The holy grail of cystic fibrosis research: pharmacological repair of the F508del-CFTR mutation

Eitemau Tebyg

• Manipulating proteostasis to repair the F508del-CFTR defect in cystic fibrosis
  gan: Esposito, Speranza, et al.
  Cyhoeddwyd: (2016)
• Restoration of CFTR function in patients with cystic fibrosis carrying the F508del-CFTR mutation
  gan: Stefano, Daniela De, et al.
  Cyhoeddwyd: (2014)
• Strategies for the etiological therapy of cystic fibrosis
  gan: Maiuri, Luigi, et al.
  Cyhoeddwyd: (2017)
• Cystic fibrosis transmembrane conductance regulator (CFTR) and autophagy: hereditary defects in cystic fibrosis versus gluten-mediated inhibition in celiac disease
  gan: Maiuri, Luigi, et al.
  Cyhoeddwyd: (2019)
• Cysteamine re-establishes the clearance of Pseudomonas aeruginosa by macrophages bearing the cystic fibrosis-relevant F508del-CFTR mutation
  gan: Ferrari, Eleonora, et al.
  Cyhoeddwyd: (2017)