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Editorial
. 2014 Aug 15;190(4):364-5.
doi: 10.1164/rccm.201407-1247ED.

Measuring mucociliary transport and mucus properties in multiple regions of airway epithelial surfaces helps clarify cystic fibrosis defects

Jeffrey J Wine  1
Affiliations
Editorial

Measuring mucociliary transport and mucus properties in multiple regions of airway epithelial surfaces helps clarify cystic fibrosis defects

Jeffrey J Wine. Am J Respir Crit Care Med. .
No abstract available

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Comment on

  • A functional anatomic defect of the cystic fibrosis airway.
    Birket SE, Chu KK, Liu L, Houser GH, Diephuis BJ, Wilsterman EJ, Dierksen G, Mazur M, Shastry S, Li Y, Watson JD, Smith AT, Schuster BS, Hanes J, Grizzle WE, Sorscher EJ, Tearney GJ, Rowe SM. Birket SE, et al. Am J Respir Crit Care Med. 2014 Aug 15;190(4):421-32. doi: 10.1164/rccm.201404-0670OC. Am J Respir Crit Care Med. 2014. PMID: 25029666 Free PMC article.

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