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Journal Abstract Search

129 related items for PubMed ID: 19350514

  • 1. [Prevalence and clinical characteristics of the mitochondrial tRNA(Leu(UUR)) gene 3243 A to G mutation in familial diabetes mellitus in Chinese population].
    Wang SJ, Wu SH, Zheng TS, Wang L, Lu HJ, Xiang KS.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Apr; 26(2):191-5. PubMed ID: 19350514
    [Abstract] [Full Text] [Related]

  • 2. Prevalence and clinical characteristics of mitochondrial tRNA leu(UUR) mt 3243 A-->G and ND-1 gene mt 3316 G-->A mutations in Chinese patients with type 2 diabetes.
    Ji L, Hou X, Han X.
    Chin Med J (Engl); 2001 Nov; 114(11):1205-7. PubMed ID: 11729521
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  • 3. 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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  • 4. [Study on the mitochondrial DNA mutations in familial diabetes mellitus in Chinese population].
    Wang SJ, Wu SH, Zheng TS, Wang L, Lu HJ, Xiang KS.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Feb; 26(1):6-10. PubMed ID: 19199242
    [Abstract] [Full Text] [Related]

  • 5. [Clinical characterizations of familial diabetes mellitus associated with mitochondrial gene mutation].
    Xiu L, Zhang Q, Yu B.
    Zhonghua Yi Xue Za Zhi; 1997 Jun; 77(6):418-21. PubMed ID: 9772504
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  • 6. 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
    [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; 21(2):168-70. PubMed ID: 15079803
    [Abstract] [Full Text] [Related]

  • 8. [Prevalence and clinical characteristics of the A to G variant at position 12026 of the mitochondrial ND4 gene in familial diabetes mellitus in Chinese population].
    Wang SJ, Wu SH, Zheng TS, Yang Z, Lu HJ.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Dec; 23(6):652-4. PubMed ID: 17160945
    [Abstract] [Full Text] [Related]

  • 9. [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]

  • 10. Auditory findings in patients with maternally inherited diabetes and deafness harboring a point mutation in the mitochondrial transfer RNA(Leu) (UUR) gene.
    Yamasoba T, Oka Y, Tsukuda K, Nakamura M, Kaga K.
    Laryngoscope; 1996 Jan; 106(1 Pt 1):49-53. PubMed ID: 8544627
    [Abstract] [Full Text] [Related]

  • 11. 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
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  • 15. Presence of mitochondrial tRNA(Leu(UUR)) A to G 3243 mutation in DNA extracted from serum and plasma of patients with type 2 diabetes mellitus.
    Zhong S, Ng MC, Lo YM, Chan JC, Johnson PJ.
    J Clin Pathol; 2000 Jun; 53(6):466-9. PubMed ID: 10911806
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  • 16. 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 Jun; 3():S124-30. PubMed ID: 7603513
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  • 17. Mitochondrial aldehyde dehydrogenase in diabetes associated with mitochondrial tRNA(Leu(UUR)) mutation at position 3243.
    Suzuki Y, Muramatsu T, Taniyama M, Atsumi Y, Suematsu M, Kawaguchi R, Higuchi S, Asahina T, Murata C, Handa M, Matsuoka K.
    Diabetes Care; 1996 Dec; 19(12):1423-5. PubMed ID: 8941476
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  • 18. 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
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