Author

A. E. Siniavin

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· 3

Signature Assays, Organisms & Methods

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Research Focus:host-pathogen & immune response· 3 Approach:experimental assay· 2 Research Focus:cell-cell communication· 1 Approach:deep learning· 1 Organism:human· 1 Organism:mouse· 1 Assay:spatial transcriptomics· 1 Approach:statistical model· 1

Frequent Co-Authors

V. A. Gushchin· 3 shared A. A. Pochtovyi· 1 shared A. V. Osipov· 1 shared D. A. Reshetnikov· 1 shared D. Mazurov· 1 shared I. V. Dolzhikova· 1 shared M. A. Nikiforova· 1 shared N. Kruglova· 1 shared

Activity by Year

2021-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 19 mutual co-author links

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3 shared papersMicrobiology

V. A. Gushchin

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Lethality of West Nile virus strains in a mouse model

A. E. Siniavin, I. V. Dolzhikova, A. A. Pochtovyi, D. A. Reshetnikov, V. A. Gushchin

This study evaluates the lethality of different West Nile virus strains in a mouse model, highlighting the impact of amino acid substitutions on pathogenesis and vaccine development.

bioRxiv · Dec 22, 2023 · PreprintMicrobiology

SARS-CoV-2 cell-to-cell infection is resistant to neutralizing antibodies

N. Kruglova, A. E. Siniavin, V. A. Gushchin, D. Mazurov

This study quantifies SARS-CoV-2 cell-to-cell infection resistance to neutralizing antibodies, finding it is more than tenfold less susceptible than cell-free infection.

bioRxiv · May 4, 2021Microbiology

Snake venom phospholipases A2 possess a strong virucidal activity against SARS-CoV-2 in vitro and block the cell fusion mediated by spike glycoprotein interaction with the ACE2 receptor

A. E. Siniavin, M. A. Nikiforova, S. D. Grinkina, V. A. Gushchin, V. G. Starkov, A. V. Osipov, V. I. Tsetlin, Y. N. Utkin

This study shows that snake venom phospholipases A2, especially dimeric forms, have strong antiviral activity against SARS-CoV-2 by inactivating the virus and blocking cell fusion.

bioRxiv · Jan 12, 2021 · PreprintMicrobiology