Limbic epileptogenesis in a mouse model of fragile X syndrome. - Test2 - elhamkhani - TriplyDB

Limbic epileptogenesis in a mouse model of fragile X syndrome.

Limbic epileptogenesis in a mouse model of fragile X syndrome.

http://www.wikidata.org/entity/Q37220443

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Genetic-background modulation of core and variable autistic-like symptoms in Fmr1 knock-out mice.Emerging pharmacotherapies for neurodevelopmental disorders Fragile X syndrome as a rare disease in China - Therapeutic challenges and opportunities Fragile X syndrome and targeted treatment trials.Stem cells and modeling of autism spectrum disorders.From FMRP function to potential therapies for fragile X syndrome.Annual Research Review: Transgenic mouse models of childhood-onset psychiatric disorders.Therapeutic strategies in fragile X syndrome: dysregulated mGluR signaling and beyond.Fragile X mental retardation protein in the driver's seat.Epilepsy in four genetically determined syndromes of intellectual disability.Involvement of Rho-family GTPases in axon branching.Genetic and Pharmacological Reversibility of Phenotypes in Mouse Models of Autism Spectrum Disorder.Differential roles of α-, β-, and γ-actin in axon growth and collateral branch formation in motoneurons.Origins of epilepsy in fragile X syndrome.Neuron-restrictive silencer factor is not required for the antiepileptic effect of the ketogenic diet.

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Limbic epileptogenesis in a mouse model of fragile X syndrome.

http://www.wikidata.org/entity/Q37220443

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on October 2008

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Limbic epileptogenesis in a mouse model of fragile X syndrome.

@en

Limbic epileptogenesis in a mouse model of fragile X syndrome.

@nl

type

label

Limbic epileptogenesis in a mouse model of fragile X syndrome.

@en

Limbic epileptogenesis in a mouse model of fragile X syndrome.

@nl

prefLabel

Limbic epileptogenesis in a mouse model of fragile X syndrome.

@en

Limbic epileptogenesis in a mouse model of fragile X syndrome.

@nl

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Cerebral Cortex

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Limbic epileptogenesis in a mouse model of fragile X syndrome.

@en

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Li-Feng Qiu

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Ting-Jia Lu

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Wei-Ping Liao

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Xiao-Ling Hu

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Yong-Hong Yi

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Zhi-Qi Xiong

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P2860

FMR1 protein: conserved RNP family domains and selective RNA binding

Abnormal dendritic spines in fragile X knockout mice: maturation and pruning deficits

Fragile X mental retardation protein is translated near synapses in response to neurotransmitter activation

Local functions for FMRP in axon growth cone motility and activity-dependent regulation of filopodia and spine synapses

New insights into fragile X syndrome: from molecules to neurobehaviors

A decade of molecular studies of fragile X syndrome

The fragile X syndrome protein FMRP associates with BC1 RNA and regulates the translation of specific mRNAs at synapses

Identification of mRNA/protein (mRNP) complexes containing Puralpha, mStaufen, fragile X protein, and myosin Va and their association with rough endoplasmic reticulum equipped with a kinesin motor

Modification of seizure activity by electrical stimulation. II. Motor seizure

Dynamic translational and proteasomal regulation of fragile X mental retardation protein controls mGluR-dependent long-term depression

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1504-1514

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scholarly article

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10.1093/CERCOR/BHN163

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7

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19

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23296898

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18832330

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2693616

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