This podcast discusses how CRISPR gene-editing technology is revolutionizing healthcare by making personalized gene therapy a reality. From treating genetic disorders to unlocking precision medicine, CRISPR could transform the way we fight disease.

Performing successful CRISPR-Cas9 experiments isn’t just about cutting DNA—it requires precision, programming, and a deep understanding of both the technology and the biology behind it.That’s where CRISPR-GPT comes in: a DNA programming assistant built in Python for automating and optimizing gene-editing experiments.Think of it as your agentic co-pilot in the lab—helping design, analyze, and streamline CRISPR workflows, so you can focus on discovery and innovation.Join us as we explore how AI-driven automation is transforming the way we approach CRISPR, stem cells, and gene editing research.Reference article: https://www.nature.com/articles/s41551-025-01463-z.pdf

How reprogrammed T cells become living medicines. In clear, science-first episodes, we trace collection → engineering → infusion, highlight successes in B-cell cancers (CD19, BCMA), unpack risks (CRS, ICANS), and preview what’s next—off-the-shelf/allogeneic CARs, safety switches, and solid-tumor strategies. Subscribe for translational takeaways you can trust.

Organoids: Growing the Future of Medicine in Your Hand explores how mini-organs built from stem cells are reshaping drug discovery, disease modeling, and regenerative medicine today.