Exploring novel combinatorial therapies for personalized management of Cystic Fibrosis using primary human airway epithelial cells
Exploring novel combinatorial therapies for personalized management of Cystic Fibrosis using primary human airway epithelial cells
批准号:
439577
负责人:
Nguyen Jenny P
金额:
$7.65万
依托单位:
依托单位国家:
加拿大
项目类别:
Studentship Programs
财政年份:
2020
资助国家:
加拿大
项目状态:
已结题
起止时间:
2020-11-01 至 2023-11-01
中文摘要
囊性纤维化是影响加拿大新生儿的最常见的遗传疾病(1/3600),是由来自父母双方的囊性纤维化跨膜传导调节因子基因突变遗传引起的。囊性纤维化患者
英文摘要
Cystic Fibrosis is the most common genetic condition affecting Canadian newborns (1 in 3600), and is caused by the inheritance of a mutation, from each parent, in the gene for the Cystic Fibrosis transmembrane conductance regulator. People with Cystic Fib
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专著(0)
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会议论文
The role of cystic fibrosis transmembrane conductance regulator in airway surface liquide pH and host defenses in human airway epithelial cells.
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批准号:474040
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项目类别:Miscellaneous Programs
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资助金额:$0.44万
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财政年份:2022
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负责人:Nguyen Jenny P
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依托单位:
海外基金