Not exact matches
These findings allowed researchers to
create a chimera virus: a mouse virus with a
human viral gene that can be used to test molecules that inhibit
human LANA protein in an
animal model of disease, treating not only
human herpes virus infection but also its associated cancers.
From accelerating the identification and validation
of novel therapeutic targets, to
creating better
animal models of human diseases in a shorter time frame, to reducing the number
of failed products, Crispr looks set to shave millions off R&D costs and boost drug discovery, she says.
One
of the most promising avenues for developing a cure, however, is through gene therapy, and to
create those therapies requires
animal models of disease that closely replicate the
human condition.