Cargando…
Network Biology Identifies Novel Regulators of CFTR Trafficking and Membrane Stability
In cystic fibrosis, the most common disease-causing mutation is F508del, which causes not only intracellular retention and degradation of CFTR, but also defective channel gating and decreased membrane stability of the small amount that reaches the plasma membrane (PM). Thus, pharmacological correcti...
Autores principales: | Loureiro, Cláudia Almeida, Santos, João D., Matos, Ana Margarida, Jordan, Peter, Matos, Paulo, Farinha, Carlos M., Pinto, Francisco R. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6559121/ https://www.ncbi.nlm.nih.gov/pubmed/31231217 http://dx.doi.org/10.3389/fphar.2019.00619 |
Ejemplares similares
-
Regulatory Crosstalk by Protein Kinases on CFTR Trafficking and Activity
por: Farinha, Carlos M., et al.
Publicado: (2016) -
Absence of EPAC1 Signaling to Stabilize CFTR in Intestinal Organoids
por: Ferreira, João F., et al.
Publicado: (2022) -
Rare Trafficking CFTR Mutations Involve Distinct Cellular Retention Machineries and Require Different Rescuing Strategies
por: Ramalho, Sofia S., et al.
Publicado: (2021) -
Decreasing Poly(ADP-Ribose) Polymerase Activity Restores ΔF508 CFTR Trafficking
por: Anjos, Suzana M., et al.
Publicado: (2012) -
Rescue of Mutant CFTR Trafficking Defect by the Investigational Compound MCG1516A
por: Lopes-Pacheco, Miquéias, et al.
Publicado: (2022)