Search results for "GABAERGIC INTERNEURON"

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An update to Hippocampome.org by integrating single-cell phenotypes with circuit function in vivo.

2021

Understanding brain operation demands linking basic behavioral traits to cell-type specific dynamics of different brain-wide subcircuits. This requires a system to classify the basic operational modes of neurons and circuits. Single-cell phenotyping of firing behavior during ongoing oscillations in vivo has provided a large body of evidence on entorhinal–hippocampal function, but data are dispersed and diverse. Here, we mined literature to search for information regarding the phase-timing dynamics of over 100 hippocampal/entorhinal neuron types defined in Hippocampome.org. We identified missing and unresolved pieces of knowledge (e.g., the preferred theta phase for a specific neuron type) a…

DYNAMICSGABAERGIC INTERNEURONPhysiologyAction PotentialsSocial SciencesHippocampal formationHippocampusNeuron typesBehavioral traitsMice0302 clinical medicineAnimal CellsMedicine and Health SciencesEntorhinal CortexPsychologyNETWORKBiology (General)Function (engineering)media_commonNeurons0303 health sciencesPHYSIOLOGICAL-PROPERTIESGeneral NeurosciencePyramidal CellsMethods and ResourcesBrainPhenotypeMOSSY CELLS3. Good healthElectrophysiologyPhenotypeAnatomyCellular TypesGeneral Agricultural and Biological SciencesGanglion CellsHeuristic (computer science)QH301-705.5media_common.quotation_subjectNeurophysiologyBiologyMembrane PotentialGeneral Biochemistry Genetics and Molecular Biology03 medical and health sciencesAnimalsin vivo -menetelmähippokampus030304 developmental biologyBehaviorNeuron typeGeneral Immunology and MicrobiologyGranule CellsTHETA OSCILLATIONShermoverkot (biologia)Biology and Life SciencesCell BiologyNeuronal DendritesSILICON PROBESRatshermosolutBrain stateCellular Neuroscience1182 Biochemistry cell and molecular biologyfenotyyppi3111 BiomedicineNeuroscience030217 neurology & neurosurgeryNeurosciencePLoS biology
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Age-dependent epileptic encephalopathy associated with an unusual co-occurrence of ZEB2 and SCN1A variants.

2020

Mowat-Wilson syndrome is a genetic disorder associated with a variable phenotype including peculiar facial features associated with intellectual disability, epilepsy, language impairment, and multiple congenital anomalies caused by heterozygous mutation of the ZEB2 gene. The ZEB2 protein is a complex transcription factor that encompasses multiple functional domains that interact with the regulatory regions of target genes including those involved in brain development. Recently, it has been documented that ZEB2 regulates the differentiation of interneuron progenitors migrating from the medial ganglionic eminence to cortical layers by repression of the Nkx2-1 homeobox transcription factor. It…

ZEB2genotype-phenotype correlationSettore MED/38 - Pediatria Generale E SpecialisticaSettore M-PSI/08 - Psicologia ClinicaIntellectual DisabilityHumansMowat-Wilson syndromeEEGgenotype-phenotype correlationSCN1AHirschsprung DiseaseEEGChildGenetic Association StudiesZEB2Zinc Finger E-box Binding Homeobox 2EpilepsyEEG; epilepsy; GABAergic interneurons; genotype-phenotype correlation; Mowat-Wilson syndrome; SCN1A; ZEB2FaciesElectroencephalographySettore MED/39 - Neuropsichiatria InfantileGABAergic interneuronsMowat-Wilson syndromeepilepsyNAV1.1 Voltage-Gated Sodium ChannelGABAergic interneuronsMicrocephalySettore MED/26 - NeurologiaFemaleEpileptic disorders : international epilepsy journal with videotape
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