The current barriers of CRISPR/Cas9 delivery and promising development of nanoparticle-based approaches for precise gene editing.
The current barriers of CRISPR/Cas9 delivery and promising development of nanoparticle-based approaches for precise gene editing.
Scientists have functionalized a simple nano-building block to form self-assembling molecular networks that exhibit exceptional properties.
Using bacteria to combat varroa mites, a common pest that can weaken honey bees and make them more susceptible to pathogens.
Researchers in labs around the world use the latest techniques to combat the Wuhan coronavirus.
Tiny ‘xenobots’ assembled from cells promise advances from drug delivery to toxic waste clean-up.
X-rays capture the ultrafast proton transfer reaction in ionized liquid water, forming the hydroxyl radical and the hydronium ion.
What were the driving factors behind organelle evolution?
We have the potential to end the HIV epidemic. But why hasn’t it happened yet?
An artificial cell, which uses a microfluidics-based approach to engineer a modular and programable artificial‐cell‐on‐chip.
In 2019, CRISPR gene-editing therapy was used for the first time to treat sickle cell disease.