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Defining molecular pathways underlying craniofacial birth defects

Defining molecular pathways underlying craniofacial birth defects
定义颅面出生缺陷的分子途径
批准号:
280007
负责人:
Cloutier Jean-Francois
金额:
$32.19万
依托单位国家:
加拿大
项目类别:
Operating Grants
财政年份:
2013
资助国家:
加拿大
项目状态:
已结题
起止时间:
2013-03-01 至 2016-03-01

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中文摘要
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英文摘要
Malformations in head structures, such as the bones and palate, are estimated to account for approximately 50% of all human birth defects and have been associated with a wide variety of syndromes including the Pierre Robin and DiGeorge syndromes. The prev
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Uncovering a novel role for the receptor Neogenin in synaptic function.
Molecular Mechanisms of Sensory Systems Development
CANADA RESEARCH CHAIRHOLDER / TITULAIRE DE CHAIRE DE RECHERCHE DU CANADA
  • 批准号:
    204241
  • 项目类别:
  • 资助金额:
    $36.43万
  • 财政年份:
    2009
  • 负责人:
    Cloutier Jean-Francois
  • 依托单位:
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