Author

B. R. Barboza

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

Biology Disciplines

Click to filter author papers

Cell Biology· 2 Microbiology· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 3 Assay:proteomics· 3 Research Focus:cell type annotation· 2 Approach:experimental assay· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:cell-cell communication· 1 Research Focus:host-pathogen & immune response· 1 Organism:mouse· 1

Frequent Co-Authors

G. Palmisano· 2 shared S. K. N. Marie· 2 shared V. d. M. Gomes· 2 shared A. de Carvalho· 1 shared A. K. Tashima· 1 shared A. M. Marques-Neto· 1 shared A. Zelanis· 1 shared C. B. Moraes· 1 shared

Activity by Year

2021-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 20 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersMicrobiology

G. Palmisano

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

ST8Sia2 polysialyltransferase protects against infection by Trypanosoma cruzi

B. R. Barboza, J. M. da Silva, L. A. M. Trajano-Silva, V. d. M. Gomes, D. M. Santos, A. M. Marques-Neto, S. N. Mule, J. Borsoi, C. B. Moraes, M. Muhlenhoff, W. Colli, S. K. N. Marie, L. V. Pereira, M. J. M. Alves, G. Palmisano

This study shows that ST8Sia2 polysialyltransferase reduces Trypanosoma cruzi infection by modulating host polysialylation.

bioRxiv · Nov 14, 2023 · PreprintMicrobiology

ArtinM Cytotoxicity in B cells derived from Non-Hodgkins Lymphoma is regulated by CD45 phosphatase activity and Src family kinases

B. R. Barboza, S. M. d. O. Thomaz, A. de Carvalho, E. M. Espreafico, J. G. Miyamoto, A. K. Tashima, M. F. Camacho, A. Zelanis, M. C. Roque-Barreira, T. A. da Silva

bioRxiv · Jul 5, 2022 · PreprintCell Biology

Protein arginylation is regulated during SARS-CoV-2 infection

J. Macedo-da-Silva, L. Rosa-Fernandes, V. d. M. Gomes, V. F. Santiago, C. M. S. Molnar, B. R. Barboza, E. E. de Sousa, E. L. Durigon, C. R. F. Marinho, C. Wrenger, S. K. N. Marie, G. Palmisano

This study investigates how protein arginylation changes during SARS-CoV-2 infection and shows that ATE1 expression and arginylated protein levels are regulated in infected cells.

bioRxiv · Nov 2, 2021Cell Biology