T Cell Receptor Signal Initiation Induced by Low-Grade Stimulation Requires the Cooperation of LAT in Human T Cells

por Dong, Shen, Corre, Béatrice, Nika, Konstantina, Pellegrini, Sandra, Michel, Frédérique
Publicado 2010

Two common disease-associated TYK2 variants impact exon splicing and TYK2 dosage

por Li, Zhi, Rotival, Maxime, Patin, Etienne, Michel, Frédérique, Pellegrini, Sandra
Publicado 2020

USP18 and ISG15 coordinately impact on SKP2 and cell cycle progression

por Vuillier, Françoise, Li, Zhi, Commere, Pierre-Henri, Dynesen, Lasse Toftdal, Pellegrini, Sandra
Publicado 2019

Assessment of mTOR-Dependent Translational Regulation of Interferon Stimulated Genes

por Livingstone, Mark, Sikström, Kristina, Robert, Philippe A., Uzé, Gilles, Larsson, Ola, Pellegrini, Sandra
Publicado 2015

IFN-I inducible miR-3614-5p targets ADAR1 isoforms and fine tunes innate immune activation

por Vuillier, Françoise, Li, Zhi, Black, Iain, Cruciani, Melania, Rubino, Erminia, Michel, Frédérique, Pellegrini, Sandra
Publicado 2022

USP18-Based Negative Feedback Control Is Induced by Type I and Type III Interferons and Specifically Inactivates Interferon α Response

por François-Newton, Véronique, Magno de Freitas Almeida, Gabriel, Payelle-Brogard, Béatrice, Monneron, Danièle, Pichard-Garcia, Lydiane, Piehler, Jacob, Pellegrini, Sandra, Uzé, Gilles
Publicado 2011

Hepatitis B virus X protein inhibits extracellular IFN-α-mediated signal transduction by downregulation of type I IFN receptor

por CHO, IL-RAE, OH, MYUNGJU, KOH, SANG SEOK, MALILAS, WARAPORN, SRISUTTEE, RATAKORN, JHUN, BYUNG HAK, PELLEGRINI, SANDRA, FUCHS, SERGE Y., CHUNG, YOUNG-HWA
Publicado 2012

The cyclin D1 carboxyl regulatory domain controls the division and differentiation of hematopoietic cells

por Chaves-Ferreira, Miguel, Krenn, Gerald, Vasseur, Florence, Barinov, Aleksandr, Gonçalves, Pedro, Azogui, Orly, Cumano, Ana, Li, Zhi, Pellegrini, Sandra, Rocha, Benedita, Laderach, Diego
Publicado 2016

Human Ubiquitin-Specific Peptidase 18 Is Regulated by microRNAs via the 3'Untranslated Region, A Sequence Duplicated in Long Intergenic Non-coding RNA Genes Residing in chr22q11.21

por Rubino, Erminia, Cruciani, Melania, Tchitchek, Nicolas, Le Tortorec, Anna, Rolland, Antoine D., Veli, Önay, Vallet, Leslie, Gaggi, Giulia, Michel, Frédérique, Dejucq-Rainsford, Nathalie, Pellegrini, Sandra
Publicado 2021

Altered Immune Phenotypes and HLA-DQB1 Gene Variation in Multiple Sclerosis Patients Failing Interferon β Treatment

por Devi-Marulkar, Priyanka, Moraes-Cabe, Carolina, Campagne, Pascal, Corre, Béatrice, Meghraoui-Kheddar, Aida, Bondet, Vincent, Llibre, Alba, Duffy, Darragh, Maillart, Elisabeth, Papeix, Caroline, Pellegrini, Sandra, Michel, Frédérique
Publicado 2021

Receptor dimerization dynamics as a regulatory valve for plasticity of type I interferon signaling

por Wilmes, Stephan, Beutel, Oliver, Li, Zhi, Francois-Newton, Véronique, Richter, Christian P., Janning, Dennis, Kroll, Cindy, Hanhart, Patrizia, Hötte, Katharina, You, Changjiang, Uzé, Gilles, Pellegrini, Sandra, Piehler, Jacob
Publicado 2015

Mycolactone subverts immunity by selectively blocking the Sec61 translocon

por Baron, Ludivine, Paatero, Anja Onerva, Morel, Jean-David, Impens, Francis, Guenin-Macé, Laure, Saint-Auret, Sarah, Blanchard, Nicolas, Dillmann, Rabea, Niang, Fatoumata, Pellegrini, Sandra, Taunton, Jack, Paavilainen, Ville O., Demangel, Caroline
Publicado 2016

Genome-Wide Gene Expression Analysis of Mtb-Infected DC Highlights the Rapamycin-Driven Modulation of Regulatory Cytokines via the mTOR/GSK-3β Axis

por Etna, Marilena P., Severa, Martina, Licursi, Valerio, Pardini, Manuela, Cruciani, Melania, Rizzo, Fabiana, Giacomini, Elena, Macchia, Gianfranco, Palumbo, Orazio, Stallone, Raffaella, Carella, Massimo, Livingstone, Mark, Negri, Rodolfo, Pellegrini, Sandra, Coccia, Eliana M.
Publicado 2021

