Author

J. May

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 Immunology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Research Focus:host-pathogen & immune response· 2 Assay:proteomics· 2 Assay:bulk RNA-seq· 1 Organism:C. elegans· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:differential expression· 1 Research Focus:drug response / drug discovery· 1

Frequent Co-Authors

A. O. Adegoke· 1 shared A. O. Olaitan· 1 shared C. C. Anderson· 1 shared D. Peigney· 1 shared G. Thangavelu· 1 shared H. Cheroutre· 1 shared H. M. Behrens· 1 shared I. Henshall· 1 shared

Activity by Year

2020-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 14 mutual co-author links

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1 shared paperImmunology

A. O. Adegoke

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Internal regulation between constitutively expressed T cell coinhibitory receptors BTLA and CD5 and tolerance in recent thymic emigrants

A. O. Adegoke, G. Thangavelu, T.-F. Chou, M. Petersen, K. Kakugawa, J. May, K. Joannou, Q. Wang, K. K. Ellestad, L. Boon, P. A. Bretscher, H. Cheroutre, M. Kronenberg, T. A. Baldwin, C. C. Anderson

This study identifies a regulatory pathway between BTLA and CD5 in T cells that calibrates their expression to establish self-tolerance in recent thymic emigrants.

Open Biology · Oct 30, 2024Peer-reviewedImmunology

Impact of different mutations on Kelch13 protein levels, ART resistance and fitness cost in Plasmodium falciparum parasites

H. M. Behrens, S. Schmidt, D. Peigney, R. Sabitzki, I. Henshall, J. May, O. Maïga-Ascofare, T. Spielmann

This study examines how mutations in K13 and related genes affect ART resistance, protein levels, and fitness cost in Plasmodium falciparum parasites, finding no benefit from double mutations but highlighting the fitness cost of ubp1R3138H.

bioRxiv · May 13, 2022 · PreprintMicrobiology

Ebselen Exhibits Antimicrobial Activity Against Clostridioides difficile By Disrupting Redox Associated Metabolism

R. K. R. Marreddy, A. O. Olaitan, J. May, M. Dong, J. G. Hurdle

This study shows ebselen inhibits C. difficile by disrupting redox metabolism and toxin production, with bactericidal effects beyond its previously known anti-toxin activity.

bioRxiv · Jul 27, 2020 · PreprintMicrobiology