Author

A. M. Mistry

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

Click to filter author papers

Cancer Biology· 2 Immunology· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 3 Research Focus:cell type annotation· 2 Approach:experimental assay· 2 Assay:proteomics· 2 Research Focus:cell-cell communication· 1 Research Focus:clustering· 1 Research Focus:differential expression· 1 Research Focus:host-pathogen & immune response· 1

Frequent Co-Authors

B. C. Mobley· 3 shared J. M. Irish· 3 shared K. D. Weaver· 3 shared L. B. Chambless· 3 shared R. A. Ihrie· 3 shared J. Sinnaeve· 2 shared M. J. Hayes· 2 shared N. Leelatian· 2 shared

Activity by Year

2019-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 42 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

3 shared papersCancer Biology

B. C. Mobley

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

IL-8 Instructs Macrophage Identity in Lateral Ventricle Contacting Glioblastoma

S. Medina, A. A. Brockman, C. E. Cross, M. J. Hayes, B. C. Mobley, A. M. Mistry, S. Chotai, K. D. Weaver, R. Thompson, L. B. Chambless, R. A. Ihrie, J. M. Irish

This study identifies IL-8 as a key factor instructing macrophage identity in glioblastoma, showing IL-8 is necessary for generating CD32+ M_IL-8 macrophages in tumors contacting the lateral ventricle.

bioRxiv · Mar 29, 2024 · PreprintCancer Biology

Immune cell regulation in stem cell niche contacting glioblastomas.

T. Bartkowiak, S. M. Lima, M. J. Hayes, A. M. Mistry, J. Sinnaeve, N. Leelatian, C. E. Roe, B. C. Mobley, K. D. Weaver, R. C. Thompson, L. B. Chambless, R. A. Ihrie, J. M. Irish

This study shows that glioblastomas contacting the lateral ventricle have distinct immune features, including elevated T cell checkpoint receptors and suppressive myeloid cells, suggesting new therapeutic targets.

bioRxiv · Feb 16, 2022 · PreprintImmunology

High risk glioblastoma cells revealed by machine learning and single cell signaling profiles

N. Leelatian, J. Sinnaeve, A. M. Mistry, S. M. Barone, K. E. Diggins, A. R. Greenplate, K. D. Weaver, R. C. Thompson, L. B. Chambless, B. C. Mobley, R. A. Ihrie, J. M. Irish

This paper introduces RAPID, an unsupervised machine learning algorithm that identifies single cell phenotypes and assesses clinical risk stratification in glioblastoma patients using single cell mass cytometry data.

bioRxiv · Jun 1, 2019Cancer Biology