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pro vyhledávání: '"Philip, Stumbles"'
Autor:
Kyle Mincham, Jonatan Leffler, Naomi Scott, Jean-Francois Lauzon-Joset, Philip Stumbles, Patrick Holt, Deborah Strickland
Publikováno v:
Bio-Protocol, Vol 9, Iss 5 (2019)
Murine models of allergic airway disease are frequently used as a tool to elucidate the cellular and molecular mechanisms of tissue-specific asthmatic disease pathogenesis. Paramount to the success of these models is the induction of experimental ant
Externí odkaz:
https://doaj.org/article/04cdd6882a2d434e9cb9e5fdd05492ff
Autor:
Kyle Mincham, Naomi Scott, Jean-Francois Lauzon-Joset, Jonatan Leffler, Philip Stumbles, Patrick Holt, Deborah Strickland
Publikováno v:
Bio-Protocol, Vol 9, Iss 5 (2019)
The early life period represents a time of immunological plasticity whereby the functionally immature immune system is highly susceptible to environmental stimulation. Perennial aeroallergen and respiratory viral infection induced sporadic episodes o
Externí odkaz:
https://doaj.org/article/14a0c7f7c30a40a1a6ee9953f5daaefe
Akademický článek
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Publikováno v:
Clinical & Experimental Medicine; Aug2023, Vol. 23 Issue 4, p1075-1088, 14p
Autor:
Angela Fonceca M, Jeff Lauzon-Joset, Naomi ScottPhD, Philip Stumbles A, Deborah Strickland, Mark Everard L
Respiratory syncytial virus (RSV) causes annual epidemics of acute respiratory disease in large part because antibody levels fall rapidly after infection. RSV is able to infect cultured dendritic cells (DCs) and persist in these cells. Given the impo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d8a91225ba87e7ec305d766706a3d7c0
https://doi.org/10.22541/au.165579307.76212895/v1
https://doi.org/10.22541/au.165579307.76212895/v1
Autor:
Robert J. J. O'Donoghue, Darryl A. Knight, Carl D. Richards, Cecilia M. Prêle, Hui Ling Lau, Andrew G. Jarnicki, Jessica Jones, Steven Bozinovski, Ross Vlahos, Stefan Thiem, Brent S. McKenzie, Bo Wang, Philip Stumbles, Geoffrey J. Laurent, Robin J. McAnulty, Stefan Rose‐John, Hong Jian Zhu, Gary P. Anderson, Matthias R. Ernst, Steven E. Mutsaers
Publikováno v:
EMBO Molecular Medicine, Vol 4, Iss 9, Pp 939-951 (2012)
Abstract Idiopathic pulmonary fibrosis (IPF) is a fatal disease that is unresponsive to current therapies and characterized by excessive collagen deposition and subsequent fibrosis. While inflammatory cytokines, including interleukin (IL)‐6, are el
Externí odkaz:
https://doaj.org/article/bc3bb7468c6647178e64c5cfbda37d78