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Molecular mechanism of pathogenic network for the onset of joint ankylosis with psoriatic dermatitis

Molecular mechanism of pathogenic network for the onset of joint ankylosis with psoriatic dermatitis
银屑病皮炎关节强直发病的致病网络分子机制
批准号:
23659198
负责人:
ONO Masao
金额:
$2.33万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Challenging Exploratory Research
财政年份:
2011
资助国家:
日本
项目状态:
已结题
起止时间:
2011 至 2012

项目摘要

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中文摘要
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英文摘要
Ankylosing arthropathy, such as ankylosing spondylitis, psoriatic arthritis, and so forth, are intractable joint diseases with present therapeutic approaches to other arthropathic disorders. To develop a new effective approach to ankylosing arthropathy, it is necessary to clarify an essential pathogenic mechanism of ankylosis and to obtain evidence for efficacy of a new therapeutic approach in an animal disease model. My previous study had characterized a proper mouse model for the study of human ankylosing diseases. The present study using experimental strains of mice with spontaneous onset of ankylosis showed genetic association of the ankylosis onset, pathogenic contribution of testis to male preponderance of this onset, histopathological characteristics of early to late phases after the ankylosis onset, and therapeutic efficacy of anti-IL-17 administration.
期刊论文(11)
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科研奖励(0)
会议论文
動物モデルの関節強直症に対する抗IL-17抗体投与の抑制効果
抗IL-17抗体给药对动物模型关节强直的抑制作用
DOI: --
发表时间: 2011
期刊:
影响因子: --
作者: [海老原伸, 小野栄夫]
通讯作者: 小野栄夫
A novel autoantibody against fibronectin leucine-rich transmembrane protein 2 expressed on the endothelial cell surface identified by retroviral vector system in systemic lupus erythematosus.
一种针对纤连蛋白亮氨酸亮氨酸的跨膜蛋白2的新型自身抗体,该蛋白2在全身性红斑狼疮的逆转录病毒载体系统鉴定出的内皮细胞表面上表达。
DOI: 10.1186/ar3897
发表时间: 2012-07-02
期刊: Arthritis research & therapy
影响因子: 4.9
作者: [Shirai T, Fujii H, Ono M, Nakamura K, Watanabe R, Tajima Y, Takasawa N, Ishii T, Harigae H]
通讯作者: Harigae H
DOI: 10.1002/art.30485
发表时间: 2011-10-01
期刊: ARTHRITIS AND RHEUMATISM
影响因子: --
作者: [Sato-Hayashizaki, Aya, Ohtsuji, Mareki, Hirose, Sachiko]
通讯作者: Hirose, Sachiko
DOI: 10.1038/onc.2012.336
发表时间: 2013-07-04
期刊: ONCOGENE
影响因子: 8
作者: [Nakanome, A., Brydun, A., Igarashi, K.]
通讯作者: Igarashi, K.
7
    Development of centrifugal isotope separation method using a solution (investigation of fractionation of molybdenum isotopes in a solution by centrifugation)
    • 批准号:
      24760722
    • 项目类别:
      Grant-in-Aid for Young Scientists (B)
    • 资助金额:
      $2.91万
    • 财政年份:
      2012
    • 负责人:
      ONO Masao
    • 依托单位:
    Platelet function and dynamics in various phases of inflammation
    • 批准号:
      19390108
    • 项目类别:
      Grant-in-Aid for Scientific Research (B)
    • 资助金额:
      $12.15万
    • 财政年份:
      2007
    • 负责人:
      ONO Masao
    • 依托单位:
    Functional and therapeutic study on inhibitory genes associated with collagen diseases
    • 批准号:
      16390113
    • 项目类别:
      Grant-in-Aid for Scientific Research (B)
    • 资助金额:
      $9.6万
    • 财政年份:
      2004
    • 负责人:
      ONO Masao
    • 依托单位:
    Development of new cloning method and its application for novel receptor identification in mast cells
    • 批准号:
      13670312
    • 项目类别:
      Grant-in-Aid for Scientific Research (C)
    • 资助金额:
      $2.18万
    • 财政年份:
      2001
    • 负责人:
      ONO Masao
    • 依托单位:
    海外基金