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Sphingolipids and plasma membrane hydrolases in human primary bronchial cells during differentiation and their altered patterns in cystic fibrosis

Human primary bronchial epithelial cells differentiated in vitro represent a valuable tool to study lung diseases such as cystic fibrosis (CF), an inherited disorder caused by mutations in the gene coding for the Cystic Fibrosis Transmembrane Conductance Regulator. In CF, sphingolipids, a ubiquitous...

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Detalles Bibliográficos
Autores principales:	Loberto, Nicoletta, Mancini, Giulia, Bassi, Rosaria, Carsana, Emma Veronica, Tamanini, Anna, Pedemonte, Nicoletta, Dechecchi, Maria Cristina, Sonnino, Sandro, Aureli, Massimo
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Springer US 2020
Materias:	Original Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7501107/ https://www.ncbi.nlm.nih.gov/pubmed/32666337 http://dx.doi.org/10.1007/s10719-020-09935-x

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