Search Results - "Bui, Nghiem"
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Marble burying reflects a repetitive and perseverative behavior more than novelty-induced anxiety
Published in Psychopharmacologia (01-06-2009)“…Rationale An increasing number of investigators utilize the marble-burying assay despite the paucity of information available regarding what underlies the…”
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Group I metabotropic glutamate receptor antagonists alter select behaviors in a mouse model for fragile X syndrome
Published in Psychopharmacologia (01-01-2012)“…Rationale Studies in the Fmr1 knockout (KO) mouse, a model of fragile X syndrome (FXS), suggest that excessive signaling through group I metabotropic glutamate…”
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Genetic reduction of group 1 metabotropic glutamate receptors alters select behaviors in a mouse model for fragile X syndrome
Published in Behavioural brain research (01-10-2011)“…► mGluR1 genetic reduction decreased Fmr1 KO locomotor activity. ► mGluR5 genetic reduction alters KO analgesic responses and active social behavior. ►…”
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Modulation of behavioral phenotypes by a muscarinic M1 antagonist in a mouse model of fragile X syndrome
Published in Psychopharmacology (01-09-2011)“…Rationale Muscarinic acetylcholine receptors (mAChR) are G protein-coupled receptors, widely expressed in the CNS. Electrophysiological and molecular studies…”
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The Modulation of Fragile X Behaviors by the Muscarinic M4 Antagonist, Tropicamide
Published in Behavioral neuroscience (01-10-2011)“…Muscarinic acetylcholine receptors (mAChR) are G protein-coupled receptors (M1-M5), grouped together into two functional classes, based on their G protein…”
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Onset and progression of behavioral and molecular phenotypes in a novel congenic R6/2 line exhibiting intergenerational CAG repeat stability
Published in PloS one (07-12-2011)“…In the present study we report on the use of speed congenics to generate a C57BL/6J congenic line of HD-model R6/2 mice carrying 110 CAG repeats, which…”
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Genetic background modulates behavioral impairments in R6/2 mice and suggests a role for dominant genetic modifiers in Huntington’s disease pathogenesis
Published in Mammalian genome (01-06-2012)“…Variability and modification of the symptoms of Huntington’s disease (HD) are commonly observed in both patient populations and animal models of the disease…”
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Genetic reduction of muscarinic M4 receptor modulates analgesic response and acoustic startle response in a mouse model of fragile X syndrome (FXS)
Published in Behavioural brain research (01-03-2012)“…The G-protein coupled muscarinic acetylcholine receptors, widely expressed in the CNS, have been implicated in fragile X syndrome (FXS). Recent studies have…”
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Genetic reduction of muscarinic M 4 receptor modulates analgesic response and acoustic startle response in a mouse model of fragile X syndrome (FXS)
Published in Behavioural brain research (01-03-2012)“…► M 4 receptor modulates select fragile X behaviors. ► Genetic reduction of M 4 rescued the analgesic response. ► Genetic reduction of M 4 partly rescued the…”
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Neuronal aggregates are associated with phenotypic onset in the R6/2 Huntington's disease transgenic mouse
Published in Behavioural brain research (15-04-2012)“…► Age of onset is delayed with increasing CAG repeat length in congenic C57BL6/J R6/2 HD model mice. ► Lower repeat lengths correlate with higher transgene…”
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Modulation of behavioral phenotypes by a muscarinic Ml antagonist in a mouse model of fragile X syndrome
Published in Psychopharmacologia (2011)Get full text
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