MiR-101 and miR-144 Regulate the Expression of the CFTR Chloride Channel in the Lung

The Cystic Fibrosis Transmembrane conductance Regulator (CFTR) is a chloride channel that plays a critical role in the lung by maintaining fluid homeostasis. Absence or malfunction of CFTR leads to Cystic Fibrosis, a disease characterized by chronic infection and inflammation. We recently reported t...

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Detalhes bibliográficos
Main Authors: Hassan, Fatemat, Nuovo, Gerard J., Crawford, Melissa, Boyaka, Prosper N., Kirkby, Stephen, Nana-Sinkam, Serge P., Cormet-Boyaka, Estelle
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2012
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3511328/
https://ncbi.nlm.nih.gov/pubmed/23226399
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0050837
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