Editing one gene extends mouse life expectancy by 23%

By modifying just one gene, researchers were able to extend the life expectancy of mice by 23%, and they think their results may translate to humans.

Full-length dystrophin restoration via targeted exon integration by AAV-CRISPR in a humanized mouse model of Duchenne muscular dystrophy: Molecular Therapy

Genome editing in the mouse brain with minimally immunogenic Cas9 RNPs: Molecular Therapy

Genes, Free Full-Text

Gene drive technology makes mouse offspring inherit specific traits from parents

New gene editing strategies developed for Duchenne muscular dystrophy : Newsroom - UT Southwestern, Dallas, Texas

Perturbations in neural stem cell function during a neurotropic viral infection in juvenile mice - Kamte - 2023 - Journal of Neurochemistry - Wiley Online Library

Cells, Free Full-Text

Frontiers Base and Prime Editing Technologies for Blood Disorders

Israeli scientists extend life of mice by 23%, say method may work on humans : r/slatestarcodex