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Journal Abstract Search

386 related items for PubMed ID: 11257730

  • 1. 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; 7(2):246-50. PubMed ID: 11257730
    [Abstract] [Full Text] [Related]

  • 2. 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; 106(6):1101-8. PubMed ID: 10366077
    [Abstract] [Full Text] [Related]

  • 3. [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]

  • 4. 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 30; 113(2):111-6. PubMed ID: 11775531
    [Abstract] [Full Text] [Related]

  • 5. 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 30; 14(6):457-60. PubMed ID: 9212310
    [Abstract] [Full Text] [Related]

  • 6. 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 30; 110(5):372-8. PubMed ID: 9594306
    [Abstract] [Full Text] [Related]

  • 7. [Study on mitochondrial DNA gene tRNA(Leu(UUR)) A3243G mutation in type 2 diabetes mellitus].
    Zhang XY, Zhang SL, Ke BS, Jiang ZS, Sun R.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Apr 30; 21(2):168-70. PubMed ID: 15079803
    [Abstract] [Full Text] [Related]

  • 8. 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 30; 1(5):368-71. PubMed ID: 1284550
    [Abstract] [Full Text] [Related]

  • 9. [Mitochondrial DNA 3243, 3316 point mutations and type 2 diabetes mellitus].
    Tang J, Li J, Tian X, Kong Q, Zhang Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Apr 30; 22(2):198-200. PubMed ID: 15793785
    [Abstract] [Full Text] [Related]

  • 10. 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 30; 14(12):1032-7. PubMed ID: 9455930
    [Abstract] [Full Text] [Related]

  • 11. Progressive sensorineural hearing impairment in maternally inherited diabetes mellitus and deafness (MIDD).
    Hendrickx JJ, Mudde AH, 't Hart LM, Huygen PL, Cremers CW.
    Otol Neurotol; 2006 Sep 30; 27(6):802-8. PubMed ID: 16788417
    [Abstract] [Full Text] [Related]

  • 12. Search for mitochondrial DNA mutation at position 3243 in German patients with a positive family history of maternal diabetes mellitus.
    Klemm T, Neumann S, Trülzsch B, Pistrosch F, Hanefeld M, Paschke R.
    Exp Clin Endocrinol Diabetes; 2001 Sep 30; 109(5):283-7. PubMed ID: 11507652
    [Abstract] [Full Text] [Related]

  • 13. 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 30; 15(11):946-52. PubMed ID: 9827849
    [Abstract] [Full Text] [Related]

  • 14. Mitochondrial gene mutations that affect the binding of the termination factor and their prevalence among Japanese diabetes mellitus.
    Odawara M, Asano M, Yamashita K.
    Nucleic Acids Symp Ser; 1995 Nov 30; (34):237-8. PubMed ID: 8841639
    [Abstract] [Full Text] [Related]

  • 15. 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]

  • 16. 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 Dec 01; 46(6):330-4. PubMed ID: 11393536
    [Abstract] [Full Text] [Related]

  • 17. 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
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