Zobrazeno 1 - 10
of 10
pro vyhledávání: '"David W, Parsons"'
Autor:
Martin Donnelley, Kaye S. Morgan, Maged Awadalla, Nigel R. Farrow, Chris Hall, David W. Parsons
Publikováno v:
Respiratory Research, Vol 18, Iss 1, Pp 1-11 (2017)
Abstract Background The Australian Synchrotron Imaging and Medical Beamline (IMBL) was designed as the world’s widest synchrotron X-ray beam, enabling both clinical imaging and therapeutic applications for humans as well as the imaging of large ani
Externí odkaz:
https://doaj.org/article/ef4bd1cfe0c14d7f9e17f20305b84911
Autor:
Martin Donnelley, David W. Parsons
Publikováno v:
Frontiers in Pharmacology, Vol 9 (2018)
Cystic fibrosis (CF) is a progressive, chronic and debilitating genetic disease caused by mutations in the CF Transmembrane-Conductance Regulator (CFTR) gene. Unrelenting airway disease begins in infancy and produces a steady deterioration in quality
Externí odkaz:
https://doaj.org/article/76a2eaca90964eff83d4135441302d3d
Autor:
Nirajan Shrestha, Alexandra McCarron, Nathan Rout-Pitt, Martin Donnelley, David W. Parsons, Deanne H. Hryciw
Publikováno v:
Nutrients. 14(21)
Adequate intake of nutrients such as essential fatty acids (EFA) are critical in cystic fibrosis (CF). The clinical course of deterioration of lung function in people with CF has been shown to relate to nutrition. Independent of the higher energy con
Autor:
Nirajan Shrestha, Nathan Rout-Pitt, Alexandra McCarron, Courtney A. Jackson, Andrew C. Bulmer, Andrew J. McAinch, Martin Donnelley, David W. Parsons, Deanne H. Hryciw
Publikováno v:
International Journal of Molecular Sciences; Volume 24; Issue 8; Pages: 7194
Cystic fibrosis (CF), the result of mutations in the CF transmembrane conductance regulator (CFTR), causes essential fatty acid deficiency. The aim of this study was to characterize fatty acid handling in two rodent models of CF; one strain which har
Autor:
Kaye S Morgan, Martin Donnelley, David M Paganin, Andreas Fouras, Naoto Yagi, Yoshio Suzuki, Akihisa Takeuchi, Kentaro Uesugi, Richard C Boucher, David W Parsons, Karen K W Siu
Publikováno v:
PLoS ONE, Vol 8, Iss 1, p e55822 (2013)
In the airways of those with cystic fibrosis (CF), the leading pathophysiological hypothesis is that an ion channel defect results in a relative decrease in airway surface liquid (ASL) volume, producing thick and sticky mucus that facilitates the est
Externí odkaz:
https://doaj.org/article/2c250819c59c4160ac35740997774c26
Long-term therapeutic and reporter gene expression in lentiviral vector treated cystic fibrosis mice
Publikováno v:
The journal of gene medicine. 16(9-10)
Persistent reporter gene and cystic fibrosis transmembrane conductance regulator (CFTR) nasal airway gene expression can be achieved with a single lentiviral (LV) gene vector dosing when coupled with a preparatory lysophosphatidylcholine (LPC) airway
Autor:
David W. Parsons
The doctrinal inertia resulting from 40 years of preparing for war with the Soviet Union, combined with several 'lessons learned' from the air campaign in Operation Desert Storm, has led some air power advocates to overstate the role of air power in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5eb1d5b8d008140e180c1df63f5c9731
https://doi.org/10.21236/ada329097
https://doi.org/10.21236/ada329097
Publikováno v:
The Journal of experimental biology. 123
The neuroendocrine bag cells of the hermaphroditic marine gastropod, Aplysia, secrete peptide hormones that induce release of ripe eggs from the ovotestis. The egg string is subsequently deposited on the substrate by means of a complex sequence of rh
Autor:
William B. Runciman, Desmond F. Gorman, Robert K. Webb, Walter J. Russell, John E. Gilligan, David W. Parsons
Publikováno v:
Chest. 94:671-672