Author
T. M. Yaron
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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2020-2022 · peak 3/yrCo-Author Collaboration Network
10 top collaborators · 39 mutual co-author links6 papers
Recent·Most cited
- MicrobiologybioRxivPreprint
Evolution of host protease interactions among SARS-CoV-2 variants of concern and related coronaviruses
E. R. Kastenhuber, M. Mercadante, J. L. Johnson…·L. C. Cantley
The paper examines how SARS-CoV-2 variants interact with host proteases and shows that some proteases remain effective against variant spike proteins.
DOI 10.1101/2022.06.16.496428 - Cell BiologybioRxivPreprint
NAK associated protein 1/NAP1 is required for mitosis and cytokinesis by activating TBK1
S. Paul, S. Sarraf, K. H. Nam…·A. M. Pickrell
This study identifies NAP1 as a critical regulator of TBK1 activation at centrosomes during mitosis and cytokinesis, revealing its role in cell division through substrate interactions and degradation.
DOI 10.1101/2022.03.09.483647 - MicrobiologybioRxivPreprint
SARS-CoV-2 hijacks p38β/MAPK11 to promote viral protein translation
C. A. Higgins, B. E. Nilsson-Payant, A. Kurland…·J. R. Johnson
This study identifies p38β as a critical host factor for SARS-CoV-2 replication and shows that inhibiting it reduces viral replication and cytokine production.
DOI 10.1101/2021.08.20.457146 - MicrobiologybioRxivPreprint
The FDA-approved drug Alectinib compromises SARS-CoV-2 nucleocapsid phosphorylation and inhibits viral infection in vitro
T. M. Yaron, B. E. Heaton, T. M. Levy…·M Kavanagh-Williamson
This study identifies Alectinib as an FDA-approved drug that inhibits SARS-CoV-2 nucleocapsid phosphorylation and viral replication in vitro by targeting host kinases.
DOI 10.1101/2020.08.14.251207 - MicrobiologybioRxivPreprint
Identification of Candidate COVID-19 Therapeutics using hPSC-derived Lung Organoids
Y. Han, L. Yang, X. Duan…·S. Chen
This study uses hPSC-derived lung organoids to identify FDA-approved drugs that inhibit SARS-CoV-2 entry and reduce infection in a model of human COVID-19.
DOI 10.1101/2020.05.05.079095