Cargando…
TMEM16A/ANO1: Current Strategies and Novel Drug Approaches for Cystic Fibrosis
Cystic fibrosis (CF) is the most common of rare hereditary diseases in Caucasians, and it is estimated to affect 75,000 patients globally. CF is a complex disease due to the multiplicity of mutations found in the CF transmembrane conductance regulator (CFTR) gene causing the CFTR protein to become d...
Autores principales: | Mitri, Christie, Sharma, Himanshu, Corvol, Harriet, Tabary, Olivier |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8616501/ https://www.ncbi.nlm.nih.gov/pubmed/34831090 http://dx.doi.org/10.3390/cells10112867 |
Ejemplares similares
-
Novel Anti-Inflammatory Approaches for Cystic Fibrosis Lung Disease: Identification of Molecular Targets and Design of Innovative Therapies
por: Mitri, Christie, et al.
Publicado: (2020) -
Emerging microRNA Therapeutic Approaches for Cystic Fibrosis
por: Bardin, Pauline, et al.
Publicado: (2018) -
MicroRNA-9 downregulates the ANO1 chloride channel and contributes to cystic fibrosis lung pathology
por: Sonneville, Florence, et al.
Publicado: (2017) -
TMEM16A in Cystic Fibrosis: Activating or Inhibiting?
por: Kunzelmann, Karl, et al.
Publicado: (2019) -
The role of TMEM16A (ANO1) and TMEM16F (ANO6) in cell migration
por: Jacobsen, K. S., et al.
Publicado: (2013)