Author

M. J. Price

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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Immunology· 2 Cancer Biology· 1

Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 3 Research Focus:cell type annotation· 3 Research Focus:differential expression· 3 Approach:experimental assay· 3 Organism:human· 2 Organism:mouse· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:cell-cell communication· 1

Frequent Co-Authors

A. K. Kania· 2 shared C. D. Scharer· 2 shared A. D. Nguyen· 1 shared C. D. Baeta· 1 shared C. Haines· 1 shared C. Lavau· 1 shared C. R. Goodwin· 1 shared D. G. Patterson· 1 shared

Activity by Year

2021-2024 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 20 mutual co-author links

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2 shared papersImmunology

A. K. Kania

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

UDP-6-glucose dehydrogenase in hormonally responsive breast cancers

M. J. Price, A. D. Nguyen, C. Haines, C. D. Baeta, J. Byemerwa, D. Mukherjee, S. Artham, V. Kumar, C. Lavau, S. Wardell, S. Varghese, C. R. Goodwin

This study shows that UGDH knockdown reduces estrogen-induced tumorigenic traits in breast cancer models and validates findings in human clinical specimens.

bioRxiv · Mar 20, 2024 · PreprintCancer Biology

An IRF4-MYC-mTORC1 integrated pathway controls cell growth and the proliferative capacity of activated B cells during B cell differentiation in vivo

D. G. Patterson, A. K. Kania, M. J. Price, J. R. Rose, C. D. Scharer, J. M. Boss

This study identifies an IRF4-MYC-mTORC1 pathway critical for B cell proliferation and growth during differentiation, showing IRF4 regulates MYC and mTORC1 to drive metabolic reprogramming and cell cycle progression.

bioRxiv · Jun 20, 2021Immunology

Conserved epigenetic programming and enhanced heme metabolism drive memory B cell reactivation

M. J. Price, C. D. Scharer, A. K. Kania, T. Randall, J. Boss

This study identifies conserved epigenetic and transcriptional signatures in memory B cells that enhance their reactivation potential, with a central role for heme metabolism.

bioRxiv · Jan 20, 2021Immunology