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应用变性高效液相色谱法检测G6PD基因G392T及C1024T 被引量:1

Detection of G6PDG392T and G6PDC1024T by using denaturing high performance liqid chromatography
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摘要 目的:通过对葡萄糖-6-磷酸脱氢酶(G6PD)基因两种已知突变的检测,观察变性高效液相色谱法(denaturing h igh perform ance liqu id chrom atography,DHPLC)的实用价值。方法:应用DHPLC方法及脱氧核糖核酸序列测定对葡萄糖-6-磷酸脱氢酶缺乏症患者和正常对照者进行已知突变的检测。结果:正常对照者第5、9-10外显子为单峰;G6PDG392T有两个峰,G6PDC1024T则有3个峰。结论:DHPLC方法敏感、自动化、使用方便而且成本低,可能成为今后检测已知和未知突变的重要方法。
出处 《中国病理生理杂志》 CAS CSCD 北大核心 2006年第10期2076-2077,共2页 Chinese Journal of Pathophysiology
关键词 葡糖磷酸脱氢酶缺乏 突变 基因 Glucose phosphate dehydrogenase deficiency Mutation Genes
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  • 1Pai G, Sprenkle J, Do T, et al. Localization of loci for hypoxanthine phosphoribosyl transferase and glucose- 6 -phosphate dehydrogenase and biochemical evidence for nonrandom X - chromosome expression from studies of human X - antosome translocation [ J ]. Proc Natl Acad SciUSA, 1980, 77(5): 2810-2813.
  • 2杜传书 芮琳.红细胞葡萄糖6—磷酸脱氢酶活性的四氮蓝定量测定法[J].中华血液学杂志,1981,2(3):188-192.
  • 3叶文红,杜传书,蒋玮莹,刘鹏,田秋红,陈路明,林群娣.突变特异性扩增系统方法检测葡萄糖-6-磷酸脱氢酶基因C1024T及G392T[J].中华血液学杂志,2003,24(4):214-215. 被引量:1
  • 4Arnold N, Gross E, Schwarz - Boeger U, et al. A highlysensitive, fast, and economical technique for mutation analysis in hereditary breast and ovarian cancers[ J ]. Hum Mutat, 1999, 14(4): 333-339.
  • 5Yamanoshita O, Kubota T, Hou J, et al. DHPLC is superior to SSCP in screening p53 mutations esophageal cancer tissues[J]. Int JCaneer, 2005, 114(1): 74 -79.
  • 6Castro RM, Landemberger MC, Walz R, et al. High capacity and low cost detection of prion protein variant allelesby denaturing HPLC[ J ]. J Neurosci Methods, 2004, 139(2) : 263 - 269.

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  • 1郑敏,罗建明.葡萄糖-6-磷酸脱氢酶基因突变的研究进展[J].医学综述,2005,11(3):266-268. 被引量:13
  • 2Chen EY, Cheng A, Lee A, et al. Sequence of human glucose6-phosphate dehydrogenase cloned in plasmids and a yeast artificial chromosome. Genomics, 1991, 10:792-800.
  • 3Luzzatto L. Glucose 6-phosphate dehydrogenase deficiency : from genotype to phenotype. Haematologica, 2006, 91 ( 10 ) : 1303- 1306.
  • 4WHO Working Group. Glucose-6-phosphate dehydrogenase deficiency. Bull WHO, 1989, 67:601-611.
  • 5Alison AC. Glucose-6-phosphate dehydrogenase deficiency in red blood cells of East Africans. Nature, 1960,186:531-532.
  • 6Yenchitsomanus P, Sumers KM, Board PG, et al. Alpha thalassaemia in Papua New Guinea. Hum Genet, 1986,74:432.
  • 7Stamatoyannopoulos G, Panayotopoulos A, Motulsky AG. The distribution of glucose-6-phosphate dehydrogenase deficiency in Greece. Am J Hum Genet, 1966, 18:296.
  • 8Siniscalco M, Bernini L, Filippi G, et al. Population genetics of haemoglobin variants, thalassaemia and glucose-6-phosphate dehydrogenase deficiency, with particular reference to the malaria hypothesis. Bull WHO, 1966,34:379-393.
  • 9Ruwende C, Khoo SC, Snow RW, et al. Natural selection of hemi-and heterozygotes for G6PD deficiency in Africa by resistance to severe malaria. Nature, 1995, 376: 246-249.
  • 10Ruwende C, Hill A. Glucose-6-phosphate dehydrogenase deficiency and malaria. J Mol Med, 1998,76:581-588.

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