Author

S. Caplan

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 Pharmacology & Toxicology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 4 Organism:human· 3 Organism:C. elegans· 2 Research Focus:cell signaling & trafficking· 2 Research Focus:cell type annotation· 2 Assay:proteomics· 2 Research Focus:clustering· 1 Research Focus:development & morphogenesis· 1

Frequent Co-Authors

N. Naslavsky· 3 shared A. B. Murakonda· 1 shared A. Bose· 1 shared A. Davis· 1 shared A. Kapur· 1 shared A. Misra· 1 shared A. Williams· 1 shared B. Ashraf· 1 shared

Activity by Year

2021-2024 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 12 mutual co-author links

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3 shared papersCell Biology

N. Naslavsky

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

Endosomal actin branching, fission and receptor recycling require FCHSD2 recruitment by MICAL-L1

D. Frisby, A. B. Murakonda, B. Ashraf, K. Dhawan, L. Almeida-Souza, N. Naslavsky, S. Caplan

This study identifies MICAL-L1's role in recruiting FCHSD2 to endosomes, which is essential for actin branching, fission, and receptor recycling.

bioRxiv · Jun 27, 2024Cell Biology

Conserved NIMA kinases regulate multiple steps of endocytic trafficking

B. B. Joseph, N. Naslavsky, S. Binti, S. Conquest, L. Robison, G. Bai, B. D. Grant, S. Caplan, D. Fay

This study shows that NIMA kinases regulate endocytic trafficking in worms and humans, affecting endosome morphology and cargo sorting, with implications for disease.

bioRxiv · Dec 22, 2022Cell Biology

The retromer complex regulates C. elegans development and mammalian ciliogenesis

S. Xie, E. Smith, C. Dierlam, D. Mathew, A. Davis, A. Williams, N. Naslavsky, J. Iyer, S. Caplan

This study shows the retromer complex is essential for C. elegans development and mammalian ciliogenesis, with a role in CP110 removal from the mother centriole.

bioRxiv · Sep 24, 2021Cell Biology

FGF21 Normalizes Plasma Glucose in Mouse Models of Type 1 Diabetes and Insulin Receptor Dysfunction

J. L. Diener, S. Mowbray, D. Yowe, J. Xu, S. Caplan, A. Misra, A. Kapur, W.-J. Huang, J. Shapiro, X. Ke, X. Wu, A. Bose, D. Panza, M. Chen, V. Beaulieu, J. Gao

This study shows that FGF21-PEG normalizes plasma glucose in two mouse diabetes models, even when insulin receptor function is impaired.

bioRxiv · Jan 4, 2021Pharmacology & Toxicology