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...

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發表在:Thorax
Main Authors: 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
格式: Artigo
語言:Inglês
出版: BMJ Publishing Group 2020
主題:
Cystic Fibrosis
在線閱讀: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
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