Author

J. Mintern

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 Cell Biology· 1 Immunology· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Research Focus:cell type annotation· 2 Approach:statistical model· 2 Research Focus:benchmarking· 1 Assay:bulk RNA-seq· 1 Research Focus:cell signaling & trafficking· 1 Approach:experimental assay· 1 Research Focus:protein folding & dynamics· 1

Frequent Co-Authors

C. Wells· 2 shared Z. Elahi· 2 shared D. M. Hatters· 1 shared H. McWilliam· 1 shared J. Choi· 1 shared K. J. Radford· 1 shared K. Radford· 1 shared L. Furic· 1 shared

Activity by Year

2022-2024 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 17 mutual co-author links

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2 shared papersCell Biology

C. Wells

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Author profile →

3 papers

Recent·Most cited

Efficient generation of human dendritic cells from iPSC by introducing a feeder-free expansion step for hematopoietic progenitors

Z. Elahi, V. Jameson, M. Sakkas, S. K. Butcher, J. Mintern, K. J. Radford, C. Wells

This paper develops an in vitro protocol to generate human dendritic cells from iPSC with a feeder-free expansion step, resulting in DC1-like cells that show functional characteristics similar to monocyte-derived DCs.

bioRxiv · Jun 4, 2024Cell Biology

The Human Dendritic Cell Atlas: An integrated transcriptional tool to study human dendritic cell biology

Z. Elahi, P. W. Angel, S. Butcher, N. Rajab, J. Choi, J. Mintern, K. Radford, C. Wells

The paper constructs a human dendritic cell (DC) transcriptional atlas by integrating 14 studies, revealing tissue-specific DC subset markers and highlighting gaps between in vitro and in vivo DC models.

bioRxiv · May 12, 2022Immunology

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