On the Hunt for the Next Breakthrough in Motor Neuron Disease

By Deanna MacNeil, PhD

Researchers leave no stone unturned in the search for a spinal muscular atrophy treatment strategy that uses base editing.

Poster: Linking Thousands of Gene Mutations to Their Transcriptional Responses

By Cellecta

With Perturb-seq, researchers analyze the effects of CRISPR-based perturbations in individual cells. Learn how this technique works in this poster from Cellecta.

Resolving Discrepancies in Mouse and Human Autoimmunity Studies

By Niki Spahich, PhD

By editing primary T cells with CRISPR, researchers begin to settle a long-standing debate about a common autoimmunity risk variant.

eBook: CRISPR Revolutionizes Cell and Gene Therapy Development

By Synthego

Explore the challenges—and their solutions—related to CRISPR in cell and gene therapies in this ebook from Synthego.

Science Philosophy in a Flash: Targeting a Genetic Accident to Treat Disease

By The Scientist’s Creative Services Team

David Liu shares how integrating chemistry and evolution in his research has directed his work on base editing techniques aimed at developing new therapeutics.