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Agonists that stimulate secretion promote the recruitment of CFTR into membrane lipid microdomains
The cystic fibrosis transmembrane conductance regulator (CFTR) is a tightly regulated anion channel that mediates secretion by epithelia and is mutated in the disease cystic fibrosis. CFTR forms macromolecular complexes with many proteins; however, little is known regarding its associations with mem...
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| Publicat a: | J Gen Physiol |
|---|---|
| Autors principals: | , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Rockefeller University Press
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6572005/ https://ncbi.nlm.nih.gov/pubmed/31048413 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1085/jgp.201812143 |
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