Researchers at the Broad Institute of MIT and Harvard have developed a gene-editing treatment for prion disease that extends ...

Researchers at the Broad Institute of MIT and Harvard have developed a gene-editing treatment for prion disease that extends lifespan by about 50 percent in a mouse model of the fatal ...

Cell therapy and gene therapy represent groundbreaking approaches to treating, preventing, and potentially curing diseases by addressing their underlying causes ... Technological advancements, ...

Scientists looked at multiple techniques used to measure the modified viruses deployed in some gene therapy research and treatments. One technique, known as SEC-MALS, was the most precise and accurate ...

From AI to gene therapy, we reached out to industry experts to get their thoughts on the trends that will shape the biotech ...

29, 2024 — For decades, scientists have dreamt of a future where genetic diseases, such as the blood ... have developed a novel version of a key CRISPR gene-editing protein that shows efficient ...

The revolution in artificial intelligence (AI) and genetic engineering represents an unprecedented turning point in human ...

Imagine a world where the genetic code is as easy to edit as a simple copy-and-paste. This is the reality of CRISPR, a ...

In October, Intellia reported phase 2 results with NTLA-2002 – which is pitching to become the first approved in vivo CRISPR ...

A gene-editing therapy may correct a defect in the DYSF gene that drives a form of limb-girdle muscular dystrophy (LGMD), per ...

CRISPR-Cas9 genome editing exploits the ... that it is theoretically possible to reduce risk of common diseases using heritable genome editing. Scientists argue that the technology involves ...