Jérémie Nsengimana
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Jérémie Nsengimana has a total of 593 co-authors. Here are the top co-authors by number of shared publications:
- Julia Newton-Bishop
Leeds Institute of Rheumatic and Musculoskeletal Medicine (LIRMM), University of Leeds, Leeds LS2 9JT, UK
112 shared publications - Nelly M. Cruz
Department of Cancer Biology and Genetics, Memorial Sloan Kettering Cancer Center
73 shared publications - Richard M. White
University of Oxford
73 shared publications - Shruthy Suresh
Department of Molecular Biology, UT Southwestern Medical Center, Dallas, Texas
73 shared publications - David James Adams
Wellcome Sanger Institute Wellcome Genome Campus Cambridge UK
52 shared publications - Manik Garg
Centre for Genomics Research, Discovery Sciences, BioPharmaceuticals R&D, AstraZeneca, Cambridge, UK
51 shared publications
Latest Publications
- Open Access
- 9 February 2026
- Published by American Association for Cancer Research (AACR)
Figure S8 from Glucocorticoids Unleash Immune-dependent Melanoma Control through Inhibition of the GARP/TGFβ Axis
Supplementary Figure 8. Topical GC treatment induces comparable systemic leukocyte reduction in parental and GRKO tumor-bearing mice.
- 9 February 2026
- Published by American Association for Cancer Research (AACR)
Open AccessFigure S8 from Glucocorticoids Unleash Immune-dependent Melanoma Control through Inhibition of the GARP/TGFβ Axis
Supplementary Figure 8. Topical GC treatment induces comparable systemic leukocyte reduction in parental and GRKO tumor-bearing mice.
- Open Access
- 9 February 2026
- Published by American Association for Cancer Research (AACR)
Figure S7 from Glucocorticoids Unleash Immune-dependent Melanoma Control through Inhibition of the GARP/TGFβ Axis
Supplementary Figure 7. GCs do not act on immune cells to trigger tumor control.
- 9 February 2026
- Published by American Association for Cancer Research (AACR)
Open AccessFigure S7 from Glucocorticoids Unleash Immune-dependent Melanoma Control through Inhibition of the GARP/TGFβ Axis
Supplementary Figure 7. GCs do not act on immune cells to trigger tumor control.
- Open Access
- 9 February 2026
- Published by American Association for Cancer Research (AACR)
Figure S2 from Glucocorticoids Unleash Immune-dependent Melanoma Control through Inhibition of the GARP/TGFβ Axis
Supplementary Figure 2. Topical GC treatment of 20967 tumors reduce leukocyte counts systemically.
- 9 February 2026
- Published by American Association for Cancer Research (AACR)
Open AccessFigure S2 from Glucocorticoids Unleash Immune-dependent Melanoma Control through Inhibition of the GARP/TGFβ Axis
Supplementary Figure 2. Topical GC treatment of 20967 tumors reduce leukocyte counts systemically.
- Open Access
- 9 February 2026
- Published by American Association for Cancer Research (AACR)
Figure S10 from Glucocorticoids Unleash Immune-dependent Melanoma Control through Inhibition of the GARP/TGFβ Axis
Supplementary Figure 10. The TGF-β activating function of GARP is required for GC-induced tumor control.
- 9 February 2026
- Published by American Association for Cancer Research (AACR)
Open AccessFigure S10 from Glucocorticoids Unleash Immune-dependent Melanoma Control through Inhibition of the GARP/TGFβ Axis
Supplementary Figure 10. The TGF-β activating function of GARP is required for GC-induced tumor control.
- Open Access
- 9 February 2026
- Published by American Association for Cancer Research (AACR)
Table S5 from Glucocorticoids Unleash Immune-dependent Melanoma Control through Inhibition of the GARP/TGFβ Axis
Cluster biomarkers used for cell classification (Fig. 3).
- 9 February 2026
- Published by American Association for Cancer Research (AACR)
Open AccessTable S5 from Glucocorticoids Unleash Immune-dependent Melanoma Control through Inhibition of the GARP/TGFβ Axis
Cluster biomarkers used for cell classification (Fig. 3).
- Open Access
- 9 February 2026
- Published by American Association for Cancer Research (AACR)
Table S6 from Glucocorticoids Unleash Immune-dependent Melanoma Control through Inhibition of the GARP/TGFβ Axis
GSEA results for control- or GC-treated 20967 melanomas for the CD8, neutrophil and monocyte clusters related to Fig. 3.
- 9 February 2026
- Published by American Association for Cancer Research (AACR)
Open AccessTable S6 from Glucocorticoids Unleash Immune-dependent Melanoma Control through Inhibition of the GARP/TGFβ Axis
GSEA results for control- or GC-treated 20967 melanomas for the CD8, neutrophil and monocyte clusters related to Fig. 3.
- Open Access
- 9 February 2026
- Published by American Association for Cancer Research (AACR)
Table S1 from Glucocorticoids Unleash Immune-dependent Melanoma Control through Inhibition of the GARP/TGFβ Axis
Overlapping DEGs following GC-treatment in vivo and in vitro, leading to development of GC-stimulated gene signature (related to Fig. 4).
- 9 February 2026
- Published by American Association for Cancer Research (AACR)
Open AccessTable S1 from Glucocorticoids Unleash Immune-dependent Melanoma Control through Inhibition of the GARP/TGFβ Axis
Overlapping DEGs following GC-treatment in vivo and in vitro, leading to development of GC-stimulated gene signature (related to Fig. 4).
- Open Access
- 9 February 2026
- Published by American Association for Cancer Research (AACR)
Table S2 from Glucocorticoids Unleash Immune-dependent Melanoma Control through Inhibition of the GARP/TGFβ Axis
Human GC-stimulated gene signature, developed from murine sequencing data (related to Supplementary Table 1).
- 9 February 2026
- Published by American Association for Cancer Research (AACR)
Open AccessTable S2 from Glucocorticoids Unleash Immune-dependent Melanoma Control through Inhibition of the GARP/TGFβ Axis
Human GC-stimulated gene signature, developed from murine sequencing data (related to Supplementary Table 1).
- Open Access
- 9 February 2026
- Published by American Association for Cancer Research (AACR)
Table S4 from Glucocorticoids Unleash Immune-dependent Melanoma Control through Inhibition of the GARP/TGFβ Axis
GSEA results for GC-treated parental and GRKO tumors in vivo related to Fig. 4.
- 9 February 2026
- Published by American Association for Cancer Research (AACR)
Open AccessTable S4 from Glucocorticoids Unleash Immune-dependent Melanoma Control through Inhibition of the GARP/TGFβ Axis
GSEA results for GC-treated parental and GRKO tumors in vivo related to Fig. 4.
- Open Access
- 9 February 2026
- Published by American Association for Cancer Research (AACR)
Figure S1 from Glucocorticoids Unleash Immune-dependent Melanoma Control through Inhibition of the GARP/TGFβ Axis
Supplementary Figure 1. The 20967 melanoma model is resistant to immune checkpoint blockade.
- 9 February 2026
- Published by American Association for Cancer Research (AACR)
Open AccessFigure S1 from Glucocorticoids Unleash Immune-dependent Melanoma Control through Inhibition of the GARP/TGFβ Axis
Supplementary Figure 1. The 20967 melanoma model is resistant to immune checkpoint blockade.