Discovery of novel WNT signaling mechanisms from the study of human genetic disease in two animal models
Discovery of novel WNT signaling mechanisms from the study of human genetic disease in two animal models
批准号:
400860
负责人:
Richman Joy M
金额:
$59.7万
依托单位国家:
加拿大
项目类别:
Operating Grants
财政年份:
2019
资助国家:
加拿大
项目状态:
已结题
起止时间:
2019-03-01 至 2024-03-01
中文摘要
现在比以往任何时候都更重要的是,人类基因组测序正在为未诊断的遗传疾病的原因提供无与伦比的见解。下一步是研究已确定的突变如何影响细胞、组织或器官的发育。通过这些研究
英文摘要
Now more than ever, human genome sequencing is providing unparalleled insights into the causes of undiagnosed genetic diseases. The next step is to investigate how identified mutations affect development of cells, tissues or organs. Through these studies
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会议论文
Canada Research Chair - Tier 1
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批准号:471068
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项目类别:
-
资助金额:$101.99万
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财政年份:2022
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负责人:Richman Joy M
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依托单位:
Biological mechanisms contributing to increased risk of facial clefting
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批准号:255940
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项目类别:Operating Grants
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资助金额:$46.55万
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财政年份:2012
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负责人:Richman Joy M
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依托单位:
Molecular controls of jaw identity and limb patterning
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批准号:191187
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项目类别:Operating Grants
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资助金额:$66.11万
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财政年份:2009
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负责人:Richman Joy M
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依托单位:
The function of TBX22 in orofacial clefting
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批准号:183806
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项目类别:Operating Grants
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资助金额:$7.29万
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财政年份:2008
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负责人:Richman Joy M
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依托单位:
海外基金