CFTR, Cell Junctions and the Cytoskeleton

The multi-organ disease cystic fibrosis (CF) is caused by mutations in the gene encoding the CF transmembrane conductance regulator (CFTR) protein, a cAMP regulated chloride (Cl(−)) and bicarbonate (HCO(3)(−)) ion channel expressed at the apical plasma membrane (PM) of epithelial cells. Reduced CFTR...

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Detalles Bibliográficos
Autores principales: Pankonien, Ines, Quaresma, Margarida C., Rodrigues, Cláudia S., Amaral, Margarida D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8910340/
https://www.ncbi.nlm.nih.gov/pubmed/35269829
http://dx.doi.org/10.3390/ijms23052688

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8910340/
https://www.ncbi.nlm.nih.gov/pubmed/35269829
http://dx.doi.org/10.3390/ijms23052688

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