This non-viral CRISPR-Cas9 delivery vector is ten times as effective at genome modification as the standard plasmid transfection techniques, down-regulating Plk1 expression over 70% to inhibit tumor growth.

This non-viral CRISPR-Cas9 delivery vector is ten times as effective at genome modification as the standard plasmid transfection techniques, down-regulating Plk1 expression over 70% to inhibit tumor growth.
The size, shape, and order of nanorods in solid-state microbial sensors are controlled using the forces of gravity and magnetism.
A smart cell-targeting approach for potential use in specific cell ablation.
Stimulation of nerves by an artificial retina toward therapeutics for blindness.
Small molecules have been used to study several mammalian RNA elements in disease. These advances encourage exploration of newly discovered RNA interactions with therapeutic potential.
A strategy to transform various photosensitizers into activatable ones for photodynamic therapy is reported.
An overview of the most recent literature relevant to mRNA delivery helps readers to obtain an overall concept and direction of nanoscale platforms for mRNA delivery.
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Complex, aqueous-stable, hydrogel ionic circuits towards transparent, flexible, biocompatible bioelectronic devices.
A new ambient drying method for aerogel fabrication is reported.