Goblet cell hyperplasia is not epithelial-autonomous in the Cftr knockout intestine
Author:
Affiliation:
1. Dalton Cardiovascular Research Center, University of Missouri, Columbia, Missouri
2. Department of Pathobiology, University of Missouri, Columbia, Missouri
3. Department of Biomedical Sciences, University of Missouri, Columbia, Missouri
Abstract
Funder
Cystic Fibrosis Foundation
HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases
Publisher
American Physiological Society
Subject
Physiology (medical),Gastroenterology,Hepatology,Physiology
Link
https://journals.physiology.org/doi/pdf/10.1152/ajpgi.00290.2021
Reference77 articles.
1. Cystic fibrosis airway secretions exhibit mucin hyperconcentration and increased osmotic pressure
2. Gastrointestinal Outcomes and Confounders in Cystic Fibrosis
3. An Animal Model for Cystic Fibrosis Made by Gene Targeting
4. Defective goblet cell exocytosis contributes to murine cystic fibrosis–associated intestinal disease
5. Bicarbonate and functional CFTR channel are required for proper mucin secretion and link cystic fibrosis with its mucus phenotype
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