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American Journal of Physiology, ISSN 1040-0605, 11/2017, Volume 313, Issue 5, p. L859
Maintenance of normal epithelial ion and water transport in the lungs includes providing a thin layer of surface liquid that coats the conducting airways. This... 
Viscosity | Respiratory function | Preservation | Pathogenesis | Batteries | pH effects | Respiratory tract | Pathology | Airway management | Lungs | Water transport | Bacteria | Ion channels | Transporter
Journal Article
American Journal of Physiology, ISSN 1040-0605, 12/2014, Volume 307, Issue 12, p. L917
  CFTR is a cAMP-activated chloride and bicarbonate channel that is critical for lung homeostasis. Decreases in CFTR expression have dire consequences in... 
Pathology | Membranes | Lungs | Homeostasis | Cystic fibrosis | Chronic obstructive pulmonary disease
Journal Article
American Journal of Physiology, ISSN 1040-0605, 12/2015, Volume 309, Issue 11, p. L1229
  In utero, fetal lung epithelial cells actively secrete Cl- ions into the lung air spaces while Na+ ions follow passively to maintain electroneutrality. This... 
Sodium | Lung diseases | Homeostasis | Cystic fibrosis | Ions | Cells
Journal Article
American Journal of Physiology, ISSN 1040-0605, 05/2013, Volume 304, Issue 9, p. L582
  The human cystic fibrosis transmembrane conductance regulator (CFTR) is a cyclic AMP-activated chloride (Cl-) channel in the lung epithelium that helps... 
Proteins | Pro bono services | Cystic fibrosis | Mutation | Gene expression | Cells
Journal Article
American Journal of Physiology, ISSN 1040-0605, 09/2014, Volume 307, Issue 6, p. L431
  Since the discovery of the cystic fibrosis (CF) gene that encodes the CF transmembrane conductance regulator (CFTR) in 1989, there has been considerable... 
Molecules | Membranes | Protein folding | Cystic fibrosis | Mutation | Drug therapy
Journal Article
Journal Article
Cellular signalling, 12/2018, Volume 54, p. 150
Solid tumor microenvironments are often subjected to various levels of hypoxia. Although regulation of gene expression has been examined extensively, most... 
Journal Article
American Journal of Physiology, ISSN 1040-0605, 06/2012, Volume 302, Issue 11, p. L1141
Cystic fibrosis (CF) is caused by the loss of the cystic fibrosis transmembrane conductance regulator (CFTR) function and results in a respiratory phenotype... 
Genotype & phenotype | Mortality | Lung diseases | Cystic fibrosis | Bacteria
Journal Article
American Journal of Physiology: Lung Cellular and Molecular Physiology, ISSN 1040-0605, 10/2013, Volume 305, Issue 8, pp. L530 - L530
Chronic obstructive pulmonary disease (COPD) is a progressive respiratory disorder consisting of chronic bronchitis and/or emphysema. COPD patients suffer from... 
Journal Article
American Journal of Physiology, ISSN 1040-0605, 11/2017, Volume 313, Issue 5, p. L845
The cystic fibrosis transmembrane conductance regulator (CFTR) and the amiloride-sensitive epithelial sodium channels (ENaC) are located in the apical... 
Respiratory function | Membranes | Pathogenesis | Epithelial cells | Homeostasis | Viruses | Mucus | Infections | Accumulation | Respiratory tract | Bicarbonate | Amiloride | Chloride | Bacteria | Influenza A | Ion channels | Carbonates | Alveoli | Edema | Sodium channels | Secretion | Complications | Ion transport | Cystic fibrosis | Pharynx | Cough | Resistance | Sodium | Lungs | Influenza | Fibrosis | Conductance | Pharyngitis | Gas exchange
Journal Article
American Journal of Physiology - Lung Cellular and Molecular Physiology, ISSN 1040-0605, 06/2012, Volume 302, Issue 11, pp. 1141 - 1146
Journal Article
American Journal of Physiology - Lung Cellular and Molecular Physiology, ISSN 1040-0605, 10/2013, Volume 305, Issue 8, pp. L530 - L541
Journal Article
Journal Article
FASEB Journal, ISSN 0892-6638, 04/2015, Volume 29, Issue 4, pp. 1467 - 1479
Journal Article