Author

F. Tay

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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Cell Biology· 3

Signature Assays, Organisms & Methods

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Research Focus:cell signaling & trafficking· 3 Research Focus:cell type annotation· 3 Assay:proteomics· 3 Approach:experimental assay· 2 Approach:genetic perturbation / CRISPR· 1 Organism:human· 1 Research Focus:protein folding & dynamics· 1

Frequent Co-Authors

F. Bard· 2 shared J. Chia· 2 shared C. S. Verma· 1 shared D. J. Gill· 1 shared F. A. Bard· 1 shared J. Gunaratne· 1 shared J. Maignel· 1 shared K. Foster· 1 shared

Activity by Year

2018-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 20 mutual co-author links

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2 shared papersCell Biology

F. Bard

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3 papers

Recent·Most cited

Botulinum toxin intoxication requires retrograde transport and membrane translocation at the ER

Y. C. Jeremy, F. Tay, R. E. Bennion, O. Loss, J. Maignel, L. Pons, K. Foster, M. Beard, F. A. Bard

This study identifies genes and trafficking processes involved in botulinum toxin A intoxication, revealing a complex route involving retrograde transport and ER membrane translocation.

bioRxiv · Oct 17, 2023Cell Biology

Src activates retrograde membrane traffic through phosphorylation of GBF1

J. Chia, S.-C. Wang, S. Wee, D. J. Gill, F. Tay, S. Kannan, C. S. Verma, J. Gunaratne, F. Bard

This study identifies how Src kinase promotes retrograde membrane traffic by phosphorylating GBF1, facilitating its interaction with Arf1 and enabling GALNTs relocation from Golgi to ER.

bioRxiv · Aug 2, 2020Cell Biology

The GalNAc-T Activation (GALA) Pathway: Drivers and Markers

J. Chia, F. Tay, F. Bard

The paper reanalyzes data to show EGF-induced GALNTs relocation is reproducible, identifies EGFR as a driver of the GALA pathway, and proposes PDIA4 glycosylation as a new marker.

bioRxiv · Aug 6, 2018Cell Biology