High lysosomal activities in cystic fibrosis tracheal gland cells corrected by adenovirus-mediated CFTR gene transfer

Author:

Kammouni W.,Naı̈mi D.,Renaud W.,Bianco N.,Figarella C.,Merten M.D.

Publisher

Elsevier BV

Subject

Molecular Biology,Molecular Medicine

Reference30 articles.

1. Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA;Riordan;Science,1989

2. Cystic fibrosis and endobronchial Pseudomonas infection;Hoiby;Curr. Opin. Pediatr.,1993

3. Submucosal glands are the predominant site of CFTR expression in human bronchus;Engelhardt;Nature Genet.,1992

4. The serous cell;Basbaum;Annu. Rev. Physiol.,1990

5. Culture and characterization of human tracheal gland cells;Tournier;Am. Rev. Respir. Dis.,1990

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1. Airway Gland Structure and Function;Physiological Reviews;2015-10

2. Airway Epithelium;Colloquium Series on Integrated Systems Physiology: From Molecule to Function;2012-11-15

3. Yet Another Role for the Cystic Fibrosis Transmembrane Conductance Regulator;American Journal of Respiratory Cell and Molecular Biology;2000-01

4. Recombinant E1-Deleted Adenoviral Vectors Induce Apoptosis in a Rat Airway Epithelial Mucous Goblet Cell Line;Japanese Journal of Pharmacology;1999

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