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Journal Abstract Search

209 related items for PubMed ID: 8121460

  • 1. A subtype of diabetes mellitus associated with a mutation of mitochondrial DNA.
    Kadowaki T, Kadowaki H, Mori Y, Tobe K, Sakuta R, Suzuki Y, Tanabe Y, Sakura H, Awata T, Goto Y.
    N Engl J Med; 1994 Apr 07; 330(14):962-8. PubMed ID: 8121460
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  • 2. A G-to-A substitution at nucleotide position 3316 in mitochondrial DNA is associated with Japanese non-insulin-dependent diabetes mellitus.
    Odawara M, Sasaki K, Yamashita K.
    Biochem Biophys Res Commun; 1996 Oct 03; 227(1):147-51. PubMed ID: 8858117
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  • 3. [Clinical characterizations of familial diabetes mellitus associated with mitochondrial gene mutation].
    Xiu L, Zhang Q, Yu B.
    Zhonghua Yi Xue Za Zhi; 1997 Jun 03; 77(6):418-21. PubMed ID: 9772504
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  • 4. 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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  • 5. 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 17; 45(11):1577-83. PubMed ID: 12436342
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  • 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 17; 110(5):372-8. PubMed ID: 9594306
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  • 7. 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 May 17; (34):237-8. PubMed ID: 8841639
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  • 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
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  • 14. 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 01; 113(2):111-6. PubMed ID: 11775531
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  • 16. [A new subtype of diabetes mellitus: maternally inherited diabetes and deafness (MIDD)].
    Maassen JA, Jansen JJ, van den Ouweland JM, Hart LM, van Essen EH, Lemkes HH.
    Ned Tijdschr Geneeskd; 1998 Jan 31; 142(5):229-33. PubMed ID: 9557035
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  • 17. 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 Jan 31; 7(2):246-50. PubMed ID: 11257730
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  • 18. [MELAS associated with diabetes mellitus and point mutation in mitochondrial DNA].
    Onishi H, Inoue K, Osaka H, Nagatomo H, Ando N, Yamada Y, Suzuki K, Hanihara T, Kawamoto S, Okuda K.
    No To Shinkei; 1992 Mar 31; 44(3):259-64. PubMed ID: 1591103
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  • 19. Heritability of diabetes mellitus in Ethiopian diabetics.
    Mengesha B, Abdulkadir J.
    East Afr Med J; 1997 Jan 31; 74(1):37-40. PubMed ID: 9145576
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  • 20. Analysis of diabetic family connection in subjects with insulin-dependent diabetes mellitus (IDDM).
    Quatraro A, Consoli G, Magno M, Caretta F, Ceriello A, Giugliano D.
    Diabete Metab; 1990 Jan 31; 16(5):449-52. PubMed ID: 2073970
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