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CRISPR Tool Targets Neuron Gene Repair
15. syyskuuta 2025
Raportoinut AI
Faktatarkistettu
Stanford researchers have created a CRISPR-based technology to target RNA in neurons, enabling repair processes for genetic diseases. The method addresses key challenges in Cas9 delivery and DNA repair. It reveals unique genome editing rules in neurons, paving the way for targeted therapies.
Tool Mechanism
Known as CRISPR-TO, it uses modified CRISPR-Cas13 for precise RNA delivery and repair initiation in neurons.
Potential Applications
This advancement could reduce reliance on ongoing treatments for neurological conditions by enabling one-time interventions.