The chemical probe CDr20 can label microglia in living cells, researchers report. Read More
Using CRISPR gene editing techniques, researchers create modified skin grafts that rapidly degrade cocaine and reduce drug seeking behaviors in mouse models of addiction. Read More
A new study confirms a mutation caused dysfunction associated with Alzheimer's and proposes a new therapeutic target. Read More
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. Read More
Researchers have successfully reduced some symptoms associated with fragile X syndrome in mice with the help of CRISPR-Cas 9 gene editing. Read More
A newly developed approach could be used to treat Duchenne muscular dystrophy, researchers believe. Read More
The human development 'clock in a dish' opens up new avenues for research and provides a way to replicate developmental disorders. Read More
Study reveals how a protein that transports essential amino acids across the placenta plays a role in fetal development. Deficiencies of the SNAT4 protein may result in developmental abnormalities and a higher risk of miscarriage. Read More
Researchers use CRISPR to convert cells isolated from mouse connective tissue into neural cells. Read More
Researchers have created a map of gene regulation in human cortical neurogenesis. The study reveals a number of factors that govern brain growth and the development of some brain disorders. Read More
CRISPR gene editing has allowed researchers to prevent angiogenesis of the retina occurring in mice. Researchers say the new technology could help prevent vision loss in those with retinal diseases. Read More
Researchers show CRISPR/Cas9 gene editing technology can be effectively used in rhesus monkey embryos. Read More
