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With extremely precise gene repair scientist succesfully converts the mutated allele that causes sickle cell disease into a non-pathogenic variant and...

Using microneedles for transdermal delivery of CRIPSR-Cas9 and glucocorticoids researchers have found a viable way to precisely treat inflammation...

Editing a single nucleotide in the largest human gene is sufficient to restore dystrophin production and myocyte function in Duchenne muscular...

Professor Jin-Soo Kim, from the Center for Genome Engineering at the Republic of Korea’s Institute for Basic Science, struggled for years to edit...

Almost complete efficiency of gene knock-in is achieved with a new CRISPR-based system developed by researchers from AstraZeneca. The system also...

DECODR's algorithm can quickly — and cheaply — make sense of Sanger sequencing data at a very precise level.

A constant battle between prokaryotes and phages has shaped how CRISPR is controlled and regulated. Haridha Shivram from Jennifer Doudna’s lab is...

Leber congenital amaurosis is a group of rare inherited retinal diseases that lead to blindness over time. Treatment options are limited,...