Cooh-Terminal Truncations Promote Proteasome-Dependent Degradation of Mature Cystic Fibrosis Transmembrane Conductance Regulator from Post-Golgi Compartments

Impaired biosynthetic processing of the cystic fibrosis (CF) transmembrane conductance regulator (CFTR), a cAMP-regulated chloride channel, constitutes the most common cause of CF. Recently, we have identified a distinct category of mutation, caused by premature stop codons and frameshift mutations,...

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Detalles Bibliográficos
Autores principales: Benharouga, Mohamed, Haardt, Martin, Kartner, Norbert, Lukacs, Gergely L.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2001
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2174331/
https://www.ncbi.nlm.nih.gov/pubmed/11381082

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2174331/
https://www.ncbi.nlm.nih.gov/pubmed/11381082

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