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Brushed nasal epithelial cells are a surrogate for bronchial epithelial CFTR studies
Recent advances in the management of cystic fibrosis (CF) target underlying defects in the CF transmembrane conductance regulator (CFTR) protein, but efficacy analyses remain limited to specific genotype–based subgroups. Patient-derived model systems may therefore aid in expanding access to these dr...
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| Опубликовано в: : | JCI Insight |
|---|---|
| Главные авторы: | , , , , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
American Society for Clinical Investigation
2018
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6124537/ https://ncbi.nlm.nih.gov/pubmed/29997283 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/jci.insight.99385 |
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