, Zhao J, Ye W, Yang L, Qian Y, Zhu Y, Guan MX.
    Biochem Biophys Res Commun; 2006 Sep 15; 348(1):115-9. PubMed ID: 16876129
    [Abstract] [Full Text] [Related]

  • 4. Mitochondrial 3243 BP mutation: a case report.
    Rigoli L, Caruso RA, Zuccarello D, Rigoli M, Barberi I.
    Diabetes Nutr Metab; 2001 Dec 15; 14(6):343-8. PubMed ID: 11853367
    [Abstract] [Full Text] [Related]

  • 5. Pigmentary retinal dystrophy and the syndrome of maternally inherited diabetes and deafness caused by the mitochondrial DNA 3243 tRNA(Leu) A to G mutation.
    Smith PR, Bain SC, Good PA, Hattersley AT, Barnett AH, Gibson JM, Dodson PM.
    Ophthalmology; 1999 Jun 15; 106(6):1101-8. PubMed ID: 10366077
    [Abstract] [Full Text] [Related]

  • 6. Mitochondrial gene variation in type 2 diabetes mellitus: detection of a novel mutation associated with maternally inherited diabetes in a Chinese family.
    Ma L, Wang H, Chen J, Jin W, Liu L, Ban B, Shen J, Hua Z, Chai J.
    Chin Med J (Engl); 2000 Feb 15; 113(2):111-6. PubMed ID: 11775531
    [Abstract] [Full Text] [Related]

  • 7. [Diabetes mellitus associated with the A3243G mutation of mitochondrial DNA. Apropos a case].
    Biarnés J, Barrientos A, Ricart W, Nunes V, Fernández-Castañer M, Soler J.
    Med Clin (Barc); 1999 Jan 30; 112(3):99-101. PubMed ID: 10074618
    [Abstract] [Full Text] [Related]

  • 8. Prevalence of A-to-G mutation at nucleotide 3243 of the mitochondrial tRNA(Leu(UUR)) gene in Japanese patients with diabetes mellitus and end stage renal disease.
    Iwasaki N, Babazono T, Tsuchiya K, Tomonaga O, Suzuki A, Togashi M, Ujihara N, Sakka Y, Yokokawa H, Ogata M, Nihei H, Iwamoto Y.
    J Hum Genet; 2001 Jan 30; 46(6):330-4. PubMed ID: 11393536
    [Abstract] [Full Text] [Related]

  • 9. A novel mitochondrial DNA missense mutation at G3421A in a family with maternally inherited diabetes and deafness.
    Chen FL, Liu Y, Song XY, Hu HY, Xu HB, Zhang XM, Shi JH, Hu J, Shen Y, Lu B, Wang XC, Hu RM.
    Mutat Res; 2006 Dec 01; 602(1-2):26-33. PubMed ID: 16949108
    [Abstract] [Full Text] [Related]

  • 10. 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
    [Abstract] [Full Text] [Related]

  • 11. Mutational analysis of the mitochondrial tRNALeu(UUR) gene in Tunisian patients with mitochondrial diseases.
    Mkaouar-Rebai E, Tlili A, Masmoudi S, Belguith N, Charfeddine I, Mnif M, Triki C, Fakhfakh F.
    Biochem Biophys Res Commun; 2007 Apr 20; 355(4):1031-7. PubMed ID: 17336924
    [Abstract] [Full Text] [Related]

  • 12. A detailed investigation of maternally inherited diabetes and deafness (MIDD) including clinical characteristics, C-peptide secretion, HLA-DR and -DQ status and autoantibody pattern.
    Hosszúfalusi N, Karcagi V, Horváth R, Palik E, Várkonyi J, Rajczy K, Prohászka Z, Szentirmai C, Karádi I, Romics L, Pánczél P.
    Diabetes Metab Res Rev; 2009 Feb 20; 25(2):127-35. PubMed ID: 19116951
    [Abstract] [Full Text] [Related]

  • 13. 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 Feb 20; 7(2):246-50. PubMed ID: 11257730
    [Abstract] [Full Text] [Related]

  • 14. 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 20; 14(12):1032-7. PubMed ID: 9455930
    [Abstract] [Full Text] [Related]

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  • 17. Maternally-inherited diabetes and deafness: report of two affected German families with the A3243G mitochondrial DNA mutation.
    Thorns C, Widjaja A, Boeck N, Skamira C, Zühlke H.
    Exp Clin Endocrinol Diabetes; 1998 Dec 20; 106(5):384-8. PubMed ID: 9831303
    [Abstract] [Full Text] [Related]

  • 18. [Evolution until death of two members of a family with A3243G mutation and MELAS phenotype versus diabetes mellitus].
    Pérez López-Fraile MI, Barrena R, Montoya J, Marta E.
    Neurologia; 2006 Dec 20; 21(6):327-32. PubMed ID: 16799910
    [Abstract] [Full Text] [Related]

  • 19. Maternally inherited diabetes and deafness: prevalence in a hospital diabetic population.
    Newkirk JE, Taylor RW, Howell N, Bindoff LA, Chinnery PF, Alberti KG, Turnbull DM, Walker M.
    Diabet Med; 1997 Jun 20; 14(6):457-60. PubMed ID: 9212310
    [Abstract] [Full Text] [Related]

  • 20. [Sequence analysis of mtDNA 12S rRNA, tRNA(Leu(UUR)),tRNA(Ser(UCN))and 16S rRNA gene of 12 nonsyndromic inherited deafness pedigrees].
    Li W, Han D, Yuan H, Wang Y, Cao J, Yang W, Jiang S.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Dec 20; 18(6):415-20. PubMed ID: 11774206
    [Abstract] [Full Text] [Related]

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