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Assessing Human Airway Epithelial Progenitor Cells for Cystic Fibrosis Cell Therapy
Cystic fibrosis (CF) is caused by loss-of-function mutations in the CFTR (CF transmembrane regulator) gene. Pharmacologic therapies directed at CFTR have been developed but are not effective for mutations that result in little or no mRNA or protein expression. Cell therapy is a potential mutation-ag...
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| Publicat a: | Am J Respir Cell Mol Biol |
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| Autors principals: | , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
American Thoracic Society
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7462339/ https://ncbi.nlm.nih.gov/pubmed/32437238 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1165/rcmb.2019-0384OC |
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