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Fate Therapeutics Features Multiple Novel Approaches to Eliminate Conditioning Chemotherapy for Off-the-shelf, iPSC-derived Cell Therapies at 2022 ASH Annual Meeting

Next-generation Engineering Strategies Designed to Resist Host Immune Cell Rejection Show Enhanced Functionality and Persistence of iPSC-derived Cells in Preclinical Allogeneic ModelsSAN DIEGO, Dec. ... | December 13, 2022
San Diego United States Karl Johan Malmberg Barbara Friedman Michels Sadelain Bob Valamehr

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Proof-of-principle study: Novel tool advances potential way to deliver gene therapy

Johns Hopkins Medicine researchers say they have successfully used a cell's natural process for making proteins to "slide" genetic instructions into a cell and produce critical proteins missing from those cells.
Seth Blackshaw Alexei Bygrave Emily Henderson Nature Communications Institute For Cell Engineering Johns Hopkins University School Of Medicine

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