Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Rachele Invernizzi"'
Autor:
Amanda Demeter, Anne-Claire Jacomin, Lejla Gul, Ashleigh Lister, James Lipscombe, Rachele Invernizzi, Priscilla Branchu, Iain Macaulay, Ioannis P. Nezis, Robert A. Kingsley, Tamas Korcsmaros, Isabelle Hautefort
Publikováno v:
Frontiers in Cellular and Infection Microbiology, Vol 12 (2022)
Macroautophagy is a ubiquitous homeostasis and health-promoting recycling process of eukaryotic cells, targeting misfolded proteins, damaged organelles and intracellular infectious agents. Some intracellular pathogens such as Salmonella enterica sero
Externí odkaz:
https://doaj.org/article/2473b25ba8984379ac6d561d72fc768c
Autor:
Karim Boustani, Poonam Ghai, Rachele Invernizzi, Richard J. Hewitt, Toby M. Maher, Quan-Zhen Li, Philip L. Molyneaux, James A. Harker
Publikováno v:
ERJ Open Research, Vol 8, Iss 1 (2022)
Background Fibrotic interstitial lung disease (fILD) has previously been associated with the presence of autoantibody. While studies have focused on systemic autoimmunity, the role of local autoantibodies in the airways remains unknown. We therefore
Externí odkaz:
https://doaj.org/article/60bd3a11a49c403c96d1deeb865cceca
Autor:
Athina Trachalaki, Eliza Tsitoura, Semeli Mastrodimou, Rachele Invernizzi, Eirini Vasarmidi, Eleni Bibaki, Nikolaos Tzanakis, Philip L. Molyneaux, Toby M. Maher, Katerina Antoniou
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
Fibrotic Interstitial lung diseases (ILDs) are complex disorders of variable clinical behaviour. The majority of them cause significant morbidity, whilst Idiopathic Pulmonary Fibrosis (IPF) is recognised as the most relentless. NLRP3, AIM2, and NLRC4
Externí odkaz:
https://doaj.org/article/b296acba02374e95aa7cccea67198371
Publikováno v:
European Respiratory Review, Vol 28, Iss 152 (2019)
Idiopathic pulmonary fibrosis (IPF) arises in genetically susceptible individuals as a result of an aberrant wound-healing response following repetitive alveolar injury. The clinical course of the disease remains both variable and unpredictable with
Externí odkaz:
https://doaj.org/article/cb191c8950dd45a38cc771c85c431b63
Autor:
Aoife N. McElroy, Rachele Invernizzi, Joanna W. Laskowska, Andrew O’Neill, Mohammad Doroudian, Mohsen Moghoofei, Shayan Mostafaei, Feng Li, Alexander A. Przybylski, David N. O’Dwyer, Andrew G. Bowie, Padraic G. Fallon, Toby M. Maher, Cory M. Hogaboam, Philip L. Molyneaux, Nik Hirani, Michelle E. Armstrong, Seamas C. Donnelly
Rationale: The Toll-like receptor 3 Leu412Phe (TLR3 L412F) polymorphism attenuates cellular anti-viral responses and is associated with accelerated disease progression in IPF. The role of TLR3 L412F in bacterial infection in IPF or in acute exacerbat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b41c2265316b26d9a627dfddc7f88401
http://hdl.handle.net/10044/1/93701
http://hdl.handle.net/10044/1/93701
Publikováno v:
The Microbiome in Respiratory Disease ISBN: 9783030871031
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd95b75bfcc237c9b343998beaf8c14e
https://doi.org/10.1007/978-3-030-87104-8_9
https://doi.org/10.1007/978-3-030-87104-8_9
Publikováno v:
Kompass Pneumologie. 8:240-251
Das respiratorische Epithel stellt eine physische Grenze zur äußeren Umgebung dar und fungiert als erste Verteidigungslinie gegen potenziell schädliche Umweltreize wie Mikroben und Allergene. Die Epithelzellen in der Lunge gelten jedoch zunehmend
Airway-specific autoantibodies identify a subset of patients with fibrotic interstitial lung disease
Autor:
Philip L. Molyneaux, Karim Boustani, Toby M. Maher, James A. Harker, Richard J. Hewitt, Quan-Zhen Li, Rachele Invernizzi, Poonam Ghai
BackgroundFibrotic interstitial lung disease (fILD) has previously been associated with the presence of autoantibody. While studies have focused on systemic autoimmunity, the role of local autoantibodies in the airway remains unknown. We therefore ex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3f5460605d56ee43b0802b7d6ad395f3
https://doi.org/10.1101/2021.07.29.21261213
https://doi.org/10.1101/2021.07.29.21261213
Autor:
Richard J. Hewitt, James A. Harker, Quan-Zhen Li, Karim Boustani, Philip L. Molyneaux, Rachele Invernizzi, Poonam Ghai, Toby M. Maher
Publikováno v:
ERJ open research. 8(1)
BackgroundFibrotic interstitial lung disease (fILD) has previously been associated with the presence of autoantibody. While studies have focused on systemic autoimmunity, the role of local autoantibodies in the airways remains unknown. We therefore e