<?xml version="1.0" encoding="ASCII"?>
<biogps><data><item><item key="slug">cln3-patients-with-differing-progression-of-the-di</item><item key="name">CLN3 patients with differing progression of the disease</item><item key="sample_count">15</item><item key="tags"><item>disease</item><item>epilepsy</item><item>genome</item><item>juvenile neuronal ceroid lipofuscinosis</item><item>neuronal ceroid lipofuscinosis</item></item><item key="species">human</item><item key="is_default">False</item><item key="geo_gse_id">E-GEOD-22225</item><item key="id">3687</item><item key="factor_count">6</item></item><item><item key="slug">expression-data-of-ffpe-peritumoral-neocortex-tiss</item><item key="name">Expression data of FFPE peritumoral neocortex tissue</item><item key="sample_count">10</item><item key="tags"><item>brain</item><item>cortex</item><item>epilepsy</item><item>genome</item></item><item key="species">human</item><item key="is_default">False</item><item key="geo_gse_id">E-GEOD-32534</item><item key="id">2657</item><item key="factor_count">3</item></item><item><item key="slug">transcription-profiling-by-array-of-human-perip-13</item><item key="name">Transcription profiling by array of human peripheral blood mononuclear cells from patients with epilepsy over a time course of dexamethasone treatment</item><item key="sample_count">16</item><item key="tags"><item>acute lymphoblastic leukemia</item><item>cell</item><item>central</item><item>epilepsy</item><item>glucose</item><item>leukemia</item><item>lymphoblastic leukemia</item><item>peripheral</item></item><item key="species">human</item><item key="is_default">False</item><item key="geo_gse_id">E-GEOD-22779</item><item key="id">3733</item><item key="factor_count">3</item></item><item><item key="slug">transcription-profiling-by-array-of-human-sk-n-a-2</item><item key="name">Transcription profiling by array of human SK-N-AS neuroblastoma cells treated with constructs expressing truncated or full-length NRSF</item><item key="sample_count">9</item><item key="tags"><item>brain</item><item>epilepsy</item><item>line</item><item>neuroblastoma</item><item>neuron</item><item>point</item><item>status epilepticus</item></item><item key="species">human</item><item key="is_default">False</item><item key="geo_gse_id">E-GEOD-22467</item><item key="id">3707</item><item key="factor_count">2</item></item><item><item key="slug">transcription-profiling-of-human-hek293-cells-tr-2</item><item key="name">Transcription profiling of human HEK293 cells transfected with CavB4 or CavB4-R482X mutant cDNA</item><item key="sample_count">9</item><item key="tags"><item>amino acid</item><item>cell</item><item>epilepsy</item><item>juvenile myoclonic epilepsy</item><item>line</item><item>myoclonic epilepsy</item></item><item key="species">human</item><item key="is_default">False</item><item key="geo_gse_id">E-MEXP-1165</item><item key="id">5090</item><item key="factor_count">1</item></item><item><item key="slug">expression-changes-in-the-absence-of-mir-128-in-st</item><item key="name">Expression changes in the absence of miR-128 in striatal D1-receptor positive neurons</item><item key="sample_count">16</item><item key="tags"><item>dopamine</item><item>epilepsy</item><item>neuron</item><item>protein</item><item>ribosome</item><item>striatum</item></item><item key="species">mouse</item><item key="is_default">False</item><item key="geo_gse_id">E-GEOD-48813</item><item key="id">7368</item><item key="factor_count">0</item></item><item><item key="slug">gene-expression-alterations-in-the-cerebellum-and</item><item key="name">Gene expression alterations in the cerebellum and granule neurons of Cstb-/- mouse are associated with early synaptic changes and inflammation</item><item key="sample_count">21</item><item key="tags"><item>cerebellum</item><item>cytoskeleton</item><item>disease</item><item>epilepsy</item><item>genome</item><item>neurodegenerative disease</item><item>progressive myoclonus epilepsy</item></item><item key="species">mouse</item><item key="is_default">False</item><item key="geo_gse_id">E-GEOD-47516</item><item key="id">7318</item><item key="factor_count">4</item></item><item><item key="slug">vpa-alleviates-neurological-deficits-and-restores</item><item key="name">VPA alleviates neurological deficits and restores gene expression in a mouse model of Rett syndrome</item><item key="sample_count">9</item><item key="tags"><item>brain</item><item>disease</item><item>epilepsy</item><item>mood disorder</item><item>rett syndrome</item><item>syndrome</item></item><item key="species">mouse</item><item key="is_default">False</item><item key="geo_gse_id">E-GEOD-56780</item><item key="id">7619</item><item key="factor_count">1</item></item></data></biogps>
