RNA-triggered chromatin shredding using Cas12a2 selectively eliminates tumor cells with mutations in critical cancer genes like TP53 and MYC in mouse models.
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RNA-triggered chromatin shredding using Cas12a2 selectively eliminates tumor cells with mutations in critical cancer genes like TP53 and MYC in mouse models.
Prime editors achieve up to 27.3% precise DNA insertions in zebrafish, enabling accurate genome modifications without exogenous DNA.
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CRISPR RNP-mediated genome editing achieves transgene-free modifications in woody plants but faces significant delivery and regeneration challenges, especially in species like bamboo.
De novo RNA-guided transposition systems using TnpB-family proteins achieve high-efficiency DNA insertion with precise control in bacteria.
CAR T cells targeting surface U5 snRNP200, an RNA-binding protein absent from normal hematopoietic precursors, effectively treat AML and B-cell ALL with improved safety.
Genomic and transcriptomic qualification of patient-derived dopaminergic neuron precursors was successfully achieved across multiple donors for Parkinson's disease therapy.
Proteolytic control of CRISPR-Cas systems achieves precise, tunable gene expression with reduced variability, enabling improved gene therapy for dosage-sensitive disorders.
Viral delivery of PRPF31 restores splicing, cellular function, and visual activity in patient-derived retinal cells, even in mature stages, offering a promising therapy for RP11.
A rapid sphingomyelin-dependent entry pathway in S. aureus alters intracellular fate, influencing bacterial replication and host cell death within minutes of contact.
Subpopulations of Acinetobacter baumannii exhibit distinct metabolic responses to polymyxins, with PI-positive cells increasing phosphatidylethanolamine and PI-negative cells upregulating arginine metabolism.
Genome-wide CRISPR screens identify 15 cancer driver alterations with numerous synthetic lethal interactions, revealing new therapeutic targets.
Ancient viral interactions likely shaped the development of modern class 1 CRISPR bacterial immune systems.
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