Related Experiment Video
Updated: Feb 8, 2026

Phage Therapy Application to Counteract Pseudomonas aeruginosa Infection in Cystic Fibrosis Zebrafish Embryos
Published on: May 12, 2020
Publisher Correction: Thymosin α1 represents a potential potent single-molecule-based therapy for cystic fibrosis
Luigina Romani1, Vasilis Oikonomou2, Silvia Moretti2
1Department of Experimental Medicine, University of Perugia, Perugia, Italy. luigina.romani@unipg.it.
Abstract:
In the version of this article originally published, the amino acid sequence for Tα1 described in the Online Methods is incorrect. The sequence is described as "Ac-SDAAVDTSSEITTJDLKEKKEVVEEAEN-OH". It should be "Ac-SDAAVDTSSEITTKDLKEKKEVVEEAEN-OH". The error has been corrected in the HTML and PDF versions of this article.
More Related Videos
Related Concept Videos
Cystic Fibrosis: Pathogenesis
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
Cystic Fibrosis: Management
Sinus disease and chronic...
The Representativeness Heuristic
Distance Corrections
Power Factor Correction
Molecules and Compounds

