Non-Invasive Airway Health Measurement Using Synchrotron X-Ray Microscopy of High Refractive Index Glass Microbeads
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Martin Donnelley | Kaye S. Morgan | David W. Parsons | Karen Siu | M. Donnelley | K. Siu | K. Morgan | N. Farrow | Nigel Farrow | D. Parsons
[1] S. Anderson,et al. Inhalation of hypertonic saline aerosol enhances mucociliary clearance in asthmatic and healthy subjects. , 1996, The European respiratory journal.
[2] Mark R Elkins,et al. A controlled trial of long-term inhaled hypertonic saline in patients with cystic fibrosis. , 2006, The New England journal of medicine.
[3] M. Donnelley,et al. Dry deposition of pollutant and marker particles onto live mouse airway surfaces enhances monitoring of individual particle mucociliary transit behaviour. , 2012, Journal of synchrotron radiation.
[4] W. Skinner,et al. A new technique to examine individual pollutant particle and fibre deposition and transit behaviour in live mouse trachea. , 2010, Journal of synchrotron radiation.
[5] G. Bellon,et al. Long-term inhaled dry powder mannitol in cystic fibrosis: an international randomized study. , 2012, American journal of respiratory and critical care medicine.
[6] R. Boucher,et al. Mucociliary transport determined by in vivo microdialysis in the airways of normal and CF mice. , 2004, American journal of physiology. Lung cellular and molecular physiology.
[7] S. Hyde,et al. Assessment of CFTR function after gene transfer in vitro and in vivo. , 2008, Methods in molecular biology.
[8] Andreas Fouras,et al. Tracking extended mucociliary transport activity of individual deposited particles: longitudinal synchrotron X-ray imaging in live mice. , 2014, Journal of synchrotron radiation.
[9] M. Knowles,et al. Mucus clearance and lung function in cystic fibrosis with hypertonic saline. , 2006, The New England journal of medicine.
[10] Richard B Thompson,et al. MRI measurement of regional lung deposition in mice exposed nose-only to nebulized superparamagnetic iron oxide nanoparticles. , 2008, Journal of aerosol medicine and pulmonary drug delivery.
[11] J. Wine. The genesis of cystic fibrosis lung disease. , 1999, The Journal of clinical investigation.