Author

G. Donofrio

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· 2 Microbiology· 2

Signature Assays, Organisms & Methods

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Approach:experimental assay· 4 Research Focus:host-pathogen & immune response· 3 Organism:chicken / avian· 2 Research Focus:cell type annotation· 1 Organism:human· 1 Assay:metagenomics· 1 Assay:proteomics· 1 Organism:virus· 1

Frequent Co-Authors

D. Cavazzini· 2 shared V. Franceschi· 2 shared A. Bolchi· 1 shared A. h. A. Mahmoud· 1 shared A. Nouvenne· 1 shared A. Telenti· 1 shared A. Ticinesi· 1 shared A. Vecchi· 1 shared

Activity by Year

2022-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 25 mutual co-author links

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2 shared papersMicrobiology

D. Cavazzini

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

Vaccination of cattle with a virus-vectored vaccine against a major membrane protein of Mycobacterium a. subsp. paratuberculosis elicits CD8 cytotoxic T cells that kill intracellular bacteria

A. h. A. Mahmoud, G. s. gabdellrazeq, V. Franceschi, D. A. Schneider, J. P. Bannantine, L. M. Fry, V. Hullubei, G. Demattis, K.-T. Park, W. C. Davis, G. Donofrio

bioRxiv · Nov 20, 2023 · PreprintImmunology

Metagenomic analysis of milk microbiota in the bovine subclinical mastitis

G. Alessandri, E. Sangalli, M. Facchi, F. Fontana, L. Mancabelli, G. Donofrio, M. Ventura

This study analyzes milk microbiota in healthy and subclinical mastitis-affected cows to identify microbial markers associated with the disease.

bioRxiv · May 9, 2023 · PreprintMicrobiology

Characterization of BoHV-4 ORF45

G. Donofrio, L. Russo, E. Capra, V. Franceschi, D. Cavazzini, R. Sala, B. Lazzari, S. Cavirani

This study characterizes BoHV-4 ORF45 as a tegument phosphoprotein essential for lytic replication, showing structural similarity to KSHV ORF45 and its impact on host cell transcriptome pathways.

bioRxiv · Dec 7, 2022Microbiology

Natural heteroclitic-like peptides are generated by SARS-CoV-2 mutations

C. Tiezzi, A. Vecchi, M. Rossi, D. Cavazzini, A. Bolchi, D. Laccabue, L. Sacchelli, F. Brillo, T. Meschi, A. Ticinesi, A. Nouvenne, G. Donofrio, P. Zanelli, M. Benecchi, S. Giuliodori, , C. Boni

The paper shows that SARS-CoV-2 mutations can create new CD8 T cell epitopes, enhancing immune responses in some individuals with weak CD8 T cell reactivity.

bioRxiv · Oct 28, 2022Immunology