CFTR High Expresser Cells in cystic fibrosis and intestinal diseases

Cystic Fibrosis Transmembrane Conductance Regulator (CFTR), the Cl(−)/HCO(3)(−) channel implicated in Cystic Fibrosis, is critical to the pathophysiology of many gastrointestinal diseases. Defects in CFTR lead to intestinal dysfunction, malabsorption, obstruction, infection, inflammation, and cancer...

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Detalles Bibliográficos
Autores principales: Carlos dos Reis, Diego, Dastoor, Parinaz, Santos, Anderson Kenedy, Sumigray, Kaelyn, Ameen, Nadia A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10031467/
https://www.ncbi.nlm.nih.gov/pubmed/36967909
http://dx.doi.org/10.1016/j.heliyon.2023.e14568

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10031467/
https://www.ncbi.nlm.nih.gov/pubmed/36967909
http://dx.doi.org/10.1016/j.heliyon.2023.e14568

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