Our lab has a long-standing interest in ion channels and synaptic transmission,
dating back to the 1985 discovery that central synapses use a previously
unrecognized set of calcium channels, exemplified by the N-type channel, to drive
neurotransmission. Studies of the diversity of Ca2+ channels led to an interest in
long-term potentiation and then to studies addressing more general questions
about synaptic physiology. We have also been fascinated by how the properties of individual synapses contribute to the dynamics of neuronal networks. Neurons and circuitry that generate healthy activity like long-term potentiation and sharp wave ripples also give rise to inappropriate excitation-inhibition ratios in disparate
disorders. What determines the dynamics of firing in and the watershed between
these forms of activity? What role do diverse excitatory and inhibitory synapses
play in shaping the flow of information in CNS circuits? How might neural circuitry
containing such synapses become dysfunctional in disorders such as autism,
epilepsy, schizophrenia and Alzheimer’s disease? We apply our expertise in
electrical, molecular, genetic and optical approaches to capitalize on genetic
discoveries of highly penetrant disorders that exemplify the more general disease.
By combining forces with systems neuroscientists and clinicians, our lab explores
the roles of interneuron-dominated circuitry and neuromodulatory state. We
provide a vigorous bridge between molecular/cellular and systems-level
approaches to vulnerable brain function.
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