Three-Dimensional Airway Spheroids and Organoids for Cystic Fibrosis Research

Cystic fibrosis (CF) is an autosomal recessive multi-organ disease caused by mutations in the <i>CF Transmembrane Conductance Regulator</i> (<i>CFTR</i>) gene, with morbidity and mortality primacy related to the lung disease. The CFTR protein, a chloride/bicarbonate channel,...

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Bibliographic Details
Main Authors: Onofrio Laselva, Massimo Conese
Format: Article
Language:English
Published: MDPI AG 2021-10-01
Series:Journal of Respiration
Subjects:
Online Access:https://www.mdpi.com/2673-527X/1/4/22