Phenotypic Alteration of an Established Human Airway Cell Line by Media Selection

Cystic Fibrosis (CF) is caused by mutations in the CF transmembrane conductance regulator (CFTR), a chloride/bicarbonate channel. Many studies utilize human airway cell models (cell lines and primary cells) to study different aspects of CFTR biology. Media selection can alter the growth and differen...

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Detalles Bibliográficos
Autores principales: Livnat, Galit, Meeker, Jessica D., Ostmann, Alicia J., Strecker, Lauren M., Clancy, John P., Brewington, John J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9862772/
https://www.ncbi.nlm.nih.gov/pubmed/36674762
http://dx.doi.org/10.3390/ijms24021246

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9862772/
https://www.ncbi.nlm.nih.gov/pubmed/36674762
http://dx.doi.org/10.3390/ijms24021246

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