Author

J. Vo

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

Click to filter author papers

Biochemistry· 3 Animal Behavior & Cognition· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Approach:experimental assay· 4 Research Focus:host-pathogen & immune response· 3 Organism:E. coli· 2 Assay:behavioral assay· 1 Research Focus:cell type annotation· 1 Research Focus:drug response / drug discovery· 1 Organism:mouse· 1

Frequent Co-Authors

A. Bermingham· 2 shared A. Frommlet· 2 shared A. Lingel· 2 shared A. O. Frank· 2 shared A. Ruzin· 2 shared B. Benton· 2 shared C. J. Balibar· 2 shared C. M. Baxter Rath· 2 shared

Activity by Year

2019-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersBiochemistry

A. Bermingham

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

Conditioned overconsumption is dependent on reinforcer type in lean, but not obese, mice.

D. Lewis-Sanders, S. Bullich, M. J. Olvera, J. Vo, Y.-S. Hwang, S. A. Stern

This study shows that context-conditioned overconsumption in mice depends on reinforcer type, occurring in lean but not obese mice.

bioRxiv · Dec 31, 2023Animal Behavior & Cognition

Fine tuning the mechanism of Antigen 43 self-association to modulate aggregation levels of Escherichia coli pathogens

J. Vo, G. C. Martinez Ortiz, M. Totsika, A. Lo, A. E. Whitten, L. Hor, K. M. Peters, V. Ageorges, N. Caccia, M. Desvaux, M. A. Schembri, J. J. Paxman, B. Heras

The paper investigates the role of Ag43 homologues in bacterial aggregation and biofilm formation, revealing a common trans-association mechanism and how variations in these interactions affect aggregation kinetics.

bioRxiv · Apr 19, 2021 · PreprintBiochemistry

Two distinct mechanisms of small molecule inhibition of LpxA acyltransferase essential for lipopolysaccharide biosynthesis

W. Han, X. Ma, C. J. Balibar, C. M. Baxter Rath, B. Benton, A. Bermingham, F. Casey, B. Chie-Leon, M.-K. Cho, A. O. Frank, A. Frommlet, C.-M. Ho, P. S. Lee, M. Li, A. Lingel, , T. Uehara

The paper identifies two distinct mechanisms by which small molecules inhibit LpxA acyltransferase, a key enzyme in lipopolysaccharide biosynthesis.

bioRxiv · Dec 17, 2019 · PreprintBiochemistry

Two distinct mechanisms of small molecule inhibition of LpxA acyltransferase essential for lipopolysaccharide biosynthesis

W. Han, X. Ma, C. J. Balibar, C. M. Baxter Rath, B. Benton, A. Bermingham, F. Casey, B. Chi-Leon, M.-K. Cho, A. O. Frank, A. Frommlet, C.-M. Ho, P. S. Lee, M. Li, A. Lingel, , T. Uehara

This study identifies two small-molecule inhibitors of LpxA, revealing distinct inhibition mechanisms and highlighting compound 2's improved properties for antibacterial development.

bioRxiv · Dec 14, 2019 · PreprintBiochemistry