Defective acidification of intracellular organelles in cystic fibrosis.

Cystic fibrosis. Acidification indication.

Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis.

Abnormalities in intracellular regulation in cystic fibrosis.

Airway acidification initiates host defense abnormalities in cystic fibrosis mice.

Defective protein kinase C-mediated actions in cystic fibrosis neutrophils.

Expression of cystic fibrosis transmembrane conductance regulator corrects defective chloride channel regulation in cystic fibrosis airway epithelial cells.

Cystic fibrosis and bone disease: defective osteoblast maturation with the F508del mutation in cystic fibrosis transmembrane conductance regulator.

Cystic fibrosis. 7. Management of cystic fibrosis in different countries. Cystic fibrosis in Leeds.

Cystic fibrosis. 7. Management of cystic fibrosis in different countries. Cystic fibrosis in Melbourne.

Cystic fibrosis. 7. Management of cystic fibrosis in different countries. Cystic fibrosis in Copenhagen.

Defective epithelial chloride transport in a gene-targeted mouse model of cystic fibrosis.

Cystic fibrosis and non-cystic fibrosis bronchiectasis.

Cystic fibrosis. 2. Lung injury in cystic fibrosis.

Defective innate immunity and hyperinflammation in newborn cystic fibrosis transmembrane conductance regulator-knockout ferret lungs.

Fungi in cystic fibrosis and non-cystic fibrosis bronchiectasis.

Nontuberculous mycobacteria in cystic fibrosis and non-cystic fibrosis bronchiectasis.

Imaging in cystic fibrosis and non-cystic fibrosis bronchiectasis.

Disposition index identifies defective beta-cell function in cystic fibrosis subjects with normal glucose tolerance.

Defective CFTR- β-catenin interaction promotes NF-κB nuclear translocation and intestinal inflammation in cystic fibrosis.

Defective cellular immunity to gram-negative bacteria in cystic fibrosis patients.

Cystic Fibrosis Foundation and European Cystic Fibrosis Society Survey of cystic fibrosis mental health care delivery.

Cystic fibrosis.

Cystic fibrosis.

Cystic fibrosis.

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Cystic fibrosis. Acidification indication.

Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis.

Abnormalities in intracellular regulation in cystic fibrosis.

Airway acidification initiates host defense abnormalities in cystic fibrosis mice.

Defective protein kinase C-mediated actions in cystic fibrosis neutrophils.

Expression of cystic fibrosis transmembrane conductance regulator corrects defective chloride channel regulation in cystic fibrosis airway epithelial cells.

Cystic fibrosis and bone disease: defective osteoblast maturation with the F508del mutation in cystic fibrosis transmembrane conductance regulator.

Cystic fibrosis. 7. Management of cystic fibrosis in different countries. Cystic fibrosis in Leeds.

Cystic fibrosis. 7. Management of cystic fibrosis in different countries. Cystic fibrosis in Melbourne.

Cystic fibrosis. 7. Management of cystic fibrosis in different countries. Cystic fibrosis in Copenhagen.

Defective epithelial chloride transport in a gene-targeted mouse model of cystic fibrosis.

Cystic fibrosis and non-cystic fibrosis bronchiectasis.

Cystic fibrosis. 2. Lung injury in cystic fibrosis.

Defective innate immunity and hyperinflammation in newborn cystic fibrosis transmembrane conductance regulator-knockout ferret lungs.

Fungi in cystic fibrosis and non-cystic fibrosis bronchiectasis.

Nontuberculous mycobacteria in cystic fibrosis and non-cystic fibrosis bronchiectasis.

Imaging in cystic fibrosis and non-cystic fibrosis bronchiectasis.

Disposition index identifies defective beta-cell function in cystic fibrosis subjects with normal glucose tolerance.

Defective CFTR- β-catenin interaction promotes NF-κB nuclear translocation and intestinal inflammation in cystic fibrosis.

Defective cellular immunity to gram-negative bacteria in cystic fibrosis patients.

Cystic Fibrosis Foundation and European Cystic Fibrosis Society Survey of cystic fibrosis mental health care delivery.

Cystic fibrosis.

Cystic fibrosis.

Cystic fibrosis.

Defective acidification of intracellular organelles in cystic fibrosis.

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