Maternal loss of Ube3a produces an excitatory/inhibitory imbalance through neuron type-specific synaptic defects.
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Mouse vision as a gateway for understanding how experience shapes neural circuitsExcitatory/Inhibitory Balance and Circuit Homeostasis in Autism Spectrum DisordersPrader-Willi, Angelman, and 15q11-q13 Duplication SyndromesAngelman Syndrome Protein Ube3a Regulates Synaptic Growth and Endocytosis by Inhibiting BMP Signaling in DrosophilaModeling a model: Mouse genetics, 22q11.2 Deletion Syndrome, and disorders of cortical circuit developmentDiscovery of Rare Mutations in Autism: Elucidating Neurodevelopmental MechanismsImpairment of TrkB-PSD-95 signaling in Angelman syndromeEssential Roles for ARID1B in Dendritic Arborization and Spine Morphology of Developing Pyramidal NeuronsA coding-independent function of an alternative Ube3a transcript during neuronal development.Stem cells and modeling of autism spectrum disorders.Behavioral deficits in an Angelman syndrome model: effects of genetic background and age.Disrupted neuronal maturation in Angelman syndrome-derived induced pluripotent stem cells.Sodium-potassium ATPase emerges as a player in hippocampal phenotypes of Angelman syndrome mice.Disruption of the LTD dialogue between the cerebellum and the cortex in Angelman syndrome model: a timing hypothesis.A fine balance: Regulation of hippocampal Arc/Arg3.1 transcription, translation and degradation in a rat model of normal cognitive aging.Gene expression patterns in the hippocampus during the development and aging of Glud1 (Glutamate Dehydrogenase 1) transgenic and wild type miceAngelman Syndrome.An Autism-Linked Mutation Disables Phosphorylation Control of UBE3A.Neurodevelopmental Underpinnings of Angelman Syndrome.Dysregulation of synaptic plasticity precedes appearance of morphological defects in a Pten conditional knockout mouse model of autism.Monogenic mouse models of autism spectrum disorders: Common mechanisms and missing links.GABAergic Neuron-Specific Loss of Ube3a Causes Angelman Syndrome-Like EEG Abnormalities and Enhances Seizure Susceptibility.Maternal Loss of Ube3a Impairs Experience-Driven Dendritic Spine Maintenance in the Developing Visual Cortex.Potential therapeutic approaches for Angelman syndrome.Impaired synaptic development in a maternal immune activation mouse model of neurodevelopmental disordersThe Angelman syndrome protein Ube3a/E6AP is required for Golgi acidification and surface protein sialylation.New Perspectives on Genomic Imprinting, an Essential and Multifaceted Mode of Epigenetic Control in the Developing and Adult Brain.Adolescent female C57BL/6 mice with vulnerability to activity-based anorexia exhibit weak inhibitory input onto hippocampal CA1 pyramidal cells.Allelic specificity of Ube3a expression in the mouse brain during postnatal development.Dysfunctional mTORC1 Signaling: A Convergent Mechanism between Syndromic and Nonsyndromic Forms of Autism Spectrum Disorder?Mechanisms underlying synaptic vulnerability and degeneration in neurodegenerative disease.Activity-dependent neuronal signalling and autism spectrum disorder.Copy-number variation in the pathogenesis of autism spectrum disorder.Convergent synaptic and circuit substrates underlying autism genetic risks.Synapse-type-specific plasticity in local circuits.Autism spectrum disorder model mice: Focus on copy number variation and epigenetics.Autism spectrum disorder: neuropathology and animal models.Neural networks with excitatory and inhibitory components: Direct and inverse problems by a mean-field approach.Autism gene Ube3a and seizures impair sociability by repressing VTA Cbln1.Decreased Axon Caliber Underlies Loss of Fiber Tract Integrity, Disproportional Reductions in White Matter Volume, and Microcephaly in Angelman Syndrome Model Mice.
P2860
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P2860
Maternal loss of Ube3a produces an excitatory/inhibitory imbalance through neuron type-specific synaptic defects.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
@zh
2012年论文
@zh-cn
name
Maternal loss of Ube3a produce ...... ype-specific synaptic defects.
@ast
Maternal loss of Ube3a produce ...... ype-specific synaptic defects.
@en
type
label
Maternal loss of Ube3a produce ...... ype-specific synaptic defects.
@ast
Maternal loss of Ube3a produce ...... ype-specific synaptic defects.
@en
prefLabel
Maternal loss of Ube3a produce ...... ype-specific synaptic defects.
@ast
Maternal loss of Ube3a produce ...... ype-specific synaptic defects.
@en
P2860
P1433
P1476
Maternal loss of Ube3a produce ...... type-specific synaptic defects
@en
P2093
Alain C Burette
Benjamin D Philpot
P2860
P304
P356
10.1016/J.NEURON.2012.03.036
P407
P577
2012-06-01T00:00:00Z