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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Dades bibliogràfiques
Publicat a:Am J Respir Crit Care Med
Autors principals: Schupp, Jonas C., Khanal, Sara, Gomez, Jose L., Sauler, Maor, Adams, Taylor S., Chupp, Geoffrey L., Yan, Xiting, Poli, Sergio, Zhao, Yujiao, Montgomery, Ruth R., Rosas, Ivan O., Dela Cruz, Charles S., Bruscia, Emanuela M., Egan, Marie E., Kaminski, Naftali, Britto, Clemente J.
Format: Artigo
Idioma:Inglês
Publicat: American Thoracic Society 2020
Matèries:
Original Articles
Accés en línia: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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