Examining the impact of endothelial BMPR2 loss on the transcriptional and functional response to BMP9 in pulmonary arterial hypertension
Examining the impact of endothelial BMPR2 loss on the transcriptional and functional response to BMP9 in pulmonary arterial hypertension
批准号:
458790
负责人:
VandenBroek Michael M
金额:
$7.65万
依托单位国家:
加拿大
项目类别:
Studentship Programs
财政年份:
2021
资助国家:
加拿大
项目状态:
已结题
起止时间:
2021-11-01 至 2024-11-01
中文摘要
肺动脉高压(PAH)是一种由肺动脉细胞生长失控引起的致命疾病。这会导致这些血管变窄,增加心脏的负荷,最终导致心力衰竭。Unfortu
英文摘要
Pulmonary arterial hypertension (PAH) is a deadly disease caused by uncontrolled growth of the cells lining the arteries in the lung. This leads to narrowing of these blood vessels, an increased workload on the heart, and ultimately heart failure. Unfortu
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会议论文
A genome-wide assessment of the transcriptional basis for the bone morphogenetic protein 9 induced endothelial hyperproliferation in pulmonary arterial hypertension.
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批准号:429177
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项目类别:Studentship Programs
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资助金额:$1.27万
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财政年份:2019
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负责人:VandenBroek Michael M
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依托单位:
国内基金
海外基金
骨形态发生蛋白(Bone Morphogenetic Proteins,BMP)信号在脊髓损伤中枢神经性疼痛中的作用
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批准号:81070994
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项目类别:面上项目
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资助金额:32.0万元
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批准年份:2010
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负责人:王亚平
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依托单位: