Zobrazeno 1 - 10
of 71
pro vyhledávání: '"C. Hubeau"'
Autor:
P. Blyszczuk, G. Kania, E. Pachera, F. Rolski, A. Hukara, V. Tela, M. Mayo, V. Dixit, B. Yang, J. Gollob, N. Mainolfi, A. Slavin, C. Hubeau, O. Distler
Publikováno v:
Annals of the Rheumatic Diseases. 81:494-495
BackgroundThe ubiquitin-proteasome system (UPS) is the endogenous intracellular mechanism for maintaining protein homeostasis through protein degradation and turnover. Heterobifunctional small molecules are a new class of compounds that form a ternar
Autor:
C. Hubeau, J. Sullivan, C. Brown, M. Mayo, V. Dixit, B. Enerson, H. Rong, B. Yang, C. De Savi, J. Gollob, N. Mainolfi, A. Slavin
Publikováno v:
Annals of the Rheumatic Diseases. 81:54.1-54
BackgroundSignal transducer and activator of transcription 3 (STAT3) is a transcription factor that belongs to a class of targets devoid of catalytic function, thus deemed “undruggable” by standard modalities such as small molecule inhibitors or
Akademický článek
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Autor:
B. Capraro, S. Frei, C. Hubeau, J. Xu, A. Umana, L. Rui, V. Massa, A. Aherrera, W. Li, Y. Li, Y. T. Hsieh
Publikováno v:
Annals of the Rheumatic Diseases. 79:195.1-195
Background:Impairment or deficiency of regulatory T cells (Treg) is associated with chronic inflammation and autoimmune diseases. Interleukin 2 (IL-2) is a cytokine indispensable for Treg expansion and immunosuppressive function. However, expansion o
Akademický článek
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Publikováno v:
Clinical & Experimental Allergy. 33:386-393
Summary Background Airway hyper-responsiveness (AHR), chronic airway inflammation and predominance of the T helper type-2 (Th2; IL-4, IL-5, IL-13) over the Th1 (IL-2, IFN-γ) immune response are hallmarks of asthma. Alveolar macrophages (AM) are the
Autor:
C. Hubeau, J. P. Couetil, D. Hubert, Dominique Gaillard, E. Puchelle, D. Dusser, M. Lorenzato
Publikováno v:
Clinical and Experimental Immunology
Clinical and Experimental Immunology, Wiley, 2001, 124 (1), pp.69-76
Clinical and Experimental Immunology, Wiley, 2001, 124 (1), pp.69-76
SUMMARYAirway inflammation represents a hallmark of the cystic fibrosis (CF) disease. However, the mucosal distribution of immune cells along the CF airways has not been clearly defined, particularly in intermediate bronchi and distal bronchioles. We
Publikováno v:
Archives de Pédiatrie. 7:343s-345s
Autor:
Dominique Gaillard, C. Hubeau, R. Le Naour, Moncef Guenounou, Jocelyne Hinnrasky, M. Abely, E. Puchelle
Publikováno v:
Clinical and Experimental Immunology
Clinical and Experimental Immunology, Wiley, 2004, 135 (3), pp.528-34. ⟨10.1111/j.1365-2249.2003.02385.x⟩
Clinical and Experimental Immunology, Wiley, 2004, 135 (3), pp.528-34. ⟨10.1111/j.1365-2249.2003.02385.x⟩
SUMMARY It is well documented that patients with cystic fibrosis (CF) are unable to clear persistent airway infections in spite of strong local inflammation, suggesting a dysregulation of immunity in CF. We and others have reported previously that T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a62bff65ab89892b40e7ddfa18becec5
https://www.hal.inserm.fr/inserm-00145671
https://www.hal.inserm.fr/inserm-00145671
Publikováno v:
Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology. 33(3)
Airway hyper-responsiveness (AHR), chronic airway inflammation and predominance of the T helper type-2 (Th2; IL-4, IL-5, IL-13) over the Th1 (IL-2, IFN-gamma) immune response are hallmarks of asthma. Alveolar macrophages (AM) are the most numerous ce