Biochemical evidence for the association of fragile X mental retardation protein with brain polyribosomal ribonucleoparticles
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Fragile X syndrome: loss of local mRNA regulation alters synaptic development and functionFMRP stalls ribosomal translocation on mRNAs linked to synaptic function and autismDysregulation and restoration of translational homeostasis in fragile X syndromeThe function of RNA-binding proteins at the synapse: implications for neurodegenerationThe unstable repeats--three evolving faces of neurological diseaseTracking the Fragile X Mental Retardation Protein in a Highly Ordered Neuronal RiboNucleoParticles Population: A Link between Stalled Polyribosomes and RNA GranulesRegulatory BC1 RNA and the fragile X mental retardation protein: convergent functionality in brainKissing complex RNAs mediate interaction between the Fragile-X mental retardation protein KH2 domain and brain polyribosomes.Nuclear Fragile X Mental Retardation Protein is localized to Cajal bodiesA novel function for fragile X mental retardation protein in translational activationThe G-quartet containing FMRP binding site in FMR1 mRNA is a potent exonic splicing enhancerTranslational regulation of the human achaete-scute homologue-1 by fragile X mental retardation proteinLocalization of FMRP-associated mRNA granules and requirement of microtubules for activity-dependent trafficking in hippocampal neuronsRNA and microRNAs in fragile X mental retardationFMR1 transcript isoforms: association with polyribosomes; regional and developmental expression in mouse brainFragile X related protein 1 clusters with ribosomes and messenger RNAs at a subset of dendritic spines in the mouse hippocampusFragile X related protein 1 isoforms differentially modulate the affinity of fragile X mental retardation protein for G-quartet RNA structureCold stress-induced protein Rbm3 binds 60S ribosomal subunits, alters microRNA levels, and enhances global protein synthesisGene and MicroRNA transcriptome analysis of Parkinson's related LRRK2 mouse modelsIMPACT is a developmentally regulated protein in neurons that opposes the eukaryotic initiation factor 2α kinase GCN2 in the modulation of neurite outgrowthThe shuttling SR protein 9G8 plays a role in translation of unspliced mRNA containing a constitutive transport element.Fragile X mental retardation protein has a unique, evolutionarily conserved neuronal function not shared with FXR1P or FXR2PA mouse model of the human Fragile X syndrome I304N mutation.BC1 regulation of metabotropic glutamate receptor-mediated neuronal excitability.Specific interaction between Sam68 and neuronal mRNAs: implication for the activity-dependent biosynthesis of elongation factor eEF1A.Conserved genes act as modifiers of invertebrate SMN loss of function defectsThe fragile X mental retardation protein and group I metabotropic glutamate receptors regulate levels of mRNA granules in brain.Emerging role of the KCNT1 Slack channel in intellectual disability.Regulation of RNA splicing by the methylation-dependent transcriptional repressor methyl-CpG binding protein 2.Loss of the fragile X mental retardation protein decouples metabotropic glutamate receptor dependent priming of long-term potentiation from protein synthesis.Desmoplakin and talin2 are novel mRNA targets of fragile X-related protein-1 in cardiac muscle.The fragile X mental retardation protein developmentally regulates the strength and fidelity of calcium signaling in Drosophila mushroom body neuronsFragile X mental retardation protein interacts with the RNA-binding protein Caprin1 in neuronal RiboNucleoProtein complexes [corrected].Analysis of translation initiation during stress conditions by polysome profiling.Increasing our understanding of human cognition through the study of Fragile X Syndrome.Increased long-term potentiation at medial-perforant path-dentate granule cell synapses induced by selective inhibition of histone deacetylase 3 requires Fragile X mental retardation proteinSynaptic signaling and aberrant RNA splicing in autism spectrum disordersA non-canonical start codon in the Drosophila fragile X gene yields two functional isoformsThe 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
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P2860
Biochemical evidence for the association of fragile X mental retardation protein with brain polyribosomal ribonucleoparticles
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 25 August 2004
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Biochemical evidence for the a ...... yribosomal ribonucleoparticles
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Biochemical evidence for the a ...... ribosomal ribonucleoparticles.
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type
label
Biochemical evidence for the a ...... yribosomal ribonucleoparticles
@en
Biochemical evidence for the a ...... ribosomal ribonucleoparticles.
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Biochemical evidence for the a ...... yribosomal ribonucleoparticles
@en
Biochemical evidence for the a ...... ribosomal ribonucleoparticles.
@nl
P2093
P2860
P356
P1476
Biochemical evidence for the a ...... yribosomal ribonucleoparticles
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P2093
Edouard W Khandjian
Laetitia Davidovic
Marc-Etienne Huot
Rachid Mazroui
Sandra Tremblay
P2860
P304
13357-13362
P356
10.1073/PNAS.0405398101
P407
P577
2004-08-25T00:00:00Z