Author

H. Schwartz

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 Immunology· 1 Microbiology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 2 Assay:proteomics· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Research Focus:cell-cell communication· 1

Frequent Co-Authors

A. K. Bashmail· 1 shared A. Magen· 1 shared A. O. Kamphorst· 1 shared A. Soares-Schanoski· 1 shared A. Tabachnikova· 1 shared A. Tsankov· 1 shared A. Vazquez· 1 shared B. Giotti· 1 shared

Activity by Year

2018-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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Curved chords = mutual co-authorship

1 shared paperMicrobiology

A. K. Bashmail

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Rewiring of the host cell metabolome and lipidome during lytic gammaherpesvirus infection is essential for infectious virus production

S. A. Clark, A. Vazquez, K. Furiya, M. K. Splattstoesser, A. K. Bashmail, H. Schwartz, M. Russell, S.-J. Bhark, O. K. Moreno, M. McGovern, E. R. Owsley, T. A. Nelson, E. Sanchez, T. Delgado

This study identifies metabolic rewiring in host cells during gammaherpesvirus infection, showing that glucose, glutamine, and lipid metabolism are essential for viral production.

Journal of Virology · Jun 29, 2023Peer-reviewedMicrobiology

Intratumoral mregDC and CXCL13 T helper niches enable local differentiation of CD8 T cells following PD-1 blockade

A. Magen, P. Hamon, N. Fiaschi, L. Troncoso, E. Humblin, D. D'souza, T. Dawson, M. D. Park, J. Kim, S. Hamel, M. Buckup, C. Chang, A. Tabachnikova, H. Schwartz, N. Malissen, , Merad

The paper identifies intratumoral niches involving mregDC and CXCL13+ Th cells that support CD8 T cell differentiation following PD-1 blockade in HCC patients.

bioRxiv · Jun 22, 2022 · PreprintImmunology

HSP90 inhibitors disrupt a transient HSP90-HSF1 interaction and identify a noncanonical model of HSP90-mediated HSF1 regulation

T. Kijima, T. L. Prince, M. Tigue, K. Yim, H. Schwartz, K. Beebe, S. Lee, M. Budzynski, H. Williams, J. Trepel, L. Sistonen, S. K. Calderwood, L. Neckers

This study shows HSP90 inhibitors disrupt a transient HSP90-HSF1 interaction, revealing a noncanonical role for HSP90 in modulating HSF1 activity by removing HSF1 trimers from DNA.

bioRxiv · Mar 2, 2018Biochemistry