A compact Cas12f nuclease shows high editing efficiency in human cells, with structural insights enabling an engineered variant potentially suited for future AAV‑compatible delivery.

NIH-funded UT team and colleagues from Metagenomi Thereapeutics discovered highly efficient enzyme could enable targeted gene editing within the human body.

CRISPR Cas9 gene therapy explained with DNA scissors, hereditary diseases treatment, and designer babies ethical dilemmas ...

The CRISPR-Cas gene-editing system has long been the focus of research as a promising tool in genome editing. However, the ...

So far, clinical applications of CRISPR-based gene editing have been largely limited to editing a person's cells outside of their body and then ...

Genomics gains momentum as breakthroughs, falling sequencing costs, and CRISPR advances drive precision medicine and fuel rapid market growth.

A research team has discovered an enhanced CRISPR gene-editing system that could enable targeted delivery inside the human ...

In the first of a new series of GEN Keynote Webinars, Professor Rodolphe Barrangou, PhD (North Carolina State; EIC, The CRISPR Journal) offers a front-row perspective of the CRISPR revolution, the ...

Migur A, Feussner M, Liao C, Alkhnbashi OS, Chauvier A, Walter NG, Backofen R, Weinberg Z, Beisel CL (2026) A leader-repeat hairpin blocks extraneous CRISPR RNA production in diverse CRISPR-Cas13 ...

Kookmin University said Tuesday that the Ministry of Science and ICT had selected a new synthetic biology project aimed at ...