Zobrazeno 1 - 10
of 60
pro vyhledávání: '"F. Dupuit"'
Autor:
Jocelyne Hinnrasky, F. Dupuit, Dominique Gaillard, E. Copreni, S. de Bentzmann, E. Puchelle, Emmanuel F. Mongodin
Publikováno v:
American Journal of Physiology-Lung Cellular and Molecular Physiology. 278:L165-L176
To investigate the regeneration process of a well-differentiated and functional human airway epithelium, we adapted an in vivo xenograft model in which adult human nasal epithelial cells adhere and progressively repopulate denuded rat tracheae grafte
CFTR and differentiation markers expression in non-CF and delta F 508 homozygous CF nasal epithelium
Publikováno v:
Journal of Clinical Investigation. 96:1601-1611
Human nasal polyps from non-CF and delta F 508 homozygous CF patients were used to compare the expression of CFTR and markers epithelial differentiation, such as cytokeratins (CK) and desmoplakins (DP), at the transcriptional and translational levels
Publikováno v:
Archives Internationales de Physiologie, de Biochimie et de Biophysique. 100:A41-A46
Airway secretions actively participate in respiratory epithelium protection. Apart from its main participation in transport of inhaled microorganisms and particles by mucociliary clearance, respiratory mucus also contributes to other protective purpo
Autor:
F. Dupuit, Hassan El'btaouri, Jacky Jacquot, Jocelyne Hinnrasky, Frank Antonicelli, E. Puchelle, Bernard Haye
Publikováno v:
FEBS Letters. 274:131-135
Evidence is obtained for the presence of lipocortin-like proteins in human tracheal gland cells in culture. Using polyclonal antibodies to lipocortin I. indirect immunofluorescence studies demonstrate that lipocortin I is mainly confined to the trach
Autor:
Noël Bonnet, Odile Bajolet, Jérôme Cutrona, F. Dupuit, Emmanuel F. Mongodin, Edith Puchelle, Sophie de Bentzmann
Publikováno v:
Infection and Immunity
Infection and Immunity, American Society for Microbiology, 2002, 70 (2), pp.620-30
Infection and Immunity, American Society for Microbiology, 2002, 70 (2), pp.620-30
This study was designed to investigate the molecular mechanisms of Staphylococcus aureus adherence to human airway epithelium. Using a humanized bronchial xenograft model in the nude mouse and primary cultures of human airway epithelial cells (HAEC),
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12cd235fd81341aade597b620f8e8d7a
https://www.hal.inserm.fr/inserm-00149318
https://www.hal.inserm.fr/inserm-00149318
Autor:
David J. Porteous, F. Dupuit, E. Puchelle, J. R. Dorin, J.M. Zahm, Dominique Gaillard, Jocelyne Hinnrasky
Publikováno v:
The American journal of physiology. 272(3 Pt 1)
In cystic fibrosis (CF), whether cystic fibrosis transmembrane conductance regulator (CFTR) dysfunction leads to decreased mucociliary clearance and mucus hypersecretion, before bacterial infection, remains an open question. To answer this question,
Autor:
E. Puchelle, S. de Bentzmann, C Fuchey, O Bajolet-Laudinat, P. Roger, F. Dupuit, M C Plotkowski
We investigated the implication of asialo GM1 as an epithelial receptor in the increased Pseudomonas aeruginosa affinity for regenerating respiratory epithelial cells from cystic fibrosis (CF) and non-CF patients. Human respiratory epithelial cells w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::099105e8831071a337bd902bb7b4bb3a
https://europepmc.org/articles/PMC173965/
https://europepmc.org/articles/PMC173965/
Autor:
J L, Imler, F, Dupuit, C, Chartier, N, Accart, A, Dieterle, H, Schultz, E, Puchelle, A, Pavirani
Publikováno v:
Gene therapy. 3(1)
In vivo gene therapy requires the development of vectors able to deliver and express therapeutic genes preferentially into specific cell populations. This can be achieved by the manipulation of viral proteins mediating target-cell recognition, as wel
Autor:
F, Dupuit, A, Bout, J, Hinnrasky, C, Fuchey, J M, Zahm, J L, Imler, A, Pavirani, D, Valerio, E, Puchelle
Publikováno v:
Gene therapy. 2(2)
The Rhesus monkey has been used as a model for evaluating the possibility of introducing the CFTR gene into the airway epithelium in vivo. We addressed the question of whether the simian airway surface epithelium exhibits a CFTR distribution and func
Publikováno v:
Laboratory investigation; a journal of technical methods and pathology. 72(2)
In normal adult pseudostratified human nasal surface epithelium, the cystic fibrosis transmembrane conductance regulator (CFTR) is localized to the apical domain of the ciliated cells, whereas in cystic fibrosis (CF), the mutated delta F 508 CFTR exh