Optimization of CFTR-mRNA transfection in human nasal epithelial cells

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Optimization of CFTR-mRNA transfection in human nasal epithelial cells

Background: Cystic fibrosis (CF) is the most common life-threatening inherited disease in the Caucasian population. It is caused by genetic defects in the cystic fibrosis transmembrane conductance regulator gene (CFTR), a cAMP regulated chloride-bicarbonate channel mainly located in the apical membrane of polarized epithelial cells. CFTR is proposed to regulate other proteins, including the epi...

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ژورنال

عنوان ژورنال: Translational Medicine Communications

سال: 2016

ISSN: 2396-832X

DOI: 10.1186/s41231-016-0006-0