Papers 3

  1. Normal nasal mucociliary clearance in CF children: evidence against a CFTR-related defect.
    McShane D et al., Eur Respir J. 2004 Jul;24(1):95-100.
  2. Airway surface pH in subjects with cystic fibrosis.
    McShane D et al., Eur Respir J. 2003 Jan;21(1):37-42.
  3. Potential difference measurements in the lower airway of children with and without cystic fibrosis.
    Davies JC et al., Am J Respir Crit Care Med. 2005 May 1;171(9):1015-9. Epub 2005 Jan 7.

 

Purifying mRNA from tissue samples.