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 ...

In a Phase I/II trial, patients with X-linked chronic granulomatous disease will receive a treatment created using a new ...

Gene-editing kicked off 2024 with a bang in the medical sector but closed the year with a whimper. It started with the FDA approval for the first CRSPR-based gene therapy treatment for sickle cell ...

Gene editing involves precise changes in DNA sequences using enzymes, revolutionizing medical, agricultural, and research ...

It feels fantastic,” said Blau, who thanked her lab members and colleagues for their support and dedication. “This ...

The new Express License service removes barriers to accessing this transformative gene editing technology for startups.An ...

Using whole genome sequencing (WGS ... so the researchers aimed to increase activity in the organoids. Next, CRISPR-Cas9 gene editing was used to effect functional changes in the organoids ...

Editas Medicine ( (EDIT) ) has provided an announcement. Editas Medicine announced new in vivo preclinical proof of concept data and outlined its strategic priorities and key milestones for 2025, ...

Kansas State University researchers have reported a breakthrough in developing wheat-based foods that contain lower amounts ...