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Three Advancing Gene Therapy Strategies for ALS
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Learn how scientists at the University of Pennsylvania are leveraging the strengths of IVT mRNA-LNPs to develop an effective vaccine against Borrelia burgdorferi, the Lyme disease causing bacteria.
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The “Promising Novel Antitumor Strategies in Early Phase Clinical Trials” session at AACR2023 highlighted progress in evaluating new immunotherapy strategies targeting solid tumor antigens.
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Learn how work presented at ACCR2023 is leveraging IVT mRNA to improve existing cancer immunotherapies or develop new therapy strategies by arming myeloid cells with CARs.
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Reducing genetic code redundancy through genetic compression, sense codon replacement, deletion of corresponding tRNAs, and genetic code swapping have emerged as innovative ways to induce viral resistance.
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A new outer membrane vesicle-based vaccine platform offers a simpler approach to antigen display by leveraging the expression of a Synthetic Antigen-Binding Protein (SNAP) to easily enable the docking of various biotinylated antigens.
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Learn how scientists at the Pritzker School of Molecular Engineering, University of Chicago, have engineered a masked Interleukin-12 protein that is preferentially unmasked at tumor sites, thereby reducing adverse events commonly associated with systemic
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Learn about molecular mechanisms underscoring Dystroglycanopathies, a type of muscular dystrophy, and a new AAV-based gene replacement strategy to restore muscle function and reduce pathology.
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Learn about NAFLD and NASH chronic liver disease states and how an AAV8 delivered E06-scfv helps reduce pathogenesis by targeting oxidized phospholipids.
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Learn how scientists at the University of Pennsylvania and Moderna are advancing the production and delivery of effective mRNA therapeutics.