Author

M. D. Camus

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

Frequent Co-Authors

F. M. Brodsky· 2 shared K. Briant· 2 shared Y. Chen· 2 shared A. Bigot· 1 shared C. Esk· 1 shared C. Figueras-Novoa· 1 shared D. Kioumourtzoglou· 1 shared E. Palomer· 1 shared

Activity by Year

2019-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 22 mutual co-author links

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2 shared papersCell Biology

F. M. Brodsky

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3 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

Clathrin light chain diversity regulates membrane deformation in vitro and synaptic vesicle formation in vivo

L. Redlingshoefer, F. McLeod, Y. Chen, M. D. Camus, J. J. Burden, E. Palomer, K. Briant, P. N. Dannhauser, P. C. Salinas, F. Brodsky

This study shows that clathrin light chain diversity affects membrane deformation and synaptic vesicle formation, with isoform mixing being necessary for optimal neuronal function.

bioRxiv · Jul 28, 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