For the past decade, scientists have relied almost exclusively on CRISPR-Cas systems for genome editing. Now, a smaller but ...

A recent breakthrough in genetic research has introduced a tool capable of delivering genetic material to developing fetal ...

People with myotonic dystrophy type 1 (DM1), the most common adult-onset form of muscular dystrophy, progressively lose ...

Editas Medicine announced proof-of-concept data for a gene-editing approach for sickle cell disease that doesn't need a stem ...

Researchers have developed a novel delivery system for sending CRISPR reagents to brain cells, where it performs its gene ...

The best gaming mouse isn't always the fastest on the market, nor is it the one with the most buttons. Pointers that ascend to legendary status on a desk setup are the ones that marry comfort with ...

KOREA MICE EXPO 2024 to be held at Songdo ConvensiA, Incheon from 6 (Wed) to 8 (Fri) November. Diverse programs including exhibition booths, business 1:1 meetings, conferences, and networking dinner.

The gene therapy, called P-KLKB1-101, edited KLKB1 to therapeutic levels in mice with just a single dose ... 25 times more reliably than the CRISPR-Cas9 approach, according to a 2022 study.

The researchers injected the LNP with the mRNA into the fetal brain's ventricles in a mouse model. The mRNA translates into CAS9, a protein that works like scissors for gene editing. The produced ...

A single treatment with a CRISPR-Cas9 based gene editing therapy is enough to replace the daily medication of patients with hereditary angioedema (HAE), a condition characterized by severe ...