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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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| Vydáno v: | JCI Insight |
|---|---|
| Hlavní autoři: | , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
American Society for Clinical Investigation
2018
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| Témata: | |
| On-line přístup: | 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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