Zobrazeno 1 - 10
of 25
pro vyhledávání: '"François, Rodrigues"'
Autor:
Samuel Lara‐Reyna, Emily A Caseley, Joanne Topping, François Rodrigues, Jorge Jimenez Macias, Sean E Lawler, Michael F McDermott
Publikováno v:
Clinical & Translational Immunology, Vol 11, Iss 7, Pp n/a-n/a (2022)
Abstract Inflammasomes are assembled by innate immune sensors that cells employ to detect a range of danger signals and respond with pro‐inflammatory signalling. Inflammasomes activate inflammatory caspases, which trigger a cascade of molecular eve
Externí odkaz:
https://doaj.org/article/01c642d3ce5a4c1a81bf365f2cefa4d8
Autor:
François Rodrigues, Tereza Coman, Guillemette Fouquet, Francine Côté, Geneviève Courtois, Thiago Trovati Maciel, Olivier Hermine
Publikováno v:
Expert Review of Hematology. 16:349-364
Autor:
François Rodrigues, Laurence Cuisset, Bérangère Cador-Rousseau, Irina Giurgea, Benedicte Neven, David Buob, Pierre Quartier, Eric Hachulla, Thierry Lequerré, Gérard Cam, Guilaine Boursier, Valérie Hervieu, Gilles Grateau, Sophie Georgin-Lavialle
Publikováno v:
Rheumatology
Rheumatology, 2022, 61 (12), pp.4827-4834. ⟨10.1093/rheumatology/keac145⟩
Rheumatology, 2022, 61 (12), pp.4827-4834. ⟨10.1093/rheumatology/keac145⟩
Objective Cryopyrin-associated periodic syndrome (CAPS) is a rare but treatable inherited autoinflammatory condition including familial cold autoinflammatory syndrome (FCAS), Muckle–Wells syndrome (MWS) and chronic infantile neurologic cutaneous ar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6f35de0cce26052accb8c794478d503
https://www.hal.inserm.fr/inserm-03875057
https://www.hal.inserm.fr/inserm-03875057
Autor:
Mathilde Lamarque, Emilie-Fleur Gautier, François Rodrigues, Flavia Guillem, Elisa Bayard, Cédric Broussard, Thiago Maciel Trovati, Jean-Benoît Arlet, Patrick Mayeux, Olivier Hermine, Geneviève Courtois
Publikováno v:
Cell death and differentiation.
Red blood cell production is negatively controlled by the rate of apoptosis at the stage of CFU-E/pro-erythroblast differentiation, depending on the balance between erythropoietin (EPO) levels and activation of the Fas/FasL pathway. At this stage, ac
Autor:
Antoine Fayand, Léa Savey, Sophie Georgin-Lavialle, François Rodrigues, Gilles Grateau, Claude Bachmeyer
Publikováno v:
La Presse Médicale
La Presse Médicale, Elsevier Masson, 2019, 48, pp.e25-e48. ⟨10.1016/j.lpm.2018.12.003⟩
La Presse Médicale, Elsevier Masson, 2019, 48, pp.e25-e48. ⟨10.1016/j.lpm.2018.12.003⟩
Autoinflammatory diseases are characterized by innate immunity abnormalities. In autoinflammatory diseases (AID), inflammatory blood biomarkers are elevated during crisis without infection and usually without autoantibodies. The first 4 described AID
Autor:
Gilles Grateau, Irina Giurgea, Dany Anglicheau, Laurence Cuisset, Jean-Jacques Roux, Nadia Hoyeau, Jean-Baptiste Philit, François Rodrigues, Sophie Georgin-Lavialle
Publikováno v:
Seminars in Arthritis and Rheumatism
Seminars in Arthritis and Rheumatism, WB Saunders, 2020, 50, pp.1370-1373. ⟨10.1016/j.semarthrit.2020.03.005⟩
Seminars in Arthritis and Rheumatism, WB Saunders, 2020, 50, pp.1370-1373. ⟨10.1016/j.semarthrit.2020.03.005⟩
Introduction Mevalonate kinase deficiency (MKD) is a rare autosomal recessive autoinflammatory disease that can lead to an inflammatory A amyloidosis (AA). Methods To study the occurrence of AA in MKD patients we performed a systemic review of the li
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d2c2fe3c649e7bbc7a3d61904dd051d
https://hal.archives-ouvertes.fr/hal-03493463
https://hal.archives-ouvertes.fr/hal-03493463
Autor:
Achille Aouba, Serge Amselem, François Rodrigues, Jérémie Delaleu, Samuel Deshayes, Sophie Georgin-Lavialle, Gilles Grateau, Nicolas Martin Silva, Etienne Rivière, Irina Giurgea, Léa Savey, Marion Rabant
Publikováno v:
Rheumatology
Rheumatology, 2021, 60 (12), pp.5775-5784. ⟨10.1093/rheumatology/keab252⟩
Rheumatology, 2021, 60 (12), pp.5775-5784. ⟨10.1093/rheumatology/keab252⟩
Objectives TNF receptor-1-associated periodic syndrome (TRAPS) is a rare autosomal dominant autoinflammatory disorder associated with mutations in the TNF receptor super family 1 A (TNFRSF1A) gene. AA amyloidosis (AA) is the most severe complication
Publikováno v:
Genes & Immunity
Inflammasomes are key regulators of the host response against microbial pathogens, in addition to limiting aberrant responses to sterile insults, as mediated by environmental agents such as toxins or nanoparticles, and also by endogenous danger signa
Autor:
S. Abbara, Claude Bachmeyer, N. Sbeih, François Rodrigues, Véronique Hentgen, Léa Savey, A. Rouet, Sophie Georgin-Lavialle, Gilles Grateau, M. Delplanque, Isabelle Koné-Paut, K Stankovic Stojanovic, P.L. Conan, T. Fraisse
Publikováno v:
La Revue de Médecine Interne. 39:240-255
Resume La fievre mediterraneenne familiale (FMF) est la plus frequente des maladies auto-inflammatoires monogeniques. Il s’agit d’une maladie a transmission autosomique recessive qui touche principalement les populations issues du pourtour medite
Autor:
Gilles Grateau, Véronique Hentgen, Isabelle Koné-Paut, François Rodrigues, Sophie Georgin-Lavialle, Guillaume Sarrabay, Alexandre Belot, Claude Bachmeyer
Publikováno v:
La Revue de Médecine Interne. 39:279-286
Introduction Les maladies auto-inflammatoires (MAI) monogeniques sont des dereglements de l’immunite innee souvent associes au phenotype de fievre recurrente hereditaire. Le but de ce travail etait de decrire les caracteristiques cliniques, biologi