Author

E. G. Lavoie

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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Cancer Biology· 1 Microbiology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 2 Research Focus:cell type annotation· 1 Research Focus:chromatin & epigenetic regulation· 1 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Research Focus:gene regulatory network inference· 1 Research Focus:host-pathogen & immune response· 1

Frequent Co-Authors

A. Blondeau· 1 shared A. Fradet-Turcotte· 1 shared A. Gravel· 1 shared A. Malina· 1 shared A. Marechal· 1 shared A. Orthwein· 1 shared A. Samiei· 1 shared B. Djerir· 1 shared

Activity by Year

2018-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperMicrobiology

A. Blondeau

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Author profile →

2 papers

Recent·Most cited

The immediate early protein 1 of human herpesvirus 6B counteracts ATM activation in an NBS1-dependent manner

V. Collin, E. Biquand, V. Tremblay, E. G. Lavoie, J. Dessapt, A. Blondeau, A. Gravel, L. Flamand, A. Fradet-Turcotte

This paper shows that HHV-6B IE1 inhibits ATM activation at double-strand breaks via NBS1 interaction, leading to genomic instability and affecting viral replication.

bioRxiv · Jul 31, 2021 · PreprintMicrobiology

FAM35A co-operates with REV7 to coordinate DNA double-strand break repair pathway choice.

A. Orthwein, S. Findlay, J. Heath, V. Luo, A. Malina, Z. Li, A. Samiei, E. S. Cheyou, M. Karam, H. Bagci, D. Rahat, D. Grapton, E. G. Lavoie, C. Dove, H. Khaled, , H. Kuasne

This study identifies FAM35A as a novel REV7 effector that promotes NHEJ and restricts HR by limiting DNA end resection at DSBs.

bioRxiv · Jul 11, 2018Cancer Biology