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Updated: Apr 8, 2026

Forskolin-induced Swelling in Intestinal Organoids: An In Vitro Assay for Assessing Drug Response in Cystic Fibrosis Patients
Published on: February 11, 2017
Recent advances in understanding and managing cystic fibrosis transmembrane conductance regulator dysfunction
Uta Griesenbach1, Eric W F W Alton1
1Department of Gene Therapy and the UK Cystic Fibrosis Gene Therapy Consortium, Imperial College London SW3 6LR UK.
Abstract:
Cystic fibrosis is the most common autosomal recessive genetic disease in Caucasians and has been extensively studied for many decades. The cystic fibrosis transmembrane conductance regulator gene was identified in 1989. It encodes a complex protein which has numerous cellular functions. Our understanding of cystic fibrosis pathophysiology and genetics is constantly expanding and being refined, leading to improved management of the disease and increased life expectancy in affected individuals.
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