Cross‐talk between CFTR and sphingolipids in cystic fibrosis

Cystic fibrosis (CF) is the most common inherited, life‐limiting disorder in Caucasian populations. It is caused by mutations in the gene encoding the cystic fibrosis transmembrane conductance regulator (CFTR), which lead to an impairment of protein expression and/or function. CFTR is a chloride/bic...

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Detalles Bibliográficos
Autores principales: Dobi, Dorina, Loberto, Nicoletta, Bassi, Rosaria, Pistocchi, Anna, Lunghi, Giulia, Tamanini, Anna, Aureli, Massimo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Reviews
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10476574/
https://www.ncbi.nlm.nih.gov/pubmed/37315117
http://dx.doi.org/10.1002/2211-5463.13660

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10476574/
https://www.ncbi.nlm.nih.gov/pubmed/37315117
http://dx.doi.org/10.1002/2211-5463.13660

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