Mouse genetic models for prepulse inhibition: an early review
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Mouse neurexin-1alpha deletion causes correlated electrophysiological and behavioral changes consistent with cognitive impairments.Generation and characterization of Rgs4 mutant miceBehavioral and regulatory abnormalities in mice deficient in the NPAS1 and NPAS3 transcription factors.The mGluR2/3 agonist LY379268 blocks the effects of GLT-1 upregulation on prepulse inhibition of the startle reflex in adult rats.Phosphodiesterase 4 inhibition enhances the dopamine D1 receptor/PKA/DARPP-32 signaling cascade in frontal cortex.Realistic expectations of prepulse inhibition in translational models for schizophrenia research.RIM1alpha and interacting proteins involved in presynaptic plasticity mediate prepulse inhibition and additional behaviors linked to schizophreniaRefinement of Experimental Design and Conduct in Laboratory Animal ResearchTspyl2 Loss-of-Function Causes Neurodevelopmental Brain and Behavior Abnormalities in Mice.Investigating the underlying mechanisms of aberrant behaviors in bipolar disorder from patients to models: Rodent and human studies.Expanded characterization of the social interaction abnormalities in mice lacking Dvl1Altered 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 microgliaGPR55, a G-protein coupled receptor for lysophosphatidylinositol, plays a role in motor coordination.A partial loss of function allele of methyl-CpG-binding protein 2 predicts a human neurodevelopmental syndromeTbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndromeModulation of the Ca2+ conductance of nicotinic acetylcholine receptors by Lypd6.The melanin-concentrating hormone (MCH) system modulates behaviors associated with psychiatric disorders.Adolescent but not adult ethanol binge drinking modulates cocaine withdrawal symptoms in miceMouse Model of Neurological Complications Resulting from Encephalitic Alphavirus Infection.Modeling bipolar disorder in mice by increasing acetylcholine or dopamine: chronic lithium treats most, but not all features.Effects of prenatal hypoxia on schizophrenia-related phenotypes in heterozygous reeler mice: a gene × environment interaction study.Both the COMT Val158Met single-nucleotide polymorphism and sex-dependent differences influence response inhibition.Animal Models of Psychosis: Current State and Future Directions.Neural circuits containing olfactory neurons are involved in the prepulse inhibition of the startle reflex in rats.Prenatal antidepressant exposure: clinical and preclinical findings.Long-term consequences of perinatal fatty acid amino hydrolase inhibition.Distinct behavioral consequences of short-term and prolonged GABAergic depletion in prefrontal cortex and dorsal hippocampus.Animal models and measures of perceptual processing in schizophrenia.Research resource: loss of the steroid receptor coactivators confers neurobehavioral consequences.Modulation of behavioral networks by selective interneuronal inactivation.Chronic anabolic androgenic steroid exposure alters corticotropin releasing factor expression and anxiety-like behaviors in the female mouseFurther evidence for ClockΔ19 mice as a model for bipolar disorder mania using cross-species tests of exploration and sensorimotor gating.Neural correlates of sensorimotor gating: a metabolic positron emission tomography study in awake rats.The GluK4 kainate receptor subunit regulates memory, mood, and excitotoxic neurodegeneration.Modulation of prepulse inhibition through both M(1) and M (4) muscarinic receptors in miceDiet-induced hyperhomocysteinemia increases amyloid-beta formation and deposition in a mouse model of Alzheimer's disease.Nicotinic mechanisms in the treatment of psychotic disorders: a focus on the α7 nicotinic receptorPrepulse inhibition in patients with fragile X-associated tremor ataxia syndrome.Behavioural and functional characterization of Kv10.1 (Eag1) knockout miceA novel mouse model of Niemann-Pick type C disease carrying a D1005G-Npc1 mutation comparable to commonly observed human mutations.
P2860
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P2860
Mouse genetic models for prepulse inhibition: an early review
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2002 nî lūn-bûn
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2002 թուականին հրատարակուած գիտական յօդուած
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2002 թվականին հրատարակված գիտական հոդված
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2002年の論文
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2002年論文
@yue
2002年論文
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2002年論文
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2002年論文
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2002年論文
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2002年论文
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name
Mouse genetic models for prepulse inhibition: an early review
@ast
Mouse genetic models for prepulse inhibition: an early review
@en
Mouse genetic models for prepulse inhibition: an early review
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type
label
Mouse genetic models for prepulse inhibition: an early review
@ast
Mouse genetic models for prepulse inhibition: an early review
@en
Mouse genetic models for prepulse inhibition: an early review
@nl
prefLabel
Mouse genetic models for prepulse inhibition: an early review
@ast
Mouse genetic models for prepulse inhibition: an early review
@en
Mouse genetic models for prepulse inhibition: an early review
@nl
P2093
P2860
P356
P1433
P1476
Mouse genetic models for prepulse inhibition: an early review
@en
P2093
P2860
P2888
P304
P356
10.1038/SJ.MP.4001159
P407
P577
2002-01-01T00:00:00Z