Mucus, mucins, and cystic fibrosis
Author:
Affiliation:
1. Marsico Lung Institute/Cystic Fibrosis Research CenterUniversity of North Carolina at Chapel HillChapel Hill North Carolina
2. Division of Pediatric PulmonologyUniversity of North Carolina at Chapel HillChapel Hill North Carolina
Funder
Cystic Fibrosis Foundation
Vertex Pharmaceuticals
National Institute of Diabetes and Digestive and Kidney Diseases
Publisher
Wiley
Subject
Pulmonary and Respiratory Medicine,Pediatrics, Perinatology, and Child Health
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ppul.24530
Reference97 articles.
1. Cystic fibrosis: a disease of vulnerability to airway surface dehydration
2. Cystic fibrosis: An inherited disease affecting mucin-producing organs
3. Cystic fibrosis: impaired bicarbonate secretion and mucoviscidosis
4. Localization of Secretory Mucins MUC5AC and MUC5B in Normal/Healthy Human Airways
5. Airway Gland Structure and Function
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