Author

H. McWilliam

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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Biochemistry· 1 Immunology· 1 Microbiology· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:cell type annotation· 1 Assay:ChIP-seq· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Organism:mouse· 1 Research Focus:protein folding & dynamics· 1

Frequent Co-Authors

A. C. Ching· 1 shared A. Hachani· 1 shared A. I. Webb· 1 shared A. M. Turner· 1 shared B. P. Howden· 1 shared C. A. McDevitt· 1 shared C. F. Macri· 1 shared C. J. Walsh· 1 shared

Activity by Year

2021-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 18 mutual co-author links

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1 shared paperImmunology

A. C. Ching

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

The two-component regulator WalKR provides an essential link between cell wall homeostasis with DNA replication in Staphylococcus aureus

L. K. R. Sharkey, R. Guerillot, C. J. Walsh, A. M. Turner, J. Y. H. Lee, S. L. Neville, S. Klatt, S. L. Baines, S. J. Pidot, F. J. Rossello, T. Seeman, H. McWilliam, E. Cho, G. P. Carter, B. P. Howden, , I. R. Monk

This study identifies the WalKR two-component system in Staphylococcus aureus as a polyfunctional regulator linking cell wall homeostasis with DNA replication and other essential processes.

bioRxiv · Feb 27, 2023 · PreprintMicrobiology

Arginine-rich C9ORF72 ALS proteins stall ribosomes in a manner distinct from a canonical ribosome-associated quality control substrate

V. Kriachkov, H. McWilliam, J. Mintern, S. L. Amarasinghe, M. E. Ritchie, L. Furic, D. M. Hatters

The paper investigates how arginine-rich DPRs from C9ORF72 expansions stall ribosomes and shows that this stalling differs from canonical RQC substrates, with no natural regulatory responses.

bioRxiv · Feb 9, 2022Biochemistry

Physiological Substrates and Ontogeny-Specific Expression of the Ubiquitin Ligases MARCH1 and MARCH8

P. Schriek, H. Liu, A. C. Ching, P. Huang, N. Gupta, K. R. Wilson, M. Tsai, Y. Yan, C. F. Macri, L. F. Dagley, G. Infusini, A. I. Webb, H. McWilliam, S. Ishido, J. D. Mintern, J. A. Villadangos

This study identifies MARCH1 and MARCH8 as specialized regulators of CD4+ T cell immunity in distinct cellular compartments by analyzing their substrates and expression in mice.

bioRxiv · Apr 15, 2021Immunology