A mouse model of the fragile X premutation: effects on behavior, dendrite morphology, and regional rates of cerebral protein synthesis. - Wikidata - awgldk - TriplyDB

A mouse model of the fragile X premutation: effects on behavior, dendrite morphology, and regional rates of cerebral protein synthesis.

A mouse model of the fragile X premutation: effects on behavior, dendrite morphology, and regional rates of cerebral protein synthesis.

http://www.wikidata.org/entity/Q35148962

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What can we learn about autism from studying fragile X syndrome?Fragile X spectrum disorders Fragile X-associated tremor/ataxia syndrome.A decade of the anaphase-promoting complex in the nervous system A Subset of Autism-Associated Genes Regulate the Structural Stability of Neurons.Using mouse models of autism spectrum disorders to study the neurotoxicology of gene-environment interactions Impaired sensorimotor gating in Fmr1 knock out and Fragile X premutation model mice.Comprehensive neurocognitive endophenotyping strategies for mouse models of genetic disorders CGG repeat in the FMR1 gene: size matters CNS expression of murine fragile X protein (FMRP) as a function of CGG-repeat size.Increased prevalence of seizures in boys who were probands with the FMR1 premutation and co-morbid autism spectrum disorder.Mouse models of the fragile X premutation and fragile X-associated tremor/ataxia syndrome Expression of an expanded CGG-repeat RNA in a single pair of primary sensory neurons impairs olfactory adaptation in Caenorhabditis elegans.Fragile X syndrome: an update on developing treatment modalities.Cerebral protein synthesis in a knockin mouse model of the fragile X premutation.Fragile X mental retardation protein expression in Alzheimer's disease Molecular Advances Leading to Treatment Implications for Fragile X Premutation Carriers Motor deficits on a ladder rung task in male and female adolescent and adult CGG knock-in mice Mouse models of the fragile x premutation and the fragile X associated tremor/ataxia syndrome.Abnormal dendrite and spine morphology in primary visual cortex in the CGG knock-in mouse model of the fragile X premutation Effects of chronic immobilization stress on anxiety-like behavior and basolateral amygdala morphology in Fmr1 knockout mice.Widespread non-central nervous system organ pathology in fragile X premutation carriers with fragile X-associated tremor/ataxia syndrome and CGG knock-in mice.FMR1 premutation and full mutation molecular mechanisms related to autism.The importance of considering all attributes of memory in behavioral endophenotyping of mouse models of genetic disease.Clustered burst firing in FMR1 premutation hippocampal neurons: amelioration with allopregnanolone.Current Gaps in Understanding the Molecular Basis of FXTAS CGG trinucleotide repeat length modulates neural plasticity and spatiotemporal processing in a mouse model of the fragile X premutation.Neuritin reverses deficits in murine novel object associative recognition memory caused by exposure to extremely low-frequency (50 Hz) electromagnetic fields.Early mitochondrial abnormalities in hippocampal neurons cultured from Fmr1 pre-mutation mouse model.Impaired activity-dependent FMRP translation and enhanced mGluR-dependent LTD in Fragile X premutation mice Neurodegeneration the RNA way Defining genetically meaningful language and personality traits in relatives of individuals with fragile X syndrome and relatives of individuals with autism.Prevalence and risk of migraine headaches in adult fragile X premutation carriers Adult microbiota-deficient mice have distinct dendritic morphological changes: differential effects in the amygdala and hippocampus.Fragile X-associated tremor/ataxia syndrome (FXTAS): pathology and mechanisms.A brief history of triplet repeat diseases.The role of ionotropic glutamate receptors in childhood neurodevelopmental disorders: autism spectrum disorders and fragile x syndrome.Translation of Expanded CGG Repeats into FMRpolyG Is Pathogenic and May Contribute to Fragile X Tremor Ataxia Syndrome.Neuropathological, clinical and molecular pathology in female fragile X premutation carriers with and without FXTAS.Effect of 1.8 GHz radiofrequency electromagnetic radiation on novel object associative recognition memory in mice

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P2860

A mouse model of the fragile X premutation: effects on behavior, dendrite morphology, and regional rates of cerebral protein synthesis.

http://www.wikidata.org/entity/Q35148962

description

2011 nî lūn-bûn

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2011 թուականի Յունուարին հրատարակուած գիտական յօդուած

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2011 թվականի հունվարին հրատարակված գիտական հոդված

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2011年の論文

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A mouse model of the fragile X ...... of cerebral protein synthesis.

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A mouse model of the fragile X ...... of cerebral protein synthesis.

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A mouse model of the fragile X ...... of cerebral protein synthesis.

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A mouse model of the fragile X ...... of cerebral protein synthesis.

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A mouse model of the fragile X ...... of cerebral protein synthesis.

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J.NBD.2011.01.008

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Neurobiology of Disease

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A mouse model of the fragile X ...... of cerebral protein synthesis.

@en

P2093

Ali Entezam

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Carolyn B Smith

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Gloria E Hoffman

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Karen Usdin

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Mei Qin

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Tianjian Huang

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Zhong-Hua Liu

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P2860

Evidence that fragile X mental retardation protein is a negative regulator of translation

Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

The FMR1 CGG repeat mouse displays ubiquitin-positive intranuclear neuronal inclusions; implications for the cerebellar tremor/ataxia syndrome

The fragile X mental retardation protein inhibits translation via interacting with mRNA

Lithium ameliorates phenotypic deficits in a mouse model of fragile X syndrome.

Fragile X premutation is a significant risk factor for premature ovarian failure: the International Collaborative POF in Fragile X study--preliminary data

Cognitive decline, neuromotor and behavioural disturbances in a mouse model for fragile-X-associated tremor/ataxia syndrome (FXTAS).

Abnormal dendritic spine characteristics in the temporal and visual cortices of patients with fragile-X syndrome: a quantitative examination.

Measurement of local cerebral protein synthesis in vivo: influence of recycling of amino acids derived from protein degradation.

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10.1016/J.NBD.2011.01.008

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1

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49741626

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21220020

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