Mouse livers were engineered via a one-time genome editing to secrete a GLP-1, cutting weight gain and improving glucose ...

In vivo base editing enables precise, single-nucleotide changes to DNA without double-strand breaks. A recent application in ...

A recent study involving researchers from the University of Basel reveals that slowing down the intracellular transport of ...

A cocktail of FDA-approved cancer drugs, trametinib and rapamycin, boosts the lifespan of lab mice by 30% and might help humans age better, new study finds.

Pheromones—chemicals produced by animals—are well-known for influencing the social and sexual behavior of members of the same species. These chemical signals convey vital information, such as gender ...

Young adult mice with a genetic form of progressive deafness can hear again after being treated with an experimental CRISPR gene therapy that its creators hope to eventually use in humans.

Now, researchers have developed a noninvasive method of delivering CRISPR/Cas9 gene editing technology to the brain to knock out a gene associated with anxiety and depression in mice.

Their results were published in the journal PLOS Biology ("Meiotic Cas9 expression mediates gene conversion in the male and female mouse germline"). Researchers discovered that CRISPR-Cas9 genetic ...

So for this new study, the team investigated how to use CRISPR-Cas9 to control which sex is born from a litter of mice.

In a recent study, researchers managed to kill resistant bacteria in mice guts. This method, which is still being researched, uses the famous Nobel Prize winning gene-editing technology, CRISPR-Cas9.

Symptoms of Myotonic dystrophy 1 reversed in mouse model after researchers used their CRISPR-mediated RNA targeting method to clear toxic RNA buildup.

In 31 of the Cas9 mouse lines, no off-target mutations were identified, but an average of 2.3 such mutations were identified in the remaining 20 lines.