Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Paul McNally"'
Autor:
Julie Renwick, Paul McNally, Bettina John, Todd DeSantis, Barry Linnane, Philip Murphy, SHIELD CF
Publikováno v:
PLoS ONE, Vol 9, Iss 12, p e109798 (2014)
Molecular techniques have uncovered vast numbers of organisms in the cystic fibrosis (CF) airways, the clinical significance of which is yet to be determined. The aim of this study was to describe and compare the microbial communities of the lower ai
Externí odkaz:
https://doaj.org/article/0a8af26aa33347aba8dd46aa07576a42
Autor:
Valia Verrière, Gerard Higgins, Mazen Al-Alawi, Richard W Costello, Paul McNally, Raphaël Chiron, Brian J Harvey, Valérie Urbach
Publikováno v:
PLoS ONE, Vol 7, Iss 5, p e37746 (2012)
Cystic Fibrosis (CF) is a genetic disease characterised by a deficit in epithelial Cl(-) secretion which in the lung leads to airway dehydration and a reduced Airway Surface Liquid (ASL) height. The endogenous lipoxin LXA(4) is a member of the newly
Externí odkaz:
https://doaj.org/article/bc09266915a84ad3b30f5cc572da7a55
Autor:
Richard W. Costello, Raphaël Chiron, Brian J. Harvey, Gerard Higgins, Valia Verriere, Valerie Urbach, Paul McNally, Mazen Al-Alawi
Publikováno v:
PLoS ONE
PLoS ONE, Public Library of Science, 2012, 7 (5), pp.e37746. ⟨10.1371/journal.pone.0037746⟩
PLoS ONE, Vol 7, Iss 5, p e37746 (2012)
PLoS ONE, Public Library of Science, 2012, 7 (5), pp.e37746. ⟨10.1371/journal.pone.0037746⟩
PLoS ONE, Vol 7, Iss 5, p e37746 (2012)
Cystic Fibrosis (CF) is a genetic disease characterised by a deficit in epithelial Cl(-) secretion which in the lung leads to airway dehydration and a reduced Airway Surface Liquid (ASL) height. The endogenous lipoxin LXA(4) is a member of the newly