Dr. Keerthi Krishnan discusses the role of MECP2 in Rett syndrome, focusing on its genetic regulation and impact on neurological development. The presentation highlights new findings on Rett syndrome phenotypes and the significance of context-dependent gene regulation.
Exploring Rett Syndrome: Insights from MECP2 Research
Key Takeaways
- Research focus: Study of Rett syndrome and MECP2 gene regulation.
- Model system: Human neurological development research.
- Research goal: Understand behavioral and molecular mechanisms of Rett syndrome.
- Presented by: Dr. Keerthi Krishnan, University of Tennessee.
- Content type: Scientific Presentation at SfN2025.
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SfN 2025 Booth Talk: Keerthi Krishnan | PNNs
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