Author

R. Fernandez-Rodriguez

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Immunology· 3

Signature Assays, Organisms & Methods

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Organism:human· 3 Assay:bulk RNA-seq· 2 Research Focus:cell signaling & trafficking· 2 Approach:biophysical modeling· 1 Approach:experimental assay· 1 Assay:flow cytometry· 1 Research Focus:host-pathogen & immune response· 1 Research Focus:metabolism & bioenergetics· 1

Frequent Co-Authors

A. de Lucas-Rius· 2 shared J. J. Garrido· 2 shared M. Montoya· 2 shared N. Redondo· 2 shared T. Garcia-Garcia· 2 shared A. Calvet· 1 shared A. Charap· 1 shared A. Jimenez-Marin· 1 shared

Activity by Year

2022-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 23 mutual co-author links

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2 shared papersImmunology

A. de Lucas-Rius

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Metabolic and mitochondria alterations induced by SARS-CoV-2 accessory proteins ORF3a, ORF9b, ORF9c and ORF10

B. D. Lopez-Ayllon, S. Marin, M. Farinas Fernandez, T. Garcia-Garcia, R. Fernandez-Rodriguez, A. de Lucas-Rius, N. Redondo, L. Mendoza-Garcia, C. Foguet, J. Grigas, A. Calvet, J. M. Villalba, M. J. Rodriguez Gomez, D. Megias, B. Mandracchia, , M. Montoya

This study identifies mitochondrial and metabolic reprogramming induced by SARS-CoV-2 accessory proteins in lung cells, revealing potential therapeutic targets.

bioRxiv · Sep 26, 2023Immunology

Antiviral immune responses, cellular metabolism and adhesion are differentially modulated by SARS-CoV-2 ORF7a or ORF7b

T. Garcia-Garcia, R. Fernandez-Rodriguez, N. Redondo, A. de Lucas-Rius, S. Zaldivar-Lopez, B. Dies Lopez-Ayllon, J. M. Suarez-Cardenas, A. Jimenez-Marin, M. Montoya, J. J. Garrido

This study investigates how SARS-CoV-2 ORF7a and ORF7b proteins modulate antiviral responses, metabolism, and adhesion in A549 cells, revealing their role in promoting viral pathogenesis.

bioRxiv · Jun 1, 2022 · PreprintImmunology

NKG2A and HLA-E define a novel alternative immune checkpoint axis in bladder cancer

B. Salome, J. P. Sfakianos, J. Daza, A. Charap, C. Hammer, R. Banchereau, A. M. Farkas, D. Geanon, G. Kelly, R. M. de Real, B. Lee, K. G. Beaumont, S. Shroff, Y. S. A. Wang, Y.-C. Wang, , Mariath

This study identifies NKG2A and HLA-E as an alternative immune checkpoint axis in bladder cancer, showing NKG2A+ CD8 T cells can bypass HLA-ABC loss through TCR-independent cytotoxicity.

bioRxiv · Mar 4, 2022 · PreprintImmunology