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cells to recall responses, specifically focusing on circulating memory cells (TCIRCM), memory cells with a tropism for lymphoid organs (TCM), and Tissue-resident memory cells (TRM). This project will be
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addressed by harnessing advances in tissue engineering, via the design of new organ-on-chip models that mimic features and functions of human lymphoid tissues in vitro. In this project, we will take advantage
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://www.guermonprezlab.org ). There is strong evidence that some populations of CD8+ cells like tissue resident memory-like (TRMs) or poorly differentiated stem-like T cells (TSL) are associated with favorable clinical
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