about
Genetic-background modulation of core and variable autistic-like symptoms in Fmr1 knock-out mice.Mouse neurexin-1alpha deletion causes correlated electrophysiological and behavioral changes consistent with cognitive impairments.Maternal immune activation alters fetal brain development through interleukin-6.Phospholipase C-β1 Hypofunction in the Pathogenesis of Schizophrenia.Therapeutic Targets for Neurodevelopmental Disorders Emerging from Animal Models with Perinatal Immune ActivationImpact of prenatal environmental stress on cortical developmentMice with deficient BK channel function show impaired prepulse inhibition and spatial learning, but normal working and spatial reference memory.Speech training alters consonant and vowel responses in multiple auditory cortex fields.Heterozygous deletion of α-neurexin I or α-neurexin II results in behaviors relevant to autism and schizophrenia.The Intense World Theory – A Unifying Theory of the Neurobiology of AutismNeuroinflammation in Autism: Plausible Role of Maternal Inflammation, Dietary Omega 3, and MicrobiotaDeletion of α-neurexin II results in autism-related behaviors in miceAltered cerebellar development in nuclear receptor TAK1/ TR4 null mice is associated with deficits in GLAST(+) glia, alterations in social behavior, motor learning, startle reactivity, and microgliaHaploinsufficiency for Pten and Serotonin transporter cooperatively influences brain size and social behavior.The disruption of Celf6, a gene identified by translational profiling of serotonergic neurons, results in autism-related behaviors.Relationships among parvalbumin-immunoreactive neuron density, phase-locked gamma oscillations, and autistic/schizophrenic symptoms in PDGFR-β knock-out and control miceSociability and motor functions in Shank1 mutant miceEvaluation of Pax6 mutant rat as a model for autism.Microbiota modulate behavioral and physiological abnormalities associated with neurodevelopmental disorders.Sensory processing in autism spectrum disorders and Fragile X syndrome-From the clinic to animal models.Behavioural abnormalities in a novel mouse model for Silver Russell Syndrome.Fast Detector/First Responder: Interactions between the Superior Colliculus-Pulvinar Pathway and Stimuli Relevant to Primates.Effects of Neonatal Dexamethasone Exposure on Adult Neuropsychiatric Traits in Rats.Validating γ oscillations and delayed auditory responses as translational biomarkers of autismIntegration of genome-wide association and extant brain expression QTL identifies candidate genes influencing prepulse inhibition in inbred F1 mice.Repetitive grooming and sensorimotor abnormalities in an ephrin-A knockout model for Autism Spectrum DisordersTargeting Glia with N-Acetylcysteine Modulates Brain Glutamate and Behaviors Relevant to Neurodevelopmental Disorders in C57BL/6J Mice.Disruption of mGluR5 in parvalbumin-positive interneurons induces core features of neurodevelopmental disorders.Altered object-in-place recognition memory, prepulse inhibition, and locomotor activity in the offspring of rats exposed to a viral mimetic during pregnancyBrain-specific Foxp1 deletion impairs neuronal development and causes autistic-like behaviour.Repetitive behavior profile and supersensitivity to amphetamine in the C58/J mouse model of autism.Nicotine effect on prepulse inhibition and prepulse facilitation in schizophrenia patientsFunctional characterization of FABP3, 5 and 7 gene variants identified in schizophrenia and autism spectrum disorder and mouse behavioral studiesThe effects of oxytocin and its analog, carbetocin, on genetic deficits in sensorimotor gating.Pre-pulse inhibition and antisaccade performance indicate impaired attention modulation of cognitive inhibition in 22q11.2 deletion syndrome (22q11DS).Children with autism spectrum disorders show abnormal conditioned response timing on delay, but not trace, eyeblink conditioning.Sociocommunicative and sensorimotor impairments in male P2X4-deficient mice.Developmental delays and reduced pup ultrasonic vocalizations but normal sociability in mice lacking the postsynaptic cell adhesion protein neuroligin2.Fragile X: leading the way for targeted treatments in autism.Hyperreactivity to weak acoustic stimuli and prolonged acoustic startle latency in children with autism spectrum disorders.
P2860
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P2860
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年学术文章
@wuu
2006年学术文章
@zh
2006年学术文章
@zh-cn
2006年学术文章
@zh-hans
2006年学术文章
@zh-my
2006年学术文章
@zh-sg
2006年學術文章
@yue
2006年學術文章
@zh-hant
name
Sensorimotor gating deficits in adults with autism.
@en
Sensorimotor gating deficits in adults with autism.
@nl
type
label
Sensorimotor gating deficits in adults with autism.
@en
Sensorimotor gating deficits in adults with autism.
@nl
prefLabel
Sensorimotor gating deficits in adults with autism.
@en
Sensorimotor gating deficits in adults with autism.
@nl
P2093
P1476
Sensorimotor gating deficits in adults with autism.
@en
P2093
Alan Lincoln
Arpi Minassian
Brian Lopez
Leeza Maron
William Perry
P304
P356
10.1016/J.BIOPSYCH.2005.09.025
P407
P577
2006-02-07T00:00:00Z