Potent in vivo gene editing in skeletal muscle of non-human primates by a novel, ultracompact CRISPR system delivered via a single AAV vector.

Scientists have successfully engineered a mouse with two fathers that went onto survive until adulthood. Researchers have attempted to create ... | Genetics And Genomics ...

Two new compounds may be able to treat retinitis pigmentosa, a group of inherited eye diseases that cause blindness. The compounds were identified using a virtual screening approach.

In two new papers, researchers from The Jackson Laboratory (JAX) report the successful use of two approaches -- gene therapy ...

More information: Meirui An et al, In vivo base editing extends lifespan of a humanized mouse model of prion disease, Nature Medicine (2025). DOI: 10.1038/s41591-024-03466-w . www.nature.com ...

A team of researchers has successfully engineered a bi-paternal mouse - a mouse with two dads - that survived until adulthood ...

Australian cancer researchers are the first to establish a next-generation gene-editing tool for modeling and interrogating human disease.

A gene-edited mouse with two male parents has survived to adulthood, pushing new progress on stem cell research.

A mouse with no biological mother has survived to adulthood in China – a major scientific achievement that's been years in ...

Peromyscus’ natural variation and interbreeding are quite unique in terms of model organisms out there ... “The work in neurobiology has been really dominated by [lab] mouse, because we have lots of ...

Using cutting-edge stem cell technology, a team of scientists from the Chinese Academy of Sciences (CAS) recently created a ...

Researchers have developed a gene-editing treatment for prion disease that extends lifespan by about 50 percent in a mouse model of the ... regardless of the genetic mutation causing their disease.