IL-6, IL-10, sFas, granulysin and indicators of intestinal permeability as early biomarkers for a fatal outcome in COVID-19

Autor: Hernández-Solis, Alejandro, Güemes-González, Azmavet M., Ruiz-Gómez, Ximena, Álvarez-Maldonado, Pablo, Castañeda-Casimiro, Jessica, Flores-López, Argelia, Ramírez-Guerra, Martha Alicia, Muñoz-Miranda, Omar, Madera-Sandoval, Ruth L., Arriaga-Pizano, Lourdes A., Nieto-Patlán, Alejandro, Estrada-Parra, Sergio, Pérez-Tapia, Sonia Mayra, Serafín-López, Jeanet, Chacón-Salinas, Rommel, Escobar-Gutiérrez, Alejandro, Soria-Castro, Rodolfo, Ruiz-Sánchez, Bibiana Patricia, Wong-Baeza, Isabel

Publikováno v: In Immunobiology November 2022 227(6)

177 ClinGen Framework for PIK3CD Variant Classification: Use of Adapted ACMG/AMP Guidelines

Autor: Nieto-Patlán, Alejandro, Worley, Lindsay, Hankey, William, Hilliard, Kyle, Siew, Justine, Wang, Lijun, Boisson, Bertrand, Maimaris, Jes, Cunningham-Rundles, Charlotte, Jordan, Michael, Ma, Cindy, Peng, Xiao, McLaughlin, Heather, Zelm, Menno van, Lucas, Carrie, Markle, Janet, Puel, Anne, Begtrup, Amber

Publikováno v: In Clinical Immunology May 2024 262 Supplement

CTLA4 variant curation using adapted ACMG/AMP guidelines

Autor: Hankey, William, Worley, Lindsay, Hilliard, Kyle, McNulty, Shannon, Peng, Xiao, Romberg, Neil, Puel, Anne, Begtrup, Amber, Nieto-Patlán, Alejandro

Publikováno v: In Clinical Immunology May 2023 250 Supplement

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

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

Publikováno v: Journal of Experimental Medicine
Journal of Experimental Medicine, 2022, 219 (4), ⟨10.1084/jem.20211273⟩
Martin-fernandez, M, Buta, S, Le Voyer, T, Li, Z, Dynesen, L T D, Vuillier, F, Franklin, L, Ailal, F, Amanico, A M, Malle, L, Gruber, C, Benhsaien, I, Altman, J, Taft, J, Deswarte, C, Roynard, M, Nieto-Patlan, A, Moriya, K, Rosain, J, Boddaert, N, Bousfiha, A, Crow, Y J, Jankovic, D, Sher, A, Casanova, J-L, Pellegrini, S, Bustamante, J & Bogunovic, D 2022, ' A partial form of inherited human USP18 deficiency underlies infection and inflammation ', Journal of Experimental Medicine . https://doi.org/10.1084/jem.20211273

International audience; Human USP18 is an interferon (IFN)-stimulated gene product and a negative regulator of type I IFN (IFN-I) signaling. It also removes covalently linked ISG15 from proteins, in a process called deISGylation. In turn, ISG15 preve

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3fa59f57c02c30b47c8521ac976ce0f6
https://doi.org/10.1084/jem.20211273

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