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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

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