Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Amélie Cumont"'
Autor:
Mehdi Abdelli, Charlotte Falaise, Valérie Morineaux-Hilaire, Amélie Cumont, Laurent Taysse, Françoise Raynaud, Vincent Ramisse
Publikováno v:
Microorganisms, Vol 11, Iss 11, p 2721 (2023)
Unexpected atypical isolates of Bacillus cereus s.l. occasionally challenge conventional microbiology and even the most advanced techniques for anthrax detection. For anticipating and gaining trust, 65 isolates of Bacillus cereus s.l. of diverse orig
Externí odkaz:
https://doaj.org/article/4f8f32149f124cdab48a23b2bbe3622b
Autor:
Laurent Savale, Olivier Sitbon, Xavier Jaïs, Marc Humbert, Athénaïs Boucly, Raphaël Thuillet, Amélie Cumont, Christophe Guignabert, Satoshi Akagi, Nihel Berrebeh, Alice Huertas, Yuichi Tamura, Ari Chaouat, Cécile Tromeur, Etienne Marie Jutant, Carole Phan, Elie Fadel, Olaf Mercier, David Montani, Vincent Cottin, Benjamin Le Vely, Ly Tu
Publikováno v:
European Respiratory Journal
European Respiratory Journal, European Respiratory Society, 2021, 58 (2), pp.2000332. ⟨10.1183/13993003.00332-2020⟩
European Respiratory Journal, 2021, 58 (2), pp.2000332. ⟨10.1183/13993003.00332-2020⟩
European Respiratory Journal, European Respiratory Society, 2021, 58 (2), pp.2000332. ⟨10.1183/13993003.00332-2020⟩
European Respiratory Journal, 2021, 58 (2), pp.2000332. ⟨10.1183/13993003.00332-2020⟩
Previous studies have suggested an association between uric acid (UA) and the severity of pulmonary arterial hypertension (PAH), but it is unknown whether UA contributes to disease pathogenesis.The aim of this study was to determine the prognostic va
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e4124d5021b0a2a1f280549593010fe8
https://www.hal.inserm.fr/inserm-03118201
https://www.hal.inserm.fr/inserm-03118201
Autor:
Nihel Berrebeh, Marc Humbert, Sabine Bailly, Christophe Guignabert, Raphaël Thuillet, Ly Tu, Alice Huertas, Benjamin Le Vely, Amélie Cumont, Ignacio Anegon
Publikováno v:
Pulmonary hypertension.
Introduction: Despite increasing evidence suggesting that the Bone Morphogenetic Protein (BMP)-9 signaling pathway is playing a role in the pulmonary hypertension (PH) pathogenesis, the data in the literature are still controversial. Aims and Objecti
Autor:
Ly Tu, Amélie Cumont, Raphaël Thuillet, Laurent Savale, Alice Huertas, Mohamed Reda Amar Djessas, Marc Humbert, Guillaume Hebert, Christophe Guignabert, Marie-Camille Chaumais, Pauline Gaignard
Publikováno v:
Cardiovascular Research
Cardiovascular Research, Oxford University Press (OUP), 2020, pp.cvaa200. ⟨10.1093/cvr/cvaa200⟩
Cardiovascular Research, Oxford University Press (OUP), 2020, pp.cvaa200. ⟨10.1093/cvr/cvaa200⟩
Aims Although right ventricular (RV) function is an important determinant of morbidity and mortality in patients with pulmonary arterial hypertension (PAH), there is no treatment targeting directly the RV. We evaluate the efficacy of sacubitril/valsa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4b3c0a74b98793b4f15307bc27c8c52
https://www.hal.inserm.fr/inserm-02907132
https://www.hal.inserm.fr/inserm-02907132
Autor:
Raphaël Thuillet, Alice Huertas, Amélie Cumont, Christophe Guignabert, Jennifer Bordenave, Nihel Berrebeh, Ly Tu, Elie Fadel, Marc Humbert, Benjamin Le Vely, Sophie Nadaud, Laurent Savale
Publikováno v:
Arteriosclerosis, Thrombosis, and Vascular Biology
Arteriosclerosis, Thrombosis, and Vascular Biology, 2020, 40 (3), pp.766-782. ⟨10.1161/ATVBAHA.119.313715⟩
Arteriosclerosis, Thrombosis, and Vascular Biology, American Heart Association, 2020, Ahead of print. ⟨10.1161/ATVBAHA.119.313715⟩
Arteriosclerosis, Thrombosis, and Vascular Biology, American Heart Association, 2020, 40 (3), pp.766-782. ⟨10.1161/ATVBAHA.119.313715⟩
Arteriosclerosis, Thrombosis, and Vascular Biology, 2020, 40 (3), pp.766-782. ⟨10.1161/ATVBAHA.119.313715⟩
Arteriosclerosis, Thrombosis, and Vascular Biology, American Heart Association, 2020, Ahead of print. ⟨10.1161/ATVBAHA.119.313715⟩
Arteriosclerosis, Thrombosis, and Vascular Biology, American Heart Association, 2020, 40 (3), pp.766-782. ⟨10.1161/ATVBAHA.119.313715⟩
