Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Maud Tusseau"'
Autor:
Jérôme Hadjadj, Carla Noemi Castro, Maud Tusseau, Marie-Claude Stolzenberg, Fabienne Mazerolles, Nathalie Aladjidi, Martin Armstrong, Houman Ashrafian, Ioana Cutcutache, Georg Ebetsberger-Dachs, Katherine S. Elliott, Isabelle Durieu, Nicole Fabien, Mathieu Fusaro, Maximilian Heeg, Yohan Schmitt, Marc Bras, Julian C. Knight, Jean-Christophe Lega, Gaetan Lesca, Anne-Laure Mathieu, Marion Moreews, Baptiste Moreira, Audrey Nosbaum, Matthew Page, Cécile Picard, T. Ronan Leahy, Isabelle Rouvet, Ethel Ryan, Damien Sanlaville, Klaus Schwarz, Andrew Skelton, Jean-Francois Viallard, Sebastien Viel, Marine Villard, Isabelle Callebaut, Capucine Picard, Thierry Walzer, Stephan Ehl, Alain Fischer, Bénédicte Neven, Alexandre Belot, Frédéric Rieux-Laucat
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-11 (2020)
SOCS1 is a potent suppressor of JAK-STAT signalling responses to IFNγ and γ-chain cytokines and thereby limits inflammation. Here the authors identify and characterize heterozygous SOCS1 mutations in 10 patients from 5 unrelated families with autoi
Externí odkaz:
https://doaj.org/article/e099b2415a024179917630ee4d4f2ec2
Autor:
Charlotte Boussard, Laure Delage, Tania Gajardo, Alexandre Kauskot, Maxime Batignes, Nicolas Goudin, Marie-Claude Stolzenberg, Camille Brunaud, Patricia Panikulam, Quentin Riller, Maryse Moya-Nilges, Jean Solarz, Christelle Reperant, Béatrice Durel, Jean-Claude Bordet, Olivier Pellé, Corinne Lebreton, Aude Magerus-Chatinet, Vithura Pirabakaran, Pablo Vargas, Sébastien Dupichaud, Marie Jeanpierre, Angélique Vinit, Mohammed Zarhrate, Cécile Masson, Nathalie Aladjidi, Peter D Arkwright, Brigitte Bader-Meunier, Sandrine Baron Joly, Joy Benadiba, Elise Bernard, Dominique Berrebi, Christine Bodemer, Martin Castelle, Fabienne Charbit-Henrion, Marwa Chbihi, Agathe Debray, Philippe Drabent, Sylvie Fraitag, Miguel Hié, Judith Landman-Parker, Ludovic Lhermitte, Despina Moshous, Pierre Rohrlich, Frank M Ruemmele, Anne Welfringer-Morin, Maud Tusseau, Alexandre Belot, Nadine Cerf-Bensussan, Marie Roelens, Capucine Picard, Bénédicte Neven, Alain Fischer, Isabelle Callebaut, Mickaël Mathieu Ménager, Fernando E Sepulveda, Frédéric Adam, Frédéric Rieux-Laucat
Publikováno v:
Blood.
Dedicator of cytokinesis (DOCK) proteins play a central role in actin cytoskeleton regulation. This is highlighted by the DOCK2 and DOCK8 deficiencies leading to actinopathies and immune deficiencies. DOCK8 and DOCK11 activate CDC42, a RHO-GTPase inv
Autor:
Samantha Innocenti, Silvia Bernardi, Maud Prévot, Antonin Saldmann, Maud Tusseau, Alexandre Belot, Jean-Paul Duong Van Huyen, Olivia Boyer
Publikováno v:
Pediatric nephrology (Berlin, Germany).
Autor:
Samantha Innocenti, Silvia Bernardi, Maud Prévot, Antonin Saldmann, Maud Tusseau, Alexandre Belot, Jean-Paul Duong Van Huyen, Olivia Boyer
Publikováno v:
Pediatric nephrology (Berlin, Germany).
