Disruption of Interleukin-1β Autocrine Signaling Rescues Complex I Activity and Improves ROS Levels in Immortalized Epithelial Cells with Impaired Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Function

Author:

Clauzure Mariángeles,Valdivieso Angel G.,Massip Copiz María M.,Schulman Gustavo,Teiber María Luz,Santa-Coloma Tomás A.

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference106 articles.

1. Identification of the cystic fibrosis gene: chromosome walking and jumping;JM Rommens;Science,1989

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

3. Demonstration that CFTR is a chloride channel by alteration of its anion selectivity;MP Anderson;Science,1991

4. Expression of cystic fibrosis transmembrane conductance regulator corrects defective chloride channel regulation in cystic fibrosis airway epithelial cells;DP Rich;Nature,1990

5. Cystic Fibrosis Centre - Hospital for Sick Children (2012) Cystic Fibrosis Mutation Database. Toronto. Canada. http://www.genet.sickkids.on.ca/cftr/StatisticsPage.html.

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