CRISPR is revolutionizing medicine by enabling precise DNA edits, treating genetic diseases like sickle cell anemia and ...

Mouse livers were engineered via a one-time genome editing to secrete a GLP-1, cutting weight gain and improving glucose ...

We spoke with the developers and manufacturers of the CRISPR gene therapy used to treat KJ Muldoon’s rare genetic condition, ...

A £10 million Wellcome Trust-funded project seeks to create artificial human genomes. Technology Networks explored the ...

The duration of expression of the gene Cdx2 is tightly regulated by a newly identified DNA sequence element called an “attenuator.” ...

Technical Lead, Genome Editing Initiative, African Union Development Agency (AUDA-NEPAD) Centre of Science, Technology and ...

The Australian researchers developed a novel mRNA-based technology capable of reaching the white blood cells where HIV lies ...

A Ph.D. student in biomolecular engineering at the University of California, Santa Cruz, has built a software program ...

New research has found a novel target with therapeutic potential for metastatic eye melanoma—an aggressive eye cancer—with ...

Genome editing technologies like CRISPR-Cas9 have transformed biology, medicine, and agriculture, but concerns remain about ...

CRISPR-Cas9 genome editing exploits the CRISPR-Cas system to modify a genome in a targeted manner. Guided by RNA, the Cas9 endonuclease breaks DNA at a target sequence. Imprecise repair of the ...