Becq F - Search Results

1

Missense mutations in SLC26A8, encoding a sperm-specific activator of CFTR, are associated with human asthenozoospermia.

Dirami T, Rode B, Jollivet M, Da Silva N, Escalier D, Gaitch N, Norez C, Tuffery P, Wolf JP, Becq F, Ray PF, Dulioust E, Gacon G, Bienvenu T, Touré A. Dirami T, et al. Among authors: becq f. Am J Hum Genet. 2013 May 2;92(5):760-6. doi: 10.1016/j.ajhg.2013.03.016. Epub 2013 Apr 11. Am J Hum Genet. 2013. PMID: 23582645 Free PMC article.

2

[The impact of hypoxia on the ion channels in cystic fibrosis bronchial epithelial cells].

Pascarel K, Colas J, Mirval S, Becq F, Vandebrouck C. Pascarel K, et al. Among authors: becq f. Rev Mal Respir. 2023 Mar;40(3):230-233. doi: 10.1016/j.rmr.2023.01.014. Epub 2023 Feb 10. Rev Mal Respir. 2023. PMID: 36775781 French.

3

Tat1, a novel sulfate transporter specifically expressed in human male germ cells and potentially linked to rhogtpase signaling.

Toure A, Morin L, Pineau C, Becq F, Dorseuil O, Gacon G. Toure A, et al. Among authors: becq f. J Biol Chem. 2001 Jun 8;276(23):20309-15. doi: 10.1074/jbc.M011740200. Epub 2001 Mar 5. J Biol Chem. 2001. PMID: 11278976 Free article.

4

Activation of G551D CFTR channel with MPB-91: regulation by ATPase activity and phosphorylation.

Dérand R, Bulteau-Pignoux L, Mettey Y, Zegarra-Moran O, Howell LD, Randak C, Galietta LJ, Cohn JA, Norez C, Romio L, Vierfond JM, Joffre M, Becq F. Dérand R, et al. Among authors: becq f. Am J Physiol Cell Physiol. 2001 Nov;281(5):C1657-66. doi: 10.1152/ajpcell.2001.281.5.C1657. Am J Physiol Cell Physiol. 2001. PMID: 11600430 Free article.

5

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

6

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.

7

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.

8

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

9

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

10

Determination of CFTR chloride channel activity and pharmacology using radiotracer flux methods.

Norez C, Heda GD, Jensen T, Kogan I, Hughes LK, Auzanneau C, Dérand R, Bulteau-Pignoux L, Li C, Ramjeesingh M, Li H, Sheppard DN, Bear CE, Riordan JR, Becq F. Norez C, et al. Among authors: becq f. J Cyst Fibros. 2004 Aug;3 Suppl 2:119-21. doi: 10.1016/j.jcf.2004.05.025. J Cyst Fibros. 2004. PMID: 15463942 Free article. Review.

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