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Analysis of susceptible genes of fatty liver

Analysis of susceptible genes of fatty liver
脂肪肝易感基因分析
批准号:
11670503
负责人:
YAMATO Eiji
金额:
$2.3万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
1999
资助国家:
日本
项目状态:
已结题
起止时间:
1999 至 2000

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中文摘要
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英文摘要
We have developed NSY mice which are models of type 2 diabetes mellitus. These mice are also developed fatty liver in time-dependent manner. In this research, we have isolated the genes which showed the differential expression in the fatty liver of NSY mice in comparison with the genes expressed in the liver in C3H/He mice using PCR-based cDNA subtraction method which we had already developed. The earlier method analyzed the BamHI fragment to avoid the undesirable bias of PCR-amplification by difference of DNA length. However this method may cause pseudo-negative cDNA because only BamHI fragments had been analyzed. Thus, in this study, we analyzed not only BamHI fragments, but also HindIII fragments of cDNA of the liver.ResultsBamHI fragmentNSY liver dominant-genes : 3 clones, glucuronosyltransferase, human EST, 1 unknown geneC3H dominant-genes : 4 clones, TFII-I, DRPLA, collagen typeIV, 1 unknown geneHindIII fragmentNSY liver dominant-genes : 3 unknown clonesC3H dominant-genes : 5 clones, Ser/Thr phosphatase, HMG CoA reductase, translation initiation factor, IAP, 1 unknown geneAlong with this subtraction analysis, the study on the position of the susceptible gene of fatty liver by linkage analysis using the crossing of NSY mice with C3H/He mice are now on going. The results of the subtraction analysis will lead a susceptible gene for fatty liver in combination with the linkage analysis.
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会议论文
Ueda H.: "Age-dependent changes in phenotypes and candidate gene analysis in a polygenic animal medel of type II diabetes ; NSY mouse."Diabetologia. 43. 932-938 (2000)
Ueda H.:“II 型糖尿病多基因动物模型中表型的年龄依赖性变化和候选基因分析;NSY 小鼠。”Diabetologia。
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Hattori M.: "Homologous recombination of the MHC class I K region defines new MHC-linked diabetogenic susceptibility gene (s) in NOD mice."J Immunol. 163. 1721-1724 (1999)
Hattori M.:“MHC I 类 K 区域的同源重组定义了 NOD 小鼠中新的 MHC 相关的糖尿病易感基因。”J 免疫学杂志。
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Fujisawa T: "Length rather than a specific allele of dinucleotide repeat in 5'upstream region of aldose reductase gene is associated with diabetic retinopathy."Diabetic Med. 16. 1044-1047 (1999)
Fujisawa T:“醛糖还原酶基因 5 上游区域的二核苷酸重复序列的长度而不是特定等位基因与糖尿病视网膜病变相关。”糖尿病医学。
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Ueda H.et.al.: "Genetic analysis of late-onset type 2 diabetes in a mouse model of human complex trait"Diabetes. 48. 1168-1174 (1999)
Ueda H.et.al.:“人类复杂性状小鼠模型中迟发性 2 型糖尿病的基因分析”糖尿病。
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16
    Analysis of Foxo1-regulated genes using Foxo1-deficient pancreatic beta cells
    Research on differentiation of endodermal cells from ES cells by introducing genes of transcription factor
    • 批准号:
      15609004
    • 项目类别:
      Grant-in-Aid for Scientific Research (C)
    • 资助金额:
      $2.3万
    • 财政年份:
      2003
    • 负责人:
      YAMATO Eiji
    • 依托单位:
    海外基金