Collins, along with Matthew Lau ’25, developed the affordable CRISPRKit to make CRISPR gene-editing technology accessible to high school students underrepresented in the sciences. The kit was ...

It may also help identify rare disease and develop gene therapies that can treat them ... There has also been a European effort to sequence 1+ Million Genomes across 24 countries. 1. Genome editing is ...

Learn more› By Erin Roberts and Ben Keough After considering new apps, we still think that Adobe Lightroom and Snapseed are the best choices for editing photos when you’re away from a desktop ...

Copyright 2025 The Associated Press. All Rights Reserved. Chicago Chess Records producer Gene Barge attends a screening of the film “Cadillac Records,” about ...

And this is just the beginning. But amid all the fervor and history-making lies a few teething issues. Namely, even with the improved specificity CRISPR-Cas9 has brought to gene-editing, accidental, ...

NHS patients with sickle cell disease will be able to benefit from a groundbreaking gene-editing treatment that offers the prospect of a cure for the condition. The one-off gene therapy, known as ...

Screen icon Gene Hackman turned 95 on January 30, kicking off another milestone year in the legendary actor's life. While the star has led his life away from the spotlight for the majority of the ...

A gene-edited mouse created with two male parents ... The International Society for Stem Cell Research currently prohibits heritable genome editing for human reproduction, and using human stem ...

Most video editing software works through re-encoding—essentially, uploading the file so it can be broken apart and stitched back together. This is necessary for advanced editing techniques but ...

Pluristyx makes and sells PluriBank™ iPSC lines as part of their tools, technologies, and services to support the development of cellular therapies, and is currently performing gene editing of ...

Though GNN has reported that several sickle cell disease patients have already been successfully treated with CRISPR gene editing technology, a new method of addressing this debilitating condition ...

These unique, branched molecules help LNPs break through the endosomal membrane, making them more effective at delivering mRNA and gene-editing tools. In a recent study in Nature Communications ...