Author

L. Fritts

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· 2 Microbiology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Research Focus:host-pathogen & immune response· 3 Organism:mouse· 2 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Assay:proteomics· 1 Organism:rat· 1 Research Focus:spatial domain detection· 1

Frequent Co-Authors

C. J. Miller· 3 shared A. Rustagi· 2 shared M. K. Morris· 2 shared T. Carroll· 2 shared Z.-M. Ma· 2 shared A. Sotomayor-Gonzalez· 1 shared C. A. Blish· 1 shared C. Di Germanio· 1 shared

Activity by Year

2021-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 41 mutual co-author links

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3 shared papersImmunology

C. J. Miller

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Administration of vaccine-boosted COVID-19 convalescent plasma to SARS-CoV-2 infected hamsters decreases virus replication in lungs and hastens resolution of the infection despite transiently enhancing disease and lung pathology.

T. Carroll, T. Wong, M. K. Morris, C. Di Germanio, Z.-M. Ma, M. Stone, E. E. Ball, L. Fritts, A. Rustagi, G. Simmons, M. P. Busch, C. J. Miller

This study shows that vaccine-boosted convalescent plasma reduces SARS-CoV-2 replication in hamsters but temporarily worsens disease and lung pathology.

bioRxiv · Aug 22, 2023 · PreprintImmunology

Loss of genital epithelial barrier function is greater with depot-medroxyprogesterone acetate than intravaginal rings that release etonogestrel and ethinyl estradiol

M. Liu, R. D. V. Miguel, N. Q. Calla, K. Aceves, L. Fritts, C. J. Miller, J. Moss, M. M. Baum, T. L. Cherpes

This study compares the effects of DMPA and NuvaRing on genital epithelial barrier function in rhesus macaques, finding greater compromise with DMPA.

bioRxiv · Jan 25, 2023 · PreprintImmunology

The B.1.427/1.429 (epsilon) SARS-CoV-2 variants are more virulent than ancestral B.1 (614G) in Syrian hamsters

T. Carroll, D. Fox, N. van Doremalen, E. Ball, M. K. Morris, A. Sotomayor-Gonzalez, V. Servellita, A. Rustagi, C. K. Yinda, L. Fritts, J. R. Port, Z.-M. Ma, M. Holbrook, J. Schulz, C. A. Blish, , C. J. Miller

This study shows that the B.1.427/1.429 (epsilon) SARS-CoV-2 variants cause more severe disease and higher viral loads in the upper respiratory tract in Syrian hamsters compared to the ancestral B.1 (614G) strain.

bioRxiv · Aug 25, 2021Microbiology