Objective: Excessive accumulation of resident cells within the pulmonary vascular wall represents the hallmark feature of the remodeling occurring in pulmonary arterial hypertension (PAH). Furthermore, we have previously demonstrated that pulmonary a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::643bbeec05347f0d050bd2efb680a7fb
https://www.hal.inserm.fr/inserm-02454982v2
https://www.hal.inserm.fr/inserm-02454982v2
Autor:
Raphaël Thuillet, Paul-Benoit Poble, Maria-Rosa Ghigna, Ly Tu, Laurent Savale, Alice Huertas, Marc Humbert, Peter Dorfmüller, Timothée Quatremare, Carole Phan, Christophe Guignabert, Jennifer Bordenave, Amélie Cumont
Publikováno v:
FASEB Journal
FASEB Journal, Federation of American Society of Experimental Biology, 2018, 33 (3), pp.3670-3679. ⟨10.1096/fj.201801659R⟩
FASEB Journal, 2018, 33 (3), pp.3670-3679. ⟨10.1096/fj.201801659R⟩
FASEB Journal, Federation of American Society of Experimental Biology, 2018, 33 (3), pp.3670-3679. ⟨10.1096/fj.201801659R⟩
FASEB Journal, 2018, 33 (3), pp.3670-3679. ⟨10.1096/fj.201801659R⟩
International audience; Heightened pulmonary artery smooth muscle cell (PA-SMC) proliferation and migration and dynamic remodeling of the extracellular matrix are hallmark pathogenic features of pulmonary arterial hypertension (PAH). Pirfenidone (PFD
Autor:
Amélie Cumont, Jean-Luc Galzi, Christophe Guignabert, Laurent Savale, Raphaël Thuillet, Claire Marsol, Ly Tu, Dominique Bonnet, Marcel Hibert, Jennifer Bordenave, Carole Phan, Marc Humbert, Nelly Frossard, Alice Huertas
Publikováno v:
Cardiovascular Research
Cardiovascular Research, Oxford University Press (OUP), 2019, ⟨10.1093/cvr/cvz153⟩
Cardiovascular Research, Oxford University Press (OUP), 2019, ⟨10.1093/cvr/cvz153⟩
Aims The progressive accumulation of cells in pulmonary vascular walls is a key pathological feature of pulmonary arterial hypertension (PAH) that results in narrowing of the vessel lumen, but treatments targeting this mechanism are lacking. The C-X-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0838b5f91cf6123daeb063459ffda912
https://hal.archives-ouvertes.fr/hal-02366304/document
https://hal.archives-ouvertes.fr/hal-02366304/document
Autor:
Raphaël Thuillet, Alice Huertas, Carole Phan, Ayumi Sekine, Christine Mallet, Ly Tu, Sabine Bailly, Christophe Guignabert, Laurent Savale, Olli Ritvos, Florian Robert, Jennifer Bordenave, Laurent Guyon, Agnès Desroches-Castan, Marc Humbert, Jean-Jacques Feige, Amélie Cumont
Publikováno v:
Circulation Research
Circulation Research, American Heart Association, 2019, 124 (6), pp.846-855. ⟨10.1161/CIRCRESAHA.118.313356⟩
HAL
Circulation Research, American Heart Association, 2019
Circulation Research, 2019, 124 (6), pp.846-855. ⟨10.1161/CIRCRESAHA.118.313356⟩
Circulation Research, 2019
Circulation Research, American Heart Association, 2019, 124 (6), pp.846-855. ⟨10.1161/CIRCRESAHA.118.313356⟩
HAL
Circulation Research, American Heart Association, 2019
Circulation Research, 2019, 124 (6), pp.846-855. ⟨10.1161/CIRCRESAHA.118.313356⟩
Circulation Research, 2019
Rationale: Although many familial cases of pulmonary arterial hypertension exhibit an autosomal dominant mode of inheritance with the majority having mutations in essential constituents of the BMP (bone morphogenetic protein) signaling, the specific
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5789222560e2a2270f911fd3b3f1fe5e
https://www.hal.inserm.fr/inserm-02581297/document
https://www.hal.inserm.fr/inserm-02581297/document
Autor:
Raphaël Thuillet, Jennifer Bordenave, Alice Huertas, Amélie Cumont, Ly Tu, Paul-Benoit Poble, Peter Dorfmüller, Marc Humbert, Timothée Quatremare, Maria-Rosa Ghigna, Christophe Guignabert, Carole Phan
Publikováno v:
Pulmonary hypertension.
Autor:
Thomas Guilbert, Thông Hua, Anh Tuan Dinh-Xuan, Raphaël Thuillet, Ly Tu, Christophe Guignabert, Marc Humbert, Jennifer Bordenave, Frédéric Batteux, Amélie Cumont, Carole Nicco, Sven Günther
Publikováno v:
Pulmonary hypertension.
Introduction: Pulmonary hypertension (PH) is a well-recognized complication of idiopathic pulmonary fibrosis (iPF) that is characterized by chronic inflammation and scar tissue formation. Macrophage migration inhibitory factor (MIF) and its signaling