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Orr Ashenberg

Researcher at Broad Institute

Publications -  61
Citations -  6645

Orr Ashenberg is an academic researcher from Broad Institute. The author has contributed to research in topics: Biology & Immune system. The author has an hindex of 28, co-authored 48 publications receiving 3568 citations. Previous affiliations of Orr Ashenberg include Massachusetts Institute of Technology & Fred Hutchinson Cancer Research Center.

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A Cancer Cell Program Promotes T Cell Exclusion and Resistance to Checkpoint Blockade

TL;DR: A resistance program expressed by malignant cells that is associated with T cell exclusion and immune evasion is identified, and this study provides a high-resolution landscape of ICI-resistant cell states, identifies clinically predictive signatures, and suggests new therapeutic strategies to overcome immunotherapy resistance.
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A Cellular Taxonomy of the Bone Marrow Stroma in Homeostasis and Leukemia

TL;DR: The data suggest that tissue stroma responds to malignant cells by disadvantaging normal parenchymal cells, and provides a comprehensive bone marrow cell census and experimental support for cancer cell crosstalk with specific stromal elements to impair normal tissue function and thereby enable emergent cancer.
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Rewiring the Specificity of Two-Component Signal Transduction Systems

TL;DR: The results shed light on the basis of molecular discrimination in two-component signaling pathways, provide a general approach for the rational rewiring of these pathways, and suggest that analyses of coevolution may facilitate the reprogramming of other signaling systems and protein-protein interactions.
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COVID-19 tissue atlases reveal SARS-CoV-2 pathology and cellular targets.

Toni Delorey, +137 more
- 29 Apr 2021 - 
TL;DR: In this article, single-cell analysis of lung, heart, kidney and liver autopsy samples shows the molecular and cellular changes and immune response resulting from severe SARS-CoV-2 infection.
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Decoding human fetal liver haematopoiesis

TL;DR: A shift in the haemopoietic composition of fetal liver during gestation away from being predominantly erythroid, accompanied by a parallel change in differentiation potential of HSC/MPPs is demonstrated, which is validated to produce an integrated map of fetal liver haematopoiesis.