Zobrazeno 1 - 10
of 119
pro vyhledávání: '"IPF, Idiopathic pulmonary fibrosis"'
Autor:
Céline-Hivda Yegen, Dominique Marchant, Jean-François Bernaudin, Carole Planes, Emilie Boncoeur, Nicolas Voituron
Publikováno v:
Frontiers in Physiology, Vol 14 (2023)
Some patients with idiopathic pulmonary fibrosis present impaired ventilatory variables characterised by low forced vital capacity values associated with an increase in respiratory rate and a decrease in tidal volume which could be related to the inc
Externí odkaz:
https://doaj.org/article/115be95e36ed477096b0811b1af35834
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
Pulmonary fibrosis is an irreversible disease, and its mechanism is unclear. The lung is a vital organ connecting the respiratory tract and the outside world. The changes in lung microbiota affect the progress of lung fibrosis. The latest research sh
Externí odkaz:
https://doaj.org/article/3344da8f10154d1b932911dddf9c5faf
Autor:
Jia He, Yue Du, Gaopeng Li, Peng Xiao, Xingzheng Sun, Wenjun Song, Lihua Lai, Meng Xia, Jianhua Zhang, Qingqing Wang
Publikováno v:
Frontiers in Immunology, Vol 12 (2022)
Idiopathic pulmonary fibrosis (IPF) is a group of chronic interstitial pulmonary diseases characterized by an inexorable decline in lung function with limited treatment options. The abnormal expression of transforming growth factor-β (TGF-β) in pro
Externí odkaz:
https://doaj.org/article/ed851bfe6c764df78dd5216ad10f0e9d
Publikováno v:
Frontiers in Medicine, Vol 8 (2022)
Objective:Lung microbiota is increasingly implicated in multiple types of respiratory diseases. However, no study has drawn a consistent conclusion regarding the relationship between changes in the microbial community and lung diseases. This study ve
Externí odkaz:
https://doaj.org/article/1efec835405e4bfeb8df9b383f98c73f
Publikováno v:
Frontiers in Pharmacology, Vol 12 (2022)
Idiopathic pulmonary fibrosis (IPF) is a chronic interstitial lung disease characterized by an abnormal reepithelialisation, an excessive tissue remodelling and a progressive fibrosis within the alveolar wall that are not due to infection or cancer.
Externí odkaz:
https://doaj.org/article/ee0f8c703ba8463287d0bf6d82e54d4a
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
Autor:
Caijuan Huan, Wangting Xu, Yaru Liu, Kexin Ruan, Yueli Shi, Hongqiang Cheng, Xue Zhang, Yuehai Ke, Jianying Zhou
Publikováno v:
Frontiers in Molecular Biosciences, Vol 8 (2021)
Idiopathic pulmonary fibrosis (IPF) is a progressive lung disease causing unremitting extracellular matrix deposition. Transforming growth factor-β (TGF-β) superfamily involves bone morphogenetic proteins (BMPs) and TGF-β, and the balance between
Externí odkaz:
https://doaj.org/article/16d21e8c07804c7da1ebe346a29fbc2b
Autor:
Silke Meiners, Mareike Lehmann
Publikováno v:
Frontiers in Medicine, Vol 7 (2020)
Externí odkaz:
https://doaj.org/article/cfb09a208ece49aeacd2f2c3f7090112
Autor:
Norihito Omote, Maor Sauler
Publikováno v:
Frontiers in Medicine, Vol 7 (2020)
Cellular senescence is a cell fate implicated in the pathogenesis of idiopathic pulmonary fibrosis (IPF) and chronic obstructive pulmonary disease (COPD). Cellular senescence occurs in response to cellular stressors such as oxidative stress, DNA dama
Externí odkaz:
https://doaj.org/article/6864f4158c174b958ca4c7fa22a8dcb5
Autor:
Stanley J. Radio, Heather M. Strah, Kristina L. Bailey, Michael J. Duryee, John D. Dickinson, Ted R. Mikuls, Bryant R. England, Todd A. Wyatt, Amy Nelson, Jill A. Poole, Dawn M. Katafiasz, Daniel R. Anderson, Rohit Gaurav, Geoffrey M. Thiele, Debra J. Romberger
Publikováno v:
Chest
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::80ff0bce2e66fbc5668733449b28b9d6
https://doi.org/10.1016/j.chest.2021.06.058
https://doi.org/10.1016/j.chest.2021.06.058