Zobrazeno 1 - 8
of 8
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::95661f3401973e8353aca4c550cbde4a
https://doi.org/10.1038/sj.bjp.0705597
https://doi.org/10.1038/sj.bjp.0705597
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::513a05ac60e122b24f32cb44d8cad61a
https://doi.org/10.1007/s00232-003-2030-z
https://doi.org/10.1007/s00232-003-2030-z
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd61bb23dcae108f42b87ef3c33da967
https://doi.org/10.1007/s00232-001-0183-1
https://doi.org/10.1007/s00232-001-0183-1
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5a8cebeffe4b6994a01dce568ebd49f
https://doi.org/10.1242/jcs.114.22.4073
https://doi.org/10.1242/jcs.114.22.4073
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3de91f9a0ed0bf8fd97b1d476e49960b
https://pubmed.ncbi.nlm.nih.gov/12124395
https://pubmed.ncbi.nlm.nih.gov/12124395
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88b3634b584e2340f4a3987c3bad35a2
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e217a0f988e90b1b40955875dd962eb2
http://www.scopus.com/inward/record.url?eid=2-s2.0-0035195682&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0035195682&partnerID=MN8TOARS
Autor:
Derand, Renaud, Bulteau-Pignoux, Laurence, Mettey, Yvette, Zegarra-Moran, Olga, Howell, L. Daniel, Randak, Christoph, Galietta, Luis J.V., Cohn, Jonathan A., Norez, Caroline, Romio, Leila, Vierfond, Jean-Michel, Joffre, Michel, Becq, Frederic
Publikováno v:
American Journal of Physiology: Cell Physiology; Nov2001, Vol. 281 Issue 5, p1657, 10p, 1 Diagram, 1 Chart, 22 Graphs