selected publications
- The pathogenic E139D mutation stabilizes a non-canonical active state of the multi-domain phosphatase SHP2. 2025 GET IT
- Multiplexed single-cell transcriptomics reveals diverse phenotypic outcomes for pathogenic SHP2 variants. 2025 GET IT
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Deep mutational scanning of the multi-domain phosphatase SHP2 reveals mechanisms of regulation and pathogenicity.
Nature communications.
2025
Academic Article
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Times cited: 1 - Proximity-labeling proteomics reveals remodeled interactomes and altered localization of pathogenic SHP2 variants. 2025 GET IT
- Allosteric inhibition rescues hydrocephalus caused by catalytically inactive Shp2. 2025 GET IT
- Deep mutational scanning of a multi-domain signaling protein reveals mechanisms of regulation and pathogenicity. 2024 GET IT
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The pathogenic T42A mutation in SHP2 rewires the interaction specificity of its N-terminal regulatory domain.
Proceedings of the National Academy of Sciences of the United States of America.
2024
Academic Article
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Times cited: 5 - The pathogenic T42A mutation in SHP2 rewires the interaction specificity of its N-terminal regulatory domain. 2024 GET IT