ΔF508 CFTR protein expression in tissues from patients with cystic fibrosis
Author:
Publisher
American Society for Clinical Investigation
Subject
General Medicine
Reference74 articles.
1. Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis
2. Maturation and function of cystic fibrosis transmembrane conductance regulator variants bearing mutations in putative nucleotide-binding domains 1 and 2.
3. Limited proteolysis as a probe for arrested conformational maturation of ΔF508 CFTR
4. Participation of the endoplasmic reticulum chaperone calnexin (p88, IP90) in the biogenesis of the cystic fibrosis transmembrane conductance regulator.
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