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Showing 1–4 of 4 results
Advanced filters: Author: Sarah Q. Crome Clear advanced filters
  • Knowledge of the transcriptional programs of human kidney cell populations at homeostasis is limited. Here, the authors show sex-based differences in gene expression of kidney parenchymal cells and examine the complexity of kidney-resident immune cells using single cell RNA sequencing of healthy living kidney donors.

    • Caitriona M. McEvoy
    • Julia M. Murphy
    • Sarah Q. Crome
    ResearchOpen Access
    Nature Communications
    Volume: 13, P: 1-18
  • Adipose tissues are increasingly recognized as dynamic hubs where immune cell–adipocyte cross-talk coordinates processes such as energy metabolism, inflammation and thermogenesis. In this issue, Krapić et al. identify a new role for the visceral adipose tissue and resident natural killer cells in tuning anti-viral immunity.

    • Sarah Q. Crome
    • Sue Tsai
    News & Views
    Nature Metabolism
    Volume: 7, P: 862-863
  • A previously uncharacterized population of innate lymphoid cells (ILCs) in the tumor microenvironment limits T cell expansion and cytokine production, and associates with early recurrence in patients with cancer. Depletion of this regulatory immunosuppressive cell population overcomes this effect, suggesting important implications for cancer immunotherapy.

    • Sarah Q Crome
    • Linh T Nguyen
    • Pamela S Ohashi
    Research
    Nature Medicine
    Volume: 23, P: 368-375