Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Ceinwen M. McNeilly"'
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
Autor:
Ceinwen M. McNeilly, M. R. Morris, Frédéric Becq, Malcolm M.C. Pereira, Yvette Mettey, Margaret A. McPherson, Iolo Doull, Robert L. Dormer, J-M Vierfond
Publikováno v:
Pfl�gers Archiv European Journal of Physiology. 443:S117-S120
Wild-type and the DeltaF508 mutation of the cystic fibrosis transmembrane conductance regulator (DeltaF508-CFTR) were localised by confocal imaging in DeltaF508/DeltaF508 native airway epithelial cells using a well-characterised CFTR antibody. Surfac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ed99eef992887e93cc66509044e3d29
https://doi.org/10.1007/s004240100657
https://doi.org/10.1007/s004240100657
Autor:
Robert L. Dormer, Ceinwen M. McNeilly, D. Russell, Malcolm M.C. Pereira, F. L. L. Stratford, Margaret A. McPherson, R. M. Morris
Publikováno v:
Pflugers Archiv : European journal of physiology. 443
The cystic fibrosis transmembrane conductance regulator (CFTR) mediates secretion of mucins and serous proteins. The aim was to correct pharmacologically the CFTR defect in protein secretion in airway gland cells and so to correct the viscous mucous
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1c87240bcb1e51ba6efcf1c4852da9a
https://pubmed.ncbi.nlm.nih.gov/11845317
https://pubmed.ncbi.nlm.nih.gov/11845317
Autor:
Robert L. Dormer, Malcolm M.C. Pereira, Chiara Folli, Thierry Métayé, Yvette Mettey, Jean Michel Vierfond, Ceinwen M. McNeilly, M. Rachel Morris, Olga Zegarra-Moran, Laurence Bulteau, Luis J. V. Galietta, Michel Joffre, Frédéric Becq, Chantal Jougla, Renaud Dérand
Publikováno v:
Scopus-Elsevier
CIÊNCIAVITAE
CIÊNCIAVITAE
The pharmacological activation of the cystic fibrosis gene protein cystic fibrosis transmembrane conductance regulator (CFTR) was studied in human airway epithelial Calu-3 cells, which express a high level of CFTR protein as assessed by Western blot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f6999eedf4fb3096647ebe528720612
http://hdl.handle.net/11588/739464
http://hdl.handle.net/11588/739464
Autor:
Bulteau, Laurence, Derand, Renaud
Publikováno v:
American Journal of Physiology: Cell Physiology; Dec2000, Vol. 279 Issue 6, pC1925, 13p, 12 Black and White Photographs, 28 Graphs