Zobrazeno 1 - 10
of 97
pro vyhledávání: '"Marcela, Moncada"'
Autor:
Sharon Banegas, Denis Escobar, Alejandra Pinto, Marcela Moncada, Gabriela Matamoros, Hugo O. Valdivia, Allan Reyes, Gustavo Fontecha
Publikováno v:
Pathogens, Vol 13, Iss 7, p 541 (2024)
Background: Efforts on a global scale for combating malaria have achieved substantial progress over the past twenty years. Two Central American nations have accomplished their goal of eliminating malaria: El Salvador and Belize. Honduras has decrease
Externí odkaz:
https://doaj.org/article/abb6178b40904bc7bb689ffc04fc8e5c
Autor:
Gabriela Matamoros, Denis Escobar, Alejandra Pinto, Delmy Serrano, Eliška Ksandrová, Nicole Grimaldi, Gabriel Juárez-Fontecha, Marcela Moncada, Hugo O. Valdivia, Gustavo Fontecha
Publikováno v:
Malaria Journal, Vol 22, Iss 1, Pp 1-10 (2023)
Abstract Background Malaria remains a main parasitic disease of humans. Although the largest number of cases is reported in the African region, there are still endemic foci in the Americas. Central America reported 36,000 malaria cases in 2020, which
Externí odkaz:
https://doaj.org/article/e45174fa9c4744ce8799a3c29900665a
Autor:
Christina Grosserichter‐Wagener, Alexander Franco‐Gallego, Fatemeh Ahmadi, Marcela Moncada‐Vélez, Virgil ASH Dalm, Jessica Lineth Rojas, Julio César Orrego, Natalia Correa Vargas, Lennart Hammarström, Marco WJ Schreurs, Willem A Dik, P Martin vanHagen, Louis Boon, Jacques JM vanDongen, Mirjam van derBurg, Qiang Pan‐Hammarström, José L Franco, Menno C vanZelm
Publikováno v:
Clinical & Translational Immunology, Vol 9, Iss 5, Pp n/a-n/a (2020)
Abstract Objective Selective IgA deficiency (sIgAD) is the most common primary immunodeficiency in Western countries. Patients can suffer from recurrent infections and autoimmune diseases because of a largely unknown aetiology. To increase insights i
Externí odkaz:
https://doaj.org/article/d7481a6cda3b47a693f06a960e2f80f0
Autor:
Jérémie Rosain, Anna-Lena Neehus, Jérémy Manry, Rui Yang, Jérémie Le Pen, Wassim Daher, Zhiyong Liu, Yi-Hao Chan, Natalia Tahuil, Özden Türel, Mathieu Bourgey, Masato Ogishi, Jean-Marc Doisne, Helena M. Izquierdo, Takayoshi Shirasaki, Tom Le Voyer, Antoine Guérin, Paul Bastard, Marcela Moncada-Vélez, Ji Eun Han, Taushif Khan, Franck Rapaport, Seon-Hui Hong, Andrew Cheung, Kathrin Haake, Barbara C. Mindt, Laura Pérez, Quentin Philippot, Danyel Lee, Peng Zhang, Darawan Rinchai, Fatima Al Ali, Manar Mahmoud Ahmad Ata, Mahbuba Rahman, Jessica N. Peel, Søren Heissel, Henrik Molina, Yasemin Kendir-Demirkol, Rasheed Bailey, Shuxiang Zhao, Jonathan Bohlen, Mathieu Mancini, Yoann Seeleuthner, Marie Roelens, Lazaro Lorenzo, Camille Soudée, María Elvira Josefina Paz, María Laura González, Mohamed Jeljeli, Jean Soulier, Serge Romana, Anne-Sophie L’Honneur, Marie Materna, Rubén Martínez-Barricarte, Mathieu Pochon, Carmen Oleaga-Quintas, Alexandre Michev, Mélanie Migaud, Romain Lévy, Marie-Alexandra Alyanakian, Flore Rozenberg, Carys A. Croft, Guillaume Vogt, Jean-François Emile, Laurent Kremer, Cindy S. Ma, Jörg H. Fritz, Stanley M. Lemon, András N. Spaan, Nicolas Manel, Laurent Abel, Margaret R. MacDonald, Stéphanie Boisson-Dupuis, Nico Marr, Stuart G. Tangye, James P. Di Santo, Qian Zhang, Shen-Ying Zhang, Charles M. Rice, Vivien Béziat, Nico Lachmann, David Langlais, Jean-Laurent Casanova, Philippe Gros, Jacinta Bustamante
Publikováno v:
Cell
Cell, 2023, 186 (3), pp.621-645.e33. ⟨10.1016/j.cell.2022.12.038⟩
Cell, 2023, 186 (3), pp.621-645.e33. ⟨10.1016/j.cell.2022.12.038⟩
Inborn errors of human IFN-γ-dependent macrophagic immunity underlie mycobacterial diseases, whereas inborn errors of IFN-α/β-dependent intrinsic immunity underlie viral diseases. Both types of IFNs induce the transcription factor IRF1. We describ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e4a4bba1d777506cff9bef2fad8f1ed
https://hal-pasteur.archives-ouvertes.fr/pasteur-04130575
https://hal-pasteur.archives-ouvertes.fr/pasteur-04130575
Autor:
Alejandra Catalina Vélez, Diana María Castaño, Rubén Darío Gómez, Julio César Orrego, Marcela Moncada, José Luis Franco
Publikováno v:
