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线粒体基因突变与糖尿病 被引量:1

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出处 《疑难病杂志》 CAS 2007年第5期308-309,共2页 Chinese Journal of Difficult and Complicated Cases
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  • 1Reardon W, Ross RTM. Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA [J]. Lancet, 1992, 340:1376 - 1379.
  • 2Guillausseau PJ, Massin P, Dubois - LaForgue D, et al. Maternally inherited diabetes and deafness : a multicenter study [ J ]. Ann Intern Med, 2001, 134:721-728.
  • 3Van den Ouweland JM, Lemkes HH, Ruitenbeek W, et al. Mutation in mitochondria tRNA^Lew(UUR) gene in a large pedigree with maternally transmitted type 2 diabetes mellitus and deafness [ J ]. Nat Genet, 1992, 1: 368.
  • 4Ji L, Hou X, Han X. Prevalence and clinical characteristics of mito- chondrial tRNA^Lew(UUR) mt 3243 A→G and ND -1 gene mt 3316 G→A mutations in Chinese patients with type 2 diabetes [ J ]. Chin Med J (Engl), 2001, 114 (11): 1905-1207.
  • 5Macdonald MJ, Fahien LA. Glutamate is not a messenger in insulin se- cretion [J]. J Biol Chem, 2000, 275:34025-34027.
  • 6Taylor RW, Chinner PF, Tumbull DM, et al. Selective inhibiton of mutant human mitochondrial DNA replication in vitro by peptide nuclei- caeids [J]. Nat Genet, 1997, 15: 212-215.
  • 7Suzuki S, Hinokio Y, Ohotomo M, et al. The effects of coenzyme QIO treatment on maternally inherited diabetes mellitus and deafness, and mitochondrial DNA 3243 ( A to G ) mutation [ J ]. Diabetologia, 1998, 41 (5): 584-588.
  • 8王乐,于国伟,李倬.我国少数民族2型糖尿病相关基因检测研究[J].疑难病杂志,2009,8(7):446-448. 被引量:4

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