Defective postsecretory maturation of MUC5B mucin in cystic fibrosis airways-Reference-Cited by-同舟云学术

Defective postsecretory maturation of MUC5B mucin in cystic fibrosis airways

Published:2017-03-23 Issue:6 Volume:2 Page:
ISSN:2379-3708
Container-title:JCI Insight
language:en
Short-container-title:

Author:

Abdullah Lubna H.,Evans Jessica R.,Wang T. Tiffany,Ford Amina A.,Makhov Alexander M.,Nguyen Kristine,Coakley Raymond D.,Griffith Jack D.,Davis C. William,Ballard Stephen T.,Kesimer Mehmet

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Reference39 articles.

1. Cystic fibrosis: a disease of vulnerability to airway surface dehydration

2. Imaging CFTR Protein Localization in Cultured Cells and Tissues

3. Expression of the cystic fibrosis gene in adult human lung.

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

5. CFTR, mucins, and mucus obstruction in cystic fibrosis;Kreda;Cold Spring Harb Perspect Med,2012

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