Study reveals how a neuropeptide called Big Dynorphin binds to the acid-sensing ion channel receptor, causing pain signals to be sent around the body.
Researchers have developed a new method for monitoring sleep cycles in mice. With help of the new method, researchers have identified a new short sleeper gene.
Researchers have successfully reduced some symptoms associated with fragile X syndrome in mice with the help of CRISPR-Cas 9 gene editing.
CRISPR technology allows researchers to illuminate and monitor alpha synuclein in the brain.
The most common messenger RNA modification in mammals helps coordinate nerve cell response to memory inducting stimulus, a new study reveals.
UC Berkeley researchers report they have successfully used CRISPR-Cas9 gene editing to delay symptoms and extend lifespan in mouse models of ALS.
Using CRISPR techniques, researchers have uncovered a genetic network linked to autism.
Researchers report that, at the molecular levels, aging may have originated at the beginning of the evolution of life. They suggest when it comes to genes, aging may not always be a negative trait, and may help an organism to survive.
Using CRISPR-Cas9 gene editing, researchers identified actionable pathways responsible for the growth of glioblastoma stem cells. By reverse engineering brain cancer cells, multiple potential new targets for cancer treatments have been uncovered.
Researchers show CRISPR/Cas9 gene editing technology can be effectively used in rhesus monkey embryos.
Researchers discover a mechanism that may underpin the progression of glioblastoma brain cancer development.
Researchers use CRISPR gene editing technology to rewire stem cells in order to fight inflammation caused by arthritis.
