Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Mada Ghanem"'
Autor:
Emmeline Marchal-Duval, Méline Homps-Legrand, Antoine Froidure, Madeleine Jaillet, Mada Ghanem, Deneuville Lou, Aurélien Justet, Arnaud Maurac, Aurelie Vadel, Emilie Fortas, Aurelie Cazes, Audrey Joannes, Laura Giersh, Herve Mal, Pierre Mordant, Tristan Piolot, Marin Truchin, Carine M Mounier, Ksenija Schirduan, Martina Korfei, Andreas Gunther, Bernard Mari, Frank Jaschinski, Bruno Crestani, Arnaud A Mailleux
Publikováno v:
eLife, Vol 12 (2023)
Matrix remodeling is a salient feature of idiopathic pulmonary fibrosis (IPF). Targeting cells driving matrix remodeling could be a promising avenue for IPF treatment. Analysis of transcriptomic database identified the mesenchymal transcription facto
Externí odkaz:
https://doaj.org/article/def471563ad64a989723cceb324f9f6d
Autor:
Antoine Froidure, Emmeline Marchal-Duval, Meline Homps-Legrand, Mada Ghanem, Aurélien Justet, Bruno Crestani, Arnaud Mailleux
Publikováno v:
European Respiratory Review, Vol 29, Iss 158 (2020)
Idiopathic pulmonary fibrosis (IPF) is characterised by an important remodelling of lung parenchyma. Current evidence indicates that the disease is triggered by alveolar epithelium activation following chronic lung injury, resulting in alveolar epith
Externí odkaz:
https://doaj.org/article/f4c93af63069452e93fd692b89b79c43
Autor:
Quentin Le Hingrat, Mada Ghanem, Aurélie Cazes, Benoit Visseaux, Gilles Collin, Diane Descamps, Charlotte Charpentier, Bruno Crestani
Publikováno v:
ERJ Open Research, Vol 6, Iss 3 (2020)
Externí odkaz:
https://doaj.org/article/c9957f7177ec442ebe218f9f69af060b
Autor:
Raphael Borie, Pierre Le Guen, Mada Ghanem, Camille Taillé, Clairelyne Dupin, Philippe Dieudé, Caroline Kannengiesser, Bruno Crestani
Publikováno v:
European Respiratory Review, Vol 28, Iss 153 (2019)
Interstitial lung diseases (ILDs) are a set of heterogeneous lung diseases characterised by inflammation and, in some cases, fibrosis. These lung conditions lead to dyspnoea, cough, abnormalities in gas exchange, restrictive physiology (characterised
Externí odkaz:
https://doaj.org/article/64c028a3a56a465c929ce9fc75750217
Publikováno v:
Orphan Lung Diseases ISBN: 9783031129490
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7f94611e13e697c1d2389597442d1e7e
https://doi.org/10.1007/978-3-031-12950-6_14
https://doi.org/10.1007/978-3-031-12950-6_14
Autor:
Mada Ghanem, Arnaud A. Mailleux
Publikováno v:
Am J Respir Cell Mol Biol
We previously identified a novel molecular subtype of idiopathic pulmonary fibrosis (IPF) defined by increased expression of cilium-associated genes, airway mucin gene MUC5B, and KRT5 marker of basal cell airway progenitors. Here we show the associat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0afdb235a217c2b1a3589305d504043
https://doi.org/10.1165/rcmb.2022-0201ed
https://doi.org/10.1165/rcmb.2022-0201ed
Publikováno v:
Current opinion in pulmonary medicine. 28(5)
The aim of this review was to summarize the recent data concerning interstitial lung disease after COVID-19, a field where knowledge is evolving very quickly.It has been found that a proportion of patients displayed fibrotic-like pattern on chest com
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c68d360a1ccdf9971adb9535e03b62e7
https://pubmed.ncbi.nlm.nih.gov/35938200
https://pubmed.ncbi.nlm.nih.gov/35938200
Publikováno v:
Revue des Maladies Respiratoires. 38:41-57
Resume Introduction L’asthme est une maladie frequente dont le diagnostic ne necessite habituellement pas le recours a l’imagerie. Celle-ci occupe en revanche une place cle dans les formes severes. Etat des connaissances Un epaississement parieta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1dc9e10da3b4e45c9b5d1c3ba19605b9
https://doi.org/10.1016/j.rmr.2020.09.010
https://doi.org/10.1016/j.rmr.2020.09.010
Autor:
Aurélien Justet, Mada Ghanem, Tiara Boghanim, Mouna Hachem, Eirini Vasarmidi, Madeleine Jaillet, Aurélie Vadel, Audrey Joannes, Pierre Mordant, Philippe Bonniaud, Martin Kolb, Lei Ling, Aurélie Cazes, Hervé Mal, Arnaud Mailleux, Bruno Crestani
Publikováno v:
American Journal of Respiratory Cell and Molecular Biology
American Journal of Respiratory Cell and Molecular Biology, 2022, ⟨10.1165/rcmb.2021-0246OC⟩
American Journal of Respiratory Cell and Molecular Biology, 2022, ⟨10.1165/rcmb.2021-0246OC⟩
International audience; IPF is a devastating lung disease with limited therapeutic possibilities. FGF19, an endocrine FGF, was recently shown to decrease liver fibrosis. To ask whether FGF19 had anti-fibrotic properties in the lung and decipher its e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65ed32efd0bbd350ce06510ea222339f
https://hal.science/hal-03706220
https://hal.science/hal-03706220
Autor:
Raphael Borie, Pierre Le Guen, Mada Ghanem, Camille Taillé, Susan Mathai, Philippe Dieudé, Caroline Kannengiesser, Bruno Crestani
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0decaa7cf068026247161a90d5156c3d
https://doi.org/10.1016/b978-0-12-801238-3.11453-9
https://doi.org/10.1016/b978-0-12-801238-3.11453-9