Author

R. Dvorsky

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 Pharmacology & Toxicology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:cancer & tumor microenvironment· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:drug response / drug discovery· 1 Organism:human· 1 Assay:proteomics· 1 Organism:rat· 1

Frequent Co-Authors

A. Lang· 1 shared A. Lautwein· 1 shared B. Sebastian· 1 shared C. Renz· 1 shared D. Buckert· 1 shared D. Müller-Enoch· 1 shared E. Belonovskaya· 1 shared E. Naruta· 1 shared

Activity by Year

2019-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperBiochemistry

A. Lang

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2 papers

Recent·Most cited

Identification of SIRT4 as a novel paralog-specific interactor and candidate suppressor of C-RAF kinase in MAPK signaling

M. Mehrabipour, R. Dvorsky, S. Nakhaei-Rad, A. Lang, P. Verhuelsdonk, M. R. Ahmadian, R. P. Piekorz

This study identifies SIRT4 as a specific interactor of C-RAF kinase, showing it suppresses MAPK signaling by stabilizing the inactive form of C-RAF.

bioRxiv · Nov 23, 2023 · PreprintBiochemistry

ω-imidazolyl-alkyl derivatives as new preclinical drug candidates for NASH therapy

T. Diesinger, A. Lautwein, V. Buko, E. Belonovskaya, O. Lukivskaya, E. Naruta, S. Kirko, V. Andreev, R. Dvorsky, D. Buckert, B. Sebastian, C. Renz, D. Müller-Enoch, T. Wirth, T. Haehner

The paper tests two new CYP2E1 inhibitors, I-ol and I-an, in a rat model of NASH, finding they reduce pathological markers and show good tolerability.

bioRxiv · Jun 28, 2019 · PreprintPharmacology & Toxicology