Author

A. G. West

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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Bioengineering· 1 Cancer Biology· 1 Microbiology· 1

Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 2 Research Focus:cell type annotation· 2 Organism:human· 2 Approach:statistical model· 2 Research Focus:cell-cell communication· 1 Research Focus:clustering· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1

Frequent Co-Authors

A. Digby· 1 shared A. F. J. M. A. Taqi· 1 shared A. M. Michie· 1 shared A. W. Santure· 1 shared B. Kader· 1 shared B. Peault· 1 shared C. C. West· 1 shared E. Ross· 1 shared

Activity by Year

2021-2022 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 22 mutual co-author links

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1 shared paperMicrobiology

A. Digby

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Capturing species-wide diversity of the gut microbiota and its relationship with genomic variation in the critically endangered kakapo

A. G. West, A. Digby, A. W. Santure, J. G. Guhlin, P. G. Dearden, K. R. Team, M. W. Taylor, L. Urban

This study analyzes the gut microbiota of kakapos to assess its relationship with host genomic diversity and identifies sex as a significant factor influencing microbiota diversity.

bioRxiv · Oct 31, 2022Microbiology

Bioengineered niches that recreate physiological extracellular matrix organisation to support long-term haematopoietic stem cells

H. Donnelly, E. Ross, Y. Xiao, R. Hermantara, A. F. J. M. A. Taqi, W. S. Doherty-Boyd, J. Cassels, P. M. Tsimbouri, K. M. Dunn, J. Hay, Z. A. Cheng, N. Jain, C. C. West, H. Wheadon, A. M. Michie, , M. J. Dalby

This study develops a bioengineered niche that maintains long-term haematopoietic stem cells by recreating physiological extracellular matrix organisation, supporting their survival and function without media supplementation.

bioRxiv · Jul 28, 2022 · PreprintBioengineering

EZH2 inhibition in glioblastoma stem cells increases the expression of neuronal genes and the neuronal developmental regulators ZIC2, ZNF423 and MAFB

B. Kader, R. DiStefano, K. L. West, A. G. West

This study shows that EZH2 inhibition in GBM stem cells increases neuronal gene expression and the expression of ZIC2, ZNF423, and MAFB, suggesting a role for EZH2 in suppressing neurogenesis in GBM.

bioRxiv · Nov 22, 2021 · PreprintCancer Biology