Author

R. A. Kamber

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· 2

Signature Assays, Organisms & Methods

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Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Assay:fluorescence / live-cell microscopy· 1 Approach:genetic perturbation / CRISPR· 1 Approach:microscopy & imaging analysis· 1 Approach:statistical model· 1 Organism:yeast· 1

Frequent Co-Authors

A. P. van Loon· 1 shared D. Vorselen· 1 shared E. Peterman· 1 shared J. A. Theriot· 1 shared J. P. Rasmussen· 1 shared J. S. Martenson· 1 shared M. C. Bassik· 1 shared M. K. Delgado· 1 shared

Activity by Year

2017-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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1 shared paperCell Biology

A. P. van Loon

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2 papers

Recent·Most cited

Cell BiologybioRxivPreprintJul 30, 2022

Cell surface receptors TREM2, CD14 and integrin αMβ2 drive sinking engulfment in phosphatidylserine-mediated phagocytosis

D. Vorselen, R. A. Kamber, R. L. D. Labitigan…·J. A. Theriot

This study identifies TREM2, CD14, and integrin αMβ2 as essential cell surface receptors for PS-mediated phagocytosis, revealing distinct mechanisms for PS and antibody-coated target uptake.

DOI 10.1101/2022.07.30.502145

genetic perturbation / CRISPRcell type annotation

𝕏 PostBluesky

Cell BiologybioRxivSep 6, 2017

The AAA Protein Msp1 Mediates Clearance of Excess Tail-Anchored Proteins from the Peroxisomal Membrane

N. R. Weir, R. A. Kamber, J. S. Martenson, V. Denic

The paper investigates how Msp1, an AAA ATPase, clears excess tail-anchored proteins from peroxisomal membranes and shows that Pex15 interacts with Pex3 to avoid Msp1 surveillance.

DOI 10.7554/elife.28507

yeastfluorescence / live-cell microscopy

𝕏 PostBluesky