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The molecular basis of trafficking defect of cystic fibrosis mutations in respiratory epithelia

The molecular basis of trafficking defect of cystic fibrosis mutations in respiratory epithelia
呼吸道上皮囊性纤维化突变运输缺陷的分子基础
批准号:
181202
负责人:
Lukacs Gergely L
金额:
$53.69万
依托单位:
依托单位国家:
加拿大
项目类别:
Operating Grants
财政年份:
2009
资助国家:
加拿大
项目状态:
已结题
起止时间:
2009-03-01 至 2014-03-01

项目摘要

项目成果

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中文摘要
翻译
囊性纤维化基因决定蛋白质(称为CFTR)的合成,该蛋白质通常位于细胞的限制膜中,并负责肺的正常含水量或水合作用。囊性纤维化基因中的基因突变可以
英文摘要
The cystic fibrosis gene dictates the synthesis of a protein (called CFTR) which is normally resides in the limiting membrane of cells and responsible for the normal water content or hydration of the lung. Genetic mutations in the cystic fibrosis gene can
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Mechanism and pharmacological modulation of intrinsic and acquired pro-inflammatory state of the airway epithelia in cystic fibrosis
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    445259
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    $61.3万
  • 财政年份:
    2021
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Molecular basis of and preclinical approaches to overcome therapy-resistant cystic fibrosis mutations
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  • 资助金额:
    $66.32万
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    2020
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Rational optimization of CFTR modulators and assessment of predictive potential of novel cystic fibrosis (CF) airway epithelial models for clinical outcome
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    358504
  • 项目类别:
    Operating Grants
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    2016
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    Lukacs Gergely L
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Molecular basis and correction of CFTR defects in respiratory epithelial cells
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    323359
  • 项目类别:
    Operating Grants
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  • 负责人:
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海外基金