Early defects of GABAergic synapses in the brain stem of a MeCP2 mouse model of Rett syndrome.
about
Pathophysiology of locus ceruleus neurons in a mouse model of Rett syndromeEmerging pharmacotherapies for neurodevelopmental disordersMECP2 disorders: from the clinic to mice and backPrenatal stress and inhibitory neuron systems: implications for neuropsychiatric disordersMolecular underpinnings of prefrontal cortex development in rodents provide insights into the etiology of neurodevelopmental disordersGABAergic signaling as therapeutic target for autism spectrum disordersTargeted pharmacological treatment of autism spectrum disorders: fragile X and Rett syndromesGABA and glutamate pathways are spatially and developmentally affected in the brain of Mecp2-deficient miceThe Intense World Theory – A Unifying Theory of the Neurobiology of AutismCommon mechanisms of excitatory and inhibitory imbalance in schizophrenia and autism spectrum disordersDysfunction in GABA signalling mediates autism-like stereotypies and Rett syndrome phenotypesMicroglia contribute to circuit defects in Mecp2 null mice independent of microglia-specific loss of Mecp2 expressionDegraded neural and behavioral processing of speech sounds in a rat model of Rett syndrome.Phosphorylation of MeCP2 at Serine 80 regulates its chromatin association and neurological function.Investigating mechanisms underlying neurodevelopmental phenotypes of autistic and intellectual disability disorders: a perspective.Brain activity mapping in Mecp2 mutant mice reveals functional deficits in forebrain circuits, including key nodes in the default mode network, that are reversed with ketamine treatment.Defective GABAergic neurotransmission and pharmacological rescue of neuronal hyperexcitability in the amygdala in a mouse model of fragile X syndromeMorphological and functional reversal of phenotypes in a mouse model of Rett syndrome.Preclinical research in Rett syndrome: setting the foundation for translational success.Twenty-four hour quantitative-EEG and in-vivo glutamate biosensor detects activity and circadian rhythm dependent biomarkers of pathogenesis in Mecp2 null mice.mGlu5 positive allosteric modulation normalizes synaptic plasticity defects and motor phenotypes in a mouse model of Rett syndromeMeCP2 is required for activity-dependent refinement of olfactory circuits.Modulation of GABAergic transmission in development and neurodevelopmental disorders: investigating physiology and pathology to gain therapeutic perspectives.The neural circuit basis of Rett syndromeMeCP2 is required for normal development of GABAergic circuits in the thalamus.Temporal and regional alterations in NMDA receptor expression in Mecp2-null mice.Neuronal MHC class I molecules are involved in excitatory synaptic transmission at the hippocampal mossy fiber synapses of marmoset monkeys.DNA methylation reader MECP2: cell type- and differentiation stage-specific protein distribution.Neural stem cell regulation, fibroblast growth factors, and the developmental origins of neuropsychiatric disorders.Neuronal activity-regulated gene transcription in synapse development and cognitive function.GluD1 is a common altered player in neuronal differentiation from both MECP2-mutated and CDKL5-mutated iPS cells.Correction of respiratory disorders in a mouse model of Rett syndrome.Respiratory rhythm generation in vivo.Experimental models of Rett syndrome based on Mecp2 dysfunction.Synaptic determinants of rett syndrome.Abnormal expression of cerebrospinal fluid cation chloride cotransporters in patients with Rett syndromeExcitation/inhibition imbalance and impaired synaptic inhibition in hippocampal area CA3 of Mecp2 knockout miceIntrauterine inflammation, insufficient to induce parturition, still evokes fetal and neonatal brain injuryNetwork models predict that reduced excitatory fluctuations can give rise to hippocampal network hyper-excitability in MeCP2-null miceAutism: a "critical period" disorder?
P2860
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P2860
Early defects of GABAergic synapses in the brain stem of a MeCP2 mouse model of Rett syndrome.
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
2007年论文
@zh
2007年论文
@zh-cn
name
Early defects of GABAergic syn ...... mouse model of Rett syndrome.
@en
type
label
Early defects of GABAergic syn ...... mouse model of Rett syndrome.
@en
prefLabel
Early defects of GABAergic syn ...... mouse model of Rett syndrome.
@en
P2093
P2860
P356
P1476
Early defects of GABAergic syn ...... 2 mouse model of Rett syndrome
@en
P2093
P2860
P304
P356
10.1152/JN.00826.2007
P407
P577
2007-11-21T00:00:00Z