Chemical chaperones correct the mutant phenotype of the ΔF508 cystic fibrosis transmembrane conductance regulator protein

Mutations in the cystic fibriosis transmembrane conductance regulator protein (CFTR) often result in a failure of the protein to be propely processed at the level of the endoplasmic reticulum (ER) and subsequently transported to the plasma membrane. The folding defect associated with the most common...

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Bibliografski detalji
Glavni autori: Brown, C. Randell, Hong-Brown, Ly Q., Biwersi, Joachim, Verkman, A. S., Welch, William. J
Format: Artigo
Jezik:Inglês
Izdano: Cell Stress Society International 1996
Teme:
Original Articles
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC248464/
https://ncbi.nlm.nih.gov/pubmed/9222597
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