Glucose uptake and its effect on gene expression in prochlorococcus.

Autor: Guadalupe Gómez-Baena, Antonio López-Lozano, Jorge Gil-Martínez, José Manuel Lucena, Jesús Diez, Pedro Candau, Jose Manuel García-Fernández

Publikováno v: PLoS ONE, Vol 3, Iss 10, p e3416 (2008)

The marine cyanobacteria Prochlorococcus have been considered photoautotrophic microorganisms, although the utilization of exogenous sugars has never been specifically addressed in them. We studied glucose uptake in different high irradiance- and low

Externí odkaz: https://doaj.org/article/33b6390d7d554d148af83f9b84a61ab7

Monitoring of kinetics and exhaustion markers of circulating CAR-T cells as early predictive factors in patients with B-cell malignancies

Autor: Clara Beatriz García-Calderón, Belén Sierro-Martínez, Estefanía García-Guerrero, Luzalba Sanoja-Flores, Raquel Muñoz-García, Victoria Ruiz-Maldonado, María Reyes Jimenez-Leon, Javier Delgado-Serrano, Águeda Molinos-Quintana, Beatriz Guijarro-Albaladejo, Inmaculada Carrasco-Brocal, José-Manuel Lucena, José-Raúl García-Lozano, Cristina Blázquez-Goñi, Juan Luis Reguera-Ortega, María-Francisca González-Escribano, Marta Reinoso-Segura, Javier Briones, José Antonio Pérez-Simón, Teresa Caballero-Velázquez

Publikováno v: Frontiers in Immunology. 14

PurposeCAR-T cell therapy has proven to be a disruptive treatment in the hematology field, however, less than 50% of patients maintain long-term response and early predictors of outcome are still inconsistently defined. Here, we aimed to optimize the

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::c9d5b8cea5d6db598b312e6a04272223
https://doi.org/10.3389/fimmu.2023.1152498

Executive Summary of the Consensus Document on the Diagnosis and Management of Patients with Primary Immunodeficiencies

Autor: Elisa Cordero, Rocío Parody, Ana Méndez-Echevarría, Juan I. Aróstegui, David Moreno-Pérez, Jan Ramakers, Francisco López-Medrano, José Manuel Lucena, Peter Olbrich, Juan Luis Santos-Pérez, Eduardo López-Granados, Walter Alfredo Goycochea-Valdivia, Juana Gil-Herrera, Rebeca Rodríguez Pena, Javier Carbone, María Bravo García-Morato, Pere Soler-Palacín, Jacques G. Rivière, Carlota Gudiol, Laia Alsina, Cristina Roca-Oporto, Jesús Fortún, José R. Regueiro, Carlos Rodríguez-Gallego, Oscar Len-Abad, Luis M. Allende, Patricia Muñoz, Luis Ignacio Gonzalez-Granado, Isabel Serra, Olaf Neth, Clara Aguilera Cros, Silvia Sánchez-Ramón

Publikováno v: JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY-IN PRACTICE
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
Digital.CSIC. Repositorio Institucional del CSIC
instname
ENFERMEDADES INFECCIOSAS Y MICROBIOLOGIA CLINICA
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
Journal of Allergy and Clinical Immunology-In Practice
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu

[EN] Primary immunodeficiencies (PIDs) are rare, undiagnosed and potentially fatal diseases. Clinical manifestations of PID can be fatal or leave sequelae that worsen the quality of life of patients. Traditionally, the treatment of PIDs has been larg

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4f386cf50392c417bd5a47bcf8a90fd
https://doi.org/10.1016/j.eimce.2020.07.004

SARS-CoV-2 infection in a pediatrics STAT1 GOF patient under Ruxolitinib therapy-a matter of balance?

Autor: Guillermo Martín Gutierrez, Beatriz de Felipe, Paloma Guisado Hernández, María Isabel Sánchez Codez, Peter Olbrich, José Manuel Lucena, María José Castro, Alicia Gutiérrez Valencia, Isabel Villaoslada, Mirella Gaboli, Olaf Neth, Pilar Blanco Lobo

Publikováno v: Digital.CSIC. Repositorio Institucional del CSIC
instname
Journal of Clinical Immunology

Recently, 94 inborn errors of immunity (IEI) patients suffering from COVID-19 have been described, overall demonstrating a mild phenotype [1] although more severe disease manifestations have been suggested for patients with alterations in the interfe

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e9c7b186dd18843a80a193af2b47325
https://link.springer.com/content/pdf/10.1007/s10875-021-01081-9.pdf

Biallelic TRAF3IP2 variants causing chronic mucocutaneous candidiasis in a child harboring a STAT1 variant

Autor: Anne Puel, Jean-Laurent Casanova, Simon J. Pelham, Isabel Villaoslada, Paloma Guisado Hernández, Wei-Te Lei, Olaf Neth, Peter Olbrich, José Manuel Lucena, Beatriz de Felipe, Pilar Blanco Lobo

Publikováno v: Digital.CSIC. Repositorio Institucional del CSIC
instname

[Background] Inherited chronic mucocutaneous candidiasis (CMC) is often caused by inborn errors of immunity, impairing the response to, or the production of IL-17A and IL-17F. About half of the cases carry STAT1 gain-of-function (GOF) mutations. Only

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c6df16bc3c2dd1b9f50e5568ca1f2fa
http://hdl.handle.net/10261/269406