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CCSP G38A polymorphism environment interactions regulate CCSP levels differentially in COPD.
Knabe L, Varilh J, Bergougnoux A, Gamez AS, Bonini J, Pommier A, Petit A, Molinari N, Vachier I, Taulan-Cadars M, Bourdin A. Knabe L, et al. Among authors: bergougnoux a. Am J Physiol Lung Cell Mol Physiol. 2016 Oct 1;311(4):L696-L703. doi: 10.1152/ajplung.00280.2016. Epub 2016 Aug 5. Am J Physiol Lung Cell Mol Physiol. 2016. PMID: 27496897 Free article.
DNA methylation at modifier genes of lung disease severity is altered in cystic fibrosis.
Magalhães M, Rivals I, Claustres M, Varilh J, Thomasset M, Bergougnoux A, Mely L, Leroy S, Corvol H, Guillot L, Murris M, Beyne E, Caimmi D, Vachier I, Chiron R, De Sario A. Magalhães M, et al. Among authors: bergougnoux a. Clin Epigenetics. 2017 Feb 14;9:19. doi: 10.1186/s13148-016-0300-8. eCollection 2017. Clin Epigenetics. 2017. PMID: 28289476 Free PMC article.
The HDAC inhibitor SAHA does not rescue CFTR membrane expression in Cystic Fibrosis.
Bergougnoux A, Petit A, Knabe L, Bribes E, Chiron R, De Sario A, Claustres M, Molinari N, Vachier I, Taulan-Cadars M, Bourdin A. Bergougnoux A, et al. Int J Biochem Cell Biol. 2017 Jul;88:124-132. doi: 10.1016/j.biocel.2017.05.002. Epub 2017 May 3. Int J Biochem Cell Biol. 2017. PMID: 28478266 Free article.
CFTR gene variants, epidemiology and molecular pathology.
Bareil C, Bergougnoux A. Bareil C, et al. Among authors: bergougnoux a. Arch Pediatr. 2020 Feb;27 Suppl 1:eS8-eS12. doi: 10.1016/S0929-693X(20)30044-0. Arch Pediatr. 2020. PMID: 32172939 Free article. Review.
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. Epigenetics. 2014 Jul;9(7):1007-17. doi: 10.4161/epi.28967. Epub 2014 Apr 29. Epigenetics. 2014. PMID: 24782114 Free PMC article.
47 results