Loss of MeCP2 in Parvalbumin-and Somatostatin-Expressing Neurons in Mice Leads to Distinct Rett Syndrome-like Phenotypes
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Developmental Dynamics of Rett SyndromeMicroglia contribute to circuit defects in Mecp2 null mice independent of microglia-specific loss of Mecp2 expressionMECP2 regulates cortical plasticity underlying a learned behaviour in adult female miceManipulations 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.Neuroanatomy in mouse models of Rett syndrome is related to the severity of Mecp2 mutation and behavioral phenotypes.Longitudinal course of epilepsy in Rett syndrome and related disorders.GABAergic Neuron-Specific Loss of Ube3a Causes Angelman Syndrome-Like EEG Abnormalities and Enhances Seizure Susceptibility.GABAergic Interneurons in the Neocortex: From Cellular Properties to Circuits.GlyT2-Dependent Preservation of MECP2-Expression in Inhibitory Neurons Improves Early Respiratory Symptoms but Does Not Rescue Survival in a Mouse Model of Rett Syndrome.Jointly reduced inhibition and excitation underlies circuit-wide changes in cortical processing in Rett syndrome.Stress and the Emerging Roles of Chromatin Remodeling in Signal Integration and Stable Transmission of Reversible Phenotypes.Cellular and Circuitry Bases of Autism: Lessons Learned from the Temporospatial Manipulation of Autism Genes in the Brain.Decreased parvalbumin mRNA levels in cerebellar Purkinje cells in autism.MeCP2-regulated miRNAs control early human neurogenesis through differential effects on ERK and AKT signaling.Targeted Interneuron Depletion in the Dorsal Striatum Produces Autism-like Behavioral Abnormalities in Male but Not Female Mice.Lessons learned from studying syndromic autism spectrum disorders.The Role of Interneurons in Autism and Tourette Syndrome.Basal ganglia and autism - a translational perspective.Male and Female Mice Lacking Neuroligin-3 Modify the Behavior of Their Wild-Type Littermates.Molecular and Neural Functions of Rai1, the Causal Gene for Smith-Magenis Syndrome.Functions and dysfunctions of neocortical inhibitory neuron subtypes.Inhibitory control of the excitatory/inhibitory balance in psychiatric disorders.Rett syndrome: a neurological disorder with metabolic components.Common Ribs of Inhibitory Synaptic Dysfunction in the Umbrella of Neurodevelopmental Disorders.Depleting Trim28 in adult mice is well tolerated and reduces levels of α-synuclein and tau.Loss of MECP2 Leads to Activation of P53 and Neuronal Senescence.Shank2 Deletion in Parvalbumin Neurons Leads to Moderate Hyperactivity, Enhanced Self-Grooming and Suppressed Seizure Susceptibility in Mice.Social Stimulus Causes Aberrant Activation of the Medial Prefrontal Cortex in a Mouse Model With Autism-Like BehaviorsLoss of Causes Atypical Synaptic and Molecular Plasticity of Parvalbumin-Expressing Interneurons Reflecting Rett Syndrome-Like Sensorimotor DefectsThe Neuroprotective Effects of 17β-Estradiol Pretreatment in a Model of Neonatal Hippocampal Injury Induced by Trimethyltin
P2860
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P2860
Loss of MeCP2 in Parvalbumin-and Somatostatin-Expressing Neurons in Mice Leads to Distinct Rett Syndrome-like Phenotypes
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2015 nî lūn-bûn
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2015 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2015 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
name
Loss of MeCP2 in Parvalbumin-a ...... Rett Syndrome-like Phenotypes
@ast
Loss of MeCP2 in Parvalbumin-a ...... Rett Syndrome-like Phenotypes
@en
type
label
Loss of MeCP2 in Parvalbumin-a ...... Rett Syndrome-like Phenotypes
@ast
Loss of MeCP2 in Parvalbumin-a ...... Rett Syndrome-like Phenotypes
@en
prefLabel
Loss of MeCP2 in Parvalbumin-a ...... Rett Syndrome-like Phenotypes
@ast
Loss of MeCP2 in Parvalbumin-a ...... Rett Syndrome-like Phenotypes
@en
P2093
P2860
P1433
P1476
Loss of MeCP2 in Parvalbumin-a ...... Rett Syndrome-like Phenotypes
@en
P2093
Hongmei Chen
John W Swann
Kerstin Ure
P2860
P304
P356
10.1016/J.NEURON.2015.10.029
P407
P577
2015-11-01T00:00:00Z