Demonstrates improved gene therapy in diabetic retinopathy, implying a new treatment avenue.
. Furthermore, it markedly attenuated VEGFA-induced inflammation while maintaining excellent biocompatibility. This study demonstrates M3-F4 LNP as a promising method for efficient CRISPR/Cas9 delivery and provides robust support for gene therapy strategies in DR treatment.
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Liu et al. (2026) studied this question.
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