Zobrazeno 1 - 10
of 84
pro vyhledávání: '"Steven E, Mutsaers"'
Autor:
Tylah Miles, Gerard F Hoyne, Darryl A Knight, Mark W Fear, Steven E Mutsaers, Cecilia M Prêle
Publikováno v:
Clinical & Translational Immunology, Vol 9, Iss 7, Pp n/a-n/a (2020)
Abstract Pulmonary fibrosis occurs in a heterogeneous group of lung disorders and is characterised by an excessive deposition of extracellular matrix proteins within the pulmonary interstitium, leading to impaired gas transfer and a loss of lung func
Externí odkaz:
https://doaj.org/article/c4411332b0ed47deac6487b7ba36ef37
Autor:
David W. Waters, Michael Schuliga, Prabuddha S. Pathinayake, Lan Wei, Hui-Ying Tan, Kaj E. C. Blokland, Jade Jaffar, Glen P. Westall, Janette K. Burgess, Cecilia M. Prêle, Steven E. Mutsaers, Christopher L. Grainge, Darryl A. Knight
Publikováno v:
Biomedicines, Vol 9, Iss 9, p 1162 (2021)
Idiopathic pulmonary fibrosis (IPF) is a chronic disease characterised by a dense fibrosing of the lung parenchyma. An association between IPF and cellular senescence is well established and several studies now describe a higher abundance of senescen
Externí odkaz:
https://doaj.org/article/9b887b3e6a684a2cbaf59851201b3ebd
Autor:
Cecilia M. Prêle, Thomas Iosifidis, Robin J. McAnulty, David R. Pearce, Bahareh Badrian, Tylah Miles, Sarra E. Jamieson, Matthias Ernst, Philip J. Thompson, Geoffrey J. Laurent, Darryl A. Knight, Steven E. Mutsaers
Publikováno v:
Biomedicines, Vol 9, Iss 5, p 498 (2021)
The interleukin (IL)-6 family of cytokines and exaggerated signal transducer and activator of transcription (STAT)3 signaling is implicated in idiopathic pulmonary fibrosis (IPF) pathogenesis, but the mechanisms regulating STAT3 expression and functi
Externí odkaz:
https://doaj.org/article/f48fa198e8004c7484e59b7e0c37a1fd
Autor:
Kaj E. C. Blokland, David W. Waters, Michael Schuliga, Jane Read, Simon D. Pouwels, Christopher L. Grainge, Jade Jaffar, Glen Westall, Steven E. Mutsaers, Cecilia M. Prêle, Janette K. Burgess, Darryl A. Knight
Publikováno v:
Pharmaceutics, Vol 12, Iss 4, p 389 (2020)
Idiopathic pulmonary fibrosis (IPF) is a progressive lung disease marked by excessive accumulation of lung fibroblasts (LFs) and collagen in the lung parenchyma. The mechanisms that underlie IPF pathophysiology are thought to reflect repeated alveola
Externí odkaz:
https://doaj.org/article/c78d3268b80d43e7a397a1b9abe04195
Autor:
Cecilia M. Prêle, Claire Thomson, Darryl A. Knight, Steven E. Mutsaers, Amama Kanwal, Kaj E C Blokland, Jane Read, Michael Schuliga, Janette K. Burgess, Christopher Grainge, Nathan W. Bartlett, Allen James
Publikováno v:
American Journal of Physiology-Lung Cellular and Molecular Physiology, 321(5), L859-L871. AMER PHYSIOLOGICAL SOC
Alveolar epithelial cell (AEC) senescence is implicated in the pathogenesis of idiopathic pulmonary fibrosis (IPF). Mitochondrial dysfunction including release of mitochondrial DNA (mtDNA) is a feature of senescence, which led us to investigate the r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9c5aa3b2b498def3fbda3c8f9e1ee71
https://research.rug.nl/en/publications/556d48b1-48e1-4762-9dc7-e55a4f14cabd
https://research.rug.nl/en/publications/556d48b1-48e1-4762-9dc7-e55a4f14cabd
Autor:
Lan Wei, Steven E. Mutsaers, Christopher Grainge, Jade Jaffar, Michael Schuliga, Prabuddha S. Pathinayake, Janette K. Burgess, Glen P. Westall, Philip M. Hansbro, Darryl A. Knight, Kaj E C Blokland, Nathan W. Bartlett, Cecilia M. Prêle, David W Waters
Publikováno v:
American Journal of Respiratory Cell and Molecular Biology, 61(1), 61-73. AMER THORACIC SOC
American Journal of Respiratory Cell and Molecular Biology
American Journal of Respiratory Cell and Molecular Biology
Copyright © 2019 by the American Thoracic Society. Idiopathic pulmonary fibrosis (IPF) is a chronic lung disease of unknown cause with a median survival of only 3 years. Other investigators and we have shown that fibroblasts derived from IPF lungs d
Autor:
Cecilia M. Prêle, Tylah Miles, David R. Pearce, Robert J. O'Donoghue, Chris Grainge, Lucy Barrett, Kimberly Birnie, Andrew D. Lucas, Svetlana Baltic, Matthias Ernst, Catherine Rinaldi, Geoffrey J. Laurent, Darryl A. Knight, Mark Fear, Gerard Hoyne, Robin J. McAnulty, Steven E. Mutsaers
Publikováno v:
European Respiratory Journal. 60:2101469
Idiopathic pulmonary fibrosis (IPF) is an interstitial lung disease associated with chronic inflammation and tissue remodelling leading to fibrosis, reduced pulmonary function, respiratory failure and death. Bleomycin (Blm)-induced lung fibrosis in m
Autor:
Geoffrey J. Laurent, Philip J. Thompson, David R. Pearce, Sarra E. Jamieson, Matthias Ernst, Tylah Miles, Cecilia M Prêle, Robin J. McAnulty, Darryl A. Knight, Bahareh Badrian, Steven E. Mutsaers, Thomas Iosifidis
Publikováno v:
Biomedicines, Vol 9, Iss 498, p 498 (2021)
Biomedicines
Volume 9
Issue 5
Biomedicines
Volume 9
Issue 5
The interleukin (IL)-6 family of cytokines and exaggerated signal transducer and activator of transcription (STAT)3 signaling is implicated in idiopathic pulmonary fibrosis (IPF) pathogenesis, but the mechanisms regulating STAT3 expression and functi
Autor:
Chuan Bian Lim, Cecilia M Prêle, Hui Min Cheah, Yuen Yee Cheng, Sonja Klebe, Glen Reid, D Neil Watkins, Svetlana Baltic, Philip J Thompson, Steven E Mutsaers
Publikováno v:
PLoS ONE, Vol 8, Iss 6, p e66685 (2013)
BACKGROUND: The Hedgehog (HH) signaling pathway is critical for embryonic development and adult homeostasis. Recent studies have identified regulatory roles for this pathway in certain cancers with mutations in the HH pathway genes. The extent to whi
Externí odkaz:
https://doaj.org/article/8fb1acf1b01742ddb64b80e1669bc29c