Author

V. Iadevaia

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 Microbiology· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

N. Locker· 2 shared A. Ruggieri· 1 shared B. Hall· 1 shared B. K. Dredge· 1 shared C. G. Proud· 1 shared C. Moller-Levet· 1 shared G. J. Goodall· 1 shared G. Lewis· 1 shared

Activity by Year

2018-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 19 mutual co-author links

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2 shared papersCell Biology

N. Locker

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Paracrine granules are cytoplasmic RNP granules distinct from stress granules assembling in response to viral infection.

V. Iadevaia, J. M. Burke, L. Eke, C. Moller-Levet, R. R. Parker, N. Locker

The paper identifies paracrine granules as distinct from stress granules, induced by viral infection and linked to antiviral activity.

bioRxiv · Aug 6, 2021 · PreprintCell Biology

capCLIP: a new tool to probe protein synthesis in human cells through capture and identification of the eIF4E-mRNA interactome.

K. B. Jensen, B. K. Dredge, J. Toubia, X. Jin, V. Iadevaia, G. J. Goodall, C. G. Proud

capCLIP captures and quantifies the eIF4E-mRNA interactome to measure translational activity, showing reduced TOP mRNA and altered eIF4E phosphorylation effects.

bioRxiv · Apr 18, 2020Biochemistry

Norovirus infection results in assembly of virus-specific G3BP1 granules and evasion of eIF2α signaling.

M. Brocard, V. Iadevaia, P. Klein, B. Hall, G. Lewis, J. Lu, J. Burke, R. Parker, A. Ruggieri, I. Goodfellow, N. Locker

This study shows that norovirus infection leads to the formation of virus-specific granules and disrupts eIF2α signaling to evade host stress responses.

bioRxiv · Dec 10, 2018 · PreprintMicrobiology