Modeling Cystic Fibrosis and Mucociliary Clearance

Abstract : 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.
Type de document :
Chapitre d'ouvrage
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〉
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https://hal.inria.fr/hal-01476216
Contributeur : Marc Thiriet <>
Soumis le : vendredi 24 février 2017 - 16:21:33
Dernière modification le : vendredi 14 septembre 2018 - 09:16:06
Document(s) archivé(s) le : jeudi 25 mai 2017 - 13:52:33

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18-Chapter5-CFMC.pdf
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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〉

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