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Current Stem Cell Research & Therapy, ISSN 1574-888X, 07/2018, Volume 13, Issue 5, p. 325
Journal Article
Endocrine, Metabolic and Immune Disorders - Drug Targets, ISSN 1871-5303, 2011, Volume 11, Issue 1, pp. 8 - 22
Cystic Fibrosis (CF), the most common autosomal lethal disorder in Caucasians, is caused by mutations in the CF transmembrane conductance regulator (CFTR)... 
Airway epithelial cells | Macrophages | Lymphocytes | Cystic fibrosis (CF) | CF transmembrane conductance regulator (CFTR) | Neutrophils
Journal Article
Journal Article
Experimental Cell Research, ISSN 0014-4827, 10/2016, Volume 348, Issue 1, pp. 46 - 55
Journal Article
Journal of Cellular and Molecular Medicine, ISSN 1582-1838, 08/2014, Volume 18, Issue 8, pp. 1631 - 1643
Cystic fibrosis ( CF ) is caused by mutations in the CF transmembrane conductance regulator ( CFTR ) gene, with most of the mortality given by the lung... 
actin | aC | amniotic membrane | cell therapy | mesenchymal stromal cells | EN | tight junctions | CFTR | Amniotic membrane | Cell therapy | Tight junctions | Actin | Mesenchymal stromal cells | ENaC | MEDICINE, RESEARCH & EXPERIMENTAL | LUNG | RESTORATION | CELL BIOLOGY | TRANSMEMBRANE-CONDUCTANCE-REGULATOR | INHIBITION | CHANNEL | CHLORIDE TRANSPORT | IN-VIVO | GENE-EXPRESSION | SECRETION | DELTA-F508 CFTR | Epithelial Cells - metabolism | Coculture Techniques | Humans | Actins - metabolism | Cystic Fibrosis - pathology | Epithelial Sodium Channels - metabolism | Respiratory Mucosa - pathology | Mesenchymal Stromal Cells - cytology | Tight Junctions - physiology | Amnion - metabolism | Epithelial Sodium Channels - genetics | Chlorides - metabolism | Cell Differentiation | Tissue Engineering | Cystic Fibrosis - metabolism | Amnion - cytology | Cells, Cultured | Mesenchymal Stromal Cells - metabolism | Epithelial Cells - pathology | Cystic Fibrosis Transmembrane Conductance Regulator - metabolism | Blotting, Western | Cystic Fibrosis - genetics | Fluorescent Antibody Technique | Cystic Fibrosis Transmembrane Conductance Regulator - genetics | Respiratory Mucosa - metabolism | Dextran | Analysis | Mortality | Therapeutics | Stem cells | Cystic fibrosis | Permeability | Epithelium | Muscle proteins | Homeopathy | Materia medica and therapeutics | Lung diseases | Rodents | Index Medicus | Original
Journal Article
Pediatric Pulmonology, ISSN 8755-6863, 07/2017, Volume 52, Issue 7, pp. 900 - 908
Journal Article
Journal of Aerosol Medicine and Pulmonary Drug Delivery, ISSN 1941-2711, 12/2016, Volume 29, Issue 6, pp. 482 - 489
Journal Article
Experimental Physiology, ISSN 0958-0670, 06/2019, Volume 104, Issue 6, pp. 866 - 875
What is the central question of this study? What is the precise subcellular localization of the epithelial sodium channel (ENaC) in human airway epithelium?... 
ENaC | cystic fibrosis | CFTR | airway epithelium | sodium absorption | Cystic fibrosis | Aprotinin | Tight junctions | Epithelial cells | Antibodies | Ions | Na+/K+-exchanging ATPase | Epithelium | Respiratory tract | Chloride conductance | Sodium | Fibrosis | Elastase | Localization
Journal Article