Becq F - Search Results

1

Focus on TRP channels in cystic fibrosis.

Grebert C, Becq F, Vandebrouck C. Grebert C, et al. Among authors: becq f. Cell Calcium. 2019 Jul;81:29-37. doi: 10.1016/j.ceca.2019.05.007. Epub 2019 May 30. Cell Calcium. 2019. PMID: 31176886 Review.

2

Development of substituted Benzo[c]quinolizinium compounds as novel activators of the cystic fibrosis chloride channel.

Becq F, Mettey Y, Gray MA, Galietta LJ, Dormer RL, Merten M, Métayé T, Chappe V, Marvingt-Mounir C, Zegarra-Moran O, Tarran R, Bulteau L, Dérand R, Pereira MM, McPherson MA, Rogier C, Joffre M, Argent BE, Sarrouilhe D, Kammouni W, Figarella C, Verrier B, Gola M, Vierfond JM. Becq F, et al. J Biol Chem. 1999 Sep 24;274(39):27415-25. doi: 10.1074/jbc.274.39.27415. J Biol Chem. 1999. PMID: 10488073 Free article.

3

[CFTR and transepithelial ionic transport abnormalities in cystic fibrosis].

Becq F. Becq F. Arch Pediatr. 2003 Sep;10 Suppl 2:325s-332s. doi: 10.1016/s0929-693x(03)90047-9. Arch Pediatr. 2003. PMID: 14671929 Review. French.

4

Synthesis, SAR, crystal structure, and biological evaluation of benzoquinoliziniums as activators of wild-type and mutant cystic fibrosis transmembrane conductance regulator channels.

Marivingt-Mounir C, Norez C, Dérand R, Bulteau-Pignoux L, Nguyen-Huy D, Viossat B, Morgant G, Becq F, Vierfond JM, Mettey Y. Marivingt-Mounir C, et al. Among authors: becq f. J Med Chem. 2004 Feb 12;47(4):962-72. doi: 10.1021/jm0308848. J Med Chem. 2004. PMID: 14761197

5

General anesthetic octanol and related compounds activate wild-type and delF508 cystic fibrosis chloride channels.

Marcet B, Becq F, Norez C, Delmas P, Verrier B. Marcet B, et al. Among authors: becq f. Br J Pharmacol. 2004 Mar;141(6):905-14. doi: 10.1038/sj.bjp.0705684. Epub 2004 Feb 16. Br J Pharmacol. 2004. PMID: 14967738 Free PMC article.

6

Regulation of the cystic fibrosis transmembrane conductance regulator channel by beta-adrenergic agonists and vasoactive intestinal peptide in rat smooth muscle cells and its role in vasorelaxation.

Robert R, Thoreau V, Norez C, Cantereau A, Kitzis A, Mettey Y, Rogier C, Becq F. Robert R, et al. Among authors: becq f. J Biol Chem. 2004 May 14;279(20):21160-8. doi: 10.1074/jbc.M312199200. Epub 2004 Mar 11. J Biol Chem. 2004. PMID: 15020588 Free article.

7

Syntaxin 8 impairs trafficking of cystic fibrosis transmembrane conductance regulator (CFTR) and inhibits its channel activity.

Bilan F, Thoreau V, Nacfer M, Dérand R, Norez C, Cantereau A, Garcia M, Becq F, Kitzis A. Bilan F, et al. Among authors: becq f. J Cell Sci. 2004 Apr 15;117(Pt 10):1923-35. doi: 10.1242/jcs.01070. Epub 2004 Mar 23. J Cell Sci. 2004. PMID: 15039462

8

The cystic fibrosis mutation G1349D within the signature motif LSHGH of NBD2 abolishes the activation of CFTR chloride channels by genistein.

Melin P, Thoreau V, Norez C, Bilan F, Kitzis A, Becq F. Melin P, et al. Among authors: becq f. Biochem Pharmacol. 2004 Jun 15;67(12):2187-96. doi: 10.1016/j.bcp.2004.02.022. Biochem Pharmacol. 2004. PMID: 15163550

9

Rescue of functional delF508-CFTR channels in cystic fibrosis epithelial cells by the alpha-glucosidase inhibitor miglustat.

Norez C, Noel S, Wilke M, Bijvelds M, Jorna H, Melin P, DeJonge H, Becq F. Norez C, et al. Among authors: becq f. FEBS Lett. 2006 Apr 3;580(8):2081-6. doi: 10.1016/j.febslet.2006.03.010. Epub 2006 Mar 10. FEBS Lett. 2006. PMID: 16546175 Free article.

10

Maintaining low Ca2+ level in the endoplasmic reticulum restores abnormal endogenous F508del-CFTR trafficking in airway epithelial cells.

Norez C, Antigny F, Becq F, Vandebrouck C. Norez C, et al. Among authors: becq f. Traffic. 2006 May;7(5):562-73. doi: 10.1111/j.1600-0854.2006.00409.x. Traffic. 2006. PMID: 16643279 Free article.

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