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Abnormal Expression of Cerebrospinal Fluid Cation Chloride Cotransporters in Patients with Rett Syndrome

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Oligodendrocyte Lineage Cells Contribute Unique Features to Rett Syndrome Neuropathology

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Dysregulation of BRD4 Function Underlies the Functional Abnormalities of MeCP2 Mutant Neurons

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MeCP2 Is Critical within HoxB1-Derived Tissues of Mice for Normal Lifespan

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Effects of Perinatal Exposure to Ketamine on the Developing Brain

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Disrupted circuits in mouse models of autism spectrum disorder and intellectual disability

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Perineuronal net degradation rescues CA2 plasticity in a mouse model of Rett syndrome

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Reduction of aberrant NF-κB signalling ameliorates Rett syndrome phenotypes in Mecp2-null mice

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Enhancing inhibitory synaptic function reverses spatial memory deficits in Shank2 mutant mice

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Early alterations in a mouse model of Rett syndrome: the GABA developmental shift is abolished at birth

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The Brain at High Altitude: From Molecular Signaling to Cognitive Performance

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Neuropathology and Animal Models of Autism: Genetic and Environmental Factors

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Subclinical Inflammatory Status in Rett Syndrome

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Imbalance of excitatory/inhibitory synaptic protein expression in iPSC-derived neurons from FOXG1+/− patients and in foxg1+/− mice

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Exclusive expression of MeCP2 in the nervous system distinguishes between brain and peripheral Rett syndrome-like phenotypes

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Forniceal deep brain stimulation induces gene expression and splicing changes that promote neurogenesis and plasticity

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GABAergic dysfunction mediates autism-like stereotypies and Rett syndrome phenotypes

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Restoration of Mecp2 expression in GABAergic neurons is sufficient to rescue multiple disease features in a mouse model of Rett syndrome

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Defective GABAergic neurotransmission in the nucleus tractus solitarius in Mecp2-null mice, a model of Rett syndrome

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GABA and Glutamate Pathways Are Spatially and Developmentally Affected in the Brain of Mecp2-Deficient Mice

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Early Defects of GABAergic Synapses in the Brain Stem of a MeCP2 Mouse Model of Rett Syndrome

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