Autor:
Franck Zekre, Anita Duncan, Audrey Laurent, Maud Tusseau, Rémi Pescarmona, Sophie Collardeau-Frachon, Camille Ohlmann, Sébastien Viel, Philippe Reix, Sarah Benezech, Alexandre Belot
Publikováno v:
Journal of Clinical Medicine. 12:2702
Introduction: Biological disease-modifying anti-rheumatic drugs (bDMARDs) targeting interleukin (IL)-6 and IL-1β represent a steroid-sparing first-line therapy used in systemic-onset juvenile idiopathic arthritis (sJIA). Recently, the occurrence of
Autor:
Guillaume Monneret, Morgane Gossez, Romain Marignier, Françoise Poitevin, Sandra Vukusic, Maud Tusseau, Julien Bancel, Estelle Cheli, Christophe Malcus
Publikováno v:
Multiple Sclerosis Journal. 27:1451-1454
Background: To demonstrate an inflammatory process in the central nervous system, the presence of at least two immunoglobulin (Ig) bands in the cerebrospinal fluid (CSF) is required. So far, the presence of a single abnormal Ig band is considered as
Autor:
Maud Tusseau, Alexandre Belot
Publikováno v:
Journal of Experimental Medicine. 219
In this issue of JEM, He et al. (2021. J. Exp. Med.https://doi.org/10.1084/jem.20211004) associate novel P2RY8 genetic variants to lupus, expanding the field of monogenic autoimmunity. The authors demonstrate that P2RY8 prevents the expansion of DNA-
Autor:
Maud Tusseau, Ema Lovšin, Charlotte Samaille, Rémi Pescarmona, Anne-Laure Mathieu, Maria-Cristina Maggio, Velma Selmanović, Marusa Debeljak, Angelique Dachy, Gregor Novljan, Alexandre Janin, Louis Januel, Jean-Baptiste Gibier, Emilie Chopin, Isabelle Rouvet, David Goncalves, Nicole Fabien, Gillian I Rice, Gaétan Lesca, Audrey Labalme, Paola Romagnani, Thierry Walzer, Sebastien Viel, Magali Perret, Yanick J. Crow, Tadej Avčin, Rolando Cimaz, Alexandre Belot
Publikováno v:
Journal of clinical immunology. 42(6)
Background: Deoxyribonuclease 1 like 3 (DNASE1L3) is a secreted enzyme that has been shown to digest the extracellular chromatin derived from apoptotic bodies, and DNASE1L3 pathogenic variants have been associated with a lupus phenotype. It is unclea
Autor:
Maud Tusseau, Carmen Oleaga-Quintas, Gonca Hancioglu, Jérémie Rosain, Caroline Deswarte, Laurie Toullec, Jacinta Bustamante, Şeyhan Kutluğ, Alisan Yildiran, Isinsu Kuzu, Jean-Laurent Casanova, Ibrahim Kartal
Publikováno v:
J Clin Immunol
KUZU, ISINSU/0000-0001-5519-1009 WOS: 000487139400010 PubMed: 31377971 … National Institute of Allergy and Infectious DiseasesUnited States Department of Health & Human ServicesNational Institutes of Health (NIH) - USANIH National Institute of Alle
Autor:
Françoise Poitevin, Sonia Lounis, Cécile Picard, Marine Villard, Christophe Malcus, Alexandre Belot, Mathieu Fusaro, Capucine Picard, Sébastien Viel, Debora Jorge Cordeiro, Emmanuel Martin, Sylvain Latour, David Goncalves, Benjamin Fournier, Anne-Laure Mathieu, Magali Perret, Nicole Fabien, Marion Moreews, Yves Bertrand, Thierry Walzer, Maud Tusseau, Nathalie Garnier, Alexandra Gauthier, Emilie Chopin, Christelle Lenoir
Publikováno v:
Journal of Allergy and Clinical Immunology
Journal of Allergy and Clinical Immunology, Elsevier, 2020, ⟨10.1016/j.jaci.2020.05.052⟩
Journal of Allergy and Clinical Immunology, Elsevier, 2020, ⟨10.1016/j.jaci.2020.05.052⟩
By studying four siblings with a null homozygous mutation in DEF6, we show that DEF6 deficiency is a new inherited immune dysregulation disorder with variable expressivity from autoimmunity/inflammation to EBV-associated viremia/lymphoproliferation/l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b5b45c4e5ad8d3474e2cde4771ebf38
https://hal.archives-ouvertes.fr/hal-03066027/document
https://hal.archives-ouvertes.fr/hal-03066027/document