Scott C. Baraban

Conditions sufficient for nonsynaptic epileptogenesis in the CA1 region of hippocampal slices.

Y5 receptors mediate neuropeptide Y actions at excitatory synapses in area CA3 of the mouse hippocampus.

Antiepileptic actions of neuropeptide Y in the mouse hippocampus require Y5 receptors.

Heterotopic neurons with altered inhibitory synaptic function in an animal model of malformation-associated epilepsy.

Effects of antiepileptic drugs on induced epileptiform activity in a rat model of dysplasia.

A review of gene expression patterns in the malformed brain.

An examination of calcium current function on heterotopic neurons in hippocampal slices from rats exposed to methylazoxymethanol.

Neuropeptide Y modulates a G protein-coupled inwardly rectifying potassium current in the mouse hippocampus.

Target-specific neuropeptide Y-ergic synaptic inhibition and its network consequences within the mammalian thalamus.

Interneuron Diversity series: Interneuronal neuropeptides--endogenous regulators of neuronal excitability.

Epileptogenesis in the Dysplastic Brain: A Revival of Familiar Themes.

Epilepsy Research Takes Flight.

Abnormal cortical cells and astrocytomas in the Eker rat model of tuberous sclerosis complex.

Prolonged NMDA-mediated responses, altered ifenprodil sensitivity, and epileptiform-like events in the malformed hippocampus of methylazoxymethanol exposed rats.

Mice lacking Dlx1 show subtype-specific loss of interneurons, reduced inhibition and epilepsy.

Pain without gain (of function): sodium channel dysfunction in epilepsy.

Dysfunction of synaptic inhibition in epilepsy associated with focal cortical dysplasia.

Embryonic and early postnatal abnormalities contributing to the development of hippocampal malformations in a rodent model of dysplasia.

A role for the mTOR pathway in surface expression of AMPA receptors.

Cortical inhibition modified by embryonic neural precursors grafted into the postnatal brain.

Stromal-derived factor-1 (CXCL12) regulates laminar position of Cajal-Retzius cells in normal and dysplastic brains.

Granule cell dispersion and aberrant neurogenesis in the adult hippocampus of an LIS1 mutant mouse.

Altered glutamate receptor - transporter expression and spontaneous seizures in rats exposed to methylazoxymethanol in utero.

Neocortical hyperexcitability in a human case of tuberous sclerosis complex and mice lacking neuronal expression of TSC1.

Emerging epilepsy models: insights from mice, flies, worms and fish.

A large-scale mutagenesis screen to identify seizure-resistant zebrafish.

Characterization of inhibitory circuits in the malformed hippocampus of Lis1 mutant mice.

Developing cell transplantation for temporal lobe epilepsy.

Aberrant dentate gyrus cytoarchitecture and fiber lamination in Lis1 mutant mice.

Inhibitory inputs to hippocampal interneurons are reorganized in Lis1 mutant mice.

Reduction of seizures by transplantation of cortical GABAergic interneuron precursors into Kv1.1 mutant mice.

Basic mechanisms of MCD in animal models.

Seizures, enhanced excitation, and increased vesicle number in Lis1 mutant mice.

Zebrafish as a model for studying genetic aspects of epilepsy.

Dlx5 and Dlx6 regulate the development of parvalbumin-expressing cortical interneurons.

Robust tonic GABA currents can inhibit cell firing in mouse newborn neocortical pyramidal cells.

Spontaneous seizures and altered gene expression in GABA signaling pathways in a mind bomb mutant zebrafish.

The promise of an interneuron-based cell therapy for epilepsy.

Deletion of Dlx1 results in reduced glutamatergic input to hippocampal interneurons.

Aberrant expression of genes necessary for neuronal development and Notch signaling in an epileptic mind bomb zebrafish.

Expression and function of KCNQ channels in larval zebrafish.

Impaired neural development in a zebrafish model for Lowe syndrome.

A novel zebrafish model of hyperthermia-induced seizures reveals a role for TRPV4 channels and NMDA-type glutamate receptors.

Familial cortical myoclonus with a mutation in NOL3.

LIS1 虚促进在发展中国家和成人海马齿状回中生成的颗粒细胞的功能失调性突触一体化。

Intrinsically determined cell death of developing cortical interneurons.

ALLN rescues an in vitro excitatory synaptic transmission deficit in Lis1 mutant mice.