Correction of CFTR function in intestinal organoids to guide treatment of cystic fibrosis

Rationale: Given the vast number of cystic fibrosis transmembrane conductance regulator (CFTR) mutations, biomarkers predicting benefit from CFTR modulator therapies are needed for subjects with cystic fibrosis (CF). Objectives: To study CFTR function in organoids of subjects with common and rare CF...

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Veröffentlicht in:The European respiratory journal 2021-01, Vol.57 (1), p.1902426, Article 1902426
Hauptverfasser: Ramalho, Anabela S., Fuerstova, Eva, Vonk, Annelotte M., Ferrante, Marc, Verfaillie, Catherine, Dupont, Lieven, Boon, Mieke, Proesmans, Marijke, Beekman, Jeffrey M., Sarouk, Ifat, Vazquez Cordero, Carlos, Vermeulen, Francois, De Boeck, Kris
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Sprache:eng
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