Japanese researchers have successfully eliminated the extra chromosome responsible for Down syndrome using CRISPR gene ...

While CRISPR/Cas9 represents a revolutionary gene editing ... a serotonin receptor known to play a role in anxiety and depression. They used a vector based on an inactivated adeno-associated ...

A new variation of the CRISPR-Cas9 gene editing system makes it easier to re-engineer massive quantities of cells for therapeutic applications. The approach, developed at Gladstone Institutes and UC ...

CRISPR Therapeutics’ CRSP first marketed product is the one-shot gene therapy Casgevy, approved in late 2023 and early 2024 ...

The CRISPR/Cas9 therapy approved today ... which used a Lentiviral vector to insert genes into the human genome. In this case, the system delivers the genetic code for a modified type of ...

A newly discovered bacterial defense protein named Cat1 reveals an extraordinary method of viral neutralization. All living ...

Here’s how it works. CRISPR, short for CRISPR-Cas9, is a genome-editing tool that allows scientists to precisely cut and modify DNA sequences. It has revolutionized the study of genes ...

Scientists at the San Raffaele Telethon Institute for Gene Therapy (SR-Tiget), Milan, have found that gene editing using CRISPR-Cas9 in combination with AAV6 vectors can trigger inflammatory and ...

Delve into what the new CRISPR tool, CAST, has to offer. CRISPR-associated transposases are already gaining traction in ...

The CRISPR-Cas9 gene editing technique allows scientists to make very precise changes to DNA. Its inventors — Emmanuelle Charpentier and Jennifer A. Doudna — won a Nobel Prize in chemistry in ...

For a decade, leading academic institutes and their associated companies fought a bruising, headline-grabbing fight over who held patent rights to CRISPR-Cas9, the revolutionary genome editing tool.