Increased extracellular vesicles mediate inflammatory signalling in cystic fibrosis

RATIONALE: Mutations in the cystic fibrosis transmembrane regulator (CFTR) gene form the basis of cystic fibrosis (CF). There remains an important knowledge gap in CF as to how diminished CFTR activity leads to the dominant inflammatory response within CF airways. OBJECTIVES: To investigate if extra...

Descrizione completa

Salvato in:
Dettagli Bibliografici
Pubblicato in:Thorax
Autori principali: Useckaite, Zivile, Ward, Mark P, Trappe, Anne, Reilly, Rebecca, Lennon, Jenny, Davage, Holly, Matallanas, David, Cassidy, Hilary, Dillon, Eugene T, Brennan, Kiva, Doyle, Sarah L, Carter, Suzanne, Donnelly, Seamas, Linnane, Barry, McKone, Edward F, McNally, Paul, Coppinger, Judith A
Natura: Artigo
Lingua:Inglês
Pubblicazione: BMJ Publishing Group 2020
Soggetti:
Cystic Fibrosis
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC7279202/
https://ncbi.nlm.nih.gov/pubmed/32265339
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/thoraxjnl-2019-214027
Tags: Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !

Documenti analoghi