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Cas9-based ribonucleoproteins engineered via directed evolution and encapsulated in optimized lipid nanoparticles improve genome-editing efficacies in the livers and lungs of mice.
High-throughput screening led to the identification of artesunate as an antifibrotic agent that targets the glycoprotein myeloid differentiation factor 2 in the infarcted heart.
RNA-targeting CRISPR screens reveal hundreds of functional long non-coding RNAs that are crucial for cell survival and implicated in cancer progression.
A large vision–language model trained to generate chest X-ray reports shows promise as an assistive tool for radiologists, particularly for typical cases in outpatient settings.
Proteins that tag surface receptors for degradation by triggering their endocytosis can be computationally designed so that they do not compete with native receptor ligands for binding.
DNA microbeads loaded with an agonist for Wnt and injected into retinal organoids allow for the spatiotemporal control of gradients of the morphogen to better direct organoid development and maturation.