By 2025, innovations such as lab-on-a-chip technology, automation, and CRISPR-Cas9 gene editing are expected to enhance ...

Treatments for rare diseases are hard to create and expensive to deliver, but there is new hope for editing the software of ...

"We’re in very different place," the CEO of Editas says, citing the CRISPR pioneer's plans to get its first treatments into ...

Lehigh University bioenginering researcher Tomas Gonzalez-Fernandez recently secured funding through the National Science ...

Human gene editing is a technique that allows the deliberate ... Gene editing is rather sui generis, with the molecular tool CRISPR (short for clustered regularly interspaced short palindromic ...

Researchers at the Experimental and Clinical Research Center in Berlin are developing a targeted treatment for muscular ...

The core components of CRISPR-based genome-editing therapies are bacterial proteins called nucleases that can stimulate ...

Ongoing launch of CASGEVY® continues to gain momentum--2025 is poised to be a catalyst-rich year with key updates across several ...

The preclinical findings, reported in “Nature Communications,” give the team confidence to move forward to human clinical trials ... Escobar uses CRISPR-Cas9, which is often described as “gene-editing ...

In this installment, we delve into one of the most debated scientific advancements of our time: CRISPR gene-editing ...

Bayer's venture will undoubtedly be playing catch-up, but it is likely to be a few years before the first CRISPR-Cas9 molecule for human therapy ... the most promising gene-editing technology ...