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The causative genes for allergy and clinical use.

The causative genes for allergy and clinical use.
过敏的致病基因和临床应用。
批准号:
10557075
负责人:
KONDO Naomi
金额:
$8.45万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (B).
财政年份:
1998
资助国家:
日本
项目状态:
已结题
起止时间:
1998 至 2000

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中文摘要
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英文摘要
The causative genes of allergy have been newly found and have been structurally analyzed.(1) In B cellsI ε region, S ε region and C ε region of Ig gene have been analyzed in the patients with allergy. As a result, it becomes clear that chromatin of I ε region is more open in the patients with allergy.(2) In T cellsThe mutations of IL-12 receptor β2 chain gene have been identified as one of the causative genes for allergy. Some patients with high levels of IgE production had the mutations of IL-12 receptor β2 chain gene. IL-12 was not able to inhibit IgE production of the patients' peripheral blood mononuclear cells. Therefore, it was indicated that these mutations induced high levels of IgE production and allergic reactions.Next, the mutations of IL-18 receptor α2 chain gene have been identified as the causative gene for allergy. Some patients with high levels of IgE production had the mutations of IL- 18 receptor α2 chain gene. IL-18 was not able to inhibit IgE production of the patients' peripheral blood mononuclear cells. Therefore, it was indicated that these mutations also induced high levels of IgE production and allergic reactions.Moreover, we have published the information of structure of IL-18 protein by NMR.Furthermore, we have published the genetical classification of atopy for clinical or prevention of allergy.
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Kondo N, et al.: "Reduced interferon gamma production by antigen stimulated cord blood mononuclear cells is a risk factor of allergic disorders. -6-year follow-up study."Clin Exp Allirgy. 28. 1340-1344 (1998)
Kondo N 等人:“抗原刺激的脐带血单核细胞产生的干扰素 γ 减少是过敏性疾病的危险因素。-6 年随访研究。”Clin Exp Allirgy。
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Tashita H, Kondo N, et al.: "Molecular basis of selective IgG2 deficiency: The mutated membrane-bound form of γ2 heavy chain caused complete IgG2 deficiency in two Japanese siblings"J Clin Invest. 101. 677-681 (1998)
Tashita H、Kondo N 等人:“选择性 IgG2 缺陷的分子基础:γ2 重链的突变膜结合形式导致两个日本兄弟姐妹完全 IgG2 缺陷”J Clin Invest。101. 677-681 (1998)
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通讯作者:
Kondo N, et al.: "Atopy and mutations of IL-12 receptor β2 chain gene."Clin Exp Allergy. (in press). (2001)
Kondo N 等人:“IL-12 受体 β2 链基因的特应性和突变。”Clin Exp Allergy(出版中)。
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通讯作者:
Fukao T, Kondo N et al: "Atayia telangiectasia in the Japanese population : identification of R1917X,W2491R,R2909G,IVS33+2T+A,and 788del5,the latter two being relatively common mutations." Hum Mutat. 12. 338-343 (1998)
Fukao T、Kondo N 等人:“日本人群中的 Atayia 毛细血管扩张症:R1917X、W2491R、R2909G、IVS33 2T A 和 788del5 的鉴定,后两个是相对常见的突变。”
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22
    Personalized prediction and prevention of allergic diseases
    • 批准号:
      15K11744
    • 项目类别:
      Grant-in-Aid for Scientific Research (C)
    • 资助金额:
      $2.75万
    • 财政年份:
      2015
    • 负责人:
      KONDO Naomi
    • 依托单位:
    Molecular genetics and proteomics for gene-environmental relationship in allergy
    • 批准号:
      21591358
    • 项目类别:
      Grant-in-Aid for Scientific Research (C)
    • 资助金额:
      $2.91万
    • 财政年份:
      2009
    • 负责人:
      KONDO Naomi
    • 依托单位:
    Structure biology for the causative genes of atopy and order-made therapy in the environment.
    • 批准号:
      13470163
    • 项目类别:
      Grant-in-Aid for Scientific Research (B)
    • 资助金额:
      $9.22万
    • 财政年份:
      2001
    • 负责人:
      KONDO Naomi
    • 依托单位:
    THE FUNCTION OF RECQ HELICASE GENE FAMILY IN DNA RECOMBINATION AND JOINING
    • 批准号:
      10216204
    • 项目类别:
      Grant-in-Aid for Scientific Research on Priority Areas
    • 资助金额:
      $23.04万
    • 财政年份:
      1998
    • 负责人:
      KONDO Naomi
    • 依托单位:
    国内基金
    海外基金
    Th1/Th2细胞失衡模式在分泌性中耳炎发病机制中作用的研究
    • 批准号:
      81070777
    • 项目类别:
      面上项目
    • 资助金额:
      32.0万元
    • 批准年份:
      2010
    • 负责人:
      赵守琴
    • 依托单位: