Author

R. Stanton

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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Immunology· 1 Microbiology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:host-pathogen & immune response· 2 Organism:human· 2 Research Focus:cell-cell communication· 1 Research Focus:drug response / drug discovery· 1 Assay:proteomics· 1

Frequent Co-Authors

B. J. Ryckman· 1 shared C. A. Fielding· 1 shared D. Harnum· 1 shared D. P. Ings· 1 shared E. Wang· 1 shared J. P. Kamil· 1 shared K. A. Holder· 1 shared K. Bentley· 1 shared

Activity by Year

2018-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperMicrobiology

B. J. Ryckman

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2 papers

Recent·Most cited

Hybrid immunity elicits potent cross-variant ADCC against SARS-CoV-2 through a combination of anti-S1 and S2 antibodies

M. D. Grant, K. Bentley, C. A. Fielding, K. M. Hatfield, D. P. Ings, D. Harnum, E. Wang, R. Stanton, K. A. Holder

This study shows that hybrid immunity, from prior infection followed by vaccination, generates stronger and broader antibody-dependent cellular cytotoxicity (ADCC) against SARS-CoV-2 variants than vaccination alone.

bioRxiv · Mar 9, 2023 · PreprintImmunology

Expression levels of glycoprotein O (gO) vary between strains of human cytomegalovirus, influencing the assembly of gH/gL complexes and virion infectivity.

L. Zhang, M. Zhou, R. Stanton, J. P. Kamil, B. J. Ryckman

This study shows that differences in gO and UL128-131 expression levels between HCMV strains affect gH/gL complex assembly and virion infectivity, with UL128-131 repression having a stronger impact on infectivity than gO expression.

bioRxiv · Apr 11, 2018Microbiology