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Intestinal organoids to model cystic fibrosis

Publication date

2019-01-01

Authors

Van Mourik, Peter
Beekman, JMISNI 0000000388915338
van der Ent, KorsISNI 0000000388008551

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DOI

https://doi.org/10.1183/13993003.02379-2018

Document Type

Article

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taverne

Abstract

CF can be studied using patient-specific intestinal organoids. CFTR protein function in intestinal organoids correlates with clinical disease severity and drug testing in organoids could aid in finding drugs for people with rare CFTR mutations.

Keywords

Taverne, Pulmonary and Respiratory Medicine

Citation

Van Mourik, P, Beekman, J M & Van Der Ent, C K 2019, 'Intestinal organoids to model cystic fibrosis', European Respiratory Journal, vol. 54, no. 1, 1802379. https://doi.org/10.1183/13993003.02379-2018

URI

https://dspace.library.uu.nl/handle/1874/392250