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ΔF508 CFTR protein expression in tissues from patients with cystic fibrosis

Heterologous expression of the cystic fibrosis transmembrane conductance regulator (CFTR) provided evidence that the major cystic fibrosis (CF) mutation ΔF508 leads to defective protein folding in the endoplasmic reticulum, which prevents its processing and targeting to the cell surface. In this stu...

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Detalhes bibliográficos
Main Authors: Kälin, Nanette, Claaß, Andreas, Sommer, Martin, Puchelle, Edith, Tümmler, Burkhard
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Clinical Investigation 1999
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC408454/
https://ncbi.nlm.nih.gov/pubmed/10330420
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