Behavioural and cognitive abnormalities in an imprinting centre deletion mouse model for Prader-Willi syndrome.
about
Channelopathy pathogenesis in autism spectrum disordersSensory processing in autism spectrum disorders and Fragile X syndrome-From the clinic to animal models.Genetic models of sensorimotor gating: relevance to neuropsychiatric disorders.Impact of serotonin (5-HT)2C receptors on executive control processes.Learning by observation and learning by doing in Prader-Willi syndrome.New translational assays for preclinical modelling of cognition in schizophrenia: the touchscreen testing method for mice and ratsImprinted DLK1-DIO3 region of 14q32 defines a schizophrenia-associated miRNA signature in peripheral blood mononuclear cells.Calorie seeking, but not hedonic response, contributes to hyperphagia in a mouse model for Prader-Willi syndrome.Paradoxical leanness in the imprinting-centre deletion mouse model for Prader-Willi syndrome.New Perspectives on Genomic Imprinting, an Essential and Multifaceted Mode of Epigenetic Control in the Developing and Adult Brain.Increased alternate splicing of Htr2c in a mouse model for Prader-Willi syndrome leads disruption of 5HT2C receptor mediated appetite.Natural breaking of the maternal silence at the mouse and human imprinted Prader-Willi locus: A whisper with functional consequences.Is there a genomically imprinted social brain?Measuring impulsivity in mice: the five-choice serial reaction time task.Genetic and epigenetic dysregulation of imprinted genes in the brain.Hypothalamic obesity in children.Dosage-sensitivity of imprinted genes expressed in the brain: 15q11-q13 and neuropsychiatric illness.Brain-expressed imprinted genes and adult behaviour: the example of Nesp and Grb10.Assessing behavioural and cognitive domains of autism spectrum disorders in rodents: current status and future perspectives.Implicit learning in individuals with autism spectrum disorders: a meta-analysis.An overview of measuring impulsive behavior in mice.Recommendations for the investigation of animal models of Prader-Willi syndrome.Spatial competences in Prader-Willi syndrome: a radial arm maze study.Altered attentional processing in male and female rats in a prenatal valproic acid exposure model of autism spectrum disorder.The interplay between DNA methylation, folate and neurocognitive development.Loss of the imprinted, non-coding Snord116 gene cluster in the interval deleted in the Prader Willi syndrome results in murine neuronal and endocrine pancreatic developmental phenotypes.Genomic imprinting and conflict-induced decanalization.
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P2860
Behavioural and cognitive abnormalities in an imprinting centre deletion mouse model for Prader-Willi syndrome.
description
2009 nî lūn-bûn
@nan
2009年の論文
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2009年学术文章
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2009年学术文章
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2009年学术文章
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2009年学术文章
@zh-my
2009年学术文章
@zh-sg
2009年學術文章
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2009年學術文章
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2009年學術文章
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name
Behavioural and cognitive abno ...... del for Prader-Willi syndrome.
@en
Behavioural and cognitive abno ...... del for Prader-Willi syndrome.
@nl
type
label
Behavioural and cognitive abno ...... del for Prader-Willi syndrome.
@en
Behavioural and cognitive abno ...... del for Prader-Willi syndrome.
@nl
prefLabel
Behavioural and cognitive abno ...... del for Prader-Willi syndrome.
@en
Behavioural and cognitive abno ...... del for Prader-Willi syndrome.
@nl
P2093
P1476
Behavioural and cognitive abno ...... del for Prader-Willi syndrome.
@en
P2093
Anthony J Holland
Christine M Doe
Dinko Relkovic
James L Resnick
Jim J Hagan
Karen A Johnstone
Lawrence S Wilkinson
P2860
P304
P356
10.1111/J.1460-9568.2009.07048.X
P407
P577
2009-12-23T00:00:00Z