Biomédica: revista del Instituto Nacional de Salud, Vol 35, Iss 1, Pp 101-16 (2015)
Introducción. La inmunodeficiencia común variable es un síndrome heterogéneo caracterizado por infecciones recurrentes, hipogammaglobulinemia y producción deficiente de anticuerpos específicos. Las anormalidades en subpoblaciones de linfocitos
Externí odkaz:
https://doaj.org/article/bb1d32dc78e24d5d8651241bca8bc212
Autor:
Gabriela Matamoros, Denis Escobar, Alejandra Pinto, Delmy Serrano, Eliška Ksandrová, Nicole Grimaldi, Gabriel Juárez-Fontecha, Marcela Moncada, Hugo O. Valdivia, Gustavo Fontecha
Background Malaria remains a main parasitic disease of humans. Although the largest number of cases is reported in the African region, there are still endemic foci in the Americas. Central America reported 36,000 malaria cases in 2020, which represen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b917f61a96baff685c9140dab956a017
https://doi.org/10.21203/rs.3.rs-2222901/v1
https://doi.org/10.21203/rs.3.rs-2222901/v1
Autor:
Carlos A. Arango-Franco, Mélanie Migaud, Isabel Cristina Ramírez-Sánchez, Karen Arango, Marcela Moncada-Vélez, Julián Rojas, Adrian Gervais, Santiago Patiño Giraldo, Lizeth J Perez-Zapata, Jesús A. Álvarez Álvarez, Julio César Orrego, Gustavo Roncancio Villamil, Stéphanie Boisson-Dupuis, Emmanuelle Jouanguy, Laurent Abel, Jean-Laurent Casanova, Jacinta Bustamante, Andrés A. Arias, José Luis Franco, Anne Puel
Abstract Background Cryptococcosis is a potentially life-threatening fungal disease caused by encapsulated yeasts of the genus Cryptococcus, mostly C. neoformans or C. gattii. Cryptococcal meningitis is the most frequent clinical manifestation in hum
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0b50c80b6e76ef9863e4d4b57b4a448
https://doi.org/10.21203/rs.3.rs-1892529/v1
https://doi.org/10.21203/rs.3.rs-1892529/v1
Autor:
Carlos Andrés Arango-Franco, Marcela Moncada-Vélez, Alexander Franco-Gallego, Lucía Victoria Erazo, Catalina Martínez, Sebastián Gutiérrez, Jesús Armando Álvarez, Manuela Molina, Diana Arboleda, Laura Naranjo, Juan Álvaro López, Juan Fernando Alzate, Felipe Cabarcas, Claudia Milena Trujillo-Vargas, Julio César Orrego, Satoshi Okada, Anne Puel, Jacinta Bustamante, Jean-Laurent Casanova, Andrés Augusto Arias, José Luis Franco
Publikováno v:
Revista Alergia México, Vol 65 suppl 1, Pp 129-130 (2018)
Background: The genetic etiology of several primary immunodeficiency diseases (PID) remains elusive. Next generation technologies represent a cost-effective and rapid first-line genetic approach for the evaluation of diseases underlying mendelian tra
Externí odkaz:
https://doaj.org/article/c28dca86cd9a48b3acdcaca2d8e8606a
Autor:
Marcela Moncada-Vélez, Lucía Victoria Erazo-Borrás, Jesús Armando Álvarez-lvarez, Carlos Andrés Arango, Miyuki Tsumura, Satoshi Okada, Sara Daniela Osorio, Lorena Castro, Natalia González, Catalina Arango, Julio César Orrego, Lina Riaño, Juan Fernando Alzate, Felipe Cabarcas, Jean-Laurent Casanova, Jacinta Bustamante, Anne Puel, Andrés Augusto Arias, José Luis Franco
Publikováno v:
Revista Alergia México, Vol 65 suppl 1, Pp 114-115 (2018)
Background: The transcription factor STAT1 plays a critical role in the immune response against mycobacterial, viral and fungal infections. Different mutations in STAT1 result in diverse clinical phenotypes: AR complete/partial biallelic mutations ar
Externí odkaz:
https://doaj.org/article/15503ab3fb4b465a85afe9b41d45fb07
Autor:
Carlos Andrés Arango-Franco, Alejandro Nieto-Patlán, Marcela Moncada-Vélez, Jesús Armando Álvarez, Carmen Oleaga-Quinta, Caroline Deswarte, Juan Fernando Alzate, Felipe Cabarcas, Carlos Garcés, Julio César Orrego, Susana Pamela Mejía, Luz Elena Cano, Jean-Laurent Casanova, Jacinta Bustamante, José Luis Franco, Andrés Augusto Arias
Publikováno v:
Revista Alergia México, Vol 65 suppl 1, Pp 134-135 (2018)
Background: Chronic granulomatous disease (CGD) is a primary immunodeficiency characterized by susceptibility to early-onset life-threatening bacterial and fungal infections as well as dysregulated chronic inflammation. CGD results from mutations in
Externí odkaz:
https://doaj.org/article/37ef6f9f88c44eeea48b8fbb13b9428a