Abnormal fluid and mucus secretion in response to inhaled bacteria contributes to cystic fibrosis airways disease pathogenesis.
Abnormal fluid and mucus secretion in response to inhaled bacteria contributes to cystic fibrosis airways disease pathogenesis.
批准号:
321334
负责人:
Ianowski Juan P
金额:
$24.45万
依托单位国家:
加拿大
项目类别:
Operating Grants
财政年份:
2015
资助国家:
加拿大
项目状态:
已结题
起止时间:
2015-03-01 至 2018-03-01
中文摘要
囊性纤维化是影响加拿大年轻人的最常见、最致命的遗传病。囊性纤维化是一种常染色体隐性遗传性疾病,由囊性纤维化跨膜电导调节蛋白(CFTR)负离子通道编码基因突变引起。它是e
英文摘要
Cystic fibrosis (CF) is the most common, fatal genetic disease affecting young Canadians. CF is an autosomal recessive condition caused by mutations in the gene encoding the cystic fibrosis transmembrane conductance regulator (CFTR) anion channel. It is e
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会议论文
Cellular bases of cystic fibrosis lung disease: epithelial ionocytes transport bicarbonate and control airway surface liquid pH; while club and goblet cells control hydration and volume
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批准号:452146
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项目类别:Operating Grants
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资助金额:$59.07万
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财政年份:2021
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负责人:Ianowski Juan P
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依托单位:
Cellular bases of cystic fibrosis lung disease: epithelial ionocytes transport bicarbonate and control airway surface liquid pH; while club and goblet cells control hydration and volume.
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批准号:448553
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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:2021
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负责人:Ianowski Juan P
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依托单位:
海外基金