Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Rita María Valdez"'
Autor:
Guadalupe Buda, Rita María Valdez, German Biagioli, Federico A. Olivieri, Nicolás Affranchino, Carolina Bouso, Vanesa Lotersztein, Dusan Bogunovic, Jacinta Bustamante, Marcelo A. Martí
Publikováno v:
Allergy, Asthma & Clinical Immunology, Vol 16, Iss 1, Pp 1-6 (2020)
Abstract Interferon-stimulated gene 15 (ISG15) was the first ubiquitin-like modifier protein identified that acts by protein conjugation (ISGylation) and is thought to modulate IFN-induced inflammation. Here, we report a new patient from a non-consan
Externí odkaz:
https://doaj.org/article/34b21fec13ae4972a0c29de3c5ea3cd7
Autor:
Marcelo A. Martí, Jacinta Bustamante, Vanesa Lotersztein, German Biagioli, Dusan Bogunovic, Guadalupe Buda, Federico A. Olivieri, Carolina Bouso, Nicolás Affranchino, Rita María Valdez
Publikováno v:
Allergy, Asthma, and Clinical Immunology : Official Journal of the Canadian Society of Allergy and Clinical Immunology
Allergy, Asthma & Clinical Immunology, Vol 16, Iss 1, Pp 1-6 (2020)
Allergy, Asthma & Clinical Immunology, Vol 16, Iss 1, Pp 1-6 (2020)
Interferon-stimulated gene 15 (ISG15) was the first ubiquitin-like modifier protein identified that acts by protein conjugation (ISGylation) and is thought to modulate IFN-induced inflammation. Here, we report a new patient from a non-consanguineous
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8bc00095c4232bbe8498158668a4d7a9
https://doi.org/10.1186/s13223-020-00473-7
https://doi.org/10.1186/s13223-020-00473-7
Autor:
Dusan Bogunovic, Sara Murias Loza, Mohamad-Hani Temsah, Jigar V. Desai, Abdullah Alakeel, Bertrand Boisson, Luz Yadira Bravo-Gallego, Ruth Olmer, Fahad Alsohime, Sergio D. Rosenzweig, Abdulkarim Alrabiaah, Mohammed Al Ayed, Muhammad Nasir Hayat Malik, Xueer Qiu, Sylvia Merkert, Elise M. N. Ferré, Frank Pessler, Montserrat Bret, Marta Feito Rodríguez, Amika K. Sood, Marta Martín-Fernández, Michail S. Lionakis, Guadalupe Buda, Margarita Larralde, Jean-Laurent Casanova, Blanca Amador-Borrero, Maya Chrabieh, Sofija Buta, Conor Gruber, Rabih Halwani, Saleh Al Muhsen, Michelle L. Hernandez, María Bravo García-Morato, Marcelo A. Martí, Jacinta Bustamante, Rita María Valdez
Publikováno v:
Cell reports
SUMMARY Most monogenic disorders have a primary clinical presentation. Inherited ISG15 deficiency, however, has manifested with two distinct presentations to date: susceptibility to mycobacterial disease and intracranial calcifications from hypomorph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ae9d56672629e13b931bdd200aada1b
https://doi.org/10.1016/j.celrep.2020.107633
https://doi.org/10.1016/j.celrep.2020.107633