Author

J. Hukelmann

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 Biochemistry· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Research Focus:cell type annotation· 2 Organism:human· 2 Assay:proteomics· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:database / resource· 1 Research Focus:differential expression· 1 Research Focus:host-pathogen & immune response· 1

Frequent Co-Authors

A. I. Lamond· 2 shared A. Brenes· 1 shared A. J. Brenes· 1 shared B. Bilanges· 1 shared B. Vanhaesebroeck· 1 shared C. J. Courreges· 1 shared C. Scudamore· 1 shared D. Bensaddek· 1 shared

Activity by Year

2018-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 19 mutual co-author links

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2 shared papersImmunology

A. I. Lamond

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Lack of phosphatidylinositol 3-kinase VPS34 in regulatory T cells leads to a fatal lymphoproliferative disorder without affecting their development

C. J. Courreges, E. C. Davenport, B. Bilanges, E. Rebollo-Gomez, J. Hukelmann, P. Schoenfelder, J. R. Edgar, D. Sansom, C. Scudamore, R. Roychoudhuri, O. A. Garden, B. Vanhaesebroeck, K. Okkenhaug

This study shows that VPS34 deficiency in regulatory T cells causes a fatal lymphoproliferative disorder by impairing metabolic and functional processes, despite normal development and in vitro suppression.

bioRxiv · Jan 8, 2024Immunology

Tissue environment, not ontogeny, defines intestinal intraepithelial T lymphocytes

A. J. Brenes, M. Vandereyken, O. J. James, J. Hukelmann, L. Spinelli, A. I. Lamond, M. Swamy

The paper uses proteomic analysis to show that the gut environment, not developmental origin, shapes the functional properties of intestinal intraepithelial T lymphocytes.

bioRxiv · Mar 15, 2021Immunology

The iPSC proteomic compendium

A. Brenes, D. Bensaddek, J. Hukelmann, V. Afzal, A. I. Lamond

The paper presents a proteomic analysis of 217 HipSci iPSC lines, identifying >16,000 protein groups and their roles in iPSC biology.

bioRxiv · Nov 14, 2018 · PreprintBiochemistry