The burgeoning industry of biological design is in the headlines every day. Yet even science journalists have had trouble explaining concepts like CRISPR in terms that everyone can understand. A new exhibition at a Silicon Valley museum skillfully explains the technically and ethically complicated field of…
Researchers from Temple University have used the CRISPR/Cas9 gene editing tool to clear out the entire HIV-1 genome from a patient’s infected immune cells. It’s a remarkable achievement that could have profound implications for the treatment of AIDS and other retroviruses.
Less than a year after scientists in China became the first to genetically modify human embryos, a research team in Britain has been given the green light to perform similar work. It’s a huge moment in biotech history—one that could eventually lead to “designer babies.”
Researchers in China are reportedly the first to use a powerful gene editing tool to produce super-muscled dogs. The goal is to create test subjects that mimic degenerative human diseases, but the breakthrough also raises the prospect of customized pets.
Editas Medicine hopes to use CRISPR—a revolutionary new gene-editing technology—to treat conditions such as sickle-cell anemia, cancer, and cystic fibrosis.
Scientists at Stanford University have found a way to program DNA in such a way that genes can be turned on or off in living cells. Incredibly, the new tool can affect two different genes at the same time, an advance that will allow scientists to treat even the most complex genetic disorders.
Sorry CRISPR, but there's a new genomic editor in town — and this one's better than you. It's a new approach to site-specific gene targeting that will allow scientists to safely replace disease-causing genes with functional copies. And they've already used it to relieve the effects of hemophilia in mice.
The treatment is considered radical, and the results were drawn from a small scale human trial, but for the first time in medical history, researchers have boosted their patients' ability to fight HIV by replacing some of their natural immune cells with genetically modified versions.