Alterations in microRNA-124 and AMPA receptors contribute to social behavioral deficits in frontotemporal dementia.
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The Use of Stem Cells to Model Amyotrophic Lateral Sclerosis and Frontotemporal Dementia: From Basic Research to Regenerative MedicineFrontotemporal Lobar Degeneration and MicroRNAsEarly microgliosis precedes neuronal loss and behavioural impairment in mice with a frontotemporal dementia-causing CHMP2B mutationThe Activity-Induced Long Non-Coding RNA Meg3 Modulates AMPA Receptor Surface Expression in Primary Cortical Neurons.Rab8, POSH, and TAK1 regulate synaptic growth in a Drosophila model of frontotemporal dementiaFunction and evolution of microRNAs in eusocial Hymenoptera.Probing disorders of the nervous system using reprogramming approaches.Distinct cognitive effects and underlying transcriptome changes upon inhibition of individual miRNAs in hippocampal neurons.FTD/ALS-associated poly(GR) protein impairs the Notch pathway and is recruited by poly(GA) into cytoplasmic inclusionsFrontotemporal dementia caused by CHMP2B mutation is characterised by neuronal lysosomal storage pathology.Dysregulated miRNA biogenesis downstream of cellular stress and ALS-causing mutations: a new mechanism for ALS.TMEM106B, a frontotemporal lobar dementia (FTLD) modifier, associates with FTD-3-linked CHMP2B, a complex of ESCRT-III.MicroRNA miR124 is required for the expression of homeostatic synaptic plasticity.α-Synuclein interferes with the ESCRT-III complex contributing to the pathogenesis of Lewy body disease.Early Cognitive/Social Deficits and Late Motor Phenotype in Conditional Wild-Type TDP-43 Transgenic Mice.miR-124, -128, and -137 Orchestrate Neural Differentiation by Acting on Overlapping Gene Sets Containing a Highly Connected Transcription Factor Network.GluA4 Dependent Plasticity Mechanisms Contribute to Developmental Synchronization of the CA3-CA1 Circuitry in the Hippocampus.Modeling the C9ORF72 repeat expansion mutation using human induced pluripotent stem cells.The role of CHMP2BIntron5 in autophagy and frontotemporal dementia.ALS and FTD: an epigenetic perspective.Review: Induced pluripotent stem cell models of frontotemporal dementia.Validation of microRNAs in Cerebrospinal Fluid as Biomarkers for Different Forms of Dementia in a Multicenter Study.A transgenic mouse expressing CHMP2Bintron5 mutant in neurons develops histological and behavioural features of amyotrophic lateral sclerosis and frontotemporal dementia.Progranulin haploinsufficiency causes biphasic social dominance abnormalities in the tube test.Anti-AMPA GluA3 antibodies in Frontotemporal dementia: a new molecular target.Dendritic Homeostasis Disruption in a Novel Frontotemporal Dementia Mouse Model Expressing Cytoplasmic Fused in Sarcoma.Cocaine-mediated downregulation of microglial miR-124 expression involves promoter DNA methylation.Neurotransmitter Switching Regulated by miRNAs Controls Changes in Social Preference.Neurotransmitter deficits from frontotemporal lobar degeneration.C9ORF72 repeat expansion causes vulnerability of motor neurons to Ca2+-permeable AMPA receptor-mediated excitotoxicity.Association of social defeat stress-induced anhedonia-like symptoms with mGluR1-dependent decrease in membrane-bound AMPA-GluR1 in the mouse ventral midbrain.Dysregulated molecular pathways in amyotrophic lateral sclerosis-frontotemporal dementia spectrum disorder.Dysregulation of Cortical Neuron DNA Methylation Profile in Autism Spectrum Disorder.Identification of MicroRNA-124-3p as a Putative Epigenetic Signature of Major Depressive Disorder.Dlgap1 knockout mice exhibit alterations of the postsynaptic density and selective reductions in sociability.Cocaine-Mediated Downregulation of miR-124 Activates Microglia by Targeting KLF4 and TLR4 Signaling.Synaptic dysfunction and altered excitability in C9ORF72 ALS/FTD.Epigenetic Mechanisms of Gene Regulation in Amyotrophic Lateral Sclerosis.miR-124 Contributes to the functional maturity of microglia.Molecular Genetics of Frontotemporal Dementia Elucidated by Drosophila Models-Defects in Endosomal⁻Lysosomal Pathway.
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Alterations in microRNA-124 and AMPA receptors contribute to social behavioral deficits in frontotemporal dementia.
description
2014 nî lūn-bûn
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2014 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Alterations in microRNA-124 an ...... ts in frontotemporal dementia.
@ast
Alterations in microRNA-124 an ...... ts in frontotemporal dementia.
@en
Alterations in microRNA-124 an ...... ts in frontotemporal dementia.
@nl
type
label
Alterations in microRNA-124 an ...... ts in frontotemporal dementia.
@ast
Alterations in microRNA-124 an ...... ts in frontotemporal dementia.
@en
Alterations in microRNA-124 an ...... ts in frontotemporal dementia.
@nl
prefLabel
Alterations in microRNA-124 an ...... ts in frontotemporal dementia.
@ast
Alterations in microRNA-124 an ...... ts in frontotemporal dementia.
@en
Alterations in microRNA-124 an ...... ts in frontotemporal dementia.
@nl
P2093
P2860
P50
P356
P1433
P1476
Alterations in microRNA-124 an ...... its in frontotemporal dementia
@en
P2093
Danqiong Sun
Dennis W Dickson
Fen-Biao Gao
Hongru Zhou
Hongyu Ruan
Jamie M Verheyden
Kelleen Lynch
Leonard Petrucelli
Sandra Almeida
P2860
P2888
P304
P356
10.1038/NM.3717
P407
P577
2014-11-17T00:00:00Z