Author

R. Sakson

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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Biochemistry· 1 Cell Biology· 1 Microbiology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Organism:human· 3 Assay:proteomics· 2 Assay:bulk RNA-seq· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Research Focus:host-pathogen & immune response· 1

Frequent Co-Authors

K. M. Alp· 2 shared T. Ruppert· 2 shared A. R. Ormsby· 1 shared A. Sickmann· 1 shared B. Katschinski· 1 shared B. Niesler· 1 shared C. J. Rosado· 1 shared C. Schuler· 1 shared

Activity by Year

2020-2022 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 18 mutual co-author links

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2 shared papersCell Biology

K. M. Alp

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Replicative aging impedes stress-induced assembly of a key human protein disaggregase

Y. Mathangasinghe, N. Alberts, C. J. Rosado, D. Cox, N. L. Payne, A. R. Ormsby, K. M. Alp, R. Sakson, S. Uthishtran, T. Ruppert, S. Arumugam, D. M. Hatters, H. H. Kampinga, N. B. Nillegoda

This study identifies a stress-induced trimeric protein disaggregase in human cells that collapses during replicative aging, contributing to pathophysiological consequences.

bioRxiv · Jun 25, 2022 · PreprintCell Biology

Universally available herbal teas based on sage and perilla elicit potent antiviral activity against SARS-CoV-2 variants of concern by HMOX-1 upregulation in human cells

V. T. K. Le-Trilling, D. Mennerich, C. Schuler, R. Sakson, J. K. Lill, D. Kopczynski, S. Loroch, Y. Flores-Martinez, B. Katschinski, K. Wohlgemuth, M. Gunzer, F. Meyer, U. Dittmer, A. Sickmann, M. Trilling

bioRxiv · Nov 18, 2020Microbiology

Targeted Proteomics Reveals Quantitative Differences in Low Abundance Glycosyltransferases of Patients with Congenital Disorders of Glycosylation

R. Sakson, L. Beedgen, P. Bernhard, K. M. Alp, N. Luebbehusen, R. Roeth, B. Niesler, M. P. Mayer, C. Thiel, T. Ruppert

This study develops a targeted proteomics assay to quantify low-abundance glycosyltransferases in CDG patients, revealing specific protein level changes in ALG1 and ALG2 mutants.

bioRxiv · Sep 15, 2020Biochemistry