Alterations of gene expression and glutamate clearance in astrocytes derived from an MeCP2-null mouse model of Rett syndrome
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Recent advances in understanding synaptic abnormalities in Rett syndromeAdvancements in the Underlying Pathogenesis of Schizophrenia: Implications of DNA Methylation in Glial CellsGABA and glutamate pathways are spatially and developmentally affected in the brain of Mecp2-deficient miceGlia, sympathetic activity and cardiovascular diseaseThe Use of Induced Pluripotent Stem Cell Technology to Advance Autism Research and TreatmentUnexpected cellular players in Rett syndrome pathologyBeyond Widespread Mecp2 Deletions to Model Rett Syndrome: Conditional Spatio-Temporal Knockout, Single-Point Mutations and Transgenic Rescue MiceAltered microtubule dynamics and vesicular transport in mouse and human MeCP2-deficient astrocytes.Astrocyte-specific regulation of hMeCP2 expression in Drosophila.Brain region-specific expression of MeCP2 isoforms correlates with DNA methylation within Mecp2 regulatory elements.Differentiation of multipotent neural stem cells derived from Rett syndrome patients is biased toward the astrocytic lineageImpaired CO2 sensitivity of astrocytes in a mouse model of Rett syndrome.Prefrontal lactate predicts exercise-induced cognitive dysfunction in Gulf War Illness.Functional evaluation of autism-associated mutations in NHE9.Recent Progress in Rett Syndrome and MeCP2 Dysfunction: Assessment of Potential Treatment OptionsSubclinical inflammatory status in Rett syndrome.Regulation of mRNA splicing by MeCP2 via epigenetic modifications in the brain.Developmental maturation of astrocytes and pathogenesis of neurodevelopmental disorders.Rett syndrome and MeCP2.Neuroinflammation in the pathogenesis of Alzheimer's disease. A rational framework for the search of novel therapeutic approaches.Astrocyte Transcriptome from the Mecp2(308)-Truncated Mouse Model of Rett Syndrome.Role of astrocyte-synapse interactions in CNS disorders.Transcriptional Regulation of Glutamate Transporters: From Extracellular Signals to Transcription Factors.Human astrocytes in the diseased brain.Deficiency of GABAergic synaptic inhibition in the Kölliker-Fuse area underlies respiratory dysrhythmia in a mouse model of Rett syndrome.Dysregulation of glutamine transporter SNAT1 in Rett syndrome microglia: a mechanism for mitochondrial dysfunction and neurotoxicity.MeCP2 Deficiency in Neuroglia: New Progress in the Pathogenesis of Rett SyndromeAstrocytic modulation of excitatory synaptic signaling in a mouse model of Rett syndrome.Brain metabolic sensing and metabolic signaling at the level of an astrocyte.MeCP2 Deficiency Leads to Loss of Glial Kir4.1.Mechanism and consequence of abnormal calcium homeostasis in Rett syndrome astrocytes.Transcriptome level analysis in Rett syndrome using human samples from different tissues.Regenerative glutamate release in the hippocampus of Rett syndrome model mice
P2860
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P2860
Alterations of gene expression and glutamate clearance in astrocytes derived from an MeCP2-null mouse model of Rett syndrome
description
2012 nî lūn-bûn
@nan
2012 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
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
name
Alterations of gene expression ...... l mouse model of Rett syndrome
@ast
Alterations of gene expression ...... l mouse model of Rett syndrome
@en
Alterations of gene expression ...... l mouse model of Rett syndrome
@nl
type
label
Alterations of gene expression ...... l mouse model of Rett syndrome
@ast
Alterations of gene expression ...... l mouse model of Rett syndrome
@en
Alterations of gene expression ...... l mouse model of Rett syndrome
@nl
prefLabel
Alterations of gene expression ...... l mouse model of Rett syndrome
@ast
Alterations of gene expression ...... l mouse model of Rett syndrome
@en
Alterations of gene expression ...... l mouse model of Rett syndrome
@nl
P2093
P2860
P1433
P1476
Alterations of gene expression ...... l mouse model of Rett syndrome
@en
P2093
Chiaki Mitsumasu
Eiichiro Tanaka
Ken-ichiro Kosai
Tomoyuki Takahashi
Toyojiro Matsuishi
Yasunori Okabe
P2860
P304
P356
10.1371/JOURNAL.PONE.0035354
P407
P577
2012-04-20T00:00:00Z