Human gene therapy has been transformed by repurposing mobile genetic elements as tools for efficient gene delivery and precise genome modification. Viruses, transposons, and retro
Adoptive transfer of gene-modified autologous T cells, for example, expressing chimeric antigen receptors (CARs), is a promising therapy option for a variety of malignant and nonma
Early-stage in vitro and ex vivo proof-of-concept work demonstrating a novel triple-target CRISPR strategy, not yet tested in vivo or clinically, with no efficacy or safety data in human subjects.
A perspective article proposing a conceptual framework for using CRISPR-based mutation correction to interrogate cancer drivers; raises mechanistic and therapeutic questions rather than presenting experimental evidence or clinical outcomes.
A systematic benchmarking study of computational tools against experimental data, showing moderate performance with substantial limitations; informs preclinical practice but does not establish a new clinical standard or definitive tool ranking.