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miR-636: A Newly-Identified Actor for the Regulation of Pulmonary Inflammation in Cystic Fibrosis

Cystic fibrosis (CF) results from deficient CF transmembrane conductance regulator (CFTR) protein activity leading to defective epithelial ion transport. Pulmonary degradation due to excessive inflammation is the main cause of morbidity and mortality in CF patients. By analysing miRNAs (small RNAseq...

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Библиографические подробности
Опубликовано в: :Front Immunol
Главные авторы: Bardin, Pauline, Foussignière, Tobias, Rousselet, Nathalie, Rebeyrol, Carine, Porter, Joanna C., Corvol, Harriet, Tabary, Olivier
Формат: Artigo
Язык:Inglês
Опубликовано: Frontiers Media S.A. 2019
Предметы:
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC6874100/
https://ncbi.nlm.nih.gov/pubmed/31803183
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fimmu.2019.02643
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