Learning and behavioral deficits associated with the absence of the fragile X mental retardation protein: what a fly and mouse model can teach us.
about
Comprehensive behavioral analysis of RNG105 (Caprin1) heterozygous mice: Reduced social interaction and attenuated response to noveltyOxidative stress-driven parvalbumin interneuron impairment as a common mechanism in models of schizophrenia.Zfrp8 forms a complex with fragile-X mental retardation protein and regulates its localization and function.VCP and ATL1 regulate endoplasmic reticulum and protein synthesis for dendritic spine formationEco-HAB as a fully automated and ecologically relevant assessment of social impairments in mouse models of autism.Augmented noncanonical BMP type II receptor signaling mediates the synaptic abnormality of fragile X syndrome.Intranasal siRNA administration reveals IGF2 deficiency contributes to impaired cognition in Fragile X syndrome mice.Multifarious Functions of the Fragile X Mental Retardation Protein.Neurotrophic Factors in Mouse Models of Autism Spectrum Disorder: Focus on BDNF and IGF-1.Hyperactive locomotion in a Drosophila model is a functional readout for the synaptic abnormalities underlying fragile X syndrome.The non-coding RNA BC1 regulates experience-dependent structural plasticity and learning.The Conserved, Disease-Associated RNA Binding Protein dNab2 Interacts with the Fragile X Protein Ortholog in Drosophila Neurons.Excitability is increased in hippocampal CA1 pyramidal cells of Fmr1 knockout mice.Treating a novel plasticity defect rescues episodic memory in Fragile X model mice.RNG105/caprin1, an RNA granule protein for dendritic mRNA localization, is essential for long-term memory formation.The role of TGF-β superfamily signaling in neurological disorders.Rapid, experience-dependent translation of neurogranin enables memory encoding.Impaired hippocampal representation of place in the Fmr1-knockout mouse model of fragile X syndrome.Reducing histone acetylation rescues cognitive deficits in a mouse model of Fragile X syndrome.Sensory Processing Phenotypes in Fragile X SyndromeThe Intracellular Cleavage Product of the NG2 Proteoglycan Modulates Translation and Cell-Cycle Kinetics via Effects on mTORC1/FMRP Signaling
P2860
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P2860
Learning and behavioral deficits associated with the absence of the fragile X mental retardation protein: what a fly and mouse model can teach us.
description
2014 nî lūn-bûn
@nan
2014 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Learning and behavioral defici ...... y and mouse model can teach us
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Learning and behavioral defici ...... and mouse model can teach us.
@ast
Learning and behavioral defici ...... and mouse model can teach us.
@en
type
label
Learning and behavioral defici ...... y and mouse model can teach us
@nl
Learning and behavioral defici ...... and mouse model can teach us.
@ast
Learning and behavioral defici ...... and mouse model can teach us.
@en
prefLabel
Learning and behavioral defici ...... y and mouse model can teach us
@nl
Learning and behavioral defici ...... and mouse model can teach us.
@ast
Learning and behavioral defici ...... and mouse model can teach us.
@en
P2860
P356
P1433
P1476
Learning and behavioral defici ...... y and mouse model can teach us
@en
P2093
Alexandros K Kanellopoulos
Ana Rita Santos
P2860
P304
P356
10.1101/LM.035956.114
P407
P577
2014-09-16T00:00:00Z