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Shu Wang

Researcher at Harvard University

Publications -  17
Citations -  1759

Shu Wang is an academic researcher from Harvard University. The author has contributed to research in topics: Immune system & Second fundamental form. The author has an hindex of 9, co-authored 16 publications receiving 1013 citations. Previous affiliations of Shu Wang include Cornell University.

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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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Highly multiplexed immunofluorescence imaging of human tissues and tumors using t-CyCIF and conventional optical microscopes

TL;DR: Tissue-based cyclic immunofluorescence method for highly multiplexed immuno-fluorescence imaging of formalin-fixed, paraffin-embedded specimens mounted on glass slides, the most widely used specimens for histopathological diagnosis of cancer and other diseases is described.
Posted ContentDOI

Highly multiplexed immunofluorescence imaging of human tissues and tumors using t-CyCIF and conventional optical microscopes

TL;DR: Tissue-based cyclic immunofluorescence method for highly multiplexed immuno-fluorescence imaging of formalin-fixed, paraffin-embedded specimens mounted on glass slides, the most widely used specimens for histopathological diagnosis of cancer and other diseases is described.
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Qualifying Antibodies for Image-Based Immune Profiling and Multiplexed Tissue Imaging

TL;DR: This protocol provides step-by-step procedures for confirming the selectivity and specificity of antibodies used in fluorescence-based tissue imaging and for the construction and validation of antibody panels for FFPE tissue sections using cyclic immunofluorescence (t-CyCIF) or other multiplexed imaging methods.
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Differences in steady-state inactivation between Na channel isoforms affect local anesthetic binding affinity

TL;DR: The results indicate that the greater sensitivity of cardiac tissue to cocaine or lidocaine is not due to a higher affinity of the LA receptor in cardiac Na channels, but that at physiological resting potentials, a greater percentage of hH1 channels than mu 1 channels are in the inactivated (i.e., high-affinity) state.