New application of DNA editing technique, CRISPR-Cas9, may open the door the new treatments for cancer and autism.
Researchers have developed a new method to accurately and rapidly locate proteins within brain cells.
A new study reports researchers have developed a quicker and more efficient method to alter mice genes with CRISPR-Cas9.
Researchers have developed a new technique that offers precise manipulation of where and when genes are targeted.
Researchers have developed a new protein that can alter DNA in living cells with much higher precision than current methods.
A new study has identified a biological pathway associated with the risk for developing an eating disorder.
Researchers use gene editing technology to help partially restore vision to blind rodents.
Researchers use CRISPR to modulate genes in order to reduce tissue damage and inflammation for people with neck and back pain.
Researchers successfully use CRISPR-Cpf1 to correct Duchenne muscular dystrophy in both animal and human cells.
Researchers use gene editing to reverse cell degeneration and restore vision in mouse models of retinitis pigmentosa.
Researchers show CRISPR/Cas9 gene editing technology can be effectively used in rhesus monkey embryos.
Researchers report they have successfully been able to shut down and eliminate the HIV-a virus from infected cells in mice, thanks to the help of CRISPR/Cas9 gene editing technology.
