Author

H. Ferry

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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Cancer Biology· 2 Immunology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Organism:human· 3 Research Focus:cell type annotation· 2 Research Focus:differential expression· 2 Approach:statistical model· 2 Research Focus:cancer & tumor microenvironment· 1 Assay:clinical cohort / trial· 1 Assay:DNA methylation· 1

Frequent Co-Authors

A. Amini· 1 shared A. Castor· 1 shared A. Ho· 1 shared A. Marciniak-Czochra· 1 shared A. Schuh· 1 shared A. Trumpp· 1 shared C. Demetriou· 1 shared C. Lutz· 1 shared

Activity by Year

2019-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 17 mutual co-author links

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1 shared paperImmunology

A. Amini

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Tissue-resident NK cells support survival in pancreatic cancer through promotion of cDC1-CD8T activity

S. Go, C. Demetriou, G. Valenzano, S. Hughes, S. Lanfredini, H. Ferry, E. Arbe-Barnes, S. Sivakumar, R. Bashford-Rogers, M. R. Middleton, S. Mukherjee, J. Morton, K. Jones, E. O'Neill

The paper shows that ionizing radiation enhances immunotherapy in pancreatic cancer by increasing tissue-resident NK cells that support CD8 T cell activity through cDC1-dependent mechanisms.

bioRxiv · Oct 14, 2023Cancer Biology

Complex genotype-phenotype relationships shape the response to treatment of Down Syndrome Childhood Acute Lymphoblastic Leukaemia

C. Lutz, V. A. Turati, R. Clifford, P. S. Woll, T. Stiehl, A. Castor, S. A. Clark, H. Ferry, V. Buckle, A. Trumpp, A. Ho, A. Marciniak-Czochra, J. Herrero, A. Schuh, S. E. W. Jacobsen, T. Enver

This study investigates genotype-phenotype relationships in Down Syndrome ALL, showing that genetic and phenotypic heterogeneity influences treatment response and relapse through clonal competition.

bioRxiv · Feb 6, 2022Cancer Biology

Human intestinal tissue-resident memory CD8+ T cells comprise transcriptionally and functionally distinct subsets

M. E. B. FitzPatrick, N. M. Provine, L. C. Garner, K. Powell, A. Amini, S. Irwin, H. Ferry, T. Ambrose, P. Friend, G. Vrakas, S. Reddy, E. J. Soilleux, P. Klenerman, P. J. Allan

This study identifies transcriptionally and functionally distinct subsets of human intestinal TRM cells, with β2-integrin marking a unique CD8+ TRM population.

bioRxiv · Dec 11, 2019Immunology