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A balance between activating and repressive histone modifications regulates cystic fibrosis transmembrane conductance regulator (CFTR) expression in vivo.
Bergougnoux A, Rivals I, Liquori A, Raynal C, Varilh J, Magalhães M, Perez MJ, Bigi N, Des Georges M, Chiron R, Squalli-Houssaini AS, Claustres M, De Sario A. Bergougnoux A, et al. Among authors: chiron r. Epigenetics. 2014 Jul;9(7):1007-17. doi: 10.4161/epi.28967. Epub 2014 Apr 29. Epigenetics. 2014. PMID: 24782114 Free PMC article.
Effectiveness of bacteriophages in the sputum of cystic fibrosis patients.
Saussereau E, Vachier I, Chiron R, Godbert B, Sermet I, Dufour N, Pirnay JP, De Vos D, Carrié F, Molinari N, Debarbieux L. Saussereau E, et al. Among authors: chiron r. Clin Microbiol Infect. 2014 Dec;20(12):O983-90. doi: 10.1111/1469-0691.12712. Epub 2014 Jul 26. Clin Microbiol Infect. 2014. PMID: 24920209 Free article.
Should diffuse bronchiectasis still be considered a CFTR-related disorder?
Bergougnoux A, Viart V, Miro J, Bommart S, Molinari N, des Georges M, Claustres M, Chiron R, Taulan-Cadars M. Bergougnoux A, et al. Among authors: chiron r. J Cyst Fibros. 2015 Sep;14(5):646-53. doi: 10.1016/j.jcf.2015.02.012. Epub 2015 Mar 18. J Cyst Fibros. 2015. PMID: 25797027 Free article.
124 results