Author

F. Spada

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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Biochemistry· 1 Cell Biology· 1 Immunology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Research Focus:cell type annotation· 2 Organism:human· 2 Research Focus:cell-cell communication· 1 Research Focus:chromatin & epigenetic regulation· 1 Assay:DNA methylation· 1 Assay:imaging· 1 Approach:microscopy & imaging analysis· 1

Frequent Co-Authors

A. Green· 1 shared A. Kirchner· 1 shared C. Bishop· 1 shared C. Cappel· 1 shared C. Ebert· 1 shared E. Kaminska· 1 shared E. Korytiakova· 1 shared F. Di Matteo· 1 shared

Activity by Year

2020-2021 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 13 mutual co-author links

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1 shared paperImmunology

A. Green

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Disrupted Peyer's patch microanatomy in COVID-19 including germinal centre atrophy independent of local virus

S. C. Trevelin, S. Pickering, K. Todd, C. Bishop, M. Pitcher, J. G. Mesa, L. Montorsi, F. Spada, N. Petrov, A. Green, M. Shankar-Hari, S. J. D. Neil, J. Spencer

This study examines the impact of COVID-19 on ileal Peyer's patches, finding disrupted microanatomy and germinal centre atrophy independent of local viral load.

bioRxiv · Dec 17, 2021Immunology

AMPylation is a specific lysosomal protein posttranslational modification in neuronal maturation.

T. Becker, C. Cappel, F. Di Matteo, G. Sonsalla, E. Kaminska, F. Spada, S. Cappello, M. Damme, P. Kielkowski

The paper identifies AMPylation as a lysosomal posttranslational modification in neuronal maturation and shows it inhibits PLD3 activity.

bioRxiv · Mar 2, 2021 · PreprintBiochemistry

Oxidative and non-oxidative active turnover of genomic methylcytosine in distinct pluripotent states

F. Spada, S. Schiffers, A. Kirchner, Y. Zhang, G. Arista, O. Kosmatchev, E. Korytiakova, R. Rahimoff, C. Ebert, T. Carell

The paper quantifies DNA methylation turnover in mouse pluripotent cells, revealing active oxidation-dependent and -independent processes in formative and primed states.

bioRxiv · Mar 9, 2020Cell Biology