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Hepatology (Baltimore, Md.)|February 1, 1997
Cystic fibrosis transmembrane conductance regulator mediates the cyclic adenosine monophosphate-induced fluid secretion but not the inhibition of resorption in mouse gallbladder epitheliumR H Peters, J H van Doorninck, P J French, et al.
The American Journal of Physiology|August 8, 1998
Restoration by intratracheal gene transfer of bicarbonate secretion in cystic fibrosis mouse gallbladderC M Curtis, L C Martin, C F Higgins, et al.
Gene Therapy|November 13, 2001
Steroid hormone enhancement of gene delivery to a human airway epithelial cell line in vitro and mouse airways in vivoJ W Wiseman, C A Goddard, W H Colledge
The American Journal of Physiology|December 1, 1996
CFTR expression and mucin secretion in cultured mouse gallbladder epithelial cellsR H Peters, P J French, J H van Doorninck, et al.
Nature Medicine|September 1, 1995
The challenge of fetal gene therapyC Coutelle, A M Douar, W H Colledge, et al.
The European Respiratory Journal|April 20, 2001
Inflammation in cystic fibrosis airways: relationship to increased bacterial adherenceP Scheid, L Kempster, U Griesenbach, et al.
Nature|March 18, 1993
Correction of the ion transport defect in cystic fibrosis transgenic mice by gene therapyS C Hyde, D R Gill, C F Higgins, et al.
The EMBO Journal|June 6, 1998
Mice deficient for the secreted glycoprotein SPARC/osteonectin/BM40 develop normally but show severe age-onset cataract formation and disruption of the lensD T Gilmour, G J Lyon, M B Carlton, et al.
Human Gene Therapy|April 10, 1997
Increased contact time improves adenovirus-mediated CFTR gene transfer to nasal epithelium of CF miceC Jiang, G Y Akita, W H Colledge, et al.
Gene Therapy|August 19, 2003
A comparison of linear and branched polyethylenimine (PEI) with DCChol/DOPE liposomes for gene delivery to epithelial cells in vitro and in vivoJ W Wiseman, C A Goddard, D McLelland, et al.
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