Title : Improved fluorescence assays to measure the defects associated with F508del-CFTR allow identification of new active compounds.

Pub. Date : 2017 Apr

PMID : 28094839






2 Functional Relationships(s)
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Protein Name
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1 BACKGROUND AND PURPOSE: Cystic fibrosis (CF) is a debilitating disease caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene, which codes for a Cl-/HCO3 - channel. Bicarbonates CF transmembrane conductance regulator Homo sapiens
2 BACKGROUND AND PURPOSE: Cystic fibrosis (CF) is a debilitating disease caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene, which codes for a Cl-/HCO3 - channel. Bicarbonates CF transmembrane conductance regulator Homo sapiens