Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Laurence Bulteau-Pignoux"'
Autor:
Renaud Dérand, Bertrand Moreau, Thierry Janet, Alicia Montoni, Laurence Bulteau-Pignoux, Jean-Marc Muller, Frédéric Becq
Publikováno v:
British Journal of Pharmacology. 141:698-708
1. In the human airway epithelium, VIP/PACAP receptors are distributed in nerve fibers and in epithelial cells but their role in transepithelial ion transport have not been reported. Here, we show that human bronchial epithelial Calu-3 cells expresse
Publikováno v:
Journal of Membrane Biology. 194:109-117
The pharmacological activation of the cystic fibrosis transmembrane conductance regulator (CFTR) chloride channel mutated at glycine 551 (G551D-CFTR) was studied in the presence of the benzimidazolone derivative NS004 and compared to that of wild-typ
Publikováno v:
The Journal of Membrane Biology. 188:175-182
We have studied the mechanism by which genistein activates cystic fibrosis transmembrane conductance regulator (CFTR) in CHO cells expressing wild type or G551D-CFTR. In wild-type CHO cells, after exposure to 2.5 microM forskolin, 25 microM genistein
Autor:
Luis J. V. Galietta, Robert L. Dormer, Iolo Doull, M. Rachel Morris, Jean-Michel Vierfond, Laurence Bulteau-Pignoux, Michael A. Gray, Renaud Dérand, Frédéric Becq, Malcolm M.C. Pereira, Thierry Métayé, Margaret A. McPherson, Ceinwen M. McNeilly, Yvette Mettey
Publikováno v:
Journal of Cell Science. 114:4073-4081
A number of genetic diseases, including cystic fibrosis, have been identified as disorders of protein trafficking associated with retention of mutant protein within the endoplasmic reticulum. In the presence of the benzo(c)quinolizinium drugs, MPB-07
Publikováno v:
The Journal of biological chemistry. 277(39)
Loss of cystic fibrosis transmembrane conductance regulator (CFTR) channel activity explains most of the manifestations of the cystic fibrosis (CF) disease. To understand the consequences of CF mutations on CFTR channel activity, we compared the phar
Autor:
Mohabir Ramjeesingh, David N. Sheppard, Céline Auzanneau, Renaud Dérand, Christine E. Bear, Caroline Norez, Canhui Li, Lauren K. Hughes, Ilana Kogan, Laurence Bulteau-Pignoux, John R. Riordan, Hongyu Li, Frédéric Becq, Ghanshyam D. Heda, Timothy J. Jensen
Publikováno v:
Journal of Cystic Fibrosis. :119-121
Flux studies using either radioisotopes or ion-selective electrodes are a convenient method to assay the function of the cystic fibrosis transmembrane conductance regulator (CFTR) Cl − channel. Here, we described three different protocols to study
Autor:
L. Daniel Howell, Jonathan A. Cohn, Christoph Randak, Yvette Mettey, Caroline Norez, Renaud Dérand, Laurence Bulteau-Pignoux, Michel Joffre, Frédéric Becq, Jean Michel Vierfond, Luis J. V. Galietta, Leila Romio, Olga Zegarra-Moran
Publikováno v:
Scopus-Elsevier
CIÊNCIAVITAE
CIÊNCIAVITAE
We have designed and synthesized benzo[c]quinolizinium derivatives and evaluated their effects on the activity of G551D cystic fibrosis transmembrane conductance regulator (CFTR) expressed in Chinese hamster ovary and Fisher rat thyroid cells. We dem
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