Abstract
applied for precision medicine of cystic fibrosis, a rare and progressive multi-organ disease caused by pathological variants of the CFTR gene. We study how novel drugs called their tissue used to create personalized intestinal organoids, despite some variation in growth rates among samples. Cells can be biobanked and propagated in culture in rectal tissue epithelium, whether a model exactly recapitulates the in vivo tissue comes from directly showing that organoid phenotypes in vitro associate with and preI am very grateful that our studies with intestinal organoids could help to get CFTR ensure that these living technologies can eventually be implemented as certified diag
Original language | English |
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Pages (from-to) | 4439-4443 |
Number of pages | 5 |
Journal | Cell |
Volume | 187 |
Issue number | 17 |
DOIs | |
Publication status | Published - 22 Aug 2024 |