Four interconnected research programs exploring neural circuit construction, balance, plasticity, and vulnerability in the developing brain.
Our lab pursues two major research directions: understanding how neural progenitor cells proliferate and differentiate to build functional circuits, and uncovering how excitation–inhibition balance shapes circuit function and underlies neurological disease. We complement these with studies on sensory-experience-driven plasticity and environmental neurotoxicity.
Radial glial cells, HDAC-mediated epigenetic regulation, Wnt/β-catenin signaling, and the assembly of newborn neurons into functional circuits.
How E/I equilibrium governs circuit function and behavior; disruption mechanisms linking to autism, epilepsy, and schizophrenia.
Visual activity drives epigenetic changes and AMPAR trafficking; homeostatic scaling mechanisms that keep circuits stable during development.
Para-xylene toxicity mechanisms; D-Glucuronolactone and oxidative stress; Xenopus as a translational toxicological screening platform.
The African clawed frog Xenopus laevis offers two powerful platforms for neuroscience:
In vivo (tadpole) — An optically transparent brain enables non-invasive imaging and clean electrophysiology, while genetic tools (electroporation, morpholino, CRISPR) allow precise manipulation during circuit development.
In vitro (oocyte) — Large cells ideal for heterologous expression of ion channels and receptors. Enable detailed biophysical analysis (TEVC), rapid pharmacological screening, and structure-function studies in a controlled membrane environment.
Transparent tadpole
Optic tectum
Protein expression in Xenopus oocyte