Track 13: Gene Editing and Stem Cell Therapy
Gene editing technologies such as CRISPR are transforming stem cell therapy by allowing precise modifications to genetic material. This approach has the potential to directly address genetic disorders at their root, significantly improving the therapeutic effectiveness of stem cells. As research advances, it will be crucial to establish strict regulatory frameworks and engage the public to responsibly harness the full potential of these innovative technologies.
- Introduction to Gene Editing in Stem Cell Therapy
- Mechanisms of Gene Editing
- Applications of Gene Editing in Stem Cell Therapy
- Therapeutic Goals and Strategies
- Challenges in Gene Editing and Stem Cell Therapy