Author

S. J. Gurczynski

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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Cell Biology· 1 Immunology· 1 Microbiology· 1

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 2 Approach:experimental assay· 2 Organism:mouse· 2 Assay:bulk RNA-seq· 1 Research Focus:cell-cell communication· 1 Approach:deep learning· 1 Research Focus:differential expression· 1 Research Focus:host-pathogen & immune response· 1

Frequent Co-Authors

B. B. Moore· 2 shared A. H. Vargo· 1 shared A. Linderholm· 1 shared A. Shikanov· 1 shared A. T. Fazleabas· 1 shared C. Emch· 1 shared C. L. Holmes· 1 shared D. F. Hannum· 1 shared

Activity by Year

2022-2024 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 19 mutual co-author links

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2 shared papersImmunology

B. B. Moore

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

CD103+ Dendritic Cell - Fibroblast Crosstalk via TLR9 and AHR Signaling Drives Lung Fibrogenesis

H. Carter, R. Medina Costa, M. Bame, T. Gilchrist, C. Emch, T. Adams, A. Linderholm, J. M. Oldham, I. Noth, N. Kaminski, B. B. Moore, S. J. Gurczynski

This study identifies CD103+ dendritic cell-fibroblast crosstalk via TLR9 and AHR signaling as a driver of lung fibrosis in IPF, showing that inhibiting AHR signaling reduces fibrosis.

bioRxiv · Mar 15, 2024 · PreprintImmunology

Cellular heterogeneity and dynamics of the human uterus in healthy premenopausal women

N. D. Ulrich, A. H. Vargo, Q. Ma, Y.-C. Shen, D. F. Hannum, S. J. Gurczynski, B. B. Moore, S. Schon, R. Lieberman, A. Shikanov, E. E. Marsh, A. T. Fazleabas, J. Z. Li, S. S. Hammoud

This paper presents a single-cell RNA sequencing atlas of the human uterus, identifying 39 cell subtypes and proposing a consensus annotation system, while highlighting dynamic changes and potential progenitor cells across menstrual cycle phases.

bioRxiv · Mar 7, 2024Cell Biology

The ADP-heptose biosynthesis enzyme GmhB is a conserved Gram-negative bacteremia fitness factor

C. L. Holmes, S. N. Smith, S. J. Gurczynski, G. B. Severin, L. Unverdorben, J. Vornhagen, H. L. Mobley, M. A. Bachman

This study identifies GmhB as a conserved Gram-negative bacteremia fitness factor that enhances bloodstream survival through LPS-mediated mechanisms, but is dispensable in the lung.

bioRxiv · Mar 8, 2022Microbiology