[HTML][HTML] Pharmacological therapy for cystic fibrosis: from bench to bedside

F Becq, MA Mall, DN Sheppard, M Conese… - Journal of Cystic …, 2011 - Elsevier
With knowledge of the molecular behaviour of the cystic fibrosis transmembrane conductance
regulator (CFTR), its physiological role and dysfunction in cystic fibrosis (CF), therapeutic …

[HTML][HTML] CFTR and Ca2+ signaling in cystic fibrosis

F Antigny, C Norez, F Becq… - Frontiers in …, 2011 - frontiersin.org
Among the diverse physiological functions exerted by calcium signaling in living cells, its role
in the regulation of protein biogenesis and trafficking remains incompletely understood. In …

Modulating innate and adaptive immunity by (R)-roscovitine: potential therapeutic opportunity in cystic fibrosis

…, AG Rossi, V Witko-Sarsat, C Norez, F Becq… - Journal of innate …, 2016 - karger.com
… <sup>a</sup>Centre de Perharidy, ManRos Therapeutics, Roscoff, France; <sup>b</sup>Department
of Pharmacological and Physiological Sciences, The University of Chicago, Chicago, Ill …

Development of a third generation shallow-water wave model with unstructured spatial meshing

M Benoit, F Marcos, F Becq - Coastal Engineering 1996, 1997 - ascelibrary.org
F to relative (or intrinsic) angular frequency a : N = F / a. The directional variance density F(f,9…
models the way the wave energy (or variance) spreads over frequency f and direction 0. _^ …

Interleukin-1β secretion is impaired by inhibitors of the ATP binding cassette transporter, ABC1

Y Hamon, MF Luciani, F Becq, B Verrier… - Blood, The Journal …, 1997 - ashpublications.org
… in Becq et al.12 For peritoneal macrophages, the procedure is essentially as described in
Becq et al.… Gabel (Pfizer Inc) for discussion and for having provided Tenidap and UK5099; F. …

9‐phenanthrol inhibits human TRPM4 but not TRPM5 cationic channels

…, C Norez, Y Mettey, P Launay, F Becq… - British journal of …, 2008 - Wiley Online Library
Background and purpose: TRPM4 and TRPM5 are calcium‐activated non‐selective cation
channels with almost identical characteristics. TRPM4 is detected in several tissues including …

[HTML][HTML] Rescue of functional delF508-CFTR channels in cystic fibrosis epithelial cells by the α-glucosidase inhibitor miglustat

…, M Bijvelds, H Jorna, P Melin, H DeJonge, F Becq - FEBS letters, 2006 - Elsevier
In the disease cystic fibrosis (CF), the most common mutation delF508 results in
endoplasmic reticulum retention of misfolded CF gene proteins (CFTR). We show that the α-1,2-…

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

…, N Gaitch, C Norez, P Tuffery, JP Wolf, F Becq… - The American Journal of …, 2013 - cell.com
The cystic fibrosis transmembrane conductance regulator (CFTR) is present in mature sperm
and is required for sperm motility and capacitation. Both these processes are controlled by …

Sildenafil (Viagra) corrects ΔF508-CFTR location in nasal epithelial cells from patients with cystic fibrosis

…, Z Clark, MMC Pereira, IJM Doull, C Norez, F Becq… - Thorax, 2005 - thorax.bmj.com
Background: Most patients with cystic fibrosis (CF) have a ΔF508 mutation resulting in
abnormal retention of mutant gene protein (ΔF508-CFTR) within the cell. This study was …

Discovery of novel potent ΔF 508‐CFTR correctors that target the nucleotide binding domain

…, G Faure, H Herrmann, M Ollero, F Becq… - EMBO Molecular …, 2013 - embopress.org
The deletion of Phe508 (ΔF508) in the first nucleotide binding domain (NBD1) of CFTR is
the most common mutation associated with cystic fibrosis. The ΔF508‐CFTR mutant is …