Acid exposure impairs mucus secretion and disrupts mucus transport in neonatal piglet airways (original) (raw)
Acid exposure disrupts mucus secretion and impairs mucociliary transport in neonatal piglet airways
Eda Eken
American Journal of Physiology-Lung Cellular and Molecular Physiology, 2020
View PDFchevron_right
Cystic fibrosis. Impaired mucus detachment disrupts mucociliary transport in a piglet model of cystic fibrosis
Eric Hoffman
Science (New York, N.Y.), 2014
View PDFchevron_right
Development of an airway mucus defect in the cystic fibrosis rat
Michelle Fanucchi
JCI insight, 2018
View PDFchevron_right
Normal mouse intestinal mucus release requires cystic fibrosis transmembrane regulatordependent bicarbonate secretion
Abigail Garcia
The Journal of clinical …, 2009
View PDFchevron_right
Paracellular bicarbonate flux across human cystic fibrosis airway epithelia tempers changes in airway surface liquid pH
TAYYAB REHMAN
The Journal of Physiology, 2020
View PDFchevron_right
Hyperconcentrated Mucus Unifies Submucosal Gland and Superficial Airway Dysfunction in Cystic Fibrosis
Henry Paul Goodell
2021
View PDFchevron_right
Submucosal gland secretions in airways from cystic fibrosis patients have normal [Na+] and pH but elevated viscosity
sujatha jayaraman
Proceedings of The National Academy of Sciences, 2001
View PDFchevron_right
Loss of Anion Transport without Increased Sodium Absorption Characterizes Newborn Porcine Cystic Fibrosis Airway Epithelia
Alejandro Pezzulo, Thomas Moninger
Cell, 2010
View PDFchevron_right
Molecular basis for pH-dependent mucosal dehydration in cystic fibrosis airways
L. Clunes
Proceedings of the National Academy of Sciences, 2013
View PDFchevron_right
Cystic Fibrosis Transmembrane Conductance Regulator Is Expressed in Mucin Granules from Calu-3 and Primary Human Airway Epithelial Cells
Scott O'Grady PhD
American Journal of Respiratory Cell and Molecular Biology, 2013
View PDFchevron_right
MUC5AC and MUC5B Mucins Increase in Cystic Fibrosis Airway Secretions during Pulmonary Exacerbation
Markus Henke
American Journal of Respiratory and Critical Care Medicine, 2007
View PDFchevron_right
Defective postsecretory maturation of MUC5B mucin in cystic fibrosis airways
Alexander Makhov
JCI insight, 2017
View PDFchevron_right
MUC5AC and MUC5B Mucins Are Decreased in Cystic Fibrosis Airway Secretions
Rudolf Huber
American Journal of Respiratory Cell and Molecular Biology, 2004
View PDFchevron_right
Cystic fibrosis gene mutation reduces epithelial cell acidification and injury in acid-perfused mouse duodenum
Marshall Montrose
Gastroenterology, 2004
View PDFchevron_right
Mucus secretion by single tracheal submucosal glands from normal and cystic fibrosis transmembrane conductance regulator knockout mice
Jeffrey Wine
The Journal of Physiology, 2007
View PDFchevron_right
Neonates with cystic fibrosis have a reduced nasal liquid pH; A small pilot study
Alejandro Pezzulo
Journal of Cystic Fibrosis, 2014
View PDFchevron_right
Airway submucosal glands from cystic fibrosis swine suffer from abnormal ion transport across the serous acini, collecting duct, and ciliated duct
Terry Machen
American Journal of Physiology-Lung Cellular and Molecular Physiology, 2020
View PDFchevron_right
Airway surface liquid pH is not acidic in children with cystic fibrosis
Stephen Stick
Nature communications, 2017
View PDFchevron_right
Mucin Release from Rabbit Tracheal Epithelium in Response to Sera from Normal and Cystic Fibrosis Subjects
Pi-wan Cheng
Pediatric Research, 1982
View PDFchevron_right
Mucous solids and liquid secretion by airways: studies with normal pig, cystic fibrosis human, and non-cystic fibrosis human bronchi
Vincent Valentine
AJP: Lung Cellular and Molecular Physiology, 2011
View PDFchevron_right
Cystic fibrosis airway secretions exhibit mucin hyperconcentration and increased osmotic pressure
Genevieve Demaria
Journal of Clinical Investigation, 2014
View PDFchevron_right
Evidence for Periciliary Liquid Layer Depletion, Not Abnormal Ion Composition, in the Pathogenesis of Cystic Fibrosis Airways Disease
Scott Randell
Cell, 1998
View PDFchevron_right
Human airway epithelial cell pH regulatory proteins in cystic fibrosis: Differential expression in nasal and bronchial airway cells
Kathleen Boyne
View PDFchevron_right
Epithelial Cell Dysfunction in Cystic Fibrosis: Implications for Airways Disease
Pi-wan Cheng
Acta Paediatrica, 1989
View PDFchevron_right
Mucin glycosylation changes in cystic fibrosis lung disease are not manifest in submucosal gland secretions
Nicolle Packer
Biochemical Journal, 2005
View PDFchevron_right
Is Cystic Fibrosis Mucus Abnormal?
Malcolm King
Pediatric Research, 1981
View PDFchevron_right
Faculty Opinions recommendation of Loss of anion transport without increased sodium absorption characterizes newborn porcine cystic fibrosis airway epithelia
Richard Naftalin
Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature, 2010
View PDFchevron_right
MUCLIN expression in the cystic fibrosis transmembrane conductance regulator knockout mouse
Abdulbaki Agbas
Gastroenterology, 1997
View PDFchevron_right