CRISPR mouse models show EML4-ALK fusion variants alter drug response, suggesting a need for variant-specific treatment.

Natural systems such as CRISPR-associated transposons (CASTs) offer a targetable, one-step way to edit genomes.

A research team led by Prof. Wang Yanli from the Institute of Biophysics of the Chinese Academy of Sciences has revealed the ...

By Milliam MurigiInternational researchers have developed an artificial intelligence (AI) system dubbed CRISPR-GPT, designed to automate and enhance CRISPR-based gene-editing experiments.Clustered ...

Scientists hope genetically modified mice will curb the spread of Lyme disease. They headed to Nantucket — home to a large ...

KAIST and the Korea Research Institute of Chemical Technology have jointly developed the world’s first new ‘CRISPR gene-editing technology (CRISPR)’ capable of simultaneously turning genes on and off.

Forecasts in biotech market indicate that by 2030, gene therapy will become more accessible, potentially generating hundreds ...

The 2020 Nobel Prize in Chemistry was awarded for the development of CRISPR/Cas9, a method also known as "gene scissors," ...

Researchers engineered a CRISPR base editor to correct the ACTA2 mutation causing multisystemic smooth muscle dysfunction ...

The field of microbiology has emerged as a cornerstone for green technology, playing a crucial role in fostering sustainable ...

Researchers engineered and screened dozens of base editors to precisely target a single mutation without editing other portions of the DNA.