Cargando…
CFTR Protein: Not Just a Chloride Channel?
Cystic fibrosis (CF) is a recessive genetic disease caused by mutations in a gene encoding a protein called Cystic Fibrosis Transmembrane Conductance Regulator (CFTR). The CFTR protein is known to acts as a chloride (Cl(−)) channel expressed in the exocrine glands of several body systems where it al...
Autores principales: | Hanssens, Laurence S., Duchateau, Jean, Casimir, Georges J. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8616376/ https://www.ncbi.nlm.nih.gov/pubmed/34831067 http://dx.doi.org/10.3390/cells10112844 |
Ejemplares similares
-
Immunoglobulin G: A useful outcome marker in the follow‐up of cystic fibrosis patients?
por: Hanssens, Laurence S., et al.
Publicado: (2021) -
The molecular evolution of function in the CFTR chloride channel
por: Infield, Daniel T., et al.
Publicado: (2021) -
Discovering the chloride pathway in the CFTR channel
por: Farkas, Bianka, et al.
Publicado: (2019) -
Reversible Silencing of CFTR Chloride Channels by Glutathionylation
por: Wang, Wei, et al.
Publicado: (2005) -
Gender differences and inflammation: an in vitro model of blood cells stimulation in prepubescent children
por: Casimir, Georges JA, et al.
Publicado: (2010)