about
A delicate balance: role of MMP-9 in brain development and pathophysiology of neurodevelopmental disordersEmerging pharmacologic treatment options for fragile X syndromeMolecular underpinnings of prefrontal cortex development in rodents provide insights into the etiology of neurodevelopmental disordersFragile X syndrome as a rare disease in China - Therapeutic challenges and opportunitiesFragile X mental retardation protein regulates olfactory sensitivity but not odorant discriminationSensory processing in autism spectrum disorders and Fragile X syndrome-From the clinic to animal models.Matrix metalloproteinase-9 deletion rescues auditory evoked potential habituation deficit in a mouse model of Fragile X SyndromeSelective Disruption of Metabotropic Glutamate Receptor 5-Homer Interactions Mimics Phenotypes of Fragile X Syndrome in Mice.In vivo synaptic transmission and morphology in mouse models of Tuberous sclerosis, Fragile X syndrome, Neurofibromatosis type 1, and Costello syndromeDeletion of Fmr1 alters function and synaptic inputs in the auditory brainstem.GABA-B Agonist Baclofen Normalizes Auditory-Evoked Neural Oscillations and Behavioral Deficits in the Fmr1 Knockout Mouse Model of Fragile X Syndrome.Autism spectrum disorders: emerging mechanisms and mechanism-based treatment.Autism Spectrum Disorder (ASD) and Fragile X Syndrome (FXS): Two Overlapping Disorders Reviewed through Electroencephalography-What Can be Interpreted from the Available Information?Elevated CaMKIIα and Hyperphosphorylation of Homer Mediate Circuit Dysfunction in a Fragile X Syndrome Mouse Model.Proteomic analyses of nucleus laminaris identified candidate targets of the fragile X mental retardation protein.mTOR in Brain Physiology and Pathologies.Developmental exposure to PCBs alters the activation of the auditory cortex in response to GABAA antagonism.Tonotopic alterations in inhibitory input to the medial nucleus of the trapezoid body in a mouse model of Fragile X syndrome.Deficits in the activity of presynaptic γ-aminobutyric acid type B receptors contribute to altered neuronal excitability in fragile X syndrome.Auditory repetition suppression alterations in relation to cognitive functioning in fragile X syndrome: a combined EEG and machine learning approach.Dendritic channelopathies contribute to neocortical and sensory hyperexcitability in Fmr1(-/y) mice.Cocaine-Induced Changes in Low-Dimensional Attractors of Local Field Potentials in Optogenetic Mice.Dysfunctional Autism Risk Genes Cause Circuit-Specific Connectivity Deficits With Distinct Developmental Trajectories.The Perineuronal 'Safety' Net? Perineuronal Net Abnormalities in Neurological DisordersSensory Processing Phenotypes in Fragile X Syndrome
P2860
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P2860
description
2014 nî lūn-bûn
@nan
2014 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի փետրվարին 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
Auditory processing in fragile x syndrome.
@ast
Auditory processing in fragile x syndrome.
@en
type
label
Auditory processing in fragile x syndrome.
@ast
Auditory processing in fragile x syndrome.
@en
prefLabel
Auditory processing in fragile x syndrome.
@ast
Auditory processing in fragile x syndrome.
@en
P2860
P356
P1476
Auditory processing in fragile x syndrome.
@en
P2093
Khaleel A Razak
Sarah E Rotschafer
P2860
P356
10.3389/FNCEL.2014.00019
P577
2014-02-04T00:00:00Z