Cargando…
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...
Autores principales: | Pankonien, Ines, Quaresma, Margarida C., Rodrigues, Cláudia S., Amaral, Margarida D. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
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 |
Ejemplares similares
-
What Role Does CFTR Play in Development, Differentiation, Regeneration and Cancer?
por: Amaral, Margarida D., et al.
Publicado: (2020) -
Exploring YAP1-centered networks linking dysfunctional CFTR to epithelial–mesenchymal transition
por: Quaresma, Margarida C, et al.
Publicado: (2022) -
Mutant CFTR Drives TWIST1 mediated epithelial–mesenchymal transition
por: Quaresma, Margarida C., et al.
Publicado: (2020) -
Personalized medicine: Function of CFTR variant p.Arg334Trp is rescued by currently available CFTR modulators
por: Railean, Violeta, et al.
Publicado: (2023) -
KLF4 Acts as a wt-CFTR Suppressor through an AKT-Mediated Pathway
por: Sousa, Luis, et al.
Publicado: (2020)