课题基金 / 基金详情

Modeling Cystic Fibrosis (CF) airway disease and therapies in patient derived tissues

Modeling Cystic Fibrosis (CF) airway disease and therapies in patient derived tissues
在患者来源的组织中模拟囊性纤维化 (CF) 气道疾病和治疗
批准号：
367377
负责人：
Xia Sunny
金额：
$1.27万
依托单位：
University of Toronto
依托单位国家：
加拿大
项目类别：
Studentship Programs
财政年份：
2016
资助国家：
加拿大
项目状态：
已结题
起止时间：
2016-12-01 至 2017-12-01
来源：
https://webapps.cihr-irsc.gc.ca/decisions/p/project_details.html?applId=367377&lang=en
关键词：
3d Organoids Airway Disease Phenotype Cftr-Mediated Fluid Secretion Channel Function Cystic Fibrosis Epithelium Health Modifier Genes Patient-Derived Primary Cultures

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中文摘要
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英文摘要
Cystic Fibrosis (CF) is caused by mutations in the Cystic Fibrosis Conductance Transmembrane Regulator ( CFTR ) gene. CFTR is a protein that is expressed at the cell surface and is responsible for maintaining hydration of respiratory and intestinal tracts
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