Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Manuel Muro-Perez"'
Autor:
Rafael Alfaro, Helios Martínez-Banaclocha, Santiago Llorente, Victor Jimenez-Coll, José Antonio Galián, Carmen Botella, María Rosa Moya-Quiles, Antonio Parrado, Manuel Muro-Perez, Alfredo Minguela, Isabel Legaz, Manuel Muro
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
BackgroundThe diagnosis of graft rejection in kidney transplantation (KT) patients is made by evaluating the histological characteristics of biopsy samples. The evolution of omics sciences and bioinformatics techniques has contributed to the advancem
Externí odkaz:
https://doaj.org/article/9b5c322549ec47b7bd01a68f516ad962
Autor:
Muro, Rafael Alfaro, Luis Rodríguez-Aguilar, Santiago Llorente, Victor Jimenez-Coll, Helios Martínez-Banaclocha, José Antonio Galián, Carmen Botella, María Rosa Moya-Quiles, Manuel Muro-Perez, Alfredo Minguela, Isabel Legaz, Manuel
Publikováno v:
International Journal of Molecular Sciences; Volume 24; Issue 13; Pages: 10491
Cytomegalovirus (CMV) infection is the most frequent infection episode in kidney transplant (KT) recipients. Reactivation usually occurs in the first three months after transplantation and is associated with higher cellular and/or antibody-mediated r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=multidiscipl::8edbd851b2e0c6709f329711307ae53b
Autor:
Isabel Legaz, Víctor Jimenez-Coll, Rosana González-López, Marina Fernández-González, María José Alegría-Marcos, José Antonio Galián, Carmen Botella, Rosa Moya-Quiles, Manuel Muro-Pérez, Alfredo Minguela, Santiago Llorente, Manuel Muro
Publikováno v:
Biomedicines, Vol 12, Iss 1, p 116 (2024)
Allograft rejection is a widespread complication in allograft recipients with chronic kidney disease. Undertreatment of subclinical and clinical rejection and later post-transplant problems are caused by an imperfect understanding of the mechanisms a
Externí odkaz:
https://doaj.org/article/8013df17a2bb472bb989d6b336df5b7c
Autor:
Irene Cuenca, Carmen Botella, María Rosa Moya-Quiles, Víctor Jimenez-Coll, José Antonio Galian, Helios Martinez-Banaclocha, Manuel Muro-Pérez, Alfredo Minguela, Isabel Legaz, Manuel Muro
Publikováno v:
Diagnostics, Vol 13, Iss 17, p 2845 (2023)
Alpha-1 antitrypsin (AAT1) deficiency (AAT1D) is an inherited disease with an increased risk of chronic obstructive pulmonary disease (COPD), liver disease, and skin and blood vessel problems. AAT1D is caused by mutations in the SERPINE1 gene (Serine
Externí odkaz:
https://doaj.org/article/e3f9a5232f9947f3a3e7c6fdf6775c20