Antibody microarrays: analysis of cystic fibrosis.
Methods Mol. Biol., 823:179-200 (2012)
N-acetylcysteine enhances cystic fibrosis sputum penetration and airway gene transfer by highly compacted DNA nanoparticles.
Mol. Ther., Nov;19(11):1981-9 (2011)
Cystic fibrosis and sinusitis in children: outcomes and socioeconomic status.
Otolaryngol Head Neck Surg., Jul;145(1):146-53 (2011)
Applications of proteomic technologies for understanding the premature proteolysis of CFTR.
Expert Rev Proteomics., Aug;7(4):473-86 (2010)
Ubiquitin C-terminal hydrolase-L1 protects cystic fibrosis transmembrane conductance regulator from early stages of proteasomal degradation.
J. Biol. Chem., Apr;285(15):11314-25 (2010)
Transient effectiveness of vitamin D2 therapy in pediatric cystic fibrosis patients.
J. Cyst. Fibros., Mar;9(2):143-9 (2010)
Pseudomonas aeruginosa: can studies in engineered cells tell us why is it such a problem in people with cystic fibrosis? Focus on "Cystic fibrosis transmembrane conductance regulator and caveolin-1 regulate epithelial cell internalization of Pseudomonas a
Am. J. Physiol., Cell Physiol., Aug;297(2):C235-7 (2009)
Description of a standardized nutrition classification plan and its relation to nutritional outcomes in children with cystic fibrosis.
J Pediatr Psychol., 35(1):6-13 (2010 Jan-Feb)
CFTR is a negative regulator of NFkappaB mediated innate immune response.
PLoS ONE., 4(2):e4664 (2009)
Proteome of synaptosome-associated proteins in spinal cord dorsal horn after peripheral nerve injury.
Proteomics., Mar;9(5):1241-53 (2009)
The penetration of fresh undiluted sputum expectorated by cystic fibrosis patients by non-adhesive polymer nanoparticles.
Biomaterials., May;30(13):2591-7 (2009)
Cystic fibrosis and estrogens: a perfect storm.
J. Clin. Invest., Dec;118(12):3841-4 (2008)
Spiperone, identified through compound screening, activates calcium-dependent chloride secretion in the airway.
Am. J. Physiol., Cell Physiol., Jan;296(1):C131-41 (2009)
Lubiprostone activates non-CFTR-dependent respiratory epithelial chloride secretion in cystic fibrosis mice.
Am. J. Physiol. Lung Cell Mol. Physiol., Nov;295(5):L933-40 (2008)
Cystic fibrosis presenting as recurrent pancreatitis in a young child with a normal sweat test and pancreas divisum: a case report.
J Med Case Rep., 2:176 (2008)
Atypical cystic fibrosis and CFTR-related diseases.
Clin Rev Allergy Immunol., Dec;35(3):116-23 (2008)
Dietary supplement use in pediatric patients with cystic fibrosis.
Am J Health Syst Pharm., Mar;65(6):562-5 (2008)
Chemical rescue of deltaF508-CFTR mimics genetic repair in cystic fibrosis bronchial epithelial cells.
Mol. Cell Proteomics., Jun;7(6):1099-110 (2008)
Protein microarray platforms for clinical proteomics.
Proteomics Clin Appl., Sep;1(9):934-52 (2007)
CHOP transcription factor mediates IL-8 signaling in cystic fibrosis bronchial epithelial cells.
Am. J. Respir. Cell Mol. Biol., Feb;38(2):176-84 (2008)