Scientists engineered nanoparticles capable of delivering genetic material to lung cells with high efficiency when administered intravenously. Based...
Researchers have refined prime editing (PE) to correct the cystic fibrosis (CF) related gene CFTR. Results demonstrated improved efficiency and...
In a new breakthrough, researchers have achieved significant advances in gene editing of lung stem cells, demonstrating the potential for durable...
In this post, we introduce our CMN disease overview, which will provide information on all the diseases that are targeted by gene-editing therapies...
Mammoth Biosciences was until recently most well known as a diagnostic company using CRISPR technology, but through a newly announced partnership with...
CRISPR and organoids are transforming science and medicine, and now dutch scientists have used CRISPR base editors to cure cystic fibrosis in...
