Author

P. De Jesus

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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Microbiology· 2

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:benchmarking· 1 Research Focus:cell type annotation· 1 Research Focus:drug response / drug discovery· 1 Organism:human· 1 Assay:proteomics· 1

Frequent Co-Authors

L. Pache· 2 shared S. Chanda· 2 shared A. Chatterjee· 1 shared A. Garcia-Sastre· 1 shared A. I. Su· 1 shared A. Rubanov· 1 shared A. Thor· 1 shared C. A. Stoneham· 1 shared

Activity by Year

2020-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersMicrobiology

L. Pache

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2 papers

Recent·Most cited

A combined EM and proteomic analysis places HIV-1 Vpu at the crossroads of retromer and ESCRT complexes: PTPN23 is a Vpu-cofactor

C. A. Stoneham, S. Langer, P. De Jesus, J. Wozniak, J. Lapek, T. Deerinck, A. Thor, L. Pache, S. Chanda, D. Gonzalez, M. Ellisman, J. Guatelli

This paper identifies PTPN23 as a Vpu-cofactor and maps Vpu's interactions with retromer and ESCRT complexes using EM and proteomics.

bioRxiv · Feb 22, 2021Microbiology

A Large-scale Drug Repositioning Survey for SARS-CoV-2 Antivirals

L. Riva, S. Yuan, X. Yin, L. Martin-Sancho, N. Matsunaga, S. Burgstaller, L. Pache, P. De Jesus, M. V. Hull, M. Chang, J. F. W. Chan, J. Cao, V. Kwok-Man Poon, K. Herbert, T.-T. Nguyen, , S. Chanda

This study identifies 30 known drugs that inhibit SARS-CoV-2 replication, with six showing effective concentrations likely to be therapeutic in patients.

bioRxiv · Apr 16, 2020 · PreprintMicrobiology