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Single-Cell Transcriptional Archetypes of Airway Inflammation in Cystic Fibrosis
Rationale: Cystic fibrosis (CF) is a life-shortening, multisystem hereditary disease caused by abnormal chloride transport. CF lung disease is driven by innate immune dysfunction and exaggerated inflammatory responses that contribute to tissue injury. To define the transcriptional profile of this ai...
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| Vydáno v: | Am J Respir Crit Care Med |
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| Hlavní autoři: | , , , , , , , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
American Thoracic Society
2020
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7667912/ https://ncbi.nlm.nih.gov/pubmed/32603604 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1164/rccm.202004-0991OC |
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