STAT2 is an essential adaptor in USP18-mediated suppression of type I interferon signaling

por Arimoto, Kei-ichiro, Löchte, Sara, Stoner, Samuel A., Burkart, Christoph, Zhang, Yue, Miyauchi, Sayuri, Wilmes, Stephan, Fan, Jun-Bao, Heinisch, Jürgen J., Li, Zhi, Yan, Ming, Pellegrini, Sandra, Colland, Frédéric, Piehler, Jacob, Zhang, Dong-Er
Publicado 2017

Type I Interferonopathy due to a Homozygous Loss-of-Inhibitory Function Mutation in STAT2

por Zhu, Gaofeng, Badonyi, Mihaly, Franklin, Lina, Seabra, Luis, Rice, Gillian I., Anne-Boland-Auge, Deleuze, Jean-François, El-Chehadeh, Salima, Anheim, Mathieu, de Saint-Martin, Anne, Pellegrini, Sandra, Marsh, Joseph A., Crow, Yanick J., El-Daher, Marie-Therese
Publicado 2023

Evolutionary Dynamics of Human Toll-Like Receptors and Their Different Contributions to Host Defense

por Barreiro, Luis B., Ben-Ali, Meriem, Quach, Hélène, Laval, Guillaume, Patin, Etienne, Pickrell, Joseph K., Bouchier, Christiane, Tichit, Magali, Neyrolles, Olivier, Gicquel, Brigitte, Kidd, Judith R., Kidd, Kenneth K., Alcaïs, Alexandre, Ragimbeau, Josiane, Pellegrini, Sandra, Abel, Laurent, Casanova, Jean-Laurent, Quintana-Murci, Lluís
Publicado 2009

Copy number variations and founder effect underlying complete IL-10Rβ deficiency in Portuguese kindreds

por Charbit-Henrion, Fabienne, Bègue, Bernadette, Sierra, Anaïs, Hanein, Sylvain, Stolzenberg, Marie-Claude, Li, Zhi, Pellegrini, Sandra, Garcelon, Nicolas, Jeanpierre, Marc, Neven, Bénédicte, Loge, Isabelle, Picard, Capucine, Rosain, Jérémie, Bustamante, Jacinta, Le Lorc’h, Marc, Pigneur, Bénédicte, Fernandes, Alicia, Rieux-Laucat, Frédéric, Amil Dias, Jorge, Ruemmele, Frank M., Cerf-Bensussan, Nadine
Publicado 2018

ISG15 deficiency and increased viral resistance in humans but not mice

por Speer, Scott D., Li, Zhi, Buta, Sofija, Payelle-Brogard, Béatrice, Qian, Li, Vigant, Frederic, Rubino, Erminia, Gardner, Thomas J., Wedeking, Tim, Hermann, Mark, Duehr, James, Sanal, Ozden, Tezcan, Ilhan, Mansouri, Nahal, Tabarsi, Payam, Mansouri, Davood, Francois-Newton, Véronique, Daussy, Coralie F., Rodriguez, Marisela R., Lenschow, Deborah J., Freiberg, Alexander N., Tortorella, Domenico, Piehler, Jacob, Lee, Benhur, García-Sastre, Adolfo, Pellegrini, Sandra, Bogunovic, Dusan
Publicado 2016

A partial form of inherited human USP18 deficiency underlies infection and inflammation

por Martin-Fernandez, Marta, Buta, Sofija, Le Voyer, Tom, Li, Zhi, Dynesen, Lasse Toftdal, Vuillier, Françoise, Franklin, Lina, Ailal, Fatima, Muglia Amancio, Alice, Malle, Louise, Gruber, Conor, Benhsaien, Ibtihal, Altman, Jennie, Taft, Justin, Deswarte, Caroline, Roynard, Manon, Nieto-Patlan, Alejandro, Moriya, Kunihiko, Rosain, Jérémie, Boddaert, Nathalie, Bousfiha, Aziz, Crow, Yanick J., Jankovic, Dragana, Sher, Alan, Casanova, Jean-Laurent, Pellegrini, Sandra, Bustamante, Jacinta, Bogunovic, Dusan
Publicado 2022

Human USP18 deficiency underlies type 1 interferonopathy leading to severe pseudo-TORCH syndrome

por Meuwissen, Marije E.C., Schot, Rachel, Buta, Sofija, Oudesluijs, Grétel, Tinschert, Sigrid, Speer, Scott D., Li, Zhi, van Unen, Leontine, Heijsman, Daphne, Goldmann, Tobias, Lequin, Maarten H., Kros, Johan M., Stam, Wendy, Hermann, Mark, Willemsen, Rob, Brouwer, Rutger W.W., Van IJcken, Wilfred F.J., Martin-Fernandez, Marta, de Coo, Irenaeus, Dudink, Jeroen, de Vries, Femke A.T., Bertoli Avella, Aida, Prinz, Marco, Crow, Yanick J., Verheijen, Frans W., Pellegrini, Sandra, Bogunovic, Dusan, Mancini, Grazia M.S.
Publicado 2016