Altered mRNA transport, docking, and protein translation in neurons lacking fragile X mental retardation protein - Test2 - elhamkhani - TriplyDB

Altered mRNA transport, docking, and protein translation in neurons lacking fragile X mental retardation protein

Altered mRNA transport, docking, and protein translation in neurons lacking fragile X mental retardation protein

http://www.wikidata.org/entity/Q34100256

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The molecular basis of cognitive deficits in pervasive developmental disorders The FMRP regulon: from targets to disease convergence Tracking the Fragile X Mental Retardation Protein in a Highly Ordered Neuronal RiboNucleoParticles Population: A Link between Stalled Polyribosomes and RNA Granules A Subset of Autism-Associated Genes Regulate the Structural Stability of Neurons.Fragile X related protein 1 clusters with ribosomes and messenger RNAs at a subset of dendritic spines in the mouse hippocampus DSCR1 interacts with FMRP and is required for spine morphogenesis and local protein synthesis Uncoupling of the endocannabinoid signalling complex in a mouse model of fragile X syndrome Computational identification of new structured cis-regulatory elements in the 3'-untranslated region of human protein coding genes Both Maintenance and Avoidance of RNA-Binding Protein Interactions Constrain Coding Sequence Evolution.From FMRP function to potential therapies for fragile X syndrome.Gestational and early postnatal hypothyroidism alters VGluT1 and VGAT bouton distribution in the neocortex and hippocampus, and behavior in rats.Comprehensive neurocognitive endophenotyping strategies for mouse models of genetic disorders Maternal genetic mutations as gestational and early life influences in producing psychiatric disease-like phenotypes in mice.G-quadruplex RNA structure as a signal for neurite mRNA targeting.Fragile X mental retardation protein is required for programmed cell death and clearance of developmentally-transient peptidergic neurons.Impaired cognitive discrimination and discoordination of coupled theta-gamma oscillations in Fmr1 knockout mice.Functionally diverse dendritic mRNAs rapidly associate with ribosomes following a novel experience.Fragile X mental retardation protein interacts with the RNA-binding protein Caprin1 in neuronal RiboNucleoProtein complexes [corrected].A role for dendritic translation of CaMKIIα mRNA in olfactory plasticity.The fragile x mental retardation syndrome 20 years after the FMR1 gene discovery: an expanding universe of knowledge.Regulation of molecular pathways in the Fragile X Syndrome: insights into Autism Spectrum Disorders Smaug1 mRNA-silencing foci respond to NMDA and modulate synapse formation.Nxf7 deficiency impairs social exploration and spatio-cognitive abilities as well as hippocampal synaptic plasticity in mice.Single-molecule insights into mRNA dynamics in neurons.Fmr1 deficiency promotes age-dependent alterations in the cortical synaptic proteome.RNA imaging in living cells - methods and applications.High-functioning autism spectrum disorder and fragile X syndrome: report of two affected sisters.Genetic removal of p70 S6 kinase 1 corrects molecular, synaptic, and behavioral phenotypes in fragile X syndrome mice.New X-chromosomal interactors of dFMRP regulate axonal and synaptic morphology of brain neurons in Drosophila melanogaster Targeting of ribosomal protein S6 to dendritic spines by in vivo high frequency stimulation to induce long-term potentiation in the dentate gyrus Neuronal profilins in health and disease: Relevance for spine plasticity and Fragile X syndrome.Resources for the Comprehensive Discovery of Functional RNA Elements.Crystal structure of a dimerization domain of human Caprin-1: insights into the assembly of an evolutionarily conserved ribonucleoprotein complex consisting of Caprin-1, FMRP and G3BP1 Fragile X mental retardation protein regulates trans-synaptic signaling in Drosophila Imaging Single-mRNA Localization and Translation in Live Neurons.Glucocorticoid receptors are localized to dendritic spines and influence local actin signaling.Imaging mRNA and protein interactions within neurons.Translation in astrocyte distal processes sets molecular heterogeneity at the gliovascular interface.Messengers, motors and mysteries: sorting of eukaryotic mRNAs by cytoskeletal transport.Control of cytoplasmic mRNA localization.

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Altered mRNA transport, docking, and protein translation in neurons lacking fragile X mental retardation protein

http://www.wikidata.org/entity/Q34100256

description

2010 nî lūn-bûn

@nan

2010 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի օգոստոսին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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name

Altered mRNA transport, dockin ...... e X mental retardation protein

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Altered mRNA transport, dockin ...... e X mental retardation protein

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Altered mRNA transport, dockin ...... e X mental retardation protein

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Altered mRNA transport, dockin ...... e X mental retardation protein

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Altered mRNA transport, dockin ...... e X mental retardation protein

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Altered mRNA transport, dockin ...... e X mental retardation protein

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Altered mRNA transport, dockin ...... e X mental retardation protein

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Altered mRNA transport, dockin ...... e X mental retardation protein

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Altered mRNA transport, dockin ...... e X mental retardation protein

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Proceedings of the National Academy of Sciences of the United States of America

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Altered mRNA transport, dockin ...... e X mental retardation protein

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P2093

Der-I Kao

http://www.w3.org/2001/XMLSchema#string

Georgina M Aldridge

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Ivan Jeanne Weiler

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William T Greenough

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P2860

FMR1 protein: conserved RNP family domains and selective RNA binding

Altered synaptic plasticity in a mouse model of fragile X mental retardation

Dendritic spines elongate after stimulation of group 1 metabotropic glutamate receptors in cultured hippocampal neurons.

A direct role for FMRP in activity-dependent dendritic mRNA transport links filopodial-spine morphogenesis to fragile X syndrome.

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

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

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

Fragile X protein controls the efficacy of mRNA transport in Drosophila neurons

The fragile X mental retardation protein binds specifically to its mRNA via a purine quartet motif.

Regulation of synaptic structure and function by FMRP-associated microRNAs miR-125b and miR-132

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scholarly article

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35

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107

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20713728

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2932564

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