Cystic Fibrosis Transmembrane Conductance Regulator Is Expressed in Mucin Granules from Calu-3 and Primary Human Airway Epithelial Cells-Reference-Cited by-同舟云学术

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Cystic Fibrosis Transmembrane Conductance Regulator Is Expressed in Mucin Granules from Calu-3 and Primary Human Airway Epithelial Cells

Published:2013-10 Issue:4 Volume:49 Page:511-516
ISSN:1044-1549
Container-title:American Journal of Respiratory Cell and Molecular Biology
language:en
Short-container-title:Am J Respir Cell Mol Biol

Author:

LeSimple Pierre,Goepp Julie,Palmer Melissa L.,Fahrenkrug Scott C.,O’Grady Scott M.,Ferraro Pasquale,Robert Renaud,Hanrahan John W.

Publisher

American Thoracic Society

Subject

Cell Biology,Clinical Biochemistry,Pulmonary and Respiratory Medicine,Molecular Biology

Reference27 articles.

1. Airway Surface Dehydration in Cystic Fibrosis: Pathogenesis and Therapy

2. A new role for bicarbonate in mucus formation

3. Birth of mucus

4. Hyperacidity of secreted fluid from submucosal glands in early cystic fibrosis

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1. Nano-scale viscometry reveals an inherent mucus defect in cystic fibrosis;2024-03-07

2. Ionocyte-Specific Regulation of Cystic Fibrosis Transmembrane Conductance Regulator;American Journal of Respiratory Cell and Molecular Biology;2023-09

3. CFTR Protein: Not Just a Chloride Channel?;Cells;2021-10-22

4. Anaerobic microbiota facilitate P. aeruginosa access to the airway epithelium in a novel co-culture model of colonization;2021-03-06

5. Generation of 13C-Labeled MUC5AC Mucin Oligosaccharides for Stable Isotope Probing of Host-Associated Microbial Communities;ACS Infectious Diseases;2019-01-09

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