
pmid: 31023844
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.https://bit.ly/2GryRl0
Pulmonary and Respiratory Medicine, Cystic Fibrosis, Primary Cell Culture, Cystic Fibrosis Transmembrane Conductance Regulator, Organoids, Animals, Humans, Biological Assay, Mutant Proteins, Intestinal Mucosa
Pulmonary and Respiratory Medicine, Cystic Fibrosis, Primary Cell Culture, Cystic Fibrosis Transmembrane Conductance Regulator, Organoids, Animals, Humans, Biological Assay, Mutant Proteins, Intestinal Mucosa
| selected citations These citations are derived from selected sources. This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 43 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Top 10% | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 10% | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 10% |
