Author

S. K. See

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 Biochemistry· 1

Signature Assays, Organisms & Methods

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Research Focus:cell signaling & trafficking· 4 Organism:human· 3 Assay:proteomics· 3 Approach:experimental assay· 2 Approach:genetic perturbation / CRISPR· 2 Research Focus:cancer & tumor microenvironment· 1 Research Focus:chromatin & epigenetic regulation· 1 Research Focus:development & morphogenesis· 1

Frequent Co-Authors

M. Kampmann· 3 shared D. R. Southworth· 2 shared E. Tse· 2 shared J. E. Gestwicki· 2 shared M. D. Leonetti· 2 shared R. Tian· 2 shared A. Woerman· 1 shared B. Martinez-Gonzalez· 1 shared

Activity by Year

2019-2022 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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3 shared papersCell Biology

M. Kampmann

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

Orphan quality control shapes network dynamics and gene expression

K. G. Mark, S. Kolla, D. Garshott, B. Martinez-Gonzalez, C. Xu, D. Akopian, D. L. Haakonsen, S. K. See, M. Rape

The paper identifies UBR5 as a quality control enzyme that degrades unpaired transcription factor subunits, shaping network dynamics and gene expression through continuous turnover.

bioRxiv · Nov 6, 2022Biochemistry

An E3 ligase network engages GCN1 to promote elongation factor-1α degradation on stalled ribosomes

K. Oltion, J. D. Carelli, T. Yang, S. K. See, H.-Y. Wang, M. Kampmann, J. Taunton

The paper identifies an E3 ligase network that promotes eEF1A degradation on stalled ribosomes through interaction with GCN1.

bioRxiv · Mar 21, 2022 · PreprintCell Biology

PIKfyve inhibition blocks endolysosomal escape of α-synuclein fibrils and spread of α-synuclein aggregation

S. K. See, M. Chen, S. Bax, R. Tian, A. Woerman, E. Tse, I. E. Johnson, C. Nowotny, E. N. Munoz, J. Sengstack, D. R. Southworth, J. E. Gestwicki, M. D. Leonetti, M. Kampmann

The paper identifies PIKfyve inhibition as a strategy to block α-synuclein fibril escape from lysosomes, reducing aggregation spread in a human cell model.

bioRxiv · Jan 21, 2021 · PreprintCell Biology

Compromised function of the ESCRT pathway promotes endolysosomal escape of tau seeds and propagation of tau aggregation

J. J. Chen, D. L. Nathaniel, P. Raghavan, M. Nelson, R. Tian, E. Tse, J. Y. Hong, S. K. See, S.-A. Mok, M. Y. Hein, D. R. Southworth, L. T. Grinberg, J. E. Gestwicki, M. D. Leonetti, M. Kampmann

The paper identifies ESCRT pathway components as regulators of tau aggregation propagation by enabling endolysosomal escape of tau seeds.

bioRxiv · Sep 26, 2019Cell Biology