Modeling Cystic Fibrosis and Mucociliary Clearance - Inria - Institut national de recherche en sciences et technologies du numérique Accéder directement au contenu
Chapitre D'ouvrage Année : 2017

Modeling Cystic Fibrosis and Mucociliary Clearance

Résumé

This chapter considers the investigation of airway clearance efficiency and dysfunction using rheological measurements, modeling and simulations of mucus flows. The work is mainly dedicated to the respiratory epithelium dysfunction subsequently to the consumption of cilia-inhibiting drugs (e.g. nicotine) or viral and/or bacterial infections, and cystic fibrosis, although many respiratory diseases are associated with an altered mucus transport.
Fichier principal
Vignette du fichier
18-Chapter5-CFMC.pdf (4.04 Mo) Télécharger le fichier
Origine : Fichiers produits par l'(les) auteur(s)

Dates et versions

hal-01476216 , version 1 (24-02-2017)

Identifiants

Citer

Dominique Anne-Archard, Robin Chatelin, Marlène Murris-Espin, David Sanchez, Marc Thiriet, et al.. Modeling Cystic Fibrosis and Mucociliary Clearance. Sid M. Becker. Modeling of microscale transport in biological processes, Academic Press, pp.113-154, 2017, 978-0-12-804595-4. ⟨10.1016/B978-0-12-804595-4.00005-5⟩. ⟨hal-01476216⟩
480 Consultations
546 Téléchargements

Altmetric

Partager

Gmail Facebook X LinkedIn More