Rett syndrome: genes, synapses, circuits, and therapeutics
about
Recent advances in understanding synaptic abnormalities in Rett syndromeDevelopmental Dynamics of Rett SyndromeInsulin-Like Growth Factor 1 and Related Compounds in the Treatment of Childhood-Onset Neurodevelopmental DisordersNeurobiology of social behavior abnormalities in autism and Williams syndromeA critical and cell-autonomous role for MeCP2 in synaptic scaling upMicroglia contribute to circuit defects in Mecp2 null mice independent of microglia-specific loss of Mecp2 expressionBeyond Widespread Mecp2 Deletions to Model Rett Syndrome: Conditional Spatio-Temporal Knockout, Single-Point Mutations and Transgenic Rescue MiceFunctional recovery with recombinant human IGF1 treatment in a mouse model of Rett Syndrome.In vivo interrogation of gene function in the mammalian brain using CRISPR-Cas9Anxiety-like behavior in Rett syndrome: characteristics and assessment by anxiety scales.Functional regulation of PI3K-associated signaling in the accumbens by binge alcohol drinking in male but not female mice.Jointly reduced inhibition and excitation underlies circuit-wide changes in cortical processing in Rett syndrome.A blueprint for research on Shankopathies: a view from research on autism spectrum disorder.New experimental treatments for core social domain in autism spectrum disorders.The Role of Noncoding RNAs in Neurodevelopmental Disorders: The Case of Rett Syndrome.Altered visual cortical processing in a mouse model of MECP2 duplication syndrome.MeCP2: making sense of missense in Rett syndrome.New challenges and frontiers in the research for neuropsychiatric disorders.MeCP2 Deficiency in Neuroglia: New Progress in the Pathogenesis of Rett SyndromeCholesterol metabolism and Rett syndrome pathogenesis.Epilepsy as a Network Disorder (2): What can we learn from other network disorders such as dementia and schizophrenia, and what are the implications for translational research?Common Ribs of Inhibitory Synaptic Dysfunction in the Umbrella of Neurodevelopmental Disorders.Loss of function of MECP2 in Rett syndromeSA4503, A Potent Sigma-1 Receptor Ligand, Ameliorates Synaptic Abnormalities and Cognitive Dysfunction in a Mouse Model of ATR-X Syndrome
P2860
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P2860
Rett syndrome: genes, synapses, circuits, and therapeutics
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
Rett syndrome: genes, synapses, circuits, and therapeutics
@ast
Rett syndrome: genes, synapses, circuits, and therapeutics
@en
type
label
Rett syndrome: genes, synapses, circuits, and therapeutics
@ast
Rett syndrome: genes, synapses, circuits, and therapeutics
@en
prefLabel
Rett syndrome: genes, synapses, circuits, and therapeutics
@ast
Rett syndrome: genes, synapses, circuits, and therapeutics
@en
P2093
P2860
P356
P1476
Rett syndrome: genes, synapses, circuits, and therapeutics
@en
P2093
Abhishek Banerjee
Jorge Castro
Mriganka Sur
P2860
P356
10.3389/FPSYT.2012.00034
P577
2012-05-08T00:00:00Z