Author

F. M. Brodsky

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· 4

Signature Assays, Organisms & Methods

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Approach:experimental assay· 4 Research Focus:cell signaling & trafficking· 3 Organism:human· 2 Organism:mouse· 2 Research Focus:development & morphogenesis· 1 Assay:proteomics· 1

Frequent Co-Authors

K. Briant· 2 shared M. D. Camus· 2 shared A. Bigot· 1 shared B. L. Parker· 1 shared B. Simonetti· 1 shared C. Esk· 1 shared C. Figueras-Novoa· 1 shared D. E. James· 1 shared

Activity by Year

2019-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 13 mutual co-author links

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2 shared papersCell Biology

K. Briant

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4 papers

Recent·Most cited

Clathrin light chains CLCa and CLCb have non-redundant roles in epithelial lumen formation

Y. Chen, K. Briant, M. D. Camus, F. M. Brodsky

This study identifies non-redundant roles of CLCa and CLCb in epithelial lumen formation through analysis of knockout mice and cell line models.

bioRxiv · Apr 25, 2023Cell Biology

CHC22 clathrin functions in the early secretory pathway by two-site interaction with SNX5 and p115

J. Greig, G. T. Bates, D. I. Yin, K. Briant, B. Simonetti, P. J. Cullen, F. M. Brodsky

This paper identifies two distinct interaction sites in CHC22 that mediate its recruitment to ERGIC membranes, enabling GLUT4 transport bypassing the Golgi.

bioRxiv · Dec 21, 2022 · PreprintCell Biology

Trafficking regulator of GLUT4-1 (TRARG1) is a GSK3 substrate

X. Duan, D. M. Norris, S. J. Humphrey, P. Yang, K. C. Cooke, W. P. Bultitude, B. L. Parker, O. J. Conway, J. G. Burchfield, J. R. Krycer, F. M. Brodsky, D. E. James, D. J. Fazakerley

This study identifies TRARG1 as a GSK3 substrate that regulates GLUT4 trafficking and insulin sensitivity through phosphorylation events.

bioRxiv · Dec 7, 2020Cell Biology

CHC22 clathrin mediates traffic from early secretory compartments for human GLUT4 pathway biogenesis

S. M. Camus, M. D. Camus, C. Figueras-Novoa, G. Boncompain, L. A. Sadacca, C. Esk, A. Bigot, G. W. Gould, D. Kioumourtzoglou, F. Perez, N. J. Bryant, S. Mukherjee, F. M. Brodsky

The paper identifies CHC22 clathrin as mediating ERGIC-derived membrane traffic essential for GLUT4 sequestration in humans, distinct from mice lacking CHC22.

bioRxiv · Aug 12, 2019Cell Biology