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Human Molecular Genetics|January 1, 1994
Somatic gene therapy for cystic fibrosisW K O'Neal, A L Beaudet
Current Molecular Medicine|June 16, 2012
Endoplasmic reticulum stress in chronic obstructive lung diseasesC M P Ribeiro, W K O'Neal
Molecular Therapy : the Journal of the American Society of Gene Therapy|December 22, 2000
Multiple advantages of alpha-fetoprotein as a marker for in vivo gene transferW K O'Neal, E Rose, H Zhou, et al.
Gene Therapy|July 20, 2007
Expression of CFTR from a ciliated cell-specific promoter is ineffective at correcting nasal potential difference in CF miceL E Ostrowski, W Yin, P S Diggs, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|October 18, 2011
Transgenic hCFTR expression fails to correct β-ENaC mouse lung diseaseB R Grubb, W K O'Neal, L E Ostrowski, et al.
The American Journal of Physiology|August 13, 1999
NSP4 elicits age-dependent diarrhea and Ca(2+)mediated I(-) influx into intestinal crypts of CF miceA P Morris, J K Scott, J M Ball, et al.
Molecular Medicine (Cambridge, Mass.)|August 31, 2000
Toxicity associated with repeated administration of first-generation adenovirus vectors does not occur with a helper-dependent vectorW K O'Neal, H Zhou, N Morral, et al.
Human Molecular Genetics|October 1, 1993
A severe phenotype in mice with a duplication of exon 3 in the cystic fibrosis locusW K O'Neal, P Hasty, P B McCray, et al.
Mucosal Immunology|March 16, 2012
Mucus clearance, MyD88-dependent and MyD88-independent immunity modulate lung susceptibility to spontaneous bacterial infection and inflammationA Livraghi-Butrico, E J Kelly, E R Klem, et al.
The Journal of Pharmacology and Experimental Therapeutics|March 22, 2001
Cloning and functional characterization of two murine uridine nucleotide receptors reveal a potential target for correcting ion transport deficiency in cystic fibrosis gallbladderE R Lazarowski, L G Rochelle, W K O'Neal, et al.
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