Author

H. Bagci

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 Cancer Biology· 1 Cell Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Research Focus:cell type annotation· 2 Organism:human· 2 Approach:biophysical modeling· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:cell-cell communication· 1 Organism:chicken / avian· 1 Research Focus:chromatin & epigenetic regulation· 1

Frequent Co-Authors

J.-F. Cote· 3 shared A. Kania· 1 shared A. Klar· 1 shared A. Malina· 1 shared A. Marechal· 1 shared A. Orthwein· 1 shared A. Pause· 1 shared A. Samiei· 1 shared

Activity by Year

2018-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 25 mutual co-author links

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3 shared papersBiochemistry

J.-F. Cote

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

The hGID GID4 E3 ubiquitin ligase complex targets ARHGAP11A to regulate cell migration

H. Bagci, M. Winkler, F. Uliana, J. Boulais, W. I. Mohamed, S. L. Park, J.-F. Cote, M. Peter

This study identifies GID4 as a substrate receptor of the hGID E3 ligase complex that targets ARHGAP11A for degradation, thereby regulating cell migration.

bioRxiv · Jul 20, 2023Biochemistry

The endosomal sorting adaptor HD-PTP is required for ephrin-B:EphB signalling in cell collapse and motor axon guidance

S. Lahaie, D. Morales, H. Bagci, N. Hamoud, C.-E. Castonguay, J. M. Kazan, G. Desrochers, A. Klar, A.-C. Gingras, A. Pause, J.-F. Cote, A. Kania

This study identifies HD-PTP as an ESCRT adaptor required for ephrin-B:EphB signalling, affecting cell collapse and axon guidance by modulating receptor clustering and degradation.

bioRxiv · Aug 7, 2018Cell Biology

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