Cellular origins of auditory event-related potential deficits in Rett syndrome
about
Genes, circuits, and precision therapies for autism and related neurodevelopmental disordersLoss of promoter IV-driven BDNF expression impacts oscillatory activity during sleep, sensory information processing and fear regulation.Sensory processing in autism spectrum disorders and Fragile X syndrome-From the clinic to animal models.MECP2 regulates cortical plasticity underlying a learned behaviour in adult female miceLoss of MeCP2 in Parvalbumin-and Somatostatin-Expressing Neurons in Mice Leads to Distinct Rett Syndrome-like PhenotypesDegraded neural and behavioral processing of speech sounds in a rat model of Rett syndrome.Automatic cortical representation of auditory pitch changes in Rett syndrome.Manipulations of MeCP2 in glutamatergic neurons highlight their contributions to Rett and other neurological disordersRestoration of Mecp2 expression in GABAergic neurons is sufficient to rescue multiple disease features in a mouse model of Rett syndrome.Replicable in vivo physiological and behavioral phenotypes of the Shank3B null mutant mouse model of autism.Characterization of spatio-temporal epidural event-related potentials for mouse models of psychiatric disorders.A Role for Diminished GABA Transporter Activity in the Cortical Discharge Phenotype of MeCP2-Deficient Mice.Jointly reduced inhibition and excitation underlies circuit-wide changes in cortical processing in Rett syndrome.Development and Experimental Validation of a Dry Non-Invasive Multi-Channel Mouse Scalp EEG Sensor through Visual Evoked Potential Recordings.Cellular and Circuitry Bases of Autism: Lessons Learned from the Temporospatial Manipulation of Autism Genes in the Brain.Rett syndrome: a complex disorder with simple roots.The Oscillopathic Nature of Language Deficits in Autism: From Genes to Language Evolution.Translational use of event-related potentials to assess circuit integrity in ASD.Loss and Gain of MeCP2 Cause Similar Hippocampal Circuit Dysfunction that Is Rescued by Deep Brain Stimulation in a Rett Syndrome Mouse ModelElevating expression of MeCP2 T158M rescues DNA binding and Rett syndrome-like phenotypes.Visual evoked potentials detect cortical processing deficits in Rett syndrome.Methyl-CpG binding-protein 2 function in cholinergic neurons mediates cardiac arrhythmogenesis.Disrupted circuits in mouse models of autism spectrum disorder and intellectual disability.Gene therapy for Rett syndrome: prospects and challengesToward the Language OscillogenomeReusable Multielectrode Array Technique for Electroencephalography in Awake Freely Moving Mice
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P2860
Cellular origins of auditory event-related potential deficits in Rett syndrome
description
2014 nî lūn-bûn
@nan
2014 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Cellular origins of auditory event-related potential deficits in Rett syndrome
@ast
Cellular origins of auditory event-related potential deficits in Rett syndrome
@en
type
label
Cellular origins of auditory event-related potential deficits in Rett syndrome
@ast
Cellular origins of auditory event-related potential deficits in Rett syndrome
@en
prefLabel
Cellular origins of auditory event-related potential deficits in Rett syndrome
@ast
Cellular origins of auditory event-related potential deficits in Rett syndrome
@en
P2093
P2860
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P1433
P1476
Cellular origins of auditory event-related potential deficits in Rett syndrome
@en
P2093
Edward S Brodkin
Julie A Blendy
Zhaolan Zhou
P2860
P2888
P304
P356
10.1038/NN.3710
P407
P577
2014-04-28T00:00:00Z
P5875
P6179
1044194594