GABAergic Neuron-Specific Loss of Ube3a Causes Angelman Syndrome-Like EEG Abnormalities and Enhances Seizure Susceptibility.
about
Delta rhythmicity is a reliable EEG biomarker in Angelman syndrome: a parallel mouse and human analysis.Dynamic changes in murine forebrain miR-211 expression associate with cholinergic imbalances and epileptiform activity.A Quantitative Electrophysiological Biomarker of Duplication 15q11.2-q13.1 Syndrome.A case of Pitt-Hopkins syndrome presented with Angelman-like syndromic phenotypesMiR-218 targets MeCP2 and inhibits heroin seeking behaviorStrain-dependence of the Angelman Syndrome phenotypes in Ube3a maternal deficiency mice.Early Origin and Evolution of the Angelman Syndrome Ubiquitin Ligase Gene Ube3a.Neurobiological bases of autism-epilepsy comorbidity: a focus on excitation/inhibition imbalance.Models and detection of spontaneous recurrent seizures in laboratory rodents.Sleep Disorders in Childhood Neurogenetic Disorders.Decreased Axon Caliber Underlies Loss of Fiber Tract Integrity, Disproportional Reductions in White Matter Volume, and Microcephaly in Angelman Syndrome Model Mice.Neuronal overexpression of Ube3a isoform 2 causes behavioral impairments and neuroanatomical pathology relevant to 15q11.2-q13.3 duplication syndrome.Enhanced Nociception in Angelman Syndrome Model Mice.Enhanced Transmission at the Calyx of Held Synapse in a Mouse Model for Angelman Syndrome.Inhibitory control of the excitatory/inhibitory balance in psychiatric disorders.Parvalbumin fast-spiking interneurons are selectively altered by pediatric traumatic brain injury.Enhanced operant extinction and prefrontal excitability in a mouse model of Angelman syndrome.Ube3a loss increases excitability and blunts orientation tuning in the visual cortex of Angelman syndrome model mice.Taurine Administration Recovers Motor and Learning Deficits in an Angelman Syndrome Mouse Model.Uncovering True Cellular Phenotypes: Using Induced Pluripotent Stem Cell-Derived Neurons to Study Early Insults in Neurodevelopmental Disorders.Common Ribs of Inhibitory Synaptic Dysfunction in the Umbrella of Neurodevelopmental Disorders.Lovastatin suppresses hyperexcitability and seizure in Angelman syndrome model.Differential 3' Processing of Specific Transcripts Expands Regulatory and Protein Diversity Across Neuronal Cell Types.Subcellular organization of UBE3A in human cerebral cortex
P2860
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P2860
GABAergic Neuron-Specific Loss of Ube3a Causes Angelman Syndrome-Like EEG Abnormalities and Enhances Seizure Susceptibility.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
GABAergic Neuron-Specific Loss ...... hances Seizure Susceptibility.
@ast
GABAergic Neuron-Specific Loss ...... hances Seizure Susceptibility.
@en
type
label
GABAergic Neuron-Specific Loss ...... hances Seizure Susceptibility.
@ast
GABAergic Neuron-Specific Loss ...... hances Seizure Susceptibility.
@en
prefLabel
GABAergic Neuron-Specific Loss ...... hances Seizure Susceptibility.
@ast
GABAergic Neuron-Specific Loss ...... hances Seizure Susceptibility.
@en
P2093
P2860
P50
P1433
P1476
GABAergic Neuron-Specific Loss ...... hances Seizure Susceptibility.
@en
P2093
Alain C Burette
Benjamin D Philpot
Geeske M van Woerden
Ji Eun Han
Mark J Zylka
Matthew C Judson
Michael S Sidorov
P2860
P356
10.1016/J.NEURON.2016.02.040
P407
P577
2016-03-22T00:00:00Z