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Moleculer mechanisms of cell differentiation and morphogenesis during early animal development

Moleculer mechanisms of cell differentiation and morphogenesis during early animal development
动物早期发育过程中细胞分化和形态发生的分子机制
批准号:
07408023
负责人:
ASASHIMA Makoto
金额:
$22.78万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (A)
财政年份:
1995
资助国家:
日本
项目状态:
已结题
起止时间:
1995 至 1997

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中文摘要
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英文摘要
We got many important results about the morphogenesis and cell differentiation using the amphibian embryos. (1) After the treatment of activin A on animal caps, we made subtraction methods to clone the neurogenesis-related genes. And we cloned and analyzed the new genes such as Xran, XHMG-2, XIRF-6, XFRP,XGS,XNLRR-1. (2) In vitro system, we succeeded to make the head structure and trunk-tail structures. These structures were made with sandwith methods, in which the activin-treated ectoderm was combined. Depend on the pre-culture time, the induced structures were different. (3) Some kinds of genes which were related with pronephros (kidney) formation were cloned and analyzed. These genes were Na-K-ATPase alpha-subunit, CIRP,XFKBP,and the expression patterns of these genes are examined. (4) Incorporations of activin, follistatin and vitellogenin were examined using the labeling of these substance with ^<125>I and gold colloid particles. (5) Treatment with high concentration of activin to animal cap induced the beating heart, and expressed many kinds of endodermal marker genes. (6) Vitellogenin receptor during oogenesis was also cloned and analyzed. Above these data were very important to understand the cell differentiation and morphogenesis at the molecular level during animal development.
期刊论文(27)
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会议论文
Ariizumi, T., et al.: "Activin treated urodele ectoderm:A model experomental system for cardiogenesis" Int.J.Develop.Biol.40. 715-718 (1996)
Ariizumi, T., 等人:“激活素处理的尿带外胚层:心脏发生的模型实验系统”Int.J.Develop.Biol.40。
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通讯作者:
Takakura,N., et al.: "PDGFRa expression during mouse embryogenesis:Immunolocalization analyzed by whole mount immunostaining using the monoclonal anti-mouse-PDGFRa antibody APA5." J.Hist.Chem.Cytochem.45. 883-892 (1997)
Takakura,N. 等人:“小鼠胚胎发生过程中的 PDGFRa 表达:使用单克隆抗小鼠 PDGFRa 抗体 APA5 通过整体免疫染色分析免疫定位。”
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通讯作者:
Nishinakamura, R., et al: "Xenopus FK 506-Binding Protein Homolog Induces a Secondary Axis in Frog Embryos,Which Is Inhibited by CoexistingBMP 4 Signaling" Biochem.Biophys.Res.Commun.239. 585-591 (1997)
Nishinakamura, R. 等人:“非洲爪蟾 FK 506 结合蛋白同源物在青蛙胚胎中诱导次级轴,该轴受到共存 BMP 4 信号传导的抑制”Biochem.Biophys.Res.Commun.239。
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通讯作者:
M.Asashima et al.: "Taniguchi Symposium on Developmental Biology IX" SEIKO Inc.ed.by T.S.Okada, 101 (1997)
M.Asashima 等:“Taniguchi Symposium on Developmental Biology IX” SEIKO Inc.ed.by T.S.Okada,101 (1997)
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22
    Mammalian organ regeneration method using the roadmap for amphibian organogenesis.
    • 批准号:
      21241048
    • 项目类别:
      Grant-in-Aid for Scientific Research (A)
    • 资助金额:
      $25.63万
    • 财政年份:
      2009
    • 负责人:
      ASASHIMA Makoto
    • 依托单位:
    Molecular bases of the body-plan in vertebrate
    • 批准号:
      09275101
    • 项目类别:
      Grant-in-Aid for Scientific Research on Priority Areas (A)
    • 资助金额:
      $48.7万
    • 财政年份:
      2001
    • 负责人:
      ASASHIMA Makoto
    • 依托单位:
    Molecular analysis of cell differentiation and morphogenesis by mesoderm inducing factor
    Mesoderm induction and gene expression by activin A (=EDF)
    • 批准号:
      02640562
    • 项目类别:
      Grant-in-Aid for General Scientific Research (C)
    • 资助金额:
      $0.96万
    • 财政年份:
      1990
    • 负责人:
      ASASHIMA Makoto
    • 依托单位: